| geneid | 25780 |
|---|---|
| ensemblid | ENSG00000152689.18 |
| hgncid | 14545 |
| symbol | RASGRP3 |
| name | RAS guanyl releasing protein 3 |
| refseq_nuc | NM_001139488.2 |
| refseq_prot | NP_001132960.1 |
| ensembl_nuc | ENST00000403687.8 |
| ensembl_prot | ENSP00000384192.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 33476649 |
| end | 33564731 |
| strand | + |
| ver | v1.2 |
| region | chr2:33476649-33564731 |
| region5000 | chr2:33471649-33569731 |
| regionname0 | RASGRP3_chr2_33476649_33564731 |
| regionname5000 | RASGRP3_chr2_33471649_33569731 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 690 | 359 | 90 | 46 | 184 | 9 | 28 | 142 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0002 | 0/0 | 690 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0003 | 0/0 | 690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0004 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0005 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0006 | 0/0 | 690 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0007 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0008 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0009 | 0/0 | 690 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2073 | 262 | 57 | 41 | 127 | 9 | 26 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0002 | 0/0 | 2073 | 76 | 13 | 4 | 57 | 0 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0003 | 0/0 | 2073 | 15 | 15 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0004 | 0/0 | 2073 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0005 | 0/0 | 2073 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0006 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0007 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0008 | 0/0 | 2073 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0009 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0010 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0011 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0012 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0013 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0014 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0015 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| c0016 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2310 | 104 | 0 | 7 | 93 | 0 | 4 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0002 | 0/0 | 2307 | 47 | 1 | 12 | 27 | 2 | 5 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0003 | 0/0 | 2303 | 27 | 3 | 5 | 11 | 3 | 5 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0004 | 0/0 | 2308 | 18 | 2 | 2 | 10 | 1 | 3 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0005 | 0/0 | 2303 | 15 | 15 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0006 | 0/0 | 2307 | 13 | 11 | 2 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0007 | 0/0 | 2303 | 12 | 0 | 3 | 8 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0008 | 0/0 | 2308 | 9 | 0 | 1 | 3 | 0 | 5 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0009 | 0/0 | 2308 | 9 | 2 | 3 | 0 | 2 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0010 | 0/0 | 2307 | 8 | 0 | 0 | 8 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0011 | 0/0 | 2303 | 7 | 7 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0012 | 0/0 | 2299 | 6 | 6 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0013 | 0/0 | 2298 | 5 | 5 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0014 | 0/0 | 2303 | 4 | 4 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0015 | 0/0 | 2303 | 4 | 0 | 0 | 4 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0016 | 0/0 | 2310 | 4 | 0 | 0 | 4 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0017 | 0/0 | 2303 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0018 | 0/0 | 2303 | 3 | 1 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0019 | 0/0 | 2303 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0020 | 0/0 | 2309 | 3 | 2 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0021 | 1/0 | 2314 | 3 | 1 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0022 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0023 | 0/0 | 2307 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0024 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0025 | 0/1 | 2305 | 2 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0026 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0027 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0028 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0029 | 0/0 | 2307 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0030 | 0/0 | 2308 | 2 | 0 | 0 | 1 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0031 | 0/0 | 2299 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0032 | 0/0 | 2310 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0033 | 0/0 | 2309 | 2 | 0 | 2 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0034 | 0/0 | 2310 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0035 | 0/0 | 2310 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0036 | 0/0 | 2314 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0037 | 0/0 | 2314 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0038 | 0/0 | 2310 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0039 | 0/0 | 2310 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0040 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0041 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0042 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0043 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0044 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0045 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0046 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0047 | 0/0 | 2311 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0048 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0049 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0050 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0051 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0052 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0053 | 0/0 | 2307 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0054 | 0/0 | 2307 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0055 | 0/0 | 2302 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0056 | 0/0 | 2307 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0057 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0058 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0059 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0060 | 0/0 | 2305 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0061 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0062 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0063 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0064 | 0/0 | 2314 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0065 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| t0066 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2073 | 262 | 57 | 41 | 127 | 9 | 26 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002 | 0/0 | 2073 | 76 | 13 | 4 | 57 | 0 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0003 | 0/0 | 2073 | 15 | 15 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0004 | 0/0 | 2073 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0006 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0008 | 0/0 | 2073 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0002c0005 | 0/0 | 2073 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0002c0007 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0003c0009 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0003c0011 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0004c0016 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0005c0014 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0006c0013 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0007c0012 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0008c0010 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0009c0015 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4382 | 62 | 0 | 6 | 53 | 0 | 3 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0002 | 0/0 | 4379 | 45 | 1 | 12 | 27 | 1 | 4 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0003 | 0/0 | 4375 | 19 | 3 | 5 | 5 | 1 | 5 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0004 | 0/0 | 4380 | 14 | 2 | 2 | 7 | 1 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0005 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0007 | 0/0 | 4375 | 12 | 0 | 3 | 8 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0008 | 0/0 | 4380 | 7 | 0 | 1 | 2 | 0 | 4 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0009 | 0/0 | 4380 | 9 | 2 | 3 | 0 | 2 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0010 | 0/0 | 4379 | 8 | 0 | 0 | 8 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0011 | 0/0 | 4375 | 7 | 7 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0012 | 0/0 | 4371 | 6 | 6 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0013 | 0/0 | 4370 | 5 | 5 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0014 | 0/0 | 4375 | 4 | 4 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0015 | 0/0 | 4375 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0016 | 0/0 | 4382 | 3 | 0 | 0 | 3 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0017 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0018 | 0/0 | 4375 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0019 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0020 | 0/0 | 4381 | 3 | 2 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0021 | 1/0 | 4386 | 3 | 1 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0022 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0023 | 0/0 | 4379 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0024 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0025 | 0/1 | 4377 | 2 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0026 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0027 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0029 | 0/0 | 4379 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0030 | 0/0 | 4380 | 2 | 0 | 0 | 1 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0031 | 0/0 | 4371 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0032 | 0/0 | 4382 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0033 | 0/0 | 4381 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0035 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0036 | 0/0 | 4386 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0038 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0039 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0040 | 0/0 | 4381 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0041 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0042 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0044 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0045 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0047 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0048 | 0/0 | 4385 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0050 | 0/0 | 4376 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0051 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0052 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0053 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0054 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0056 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0057 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0058 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0059 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0060 | 0/0 | 4377 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0061 | 0/0 | 4381 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0065 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0001t0066 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0001 | 0/0 | 4382 | 41 | 0 | 1 | 39 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0003 | 0/0 | 4375 | 6 | 0 | 0 | 6 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0004 | 0/0 | 4380 | 4 | 0 | 0 | 3 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0006 | 0/0 | 4379 | 13 | 11 | 2 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0015 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0016 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0017 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0028 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0034 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0037 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0038 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0055 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0063 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0002t0064 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0003t0005 | 0/0 | 4375 | 12 | 12 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0003t0018 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0003t0026 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0003t0028 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0004t0019 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0004t0043 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0006t0005 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0001c0008t0033 | 0/0 | 4381 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0002c0005t0003 | 0/0 | 4375 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0002c0007t0008 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0003c0009t0049 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0003c0011t0046 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0004c0016t0062 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0005c0014t0001 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0006c0013t0002 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0007c0012t0015 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0008c0010t0008 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| a0009c0015t0002 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | copy fasta | chr2 | 33471649 | 33569731 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0007g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0009g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0014g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0015g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0015g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0016g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0016g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0017g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0018g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0018g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0020g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0021g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0021g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0021g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0022g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0022g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0023g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0024g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0024g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0025g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0025g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0026g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0027g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0027g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0029g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0029g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0030g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0030g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0031g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0031g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0032g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0032g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0033g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0035g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0035g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0036g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0036g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0038g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0039g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0039g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0040g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0041g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0042g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0044g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0045g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0047g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0048g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0050g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0051g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0052g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0053g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0054g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0056g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0057g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0058g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0059g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0060g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0061g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0065g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0001t0066g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0015g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0017g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0028g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0034g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0034g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0037g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0037g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0038g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0055g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0063g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0002t0064g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0018g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0026g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0003t0028g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0004t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0004t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0004t0043g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0006t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0006t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0001c0008t0033g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0002c0005t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0002c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0002c0007t0008g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0003c0009t0049g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0003c0011t0046g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0004c0016t0062g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0005c0014t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0006c0013t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0007c0012t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0008c0010t0008g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| a0009c0015t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0053 | g0088 | EUR | FIN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0062 | EUR | FIN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00438 | hp1 | a0001 | c0002 | t0034 | g0152 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00558 | hp2 | a0001 | c0001 | t0039 | g0264 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00609 | hp2 | a0001 | c0002 | t0064 | g0217 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00639 | hp1 | a0001 | c0002 | t0055 | g0057 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0188 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0244 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0076 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01074 | hp1 | a0001 | c0001 | t0009 | g0110 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0071 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01099 | hp1 | a0001 | c0001 | t0054 | g0036 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01099 | hp2 | a0001 | c0001 | t0036 | g0274 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01109 | hp1 | a0001 | c0001 | t0023 | g0138 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01168 | hp2 | a0001 | c0001 | t0047 | g0105 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0246 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0016 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01255 | hp1 | a0001 | c0008 | t0033 | g0063 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01255 | hp2 | a0001 | c0002 | t0006 | g0189 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01256 | hp2 | a0001 | c0001 | t0033 | g0280 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0363 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01361 | hp1 | a0001 | c0001 | t0048 | g0087 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01361 | hp2 | a0001 | c0001 | t0032 | g0316 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01433 | hp1 | a0001 | c0001 | t0056 | g0248 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01496 | hp1 | a0001 | c0001 | t0020 | g0142 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01515 | hp1 | a0001 | c0001 | t0021 | g0336 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01515 | hp2 | a0001 | c0001 | t0029 | g0308 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0017 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01516 | hp2 | a0002 | c0005 | t0003 | g0206 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01517 | hp1 | a0002 | c0005 | t0003 | g0216 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01517 | hp2 | a0001 | c0001 | t0029 | g0307 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01884 | hp1 | a0001 | c0001 | t0040 | g0128 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01884 | hp2 | a0001 | c0004 | t0019 | g0118 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0156 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0193 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0093 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02015 | hp1 | a0001 | c0001 | t0035 | g0276 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02027 | hp2 | a0001 | c0001 | t0066 | g0001 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0342 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02055 | hp2 | a0001 | c0003 | t0005 | g0252 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02056 | hp1 | a0008 | c0010 | t0008 | g0319 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02071 | hp2 | a0001 | c0002 | t0063 | g0288 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02074 | hp2 | a0001 | c0001 | t0030 | g0362 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02080 | hp2 | a0001 | c0001 | t0039 | g0146 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02083 | hp1 | a0001 | c0002 | t0038 | g0346 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02083 | hp2 | a0001 | c0002 | t0034 | g0072 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | CDX | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0194 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0310 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0157 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0109 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0121 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02280 | hp2 | a0001 | c0002 | t0028 | g0137 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0040 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02451 | hp2 | a0001 | c0002 | t0017 | g0147 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02523 | hp2 | a0005 | c0014 | t0001 | g0007 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0238 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0133 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02615 | hp1 | a0001 | c0002 | t0006 | g0174 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02630 | hp1 | a0001 | c0003 | t0018 | g0178 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0132 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0304 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0180 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0306 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0123 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0301 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0323 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02735 | hp1 | a0001 | c0001 | t0036 | g0218 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02809 | hp1 | a0001 | c0003 | t0005 | g0192 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0130 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02818 | hp1 | a0001 | c0001 | t0031 | g0125 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02818 | hp2 | a0001 | c0001 | t0057 | g0079 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0168 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02886 | hp2 | a0001 | c0001 | t0027 | g0199 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0139 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02895 | hp2 | a0001 | c0006 | t0005 | g0255 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0127 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02896 | hp2 | a0001 | c0001 | t0022 | g0260 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02897 | hp1 | a0001 | c0001 | t0022 | g0259 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02897 | hp2 | a0001 | c0006 | t0005 | g0254 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02922 | hp1 | a0001 | c0001 | t0052 | g0303 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0195 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02970 | hp1 | a0001 | c0003 | t0005 | g0175 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02970 | hp2 | a0001 | c0001 | t0044 | g0172 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0167 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0176 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0335 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03041 | hp1 | a0003 | c0011 | t0046 | g0202 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03041 | hp2 | a0001 | c0003 | t0005 | g0119 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0153 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0239 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03130 | hp2 | a0001 | c0001 | t0051 | g0299 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03139 | hp1 | a0001 | c0001 | t0042 | g0122 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03139 | hp2 | a0001 | c0001 | t0058 | g0124 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03195 | hp1 | a0001 | c0001 | t0041 | g0322 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03195 | hp2 | a0001 | c0001 | t0050 | g0313 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0159 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0080 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0241 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0253 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0220 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03491 | hp2 | a0009 | c0015 | t0002 | g0038 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0257 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0311 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0155 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03579 | hp1 | a0001 | c0001 | t0026 | g0196 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03579 | hp2 | a0001 | c0004 | t0019 | g0042 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03669 | hp1 | a0001 | c0001 | t0030 | g0051 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0090 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03831 | hp2 | a0001 | c0001 | t0060 | g0020 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03927 | hp1 | a0001 | c0001 | t0025 | g0182 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03927 | hp2 | a0001 | c0001 | t0032 | g0235 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03942 | hp1 | a0002 | c0007 | t0008 | g0081 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | STU | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0035 | SAS | STU | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0204 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18906 | hp1 | a0001 | c0003 | t0026 | g0165 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0166 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18943 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18946 | hp1 | a0001 | c0001 | t0018 | g0281 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0296 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18950 | hp1 | a0001 | c0002 | t0037 | g0271 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18951 | hp1 | a0001 | c0001 | t0061 | g0095 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18954 | hp2 | a0001 | c0001 | t0018 | g0249 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18956 | hp2 | a0001 | c0002 | t0015 | g0278 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0169 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18962 | hp1 | a0001 | c0001 | t0035 | g0348 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18964 | hp2 | a0001 | c0001 | t0045 | g0106 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18968 | hp1 | a0001 | c0001 | t0016 | g0032 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18971 | hp1 | a0001 | c0002 | t0037 | g0272 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0229 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0309 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18981 | hp1 | a0001 | c0001 | t0010 | g0344 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18984 | hp1 | a0001 | c0001 | t0016 | g0369 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0338 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0367 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18998 | hp1 | a0001 | c0001 | t0015 | g0050 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18998 | hp2 | a0001 | c0001 | t0065 | g0357 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19002 | hp1 | a0007 | c0012 | t0015 | g0117 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0320 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0219 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19030 | hp1 | a0001 | c0001 | t0023 | g0154 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19030 | hp2 | a0001 | c0003 | t0005 | g0256 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19043 | hp1 | a0001 | c0003 | t0028 | g0173 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0240 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0361 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0326 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19083 | hp2 | a0001 | c0001 | t0038 | g0282 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19085 | hp1 | a0001 | c0002 | t0016 | g0205 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19087 | hp2 | a0001 | c0001 | t0016 | g0092 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19089 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA19091 | hp2 | a0004 | c0016 | t0062 | g0026 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20752 | hp1 | a0006 | c0013 | t0002 | g0069 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0089 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0010 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0221 | SAS | GIH | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0185 | SAS | GIH | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02109 | hp1 | a0001 | c0001 | t0059 | g0203 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0039 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02486 | hp2 | a0001 | c0003 | t0005 | g0198 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02559 | hp1 | a0001 | c0001 | t0031 | g0141 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG02559 | hp2 | a0001 | c0003 | t0005 | g0258 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0148 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG03471 | hp2 | a0001 | c0004 | t0043 | g0201 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0135 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| HG06807 | hp2 | a0001 | c0002 | t0006 | g0200 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0134 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0120 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0074 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| NA21309 | hp2 | a0003 | c0009 | t0049 | g0070 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0025 | g0170 | REF | REF | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0021 | g0265 | REF | REF | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33516634
|
C | T | 1 | a0004 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.163C>T | p.Leu55Phe | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/18 | 482/4386 | 163/2073 | 55/690 | chr2 | 33516634 | ||
| chr2:33524042
|
A | G | 1 | a0009 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.680A>G | p.Asn227Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/18 | 999/4386 | 680/2073 | 227/690 | chr2 | 33524042 | ||
| chr2:33527152
|
A | G | 1 | a0005 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.823A>G | p.Thr275Ala | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1142/4386 | 823/2073 | 275/690 | chr2 | 33527152 | ||
| chr2:33527173
|
G | A | 1 | a0002 | 3 | HG01516.hp2 HG01517.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.844G>A | p.Gly282Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1163/4386 | 844/2073 | 282/690 | chr2 | 33527173 | ||
| chr2:33539109
|
A | G | 1 | a0006 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1177A>G | p.Thr393Ala | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/18 | 1496/4386 | 1177/2073 | 393/690 | chr2 | 33539109 | ||
| chr2:33558303
|
G | A | 1 | a0008 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1672G>A | p.Gly558Arg | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/18 | 1991/4386 | 1672/2073 | 558/690 | chr2 | 33558303 | ||
| chr2:33558682
|
G | C | 1 | a0003 | 2 | HG03041.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1716G>C | p.Glu572Asp | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/18 | 2035/4386 | 1716/2073 | 572/690 | chr2 | 33558682 | ||
| chr2:33559021
|
G | T | 1 | a0007 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.2055G>T | p.Gln685His | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/18 | 2374/4386 | 2055/2073 | 685/690 | chr2 | 33559021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33527232
|
C | A | 1 | a0001c0008 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.903C>A | p.Ile301Ile | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1222/4386 | 903/2073 | 301/690 | chr2 | 33527232 | ||
| chr2:33534328
|
C | T | 1 | a0001c0004 | 3 | HG01884.hp2 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1089C>T | p.Ser363Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/18 | 1408/4386 | 1089/2073 | 363/690 | chr2 | 33534328 | ||
| chr2:33549694
|
T | C | 4 | a0001c0002a0001c0006a0002c0005others(1): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
synonymous_variant | LOW | c.1485T>C | p.His495His | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/18 | 1804/4386 | 1485/2073 | 495/690 | chr2 | 33549694 | ||
| chr2:33558326
|
G | A | 2 | a0001c0003a0001c0006 | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
synonymous_variant | LOW | c.1695G>A | p.Ser565Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/18 | 2014/4386 | 1695/2073 | 565/690 | chr2 | 33558326 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33511727
|
T | A | 7 | a0001c0001t0012a0001c0001t0014a0001c0001t0022others(4): Show | 16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-243T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/18 | 3410 | chr2 | 33511727 | |||||
| chr2:33511790
|
G | A | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | 367 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(364): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/18 | 3347 | chr2 | 33511790 | |||||
| chr2:33515057
|
A | G | 1 | a0001c0001t0039 | 2 | HG00558.hp2 HG02080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 80 | chr2 | 33515057 | |||||
| chr2:33515058
|
T | G | 2 | a0001c0001t0023a0001c0001t0044 | 3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 79 | chr2 | 33515058 | |||||
| chr2:33515122
|
A | G | 3 | a0001c0001t0038a0001c0001t0066a0001c0002t0038 | 3 | HG02027.hp2 HG02083.hp1 NA19083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-15A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 15 | chr2 | 33515122 | |||||
| chr2:33562748
|
C | T | 1 | a0001c0001t0065 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 11 | chr2 | 33562748 | |||||
| chr2:33562801
|
T | A | 1 | a0001c0001t0045 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 64 | chr2 | 33562801 | |||||
| chr2:33562811
|
T | G | 1 | a0001c0001t0040 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 74 | chr2 | 33562811 | |||||
| chr2:33562909
|
CCTAA | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 348 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*184_*187delACTA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 184 | INFO_REALIGN_3_PRIME | chr2 | 33562909 | ||||
| chr2:33562993
|
CTT | C | 65 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(62): Show | 237 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*261_*262delTT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 261 | INFO_REALIGN_3_PRIME | chr2 | 33562993 | ||||
| chr2:33563038
|
A | G | 6 | a0001c0001t0011a0001c0001t0044a0001c0001t0056others(3): Show | 12 | HG01433.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 301 | chr2 | 33563038 | |||||
| chr2:33563065
|
TACTC | T | 3 | a0001c0001t0012a0001c0001t0013a0001c0001t0031 | 13 | HG02280.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*330_*333delCTCA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 330 | INFO_REALIGN_3_PRIME | chr2 | 33563065 | ||||
| chr2:33563089
|
C | T | 18 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(15): Show | 73 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 352 | chr2 | 33563089 | |||||
| chr2:33563137
|
T | G | 1 | a0003c0011t0046 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 400 | chr2 | 33563137 | |||||
| chr2:33563163
|
A | G | 1 | a0003c0011t0046 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 426 | chr2 | 33563163 | |||||
| chr2:33563203
|
CTTGTT | C | 67 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(64): Show | 213 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*487_*491delTTGTT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 487 | INFO_REALIGN_3_PRIME | chr2 | 33563203 | ||||
| chr2:33563399
|
G | A | 1 | a0001c0002t0034 | 2 | HG00438.hp1 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 662 | chr2 | 33563399 | |||||
| chr2:33563520
|
G | C | 1 | a0001c0001t0024 | 2 | HG03209.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 783 | chr2 | 33563520 | |||||
| chr2:33563548
|
G | C | 1 | a0003c0009t0049 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 811 | chr2 | 33563548 | |||||
| chr2:33563588
|
C | T | 30 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(27): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 851 | chr2 | 33563588 | |||||
| chr2:33563592
|
T | TAACA | 12 | a0001c0001t0002a0001c0001t0029a0001c0001t0033others(9): Show | 58 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*859dupAACA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 860 | INFO_REALIGN_3_PRIME | chr2 | 33563592 | ||||
| chr2:33563662
|
T | TAA | 2 | a0001c0001t0025a0001c0001t0040 | 3 | HG01884.hp1 HG03927.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927_*928dupAA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 929 | INFO_REALIGN_3_PRIME | chr2 | 33563662 | ||||
| chr2:33563680
|
G | GA | 7 | a0001c0001t0008a0001c0001t0020a0001c0001t0032others(4): Show | 16 | HG01070.hp1 HG01361.hp2 HG01496.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*953dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 954 | INFO_REALIGN_3_PRIME | chr2 | 33563680 | ||||
| chr2:33563680
|
GA | G | 3 | a0001c0001t0013a0001c0002t0055a0004c0016t0062 | 7 | HG00639.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*953delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 953 | INFO_REALIGN_3_PRIME | chr2 | 33563680 | ||||
| chr2:33563965
|
A | G | 9 | a0001c0001t0003a0001c0001t0011a0001c0001t0014others(6): Show | 44 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1228 | chr2 | 33563965 | |||||
| chr2:33564001
|
C | G | 38 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(35): Show | 129 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1264C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1264 | chr2 | 33564001 | |||||
| chr2:33564002
|
G | A | 1 | a0001c0001t0051 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1265 | chr2 | 33564002 | |||||
| chr2:33564032
|
G | T | 5 | a0001c0001t0005a0001c0001t0023a0001c0001t0052others(2): Show | 18 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1295G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1295 | chr2 | 33564032 | |||||
| chr2:33564082
|
G | A | 1 | a0001c0001t0053 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1345 | chr2 | 33564082 | |||||
| chr2:33564138
|
T | C | 2 | a0001c0001t0052a0003c0009t0049 | 2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1401T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1401 | chr2 | 33564138 | |||||
| chr2:33564178
|
A | AAGTT | 7 | a0001c0001t0010a0001c0001t0045a0001c0001t0061others(4): Show | 15 | HG00597.hp1 HG00609.hp2 HG02027.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1443_*1446dupGTTA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1447 | INFO_REALIGN_3_PRIME | chr2 | 33564178 | ||||
| chr2:33564316
|
A | C | 2 | a0001c0001t0052a0003c0009t0049 | 2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1579A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1579 | chr2 | 33564316 | |||||
| chr2:33564335
|
T | TATCA | 4 | a0001c0001t0008a0001c0001t0032a0002c0007t0008others(1): Show | 11 | HG01070.hp1 HG01361.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1599_*1602dupATCA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1603 | INFO_REALIGN_3_PRIME | chr2 | 33564335 | ||||
| chr2:33564344
|
G | A | 2 | a0001c0001t0017a0001c0002t0017 | 3 | HG02451.hp2 HG02572.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1607 | chr2 | 33564344 | |||||
| chr2:33564426
|
T | C | 2 | a0001c0001t0052a0003c0009t0049 | 2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1689 | chr2 | 33564426 | |||||
| chr2:33564467
|
A | G | 40 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(37): Show | 133 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1730A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1730 | chr2 | 33564467 | |||||
| chr2:33564650
|
A | G | 1 | a0001c0002t0063 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1913A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1913 | chr2 | 33564650 | |||||
| chr2:33564723
|
A | G | 1 | a0001c0001t0054 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1986A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1986 | chr2 | 33564723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33476728
|
C | CCT | 137 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(134): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-261+36_-261+37dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476728 | |||||
| chr2:33476757
|
C | CCGTG | 9 | a0001c0001t0001g0115a0001c0001t0002g0108a0001c0001t0002g0111others(6): Show | 9 | HG00558.hp1 HG01074.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+51_-261+54dup others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476757 | |||||
| chr2:33476758
|
C | CGT | 19 | a0001c0001t0002g0243a0001c0001t0002g0245a0001c0001t0002g0247others(16): Show | 19 | HG00642.hp2 HG01070.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+88_-261+89dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGCGT | 21 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0099others(18): Show | 21 | HG00323.hp1 HG00423.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGCGTG others(1): Show |
49 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(46): Show | 49 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGCGTG others(3): Show |
22 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0028others(19): Show | 22 | HG01099.hp1 HG01175.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGCGTG others(5): Show |
14 | a0001c0001t0001g0014a0001c0001t0002g0006a0001c0001t0002g0013others(11): Show | 14 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGCGTG others(7): Show |
1 | a0001c0001t0066g0001 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+54_-261+55ins others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGT | 5 | a0001c0001t0003g0237a0001c0001t0013g0240a0001c0001t0017g0238others(2): Show | 5 | HG01993.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+86_-261+89dup others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGT | 25 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0227others(22): Show | 25 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-261+84_-261+89dup others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(1): Show |
15 | a0001c0001t0002g0209a0001c0001t0003g0210a0001c0001t0003g0211others(12): Show | 15 | HG01516.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+82_-261+89dup others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(3): Show |
8 | a0001c0001t0004g0197a0001c0001t0011g0195a0001c0001t0012g0123others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-261+80_-261+89dup others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0002g0187a0001c0001t0002g0190a0001c0001t0004g0191others(3): Show | 6 | HG00738.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+78_-261+89dup others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(7): Show |
14 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0184others(11): Show | 14 | HG01071.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+76_-261+89dup others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(9): Show |
9 | a0001c0001t0001g0171a0001c0001t0010g0169a0001c0001t0013g0121others(6): Show | 9 | HG01070.hp2 HG02280.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+74_-261+89dup others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(11): Show |
13 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0163others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.-261+72_-261+89dup others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(13): Show |
7 | a0001c0001t0003g0149a0001c0001t0004g0150a0001c0001t0004g0151others(4): Show | 7 | HG00438.hp1 HG01952.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+70_-261+89dup others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(15): Show |
6 | a0001c0001t0002g0144a0001c0001t0004g0143a0001c0001t0004g0145others(3): Show | 6 | HG00639.hp2 HG01496.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+68_-261+89dup others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(17): Show |
3 | a0001c0001t0003g0140a0001c0001t0023g0138a0001c0002t0006g0139 | 3 | HG01109.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+66_-261+89dup others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
C | CGTGTGTG others(19): Show |
1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-261+64_-261+89dup others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
CGT | C | 9 | a0001c0001t0009g0306a0001c0001t0010g0309a0001c0001t0011g0310others(6): Show | 9 | HG01515.hp2 HG01517.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+88_-261+89del others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
CGTGT | C | 10 | a0001c0001t0004g0129a0001c0001t0011g0312a0001c0001t0012g0132others(7): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+86_-261+89del others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0002g0315others(3): Show | 6 | HG01361.hp2 HG03195.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+82_-261+89del others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476758
|
CGTGTGTG others(3): Show |
C | 52 | a0001c0001t0001g0321a0001c0001t0001g0324a0001c0001t0001g0325others(49): Show | 52 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-261+80_-261+89del others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | |||||
| chr2:33476764
|
T | C | 1 | a0007c0012t0015g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-261+57T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476764 | ||||||
| chr2:33476823
|
T | C | 40 | a0001c0001t0001g0321a0001c0001t0001g0324a0001c0001t0001g0325others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-261+116T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476823 | ||||||
| chr2:33476846
|
G | A | 1 | a0001c0001t0048g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-261+139G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476846 | ||||||
| chr2:33476930
|
C | CG | 141 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-261+224dupG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476930 | |||||
| chr2:33477035
|
T | G | 144 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-261+328T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477035 | ||||||
| chr2:33477050
|
G | GA | 141 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-261+343_-261+344i others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477050 | ||||||
| chr2:33477059
|
A | G | 3 | a0001c0001t0012g0186a0001c0001t0044g0172a0001c0003t0005g0192 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-261+352A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477059 | ||||||
| chr2:33477136
|
C | T | 38 | a0001c0001t0001g0321a0001c0001t0001g0324a0001c0001t0001g0325others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-261+429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477136 | ||||||
| chr2:33477308
|
C | T | 4 | a0001c0001t0012g0123a0001c0001t0031g0125a0001c0001t0042g0122others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+601C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477308 | ||||||
| chr2:33477339
|
T | A | 6 | a0001c0001t0013g0166a0001c0001t0020g0155a0001c0002t0006g0139others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+632T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477339 | ||||||
| chr2:33477344
|
T | C | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-261+637T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477344 | ||||||
| chr2:33477366
|
C | T | 5 | a0001c0001t0020g0148a0001c0001t0023g0138a0001c0001t0023g0154others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+659C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477366 | ||||||
| chr2:33477419
|
C | G | 87 | a0001c0001t0001g0107a0001c0001t0001g0161a0001c0001t0001g0162others(84): Show | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-261+712C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477419 | ||||||
| chr2:33477439
|
G | T | 30 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0234others(27): Show | 30 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261+732G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477439 | ||||||
| chr2:33477448
|
C | A | 1 | a0001c0001t0007g0261 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-261+741C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477448 | ||||||
| chr2:33477612
|
G | A | 3 | a0001c0001t0004g0143a0001c0001t0020g0142a0001c0002t0006g0167 | 3 | HG01496.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-261+905G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477612 | ||||||
| chr2:33477612
|
G | T | 139 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(136): Show | 139 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-261+905G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477612 | ||||||
| chr2:33477795
|
C | G | 1 | a0001c0002t0028g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-261+1088C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477795 | ||||||
| chr2:33477835
|
C | T | 262 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(259): Show | 262 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-261+1128C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477835 | ||||||
| chr2:33477838
|
G | A | 6 | a0001c0001t0013g0166a0001c0001t0020g0155a0001c0002t0006g0139others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+1131G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477838 | ||||||
| chr2:33477878
|
T | C | 16 | a0001c0001t0004g0129a0001c0001t0012g0127a0001c0001t0012g0132others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-261+1171T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477878 | ||||||
| chr2:33477936
|
C | T | 91 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(88): Show | 91 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-261+1229C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477936 | ||||||
| chr2:33477986
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0011g0204a0001c0001t0026g0196others(2): Show | 5 | HG02109.hp1 HG02129.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+1279C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477986 | ||||||
| chr2:33478013
|
C | T | 1 | a0002c0007t0008g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-261+1306C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478013 | ||||||
| chr2:33478142
|
G | A | 4 | a0001c0001t0005g0177a0001c0003t0005g0175a0001c0003t0005g0176others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+1435G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478142 | ||||||
| chr2:33478150
|
C | G | 24 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0171others(21): Show | 24 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-261+1443C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478150 | ||||||
| chr2:33478322
|
G | A | 54 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0227others(51): Show | 54 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-261+1615G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478322 | ||||||
| chr2:33478472
|
C | T | 34 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(31): Show | 34 | HG01358.hp2 HG02071.hp2 HG02074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-261+1765C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478472 | ||||||
| chr2:33478490
|
C | T | 202 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(199): Show | 202 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.-261+1783C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478490 | ||||||
| chr2:33478536
|
G | A | 1 | a0001c0002t0001g0354 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-261+1829G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478536 | ||||||
| chr2:33478644
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-261+1937C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478644 | ||||||
| chr2:33478682
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-261+1975A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478682 | ||||||
| chr2:33478708
|
G | A | 3 | a0001c0001t0031g0141a0001c0002t0006g0188a0001c0003t0028g0173 | 3 | HG00738.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-261+2001G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478708 | ||||||
| chr2:33478721
|
C | T | 28 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0171others(25): Show | 28 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-261+2014C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478721 | ||||||
| chr2:33478788
|
C | T | 56 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(53): Show | 56 | HG01358.hp2 HG01884.hp1 HG02071.hp2 others(53): Show |
intron_variant | MODIFIER | c.-261+2081C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478788 | ||||||
| chr2:33478829
|
A | C | 3 | a0001c0001t0012g0186a0001c0001t0044g0172a0001c0003t0005g0192 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-261+2122A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478829 | ||||||
| chr2:33478833
|
T | C | 1 | a0001c0001t0009g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-261+2126T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478833 | ||||||
| chr2:33478863
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(139): Show | 142 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-261+2156G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478863 | ||||||
| chr2:33479056
|
A | G | 45 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0227others(42): Show | 45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-261+2349A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479056 | ||||||
| chr2:33479206
|
C | A | 4 | a0001c0001t0012g0123a0001c0001t0020g0155a0001c0001t0031g0125others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+2499C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479206 | ||||||
| chr2:33479253
|
G | T | 5 | a0001c0001t0005g0177a0001c0002t0006g0168a0001c0003t0005g0175others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+2546G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479253 | ||||||
| chr2:33479363
|
G | A | 1 | a0008c0010t0008g0319 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-261+2656G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479363 | ||||||
| chr2:33479411
|
A | ACTC | 54 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+2706_-261+270 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33479411 | |||||
| chr2:33479417
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-261+2710C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479417 | ||||||
| chr2:33479551
|
G | A | 4 | a0001c0001t0014g0193a0001c0001t0027g0194a0001c0001t0027g0199others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+2844G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479551 | ||||||
| chr2:33479665
|
T | C | 1 | a0001c0001t0021g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-261+2958T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479665 | ||||||
| chr2:33479694
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0213a0001c0001t0001g0234others(12): Show | 15 | HG00544.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+2987A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479694 | ||||||
| chr2:33479718
|
C | A | 94 | a0001c0001t0001g0018a0001c0001t0001g0262a0001c0001t0001g0263others(91): Show | 94 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.-261+3011C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479718 | ||||||
| chr2:33479782
|
C | G | 1 | a0001c0001t0031g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-261+3075C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479782 | ||||||
| chr2:33479874
|
A | ATTACAT | 4 | a0001c0001t0009g0215a0001c0001t0011g0080a0001c0001t0044g0172others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+3167_-261+316 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479874 | ||||||
| chr2:33479875
|
G | A | 4 | a0001c0001t0009g0215a0001c0001t0011g0080a0001c0001t0044g0172others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+3168G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479875 | ||||||
| chr2:33479883
|
T | C | 24 | a0001c0001t0001g0115a0001c0001t0001g0262a0001c0001t0001g0334others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-261+3176T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479883 | ||||||
| chr2:33479902
|
A | G | 42 | a0001c0001t0001g0115a0001c0001t0001g0262a0001c0001t0001g0334others(39): Show | 42 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-261+3195A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479902 | ||||||
| chr2:33479909
|
T | G | 9 | a0001c0001t0004g0143a0001c0001t0022g0259a0001c0001t0022g0260others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+3202T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479909 | ||||||
| chr2:33480042
|
A | AT | 92 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0083others(89): Show | 92 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-261+3355dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | |||||
| chr2:33480042
|
A | ATT | 46 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0161others(43): Show | 46 | HG00323.hp1 HG00423.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+3354_-261+335 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | |||||
| chr2:33480042
|
AT | A | 12 | a0001c0001t0001g0333a0001c0001t0004g0143a0001c0001t0009g0306others(9): Show | 12 | HG01168.hp2 HG01256.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+3355delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | |||||
| chr2:33480042
|
ATTT | A | 28 | a0001c0001t0001g0115a0001c0001t0001g0334a0001c0001t0002g0144others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-261+3353_-261+335 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | |||||
| chr2:33480074
|
G | A | 1 | a0001c0001t0004g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-261+3367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480074 | ||||||
| chr2:33480105
|
A | C | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+3398A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480105 | ||||||
| chr2:33480108
|
T | A | 1 | a0001c0002t0006g0174 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-261+3401T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480108 | ||||||
| chr2:33480128
|
C | T | 3 | a0001c0001t0005g0177a0001c0001t0011g0195a0001c0001t0019g0311 | 3 | HG02965.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-261+3421C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480128 | ||||||
| chr2:33480167
|
T | C | 71 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0115others(68): Show | 71 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-261+3460T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480167 | ||||||
| chr2:33480188
|
G | A | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+3481G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480188 | ||||||
| chr2:33480199
|
T | G | 1 | a0001c0001t0001g0345 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-261+3492T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480199 | ||||||
| chr2:33480318
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0036g0274 | 2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-261+3611C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480318 | ||||||
| chr2:33480322
|
C | T | 47 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(44): Show | 47 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-261+3615C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480322 | ||||||
| chr2:33480376
|
A | T | 1 | a0001c0001t0007g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-261+3669A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480376 | ||||||
| chr2:33480436
|
A | G | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+3729A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480436 | ||||||
| chr2:33480497
|
T | C | 51 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(48): Show | 51 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-261+3790T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480497 | ||||||
| chr2:33480513
|
G | C | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+3806G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480513 | ||||||
| chr2:33480524
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-261+3817G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480524 | ||||||
| chr2:33480531
|
G | A | 1 | a0001c0002t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-261+3824G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480531 | ||||||
| chr2:33480538
|
G | A | 1 | a0001c0001t0020g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-261+3831G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480538 | ||||||
| chr2:33480565
|
A | G | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+3858A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480565 | ||||||
| chr2:33480638
|
A | G | 1 | a0001c0001t0066g0001 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+3931A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480638 | ||||||
| chr2:33480853
|
T | C | 1 | a0001c0001t0002g0360 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-261+4146T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480853 | ||||||
| chr2:33480923
|
G | A | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+4216G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480923 | ||||||
| chr2:33480931
|
G | C | 9 | a0001c0001t0004g0143a0001c0001t0011g0080a0001c0001t0044g0172others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+4224G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480931 | ||||||
| chr2:33480944
|
T | A | 21 | a0001c0001t0003g0041a0001c0001t0003g0140a0001c0001t0009g0110others(18): Show | 21 | HG01074.hp1 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+4237T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480944 | ||||||
| chr2:33481019
|
T | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4312T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481019 | ||||||
| chr2:33481041
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0060a0001c0001t0004g0359others(2): Show | 5 | NA18944.hp2 NA18945.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+4334C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481041 | ||||||
| chr2:33481075
|
G | C | 1 | a0001c0001t0042g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-261+4368G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481075 | ||||||
| chr2:33481247
|
C | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-261+4540C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481247 | ||||||
| chr2:33481254
|
C | T | 1 | a0001c0001t0031g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-261+4547C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481254 | ||||||
| chr2:33481299
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4592C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481299 | ||||||
| chr2:33481452
|
C | T | 1 | a0006c0013t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-261+4745C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481452 | ||||||
| chr2:33481519
|
C | T | 1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+4812C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481519 | ||||||
| chr2:33481588
|
G | A | 4 | a0001c0002t0006g0168a0001c0002t0017g0147a0001c0004t0019g0042others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+4881G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481588 | ||||||
| chr2:33481611
|
C | T | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+4904C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481611 | ||||||
| chr2:33481682
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-261+4975C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481682 | ||||||
| chr2:33481894
|
G | A | 1 | a0001c0002t0006g0174 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-261+5187G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481894 | ||||||
| chr2:33481896
|
T | C | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+5189T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481896 | ||||||
| chr2:33481923
|
C | T | 3 | a0001c0001t0003g0041a0001c0001t0011g0312a0001c0002t0028g0137 | 3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-261+5216C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481923 | ||||||
| chr2:33482017
|
AT | A | 12 | a0001c0001t0004g0143a0001c0001t0011g0080a0001c0001t0027g0194others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+5324delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33482017 | |||||
| chr2:33482087
|
C | T | 1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+5380C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482087 | ||||||
| chr2:33482114
|
T | A | 9 | a0001c0001t0004g0143a0001c0001t0011g0080a0001c0001t0044g0172others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+5407T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482114 | ||||||
| chr2:33482114
|
T | C | 67 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(64): Show | 67 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-261+5407T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482114 | ||||||
| chr2:33482158
|
C | T | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+5451C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482158 | ||||||
| chr2:33482289
|
G | C | 74 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(71): Show | 74 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-261+5582G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482289 | ||||||
| chr2:33482307
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+5600C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482307 | ||||||
| chr2:33482314
|
G | T | 1 | a0001c0001t0011g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-261+5607G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482314 | ||||||
| chr2:33482332
|
T | C | 16 | a0001c0001t0003g0140a0001c0001t0009g0110a0001c0001t0011g0077others(13): Show | 16 | HG01074.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-261+5625T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482332 | ||||||
| chr2:33482416
|
G | A | 1 | a0001c0001t0011g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+5709G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482416 | ||||||
| chr2:33482419
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0004g0089a0001c0001t0009g0010others(2): Show | 5 | HG01515.hp1 HG02258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+5712A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482419 | ||||||
| chr2:33482557
|
G | T | 10 | a0001c0001t0002g0209a0001c0001t0002g0228a0001c0001t0002g0231others(7): Show | 10 | HG02132.hp2 NA18747.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+5850G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482557 | ||||||
| chr2:33482608
|
C | A | 1 | a0001c0002t0001g0113 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-261+5901C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482608 | ||||||
| chr2:33482667
|
T | C | 47 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(44): Show | 47 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-261+5960T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482667 | ||||||
| chr2:33482717
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-261+6010G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482717 | ||||||
| chr2:33482778
|
A | T | 1 | a0001c0001t0042g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-261+6071A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482778 | ||||||
| chr2:33483013
|
G | A | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+6306G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483013 | ||||||
| chr2:33483034
|
A | AT | 15 | a0001c0001t0003g0140a0001c0001t0009g0110a0001c0001t0011g0077others(12): Show | 15 | HG01074.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+6329dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483034 | |||||
| chr2:33483036
|
TA | T | 86 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0098others(83): Show | 86 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.-261+6341delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483036 | |||||
| chr2:33483038
|
A | T | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+6331A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483038 | ||||||
| chr2:33483273
|
G | A | 1 | a0001c0001t0059g0203 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-261+6566G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483273 | ||||||
| chr2:33483347
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(51): Show | 54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+6640T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483347 | ||||||
| chr2:33483424
|
A | G | 79 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-261+6717A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483424 | ||||||
| chr2:33483475
|
T | C | 15 | a0001c0001t0003g0140a0001c0001t0009g0110a0001c0001t0011g0077others(12): Show | 15 | HG01074.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+6768T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483475 | ||||||
| chr2:33483486
|
A | AT | 138 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(135): Show | 138 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-261+6799dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483486
|
A | ATT | 50 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0171others(47): Show | 50 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-261+6798_-261+679 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483486
|
A | ATTT | 8 | a0001c0001t0001g0067a0001c0001t0002g0066a0001c0001t0002g0315others(5): Show | 8 | HG02132.hp1 HG03516.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.-261+6797_-261+679 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483486
|
AT | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0100a0001c0001t0001g0337others(20): Show | 23 | HG00323.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-261+6799delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483486
|
ATTTTTT | A | 45 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(42): Show | 45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-261+6794_-261+679 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483486
|
ATTTTTTT | A | 6 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(3): Show | 6 | HG01884.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+6793_-261+679 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | |||||
| chr2:33483511
|
C | T | 2 | a0001c0001t0016g0369a0001c0001t0060g0020 | 2 | HG03831.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-261+6804C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483511 | ||||||
| chr2:33483582
|
G | A | 2 | a0001c0001t0042g0122a0001c0002t0001g0361 | 2 | HG03139.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-261+6875G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483582 | ||||||
| chr2:33483583
|
G | C | 1 | a0001c0001t0039g0264 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-261+6876G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483583 | ||||||
| chr2:33483586
|
T | TC | 54 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(51): Show | 54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+6880dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483586 | |||||
| chr2:33483591
|
T | C | 70 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(67): Show | 70 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-261+6884T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483591 | ||||||
| chr2:33483611
|
C | G | 1 | a0001c0001t0014g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-261+6904C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483611 | ||||||
| chr2:33483682
|
T | C | 1 | a0001c0001t0011g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+6975T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483682 | ||||||
| chr2:33483696
|
T | A | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+6989T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483696 | ||||||
| chr2:33483793
|
C | G | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+7086C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483793 | ||||||
| chr2:33483891
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-261+7184G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483891 | ||||||
| chr2:33484131
|
C | A | 1 | a0001c0001t0011g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-261+7424C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484131 | ||||||
| chr2:33484160
|
C | A | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+7453C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484160 | ||||||
| chr2:33484219
|
G | A | 1 | a0001c0001t0038g0282 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-261+7512G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484219 | ||||||
| chr2:33484280
|
G | T | 1 | a0001c0001t0038g0282 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-261+7573G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484280 | ||||||
| chr2:33484376
|
A | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+7669A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484376 | ||||||
| chr2:33484509
|
A | G | 1 | a0001c0004t0019g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+7802A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484509 | ||||||
| chr2:33484536
|
A | AT | 17 | a0001c0001t0002g0250a0001c0001t0003g0140a0001c0001t0009g0110others(14): Show | 17 | HG01074.hp1 HG02257.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-261+7841dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33484536 | |||||
| chr2:33484713
|
C | T | 1 | a0001c0002t0001g0366 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-261+8006C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484713 | ||||||
| chr2:33484730
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0002g0102a0001c0002t0001g0101others(1): Show | 4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+8023C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484730 | ||||||
| chr2:33484822
|
A | G | 37 | a0001c0001t0001g0059a0001c0001t0001g0107a0001c0001t0001g0179others(34): Show | 37 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.-261+8115A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484822 | ||||||
| chr2:33484894
|
T | C | 56 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(53): Show | 56 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-261+8187T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484894 | ||||||
| chr2:33484973
|
T | C | 160 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0067others(157): Show | 160 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.-261+8266T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484973 | ||||||
| chr2:33484975
|
G | T | 56 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(53): Show | 56 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-261+8268G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484975 | ||||||
| chr2:33485158
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0003g0298 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-261+8451A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485158 | ||||||
| chr2:33485222
|
A | C | 38 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0048others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-261+8515A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485222 | ||||||
| chr2:33485356
|
G | A | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+8649G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485356 | ||||||
| chr2:33485493
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+8786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485493 | ||||||
| chr2:33485510
|
G | A | 118 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0098others(115): Show | 118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.-261+8803G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485510 | ||||||
| chr2:33485530
|
G | C | 3 | a0001c0001t0001g0266a0001c0002t0001g0267a0001c0002t0001g0352 | 3 | HG00423.hp2 NA18948.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-261+8823G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485530 | ||||||
| chr2:33485761
|
T | C | 3 | a0001c0001t0011g0080a0001c0001t0044g0172a0001c0004t0043g0201 | 3 | HG02970.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-261+9054T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485761 | ||||||
| chr2:33485768
|
A | G | 2 | a0001c0001t0003g0140a0001c0002t0006g0167 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+9061A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485768 | ||||||
| chr2:33485796
|
G | A | 2 | a0001c0001t0052g0303a0001c0002t0006g0153 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-261+9089G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485796 | ||||||
| chr2:33486042
|
C | T | 5 | a0001c0001t0001g0321a0001c0001t0002g0027a0001c0001t0010g0009others(2): Show | 5 | NA18952.hp1 NA18998.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+9335C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486042 | ||||||
| chr2:33486120
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-261+9413C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486120 | ||||||
| chr2:33486164
|
AT | A | 250 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(247): Show | 250 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-261+9471delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | |||||
| chr2:33486164
|
ATT | A | 28 | a0001c0001t0002g0111a0001c0001t0002g0233a0001c0001t0003g0140others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-261+9470_-261+947 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | |||||
| chr2:33486164
|
ATTT | A | 23 | a0001c0001t0001g0059a0001c0001t0001g0183a0001c0001t0001g0262others(20): Show | 23 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.-261+9469_-261+947 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | |||||
| chr2:33486166
|
T | A | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+9459T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486166 | ||||||
| chr2:33486169
|
T | A | 7 | a0001c0001t0001g0268a0001c0001t0001g0318a0001c0001t0002g0287others(4): Show | 7 | HG00423.hp1 NA18949.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+9462T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486169 | ||||||
| chr2:33486170
|
T | A | 10 | a0001c0001t0012g0123a0001c0001t0013g0300a0001c0001t0024g0159others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+9463T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486170 | ||||||
| chr2:33486178
|
T | TGA | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | NA18945.hp2 NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-261+9483_-261+948 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486178 | |||||
| chr2:33486222
|
T | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0161a0001c0001t0001g0162others(2): Show | 5 | NA18956.hp1 NA18960.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+9515T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486222 | ||||||
| chr2:33486310
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+9603C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486310 | ||||||
| chr2:33486318
|
C | G | 51 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(48): Show | 51 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-261+9611C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486318 | ||||||
| chr2:33486327
|
C | T | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+9620C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486327 | ||||||
| chr2:33486492
|
C | CT | 73 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(70): Show | 73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-261+9788dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486492 | |||||
| chr2:33486552
|
G | T | 1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+9845G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486552 | ||||||
| chr2:33486698
|
G | A | 2 | a0001c0001t0050g0313a0001c0001t0060g0020 | 2 | HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-261+9991G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486698 | ||||||
| chr2:33486716
|
G | A | 49 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-261+10009G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486716 | ||||||
| chr2:33486852
|
C | T | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10145C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486852 | ||||||
| chr2:33486854
|
G | A | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-261+10147G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486854 | ||||||
| chr2:33486900
|
T | C | 107 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0082others(104): Show | 107 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-261+10193T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486900 | ||||||
| chr2:33486922
|
C | T | 10 | a0001c0001t0012g0123a0001c0001t0013g0300a0001c0001t0024g0159others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+10215C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486922 | ||||||
| chr2:33486939
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-261+10232G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486939 | ||||||
| chr2:33486964
|
A | G | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10257A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486964 | ||||||
| chr2:33486990
|
A | T | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+10283A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486990 | ||||||
| chr2:33487002
|
C | A | 1 | a0001c0001t0002g0360 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-261+10295C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487002 | ||||||
| chr2:33487048
|
T | C | 1 | a0001c0002t0034g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-261+10341T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487048 | ||||||
| chr2:33487069
|
G | A | 2 | a0001c0001t0002g0305a0001c0001t0003g0304 | 2 | HG00642.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-261+10362G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487069 | ||||||
| chr2:33487118
|
A | G | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+10411A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487118 | ||||||
| chr2:33487144
|
A | G | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+10437A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487144 | ||||||
| chr2:33487175
|
A | G | 1 | a0001c0001t0013g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-261+10468A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487175 | ||||||
| chr2:33487271
|
A | T | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10564A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487271 | ||||||
| chr2:33487336
|
C | T | 1 | a0001c0001t0060g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-261+10629C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487336 | ||||||
| chr2:33487346
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-261+10639C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487346 | ||||||
| chr2:33487387
|
G | C | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+10680G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487387 | ||||||
| chr2:33487418
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0277a0001c0001t0002g0066others(2): Show | 5 | HG02132.hp1 NA18991.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+10711A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487418 | ||||||
| chr2:33487580
|
A | G | 1 | a0001c0001t0010g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-261+10873A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487580 | ||||||
| chr2:33487602
|
C | A | 3 | a0001c0002t0006g0168a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+10895C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487602 | ||||||
| chr2:33487898
|
T | C | 242 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0044others(239): Show | 242 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(239): Show |
intron_variant | MODIFIER | c.-261+11191T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487898 | ||||||
| chr2:33487962
|
G | A | 2 | a0001c0001t0015g0050a0007c0012t0015g0117 | 2 | NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-261+11255G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487962 | ||||||
| chr2:33487968
|
A | C | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+11261A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487968 | ||||||
| chr2:33488080
|
A | C | 43 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(40): Show | 43 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-261+11373A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488080 | ||||||
| chr2:33488083
|
C | G | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+11376C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488083 | ||||||
| chr2:33488142
|
A | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11435A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488142 | ||||||
| chr2:33488242
|
T | A | 1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+11535T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488242 | ||||||
| chr2:33488352
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11645C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488352 | ||||||
| chr2:33488392
|
T | C | 1 | a0001c0002t0006g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-261+11685T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488392 | ||||||
| chr2:33488398
|
A | C | 2 | a0001c0001t0011g0080a0001c0004t0019g0042 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-261+11691A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488398 | ||||||
| chr2:33488460
|
G | A | 2 | a0001c0001t0002g0251a0001c0001t0002g0347 | 2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-261+11753G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488460 | ||||||
| chr2:33488493
|
G | A | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11786G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488493 | ||||||
| chr2:33488581
|
C | A | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+11874C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488581 | ||||||
| chr2:33488669
|
G | A | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11962G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488669 | ||||||
| chr2:33488670
|
C | A | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11963C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488670 | ||||||
| chr2:33488678
|
C | T | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-261+11971C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488678 | ||||||
| chr2:33488719
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-261+12012C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488719 | ||||||
| chr2:33488734
|
A | T | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+12027A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488734 | ||||||
| chr2:33488740
|
G | A | 2 | a0001c0002t0017g0147a0003c0009t0049g0070 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+12033G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488740 | ||||||
| chr2:33488954
|
A | AT | 38 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(35): Show | 38 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(35): Show |
intron_variant | MODIFIER | c.-261+12259dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33488954 | |||||
| chr2:33488954
|
AT | A | 9 | a0001c0001t0007g0093a0001c0001t0009g0017a0001c0001t0009g0215others(6): Show | 9 | HG01361.hp1 HG01516.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+12259delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33488954 | |||||
| chr2:33489038
|
G | A | 46 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+12331G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489038 | ||||||
| chr2:33489097
|
G | C | 1 | a0001c0001t0011g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+12390G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489097 | ||||||
| chr2:33489129
|
A | G | 2 | a0001c0001t0044g0172a0001c0004t0043g0201 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-261+12422A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489129 | ||||||
| chr2:33489171
|
A | G | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+12464A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489171 | ||||||
| chr2:33489227
|
A | T | 14 | a0001c0001t0003g0140a0001c0001t0009g0110a0001c0001t0011g0077others(11): Show | 14 | HG01074.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-261+12520A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489227 | ||||||
| chr2:33489280
|
A | G | 1 | a0001c0002t0006g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-261+12573A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489280 | ||||||
| chr2:33489333
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-261+12626A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489333 | ||||||
| chr2:33489336
|
G | T | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+12629G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489336 | ||||||
| chr2:33489367
|
C | T | 3 | a0001c0001t0002g0349a0001c0001t0044g0172a0001c0004t0043g0201 | 3 | HG02970.hp2 HG03471.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-261+12660C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489367 | ||||||
| chr2:33489489
|
C | G | 1 | a0001c0003t0005g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-261+12782C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489489 | ||||||
| chr2:33489531
|
T | G | 2 | a0001c0001t0018g0281a0001c0002t0001g0024 | 2 | NA18946.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-261+12824T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489531 | ||||||
| chr2:33489542
|
T | C | 59 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(56): Show | 59 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-261+12835T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489542 | ||||||
| chr2:33489602
|
A | G | 35 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(32): Show | 35 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.-261+12895A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489602 | ||||||
| chr2:33489796
|
C | G | 1 | a0001c0002t0006g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+13089C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489796 | ||||||
| chr2:33489952
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0004g0089a0001c0001t0009g0010others(2): Show | 5 | HG01515.hp1 HG02258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+13245A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489952 | ||||||
| chr2:33490000
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13293C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490000 | ||||||
| chr2:33490021
|
CT | C | 32 | a0001c0001t0001g0059a0001c0001t0001g0179a0001c0001t0001g0183others(29): Show | 32 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.-261+13315delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490021 | ||||||
| chr2:33490203
|
T | G | 6 | a0001c0001t0011g0204a0001c0001t0013g0121a0001c0001t0058g0124others(3): Show | 6 | HG01255.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13496T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490203 | ||||||
| chr2:33490360
|
G | A | 2 | a0001c0001t0050g0313a0001c0001t0060g0020 | 2 | HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-261+13653G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490360 | ||||||
| chr2:33490365
|
C | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13658C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490365 | ||||||
| chr2:33490549
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-261+13842C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490549 | ||||||
| chr2:33490610
|
C | G | 44 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(41): Show | 44 | HG01074.hp1 HG01255.hp1 HG01358.hp2 others(41): Show |
intron_variant | MODIFIER | c.-261+13903C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490610 | ||||||
| chr2:33490675
|
T | G | 159 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(156): Show | 159 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-261+13968T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490675 | ||||||
| chr2:33490718
|
G | A | 2 | a0001c0001t0023g0138a0001c0001t0023g0154 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-261+14011G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490718 | ||||||
| chr2:33490721
|
G | A | 1 | a0001c0001t0002g0243 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-261+14014G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490721 | ||||||
| chr2:33490861
|
G | A | 2 | a0001c0001t0039g0146a0001c0002t0034g0152 | 2 | HG00438.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-261+14154G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490861 | ||||||
| chr2:33490878
|
C | T | 3 | a0001c0001t0005g0177a0001c0001t0011g0195a0001c0001t0019g0311 | 3 | HG02965.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-261+14171C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490878 | ||||||
| chr2:33491043
|
C | T | 2 | a0001c0001t0004g0191a0001c0001t0004g0197 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-261+14336C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491043 | ||||||
| chr2:33491066
|
A | G | 4 | a0001c0001t0003g0302a0001c0001t0026g0196a0001c0001t0040g0128others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+14359A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491066 | ||||||
| chr2:33491105
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+14398C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491105 | ||||||
| chr2:33491172
|
T | TG | 368 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(365): Show | 368 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(365): Show |
intron_variant | MODIFIER | c.-261+14467dupG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33491172 | |||||
| chr2:33491172
|
T | TGGGTGTG others(8238): Show |
1 | a0001c0002t0016g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-261+14467_-261+14 others(8251): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33491172 | |||||
| chr2:33491399
|
A | G | 6 | a0001c0001t0001g0321a0001c0001t0002g0027a0001c0001t0010g0009others(3): Show | 6 | HG02027.hp2 NA18952.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+14692A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491399 | ||||||
| chr2:33491438
|
ATTAATAC | A | 11 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-261+14737_-261+14 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33491438 | |||||
| chr2:33491630
|
A | G | 19 | a0001c0001t0003g0140a0001c0001t0004g0143a0001c0001t0009g0110others(16): Show | 19 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+14923A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491630 | ||||||
| chr2:33491642
|
G | A | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-261+14935G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491642 | ||||||
| chr2:33491778
|
C | T | 1 | a0001c0002t0006g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+15071C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491778 | ||||||
| chr2:33491851
|
G | A | 2 | a0001c0001t0013g0300a0001c0001t0024g0159 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-261+15144G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491851 | ||||||
| chr2:33492362
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-261+15655A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492362 | ||||||
| chr2:33492368
|
A | G | 46 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+15661A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492368 | ||||||
| chr2:33492474
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-261+15767C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492474 | ||||||
| chr2:33492488
|
C | G | 2 | a0001c0001t0004g0191a0001c0001t0004g0197 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-261+15781C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492488 | ||||||
| chr2:33492616
|
G | A | 150 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0067others(147): Show | 150 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.-261+15909G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492616 | ||||||
| chr2:33492724
|
T | A | 10 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+16017T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492724 | ||||||
| chr2:33492879
|
A | C | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+16172A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492879 | ||||||
| chr2:33492919
|
C | T | 3 | a0001c0001t0003g0140a0001c0001t0051g0299a0001c0002t0006g0168 | 3 | HG02886.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+16212C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492919 | ||||||
| chr2:33492922
|
A | G | 2 | a0001c0001t0023g0138a0001c0001t0023g0154 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-261+16215A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492922 | ||||||
| chr2:33492996
|
A | T | 43 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(40): Show | 43 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(40): Show |
intron_variant | MODIFIER | c.-261+16289A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492996 | ||||||
| chr2:33493046
|
T | C | 2 | a0001c0002t0017g0147a0003c0009t0049g0070 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+16339T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493046 | ||||||
| chr2:33493065
|
A | G | 1 | a0001c0002t0006g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+16358A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493065 | ||||||
| chr2:33493188
|
T | C | 135 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(132): Show | 135 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.-261+16481T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493188 | ||||||
| chr2:33493189
|
G | A | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+16482G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493189 | ||||||
| chr2:33493251
|
C | T | 42 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-261+16544C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493251 | ||||||
| chr2:33493259
|
C | T | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+16552C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493259 | ||||||
| chr2:33493264
|
C | T | 42 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-261+16557C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493264 | ||||||
| chr2:33493456
|
T | C | 1 | a0001c0004t0019g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+16749T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493456 | ||||||
| chr2:33493550
|
A | C | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+16843A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493550 | ||||||
| chr2:33493592
|
T | C | 14 | a0001c0001t0004g0129a0001c0001t0012g0123a0001c0003t0005g0040others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+16885T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493592 | ||||||
| chr2:33493605
|
G | GA | 165 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(162): Show | 165 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-261+16898_-261+16 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493605 | ||||||
| chr2:33493612
|
C | T | 50 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-261+16905C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493612 | ||||||
| chr2:33493682
|
G | A | 6 | a0001c0001t0002g0163a0001c0001t0003g0164a0001c0001t0009g0016others(3): Show | 6 | HG01192.hp2 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+16975G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493682 | ||||||
| chr2:33493756
|
TA | T | 7 | a0001c0001t0009g0110a0001c0001t0011g0077a0001c0001t0031g0125others(4): Show | 7 | HG01074.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+17060delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33493756 | |||||
| chr2:33493789
|
T | C | 67 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(64): Show | 67 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-261+17082T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493789 | ||||||
| chr2:33493874
|
A | G | 1 | a0001c0001t0016g0369 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-261+17167A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493874 | ||||||
| chr2:33493975
|
G | A | 33 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(30): Show | 33 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(30): Show |
intron_variant | MODIFIER | c.-261+17268G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493975 | ||||||
| chr2:33493998
|
A | G | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+17291A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493998 | ||||||
| chr2:33494042
|
A | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(51): Show | 54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+17335A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494042 | ||||||
| chr2:33494156
|
C | A | 33 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(30): Show | 33 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(30): Show |
intron_variant | MODIFIER | c.-261+17449C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494156 | ||||||
| chr2:33494301
|
G | T | 1 | a0001c0002t0001g0029 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-260-17409G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494301 | ||||||
| chr2:33494406
|
C | T | 14 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-17304C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494406 | ||||||
| chr2:33494407
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-260-17303G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494407 | ||||||
| chr2:33494584
|
A | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-17126A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494584 | ||||||
| chr2:33494772
|
A | T | 2 | a0001c0001t0004g0191a0001c0001t0004g0197 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-260-16938A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494772 | ||||||
| chr2:33494908
|
A | T | 6 | a0001c0001t0039g0146a0001c0001t0039g0264a0001c0001t0045g0106others(3): Show | 6 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-16802A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494908 | ||||||
| chr2:33494942
|
T | C | 14 | a0001c0001t0001g0268a0001c0001t0001g0318a0001c0001t0003g0041others(11): Show | 14 | HG00738.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-16768T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494942 | ||||||
| chr2:33495067
|
C | A | 8 | a0001c0001t0001g0292a0001c0001t0003g0149a0001c0002t0001g0295others(5): Show | 8 | HG01952.hp1 NA18944.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-16643C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495067 | ||||||
| chr2:33495091
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-260-16619A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495091 | ||||||
| chr2:33495217
|
A | G | 1 | a0001c0001t0031g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-260-16493A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495217 | ||||||
| chr2:33495287
|
T | C | 2 | a0001c0001t0013g0301a0001c0003t0005g0119 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-260-16423T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495287 | ||||||
| chr2:33495289
|
G | T | 42 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-260-16421G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495289 | ||||||
| chr2:33495292
|
G | A | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-260-16418G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495292 | ||||||
| chr2:33495463
|
C | T | 1 | a0001c0002t0006g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-16247C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495463 | ||||||
| chr2:33495508
|
A | ACCAGGCC others(5): Show |
4 | a0001c0001t0009g0215a0001c0001t0011g0080a0001c0001t0044g0172others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-16196_-260-16 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33495508 | |||||
| chr2:33495567
|
A | G | 21 | a0001c0001t0001g0268a0001c0001t0001g0285a0001c0001t0001g0318others(18): Show | 21 | HG00738.hp1 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-260-16143A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495567 | ||||||
| chr2:33495568
|
T | C | 2 | a0001c0001t0013g0166a0001c0001t0057g0079 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-260-16142T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495568 | ||||||
| chr2:33495613
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-260-16097G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495613 | ||||||
| chr2:33495671
|
T | A | 1 | a0001c0001t0009g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-260-16039T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495671 | ||||||
| chr2:33495727
|
T | TA | 14 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-15979dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33495727 | |||||
| chr2:33495742
|
A | G | 22 | a0001c0001t0011g0204a0001c0001t0011g0310a0001c0001t0012g0127others(19): Show | 22 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-260-15968A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495742 | ||||||
| chr2:33495746
|
T | C | 1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-260-15964T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495746 | ||||||
| chr2:33495935
|
C | G | 1 | a0001c0001t0035g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-260-15775C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495935 | ||||||
| chr2:33496101
|
T | C | 1 | a0001c0002t0006g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-260-15609T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496101 | ||||||
| chr2:33496180
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-260-15530A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496180 | ||||||
| chr2:33496248
|
G | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0053others(29): Show | 32 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-260-15462G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496248 | ||||||
| chr2:33496264
|
A | G | 1 | a0001c0003t0005g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-260-15446A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496264 | ||||||
| chr2:33496276
|
G | T | 38 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(35): Show | 38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-260-15434G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496276 | ||||||
| chr2:33496390
|
A | T | 6 | a0001c0001t0001g0284a0001c0001t0002g0247a0001c0001t0002g0250others(3): Show | 6 | HG01192.hp1 HG01433.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-15320A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496390 | ||||||
| chr2:33496429
|
A | G | 26 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0277others(23): Show | 26 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-260-15281A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496429 | ||||||
| chr2:33496479
|
T | A | 84 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0067others(81): Show | 84 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.-260-15231T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496479 | ||||||
| chr2:33496538
|
T | G | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-15172T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496538 | ||||||
| chr2:33496683
|
C | T | 1 | a0001c0001t0039g0264 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-260-15027C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496683 | ||||||
| chr2:33496718
|
G | A | 26 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0277others(23): Show | 26 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-260-14992G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496718 | ||||||
| chr2:33496722
|
C | T | 1 | a0001c0001t0032g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-260-14988C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496722 | ||||||
| chr2:33496799
|
G | A | 23 | a0001c0001t0001g0268a0001c0001t0001g0318a0001c0001t0002g0187others(20): Show | 23 | HG00738.hp1 HG01496.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-14911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496799 | ||||||
| chr2:33496851
|
T | C | 6 | a0001c0001t0009g0110a0001c0001t0011g0077a0001c0001t0022g0259others(3): Show | 6 | HG01074.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-14859T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496851 | ||||||
| chr2:33496862
|
G | C | 137 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0082others(134): Show | 137 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.-260-14848G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496862 | ||||||
| chr2:33496896
|
C | G | 41 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(38): Show | 41 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(38): Show |
intron_variant | MODIFIER | c.-260-14814C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496896 | ||||||
| chr2:33496936
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0002g0102a0001c0002t0001g0101others(1): Show | 4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-14774G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496936 | ||||||
| chr2:33496948
|
G | C | 2 | a0001c0001t0002g0339a0001c0001t0025g0182 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-260-14762G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496948 | ||||||
| chr2:33496978
|
C | T | 36 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(33): Show | 36 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.-260-14732C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496978 | ||||||
| chr2:33497003
|
T | C | 1 | a0001c0001t0002g0347 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-260-14707T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497003 | ||||||
| chr2:33497033
|
T | C | 73 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(70): Show | 73 | HG01074.hp1 HG01255.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-14677T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497033 | ||||||
| chr2:33497085
|
C | G | 1 | a0001c0001t0008g0244 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-260-14625C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497085 | ||||||
| chr2:33497225
|
A | G | 1 | a0001c0001t0004g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-260-14485A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497225 | ||||||
| chr2:33497402
|
T | C | 1 | a0001c0002t0001g0370 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-260-14308T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497402 | ||||||
| chr2:33497498
|
A | T | 48 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(45): Show | 48 | HG01255.hp1 HG01358.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-260-14212A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497498 | ||||||
| chr2:33497610
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-260-14100T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497610 | ||||||
| chr2:33497745
|
T | C | 1 | a0001c0001t0015g0219 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-260-13965T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497745 | ||||||
| chr2:33497787
|
A | G | 67 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0171others(64): Show | 67 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-260-13923A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497787 | ||||||
| chr2:33497790
|
G | C | 1 | a0001c0002t0003g0291 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-260-13920G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497790 | ||||||
| chr2:33497849
|
G | C | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-13861G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497849 | ||||||
| chr2:33497912
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-260-13798G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497912 | ||||||
| chr2:33497950
|
G | A | 27 | a0001c0001t0001g0059a0001c0001t0001g0179a0001c0001t0001g0183others(24): Show | 27 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.-260-13760G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497950 | ||||||
| chr2:33497973
|
C | CCCTTTCT others(13): Show |
37 | a0001c0001t0001g0059a0001c0001t0001g0179a0001c0001t0001g0183others(34): Show | 37 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.-260-13707_-260-13 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33497973 | |||||
| chr2:33498081
|
C | A | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-260-13629C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498081 | ||||||
| chr2:33498117
|
A | G | 124 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0067others(121): Show | 124 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-260-13593A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498117 | ||||||
| chr2:33498126
|
C | T | 1 | a0001c0002t0006g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-13584C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498126 | ||||||
| chr2:33498127
|
T | C | 5 | a0001c0001t0001g0285a0001c0001t0002g0073a0001c0001t0008g0180others(2): Show | 5 | HG01099.hp1 HG01358.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-13583T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498127 | ||||||
| chr2:33498190
|
G | A | 1 | a0001c0001t0004g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-260-13520G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498190 | ||||||
| chr2:33498443
|
C | T | 36 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(33): Show | 36 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-260-13267C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498443 | ||||||
| chr2:33498498
|
G | C | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-260-13212G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498498 | ||||||
| chr2:33498566
|
T | A | 4 | a0001c0001t0001g0100a0001c0001t0002g0102a0001c0002t0001g0101others(1): Show | 4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-13144T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498566 | ||||||
| chr2:33498624
|
C | G | 79 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0067others(76): Show | 79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-260-13086C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498624 | ||||||
| chr2:33498699
|
C | T | 1 | a0001c0001t0032g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-260-13011C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498699 | ||||||
| chr2:33498873
|
T | A | 1 | a0001c0002t0001g0365 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-260-12837T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498873 | ||||||
| chr2:33499275
|
C | A | 3 | a0001c0001t0024g0074a0001c0002t0017g0147a0003c0009t0049g0070 | 3 | HG02451.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-260-12435C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499275 | ||||||
| chr2:33499452
|
G | A | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-12258G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499452 | ||||||
| chr2:33499527
|
C | T | 5 | a0001c0001t0011g0195a0001c0001t0027g0194a0001c0001t0050g0313others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-12183C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499527 | ||||||
| chr2:33499539
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-260-12171C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499539 | ||||||
| chr2:33499706
|
T | G | 12 | a0001c0001t0001g0059a0001c0001t0001g0262a0001c0001t0001g0317others(9): Show | 12 | HG00544.hp2 HG02074.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-260-12004T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499706 | ||||||
| chr2:33499744
|
C | G | 1 | a0001c0002t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-260-11966C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499744 | ||||||
| chr2:33499763
|
C | CA | 35 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-11936dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499763 | |||||
| chr2:33499773
|
A | AAAGAG | 13 | a0001c0001t0003g0140a0001c0001t0004g0143a0001c0001t0013g0240others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-11936_-260-11 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499773 | |||||
| chr2:33499773
|
A | AAGAG | 23 | a0001c0001t0004g0129a0001c0001t0009g0215a0001c0001t0011g0080others(20): Show | 23 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-11934_-260-11 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499773 | |||||
| chr2:33499776
|
A | AGAGG | 50 | a0001c0001t0001g0065a0001c0001t0001g0171a0001c0001t0001g0184others(47): Show | 50 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-260-11933_-260-11 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499776 | |||||
| chr2:33499815
|
A | G | 1 | a0001c0001t0061g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-260-11895A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499815 | ||||||
| chr2:33499862
|
G | A | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-11848G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499862 | ||||||
| chr2:33499949
|
G | A | 1 | a0001c0004t0043g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-260-11761G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499949 | ||||||
| chr2:33500030
|
A | G | 122 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0098others(119): Show | 122 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.-260-11680A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500030 | ||||||
| chr2:33500212
|
T | C | 6 | a0001c0001t0002g0163a0001c0001t0002g0233a0001c0001t0003g0164others(3): Show | 6 | HG01109.hp2 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-11498T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500212 | ||||||
| chr2:33500381
|
T | C | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-11329T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500381 | ||||||
| chr2:33500385
|
A | T | 1 | a0007c0012t0015g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-260-11325A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500385 | ||||||
| chr2:33500419
|
G | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-11291G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500419 | ||||||
| chr2:33500630
|
T | C | 1 | a0001c0001t0010g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-260-11080T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500630 | ||||||
| chr2:33500639
|
A | T | 3 | a0001c0001t0009g0010a0001c0001t0021g0109a0001c0001t0021g0336 | 3 | HG01515.hp1 HG02258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-260-11071A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500639 | ||||||
| chr2:33500679
|
T | C | 3 | a0001c0001t0029g0307a0001c0001t0029g0308a0001c0001t0033g0280 | 3 | HG01256.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-260-11031T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500679 | ||||||
| chr2:33500709
|
G | A | 5 | a0001c0001t0011g0195a0001c0001t0027g0194a0001c0001t0050g0313others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-11001G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500709 | ||||||
| chr2:33500788
|
G | A | 2 | a0002c0005t0003g0206a0002c0005t0003g0216 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-260-10922G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500788 | ||||||
| chr2:33500802
|
C | T | 1 | a0001c0002t0001g0003 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-260-10908C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500802 | ||||||
| chr2:33500866
|
G | A | 35 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-10844G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500866 | ||||||
| chr2:33500875
|
A | G | 23 | a0001c0001t0003g0140a0001c0001t0004g0143a0001c0001t0009g0110others(20): Show | 23 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-10835A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500875 | ||||||
| chr2:33500910
|
G | A | 2 | a0001c0002t0001g0361a0001c0002t0006g0200 | 2 | HG06807.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-260-10800G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500910 | ||||||
| chr2:33500927
|
C | G | 1 | a0001c0001t0002g0247 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-260-10783C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500927 | ||||||
| chr2:33500936
|
AAAAT | A | 4 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155others(1): Show | 4 | HG00738.hp1 HG01496.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-10762_-260-10 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33500936 | |||||
| chr2:33501136
|
C | T | 5 | a0001c0001t0024g0074a0001c0001t0052g0303a0001c0002t0006g0153others(2): Show | 5 | HG02451.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-10574C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501136 | ||||||
| chr2:33501299
|
A | G | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-10411A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501299 | ||||||
| chr2:33501391
|
C | G | 35 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-10319C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501391 | ||||||
| chr2:33501393
|
A | G | 5 | a0001c0001t0002g0305a0001c0001t0003g0304a0001c0001t0009g0071others(2): Show | 5 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-10317A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501393 | ||||||
| chr2:33501403
|
G | A | 1 | a0001c0001t0023g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-260-10307G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501403 | ||||||
| chr2:33501543
|
C | T | 91 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(88): Show | 91 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.-260-10167C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501543 | ||||||
| chr2:33501546
|
C | T | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-260-10164C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501546 | ||||||
| chr2:33501577
|
C | T | 1 | a0001c0001t0007g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-260-10133C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501577 | ||||||
| chr2:33501657
|
G | A | 3 | a0001c0001t0001g0345a0001c0002t0001g0003a0001c0002t0001g0004 | 3 | HG00597.hp2 HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-260-10053G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501657 | ||||||
| chr2:33501692
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-260-10018C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501692 | ||||||
| chr2:33501799
|
C | T | 1 | a0001c0002t0006g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-9911C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501799 | ||||||
| chr2:33502059
|
G | T | 1 | a0001c0001t0002g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-260-9651G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502059 | ||||||
| chr2:33502246
|
C | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-9464C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502246 | ||||||
| chr2:33502310
|
G | T | 1 | a0001c0002t0001g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-260-9400G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502310 | ||||||
| chr2:33502443
|
A | T | 1 | a0001c0001t0027g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-260-9267A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502443 | ||||||
| chr2:33502501
|
C | CT | 89 | a0001c0001t0001g0061a0001c0001t0001g0115a0001c0001t0001g0161others(86): Show | 89 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.-260-9195dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33502501 | |||||
| chr2:33502501
|
C | CTT | 30 | a0001c0001t0001g0065a0001c0001t0001g0098a0001c0001t0001g0099others(27): Show | 30 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.-260-9196_-260-919 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33502501 | |||||
| chr2:33502542
|
T | G | 121 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0098others(118): Show | 121 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.-260-9168T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502542 | ||||||
| chr2:33502555
|
G | C | 4 | a0001c0001t0011g0195a0001c0001t0031g0141a0001c0001t0050g0313others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-9155G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502555 | ||||||
| chr2:33502584
|
C | G | 1 | a0001c0001t0035g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-260-9126C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502584 | ||||||
| chr2:33502599
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-260-9111G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502599 | ||||||
| chr2:33502604
|
C | T | 6 | a0001c0001t0011g0204a0001c0001t0013g0121a0001c0001t0058g0124others(3): Show | 6 | HG01255.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-9106C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502604 | ||||||
| chr2:33502606
|
G | A | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-260-9104G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502606 | ||||||
| chr2:33502621
|
T | C | 1 | a0001c0002t0001g0029 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-260-9089T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502621 | ||||||
| chr2:33502671
|
C | A | 2 | a0001c0001t0001g0107a0001c0002t0001g0364 | 2 | NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-260-9039C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502671 | ||||||
| chr2:33502784
|
G | A | 27 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0179others(24): Show | 27 | HG00544.hp2 HG01255.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-8926G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502784 | ||||||
| chr2:33502913
|
A | T | 64 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0031others(61): Show | 64 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.-260-8797A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502913 | ||||||
| chr2:33503048
|
T | G | 43 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(40): Show | 43 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-260-8662T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503048 | ||||||
| chr2:33503108
|
A | G | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0063g0288 | 3 | HG00621.hp1 HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.-260-8602A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503108 | ||||||
| chr2:33503138
|
G | C | 2 | a0001c0001t0011g0080a0001c0001t0044g0172 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-8572G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503138 | ||||||
| chr2:33503371
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-260-8339C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503371 | ||||||
| chr2:33503419
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0226others(6): Show | 9 | HG02129.hp1 HG02523.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-8291A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503419 | ||||||
| chr2:33503499
|
A | G | 35 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0179others(32): Show | 35 | HG00544.hp2 HG01255.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-8211A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503499 | ||||||
| chr2:33503526
|
G | T | 2 | a0001c0001t0003g0103a0001c0001t0003g0210 | 2 | HG00423.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-260-8184G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503526 | ||||||
| chr2:33503541
|
G | A | 2 | a0001c0001t0027g0194a0001c0004t0019g0042 | 2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-260-8169G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503541 | ||||||
| chr2:33503587
|
A | T | 13 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-8123A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503587 | ||||||
| chr2:33503592
|
C | CT | 49 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(46): Show | 49 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.-260-8108dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33503592 | |||||
| chr2:33503592
|
C | CTT | 46 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-260-8109_-260-810 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33503592 | |||||
| chr2:33503612
|
A | G | 2 | a0001c0001t0052g0303a0001c0002t0006g0153 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-260-8098A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503612 | ||||||
| chr2:33503832
|
C | T | 2 | a0001c0001t0011g0080a0001c0001t0044g0172 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-7878C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503832 | ||||||
| chr2:33504093
|
G | A | 9 | a0001c0001t0004g0143a0001c0001t0013g0240a0001c0001t0017g0238others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-260-7617G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504093 | ||||||
| chr2:33504188
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-260-7522C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504188 | ||||||
| chr2:33504391
|
C | T | 1 | a0003c0009t0049g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-7319C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504391 | ||||||
| chr2:33504555
|
T | C | 1 | a0001c0001t0023g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-260-7155T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504555 | ||||||
| chr2:33504607
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-260-7103T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504607 | ||||||
| chr2:33504722
|
C | G | 1 | a0001c0001t0010g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-260-6988C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504722 | ||||||
| chr2:33504745
|
T | C | 54 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0082others(51): Show | 54 | HG00423.hp1 HG00544.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.-260-6965T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504745 | ||||||
| chr2:33504793
|
A | T | 6 | a0001c0001t0004g0143a0001c0002t0006g0139a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-6917A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504793 | ||||||
| chr2:33505119
|
C | T | 19 | a0001c0001t0004g0129a0001c0001t0005g0177a0001c0001t0012g0123others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6591C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505119 | ||||||
| chr2:33505153
|
T | TCAC | 51 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(48): Show | 51 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-260-6533_-260-653 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | |||||
| chr2:33505153
|
T | TCACCAC | 10 | a0001c0001t0004g0129a0001c0001t0012g0123a0001c0003t0005g0040others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-260-6536_-260-653 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | |||||
| chr2:33505153
|
T | TCACCACC others(14): Show |
4 | a0001c0003t0005g0175a0001c0003t0005g0176a0001c0003t0005g0253others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-6551_-260-653 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | |||||
| chr2:33505153
|
T | TCATCAC | 14 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0213others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-6555_-260-655 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | |||||
| chr2:33505224
|
A | G | 47 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(44): Show | 47 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-260-6486A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505224 | ||||||
| chr2:33505291
|
C | T | 19 | a0001c0001t0004g0129a0001c0001t0005g0177a0001c0001t0012g0123others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6419C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505291 | ||||||
| chr2:33505299
|
A | AT | 40 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0082others(37): Show | 40 | HG00423.hp1 HG00544.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.-260-6395dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | |||||
| chr2:33505299
|
AT | A | 19 | a0001c0001t0001g0171a0001c0001t0002g0347a0001c0001t0003g0140others(16): Show | 19 | HG00738.hp2 HG01070.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6395delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | |||||
| chr2:33505299
|
ATT | A | 19 | a0001c0001t0004g0129a0001c0001t0005g0177a0001c0001t0012g0123others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6396_-260-639 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | |||||
| chr2:33505364
|
G | A | 8 | a0001c0001t0011g0195a0001c0001t0022g0259a0001c0001t0022g0260others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-6346G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505364 | ||||||
| chr2:33505395
|
C | T | 2 | a0001c0001t0011g0080a0001c0001t0044g0172 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-6315C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505395 | ||||||
| chr2:33505436
|
G | C | 1 | a0001c0001t0007g0335 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-260-6274G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505436 | ||||||
| chr2:33505558
|
T | C | 233 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0048others(230): Show | 233 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-260-6152T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505558 | ||||||
| chr2:33505606
|
C | T | 3 | a0001c0001t0013g0240a0001c0001t0017g0238a0001c0002t0006g0239 | 3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-260-6104C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505606 | ||||||
| chr2:33505633
|
G | A | 38 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(35): Show | 38 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-260-6077G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505633 | ||||||
| chr2:33505730
|
C | T | 4 | a0001c0001t0011g0195a0001c0001t0031g0141a0001c0001t0050g0313others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-5980C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505730 | ||||||
| chr2:33505873
|
A | G | 1 | a0001c0001t0004g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-260-5837A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505873 | ||||||
| chr2:33506173
|
A | G | 55 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0179others(52): Show | 55 | HG00423.hp1 HG00544.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.-260-5537A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506173 | ||||||
| chr2:33506175
|
C | A | 1 | a0001c0001t0004g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-260-5535C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506175 | ||||||
| chr2:33506367
|
T | A | 2 | a0001c0002t0006g0168a0001c0002t0006g0174 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-260-5343T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506367 | ||||||
| chr2:33506494
|
A | G | 18 | a0001c0001t0003g0140a0001c0001t0009g0110a0001c0001t0011g0077others(15): Show | 18 | HG01074.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-260-5216A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506494 | ||||||
| chr2:33506574
|
G | C | 146 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0067others(143): Show | 146 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-260-5136G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506574 | ||||||
| chr2:33506655
|
A | G | 3 | a0001c0001t0003g0041a0001c0001t0011g0312a0001c0002t0028g0137 | 3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-260-5055A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506655 | ||||||
| chr2:33506718
|
T | C | 1 | a0001c0001t0008g0220 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-260-4992T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506718 | ||||||
| chr2:33506879
|
G | A | 5 | a0001c0001t0011g0195a0001c0001t0027g0194a0001c0001t0031g0141others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-4831G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506879 | ||||||
| chr2:33506901
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-260-4809A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506901 | ||||||
| chr2:33506928
|
G | C | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-260-4782G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506928 | ||||||
| chr2:33506936
|
G | C | 1 | a0003c0009t0049g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-4774G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506936 | ||||||
| chr2:33506937
|
T | C | 1 | a0001c0001t0060g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-260-4773T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506937 | ||||||
| chr2:33507019
|
C | A | 1 | a0001c0002t0006g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-260-4691C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507019 | ||||||
| chr2:33507143
|
T | C | 1 | a0006c0013t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-260-4567T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507143 | ||||||
| chr2:33507193
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-260-4517C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507193 | ||||||
| chr2:33507198
|
C | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0228 | 2 | NA18984.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-260-4512C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507198 | ||||||
| chr2:33507211
|
A | G | 1 | a0001c0001t0015g0219 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-260-4499A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507211 | ||||||
| chr2:33507282
|
G | C | 4 | a0001c0002t0001g0236a0001c0002t0037g0271a0001c0002t0037g0272others(1): Show | 4 | HG00639.hp1 HG01928.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-4428G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507282 | ||||||
| chr2:33507379
|
A | G | 12 | a0001c0001t0001g0060a0001c0001t0001g0268a0001c0001t0001g0285others(9): Show | 12 | HG01175.hp1 HG01358.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-260-4331A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507379 | ||||||
| chr2:33507571
|
G | A | 2 | a0001c0002t0006g0167a0001c0004t0043g0201 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-260-4139G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507571 | ||||||
| chr2:33507573
|
A | T | 27 | a0001c0001t0001g0053a0001c0001t0001g0266a0001c0001t0001g0324others(24): Show | 27 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-4137A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507573 | ||||||
| chr2:33507595
|
G | T | 22 | a0001c0001t0004g0129a0001c0001t0011g0080a0001c0001t0011g0310others(19): Show | 22 | HG01255.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-260-4115G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507595 | ||||||
| chr2:33507629
|
G | A | 1 | a0001c0001t0002g0367 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-260-4081G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507629 | ||||||
| chr2:33507714
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0007g0320 | 2 | NA18993.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-260-3996T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507714 | ||||||
| chr2:33507715
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0007g0320 | 2 | NA18993.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-260-3995G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507715 | ||||||
| chr2:33507741
|
G | C | 17 | a0001c0001t0004g0143a0001c0001t0009g0110a0001c0001t0011g0077others(14): Show | 17 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-260-3969G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507741 | ||||||
| chr2:33507748
|
A | G | 3 | a0001c0001t0003g0302a0001c0001t0009g0215a0001c0001t0051g0299 | 3 | HG02615.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-260-3962A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507748 | ||||||
| chr2:33507751
|
C | A | 1 | a0001c0003t0026g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-260-3959C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507751 | ||||||
| chr2:33507805
|
C | T | 27 | a0001c0001t0003g0041a0001c0001t0004g0129a0001c0001t0011g0080others(24): Show | 27 | HG01255.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-3905C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507805 | ||||||
| chr2:33507860
|
A | G | 4 | a0001c0001t0009g0110a0001c0001t0011g0077a0001c0001t0011g0195others(1): Show | 4 | HG01074.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-3850A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507860 | ||||||
| chr2:33507877
|
G | A | 1 | a0001c0003t0005g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-260-3833G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507877 | ||||||
| chr2:33508031
|
G | T | 1 | a0001c0001t0035g0348 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-260-3679G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508031 | ||||||
| chr2:33508042
|
C | T | 4 | a0001c0001t0009g0017a0001c0001t0020g0142a0001c0001t0020g0148others(1): Show | 4 | HG01496.hp1 HG01516.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-3668C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508042 | ||||||
| chr2:33508117
|
G | A | 1 | a0001c0001t0009g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-260-3593G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508117 | ||||||
| chr2:33508129
|
C | T | 1 | a0001c0003t0005g0241 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-260-3581C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508129 | ||||||
| chr2:33508354
|
C | A | 25 | a0001c0001t0001g0053a0001c0001t0002g0037a0001c0001t0003g0011others(22): Show | 25 | HG00323.hp2 HG00423.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.-260-3356C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508354 | ||||||
| chr2:33508447
|
C | T | 23 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(20): Show | 23 | HG00323.hp2 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-3263C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508447 | ||||||
| chr2:33508480
|
G | A | 1 | a0001c0003t0005g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-3230G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508480 | ||||||
| chr2:33508487
|
T | C | 111 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0048others(108): Show | 111 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.-260-3223T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508487 | ||||||
| chr2:33508528
|
T | C | 1 | a0001c0002t0006g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-260-3182T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508528 | ||||||
| chr2:33508546
|
T | C | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-260-3164T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508546 | ||||||
| chr2:33508652
|
C | G | 300 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0045others(297): Show | 300 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.-260-3058C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508652 | ||||||
| chr2:33508660
|
G | A | 1 | a0001c0001t0024g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-260-3050G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508660 | ||||||
| chr2:33508686
|
T | G | 15 | a0001c0001t0001g0353a0001c0001t0002g0126a0001c0001t0002g0190others(12): Show | 15 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.-260-3024T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508686 | ||||||
| chr2:33508756
|
C | A | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-260-2954C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508756 | ||||||
| chr2:33508850
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-260-2860A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508850 | ||||||
| chr2:33508893
|
G | A | 1 | a0001c0001t0025g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-260-2817G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508893 | ||||||
| chr2:33508920
|
A | G | 2 | a0001c0002t0017g0147a0003c0011t0046g0202 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-260-2790A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508920 | ||||||
| chr2:33508942
|
T | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0234 | 3 | HG02015.hp2 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-260-2768T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508942 | ||||||
| chr2:33508976
|
G | A | 2 | a0001c0002t0017g0147a0003c0011t0046g0202 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-260-2734G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508976 | ||||||
| chr2:33508995
|
G | A | 16 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-2715G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508995 | ||||||
| chr2:33509055
|
G | C | 14 | a0001c0002t0001g0021a0001c0002t0001g0029a0001c0002t0001g0047others(11): Show | 14 | HG00558.hp1 HG00639.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-2655G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509055 | ||||||
| chr2:33509059
|
T | G | 16 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0003g0302others(13): Show | 16 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-2651T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509059 | ||||||
| chr2:33509141
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-260-2569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509141 | ||||||
| chr2:33509230
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0234others(6): Show | 9 | HG02015.hp2 HG02129.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-2480C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509230 | ||||||
| chr2:33509399
|
C | CA | 47 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(44): Show | 47 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-260-2299dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33509399 | |||||
| chr2:33509425
|
A | C | 1 | a0001c0002t0006g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-260-2285A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509425 | ||||||
| chr2:33509452
|
T | C | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-260-2258T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509452 | ||||||
| chr2:33509560
|
C | G | 2 | a0001c0001t0041g0322a0001c0001t0042g0122 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-260-2150C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509560 | ||||||
| chr2:33509762
|
C | G | 4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0110others(1): Show | 4 | HG01074.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-1948C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509762 | ||||||
| chr2:33509815
|
G | A | 285 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0082others(282): Show | 285 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.-260-1895G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509815 | ||||||
| chr2:33509840
|
A | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-1870A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509840 | ||||||
| chr2:33509899
|
A | G | 5 | a0001c0001t0002g0144a0001c0001t0002g0232a0001c0001t0002g0305others(2): Show | 5 | HG00323.hp1 HG00642.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-1811A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509899 | ||||||
| chr2:33510179
|
T | G | 1 | a0003c0009t0049g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-1531T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510179 | ||||||
| chr2:33510216
|
A | T | 4 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-1494A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510216 | ||||||
| chr2:33510243
|
C | G | 16 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-1467C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510243 | ||||||
| chr2:33510284
|
C | CA | 6 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(3): Show | 6 | HG01109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-1422dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33510284 | |||||
| chr2:33510324
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0039a0001c0001t0009g0071others(3): Show | 6 | HG01074.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-1386C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510324 | ||||||
| chr2:33510345
|
A | G | 4 | a0001c0001t0003g0302a0001c0001t0017g0120a0001c0001t0024g0159others(1): Show | 4 | HG03130.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-1365A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510345 | ||||||
| chr2:33510394
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-260-1316G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510394 | ||||||
| chr2:33510426
|
G | C | 1 | a0001c0002t0001g0366 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-260-1284G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510426 | ||||||
| chr2:33510490
|
G | C | 9 | a0001c0001t0003g0041a0001c0001t0003g0140a0001c0001t0011g0080others(6): Show | 9 | HG01256.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-1220G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510490 | ||||||
| chr2:33510493
|
C | T | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-260-1217C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510493 | ||||||
| chr2:33510780
|
T | A | 1 | a0001c0001t0025g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-260-930T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510780 | ||||||
| chr2:33510970
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-260-740T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510970 | ||||||
| chr2:33511009
|
C | A | 1 | a0001c0001t0052g0303 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-260-701C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511009 | ||||||
| chr2:33511010
|
G | A | 100 | a0001c0001t0001g0067a0001c0001t0001g0179a0001c0001t0001g0213others(97): Show | 100 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-260-700G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511010 | ||||||
| chr2:33511214
|
C | T | 280 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0100others(277): Show | 280 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-260-496C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511214 | ||||||
| chr2:33511289
|
T | G | 16 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-421T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511289 | ||||||
| chr2:33511321
|
T | A | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-260-389T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511321 | ||||||
| chr2:33511644
|
A | G | 6 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-66A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511644 | ||||||
| chr2:33511656
|
T | C | 15 | a0001c0001t0001g0353a0001c0001t0002g0126a0001c0001t0002g0190others(12): Show | 15 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.-260-54T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511656 | ||||||
| chr2:33511686
|
G | A | 1 | a0001c0002t0006g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-260-24G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511686 | ||||||
| chr2:33511922
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-128+80C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33511922 | ||||||
| chr2:33512022
|
G | A | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128+180G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512022 | ||||||
| chr2:33512039
|
C | T | 28 | a0001c0001t0001g0353a0001c0001t0002g0190a0001c0001t0003g0015others(25): Show | 28 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-128+197C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512039 | ||||||
| chr2:33512177
|
G | A | 127 | a0001c0001t0001g0067a0001c0001t0001g0179a0001c0001t0001g0183others(124): Show | 127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-128+335G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512177 | ||||||
| chr2:33512347
|
G | T | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+505G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512347 | ||||||
| chr2:33512364
|
C | G | 1 | a0001c0004t0043g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-128+522C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512364 | ||||||
| chr2:33512561
|
C | G | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+719C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512561 | ||||||
| chr2:33512633
|
C | T | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+791C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512633 | ||||||
| chr2:33512753
|
G | A | 2 | a0001c0001t0041g0322a0001c0001t0042g0122 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-128+911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512753 | ||||||
| chr2:33512820
|
T | A | 161 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(158): Show | 161 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-128+978T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512820 | ||||||
| chr2:33512884
|
A | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128+1042A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512884 | ||||||
| chr2:33512902
|
A | G | 121 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(118): Show | 121 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.-128+1060A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512902 | ||||||
| chr2:33512977
|
A | G | 17 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.-128+1135A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512977 | ||||||
| chr2:33513224
|
C | T | 1 | a0001c0002t0034g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-128+1382C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513224 | ||||||
| chr2:33513382
|
C | T | 6 | a0001c0001t0003g0302a0001c0001t0017g0120a0001c0001t0031g0125others(3): Show | 6 | HG02559.hp1 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128+1540C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513382 | ||||||
| chr2:33513483
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-127-1527T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513483 | ||||||
| chr2:33513546
|
C | T | 103 | a0001c0001t0001g0060a0001c0001t0001g0100a0001c0001t0001g0227others(100): Show | 103 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.-127-1464C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513546 | ||||||
| chr2:33514032
|
A | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-978A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514032 | ||||||
| chr2:33514230
|
T | G | 126 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(123): Show | 126 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.-127-780T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514230 | ||||||
| chr2:33514245
|
A | C | 14 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-765A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514245 | ||||||
| chr2:33514294
|
A | T | 5 | a0001c0001t0003g0302a0001c0001t0017g0120a0001c0001t0031g0125others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-716A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514294 | ||||||
| chr2:33514333
|
G | A | 1 | a0001c0001t0010g0019 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-127-677G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514333 | ||||||
| chr2:33514489
|
T | C | 159 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(156): Show | 159 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.-127-521T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514489 | ||||||
| chr2:33514505
|
C | CA | 94 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0060others(91): Show | 94 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.-127-483dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | |||||
| chr2:33514505
|
C | CAA | 116 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(113): Show | 116 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-127-484_-127-483d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | |||||
| chr2:33514505
|
C | CAAA | 42 | a0001c0001t0001g0100a0001c0001t0001g0213a0001c0001t0001g0317others(39): Show | 42 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-127-485_-127-483d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | |||||
| chr2:33514505
|
C | CAAAAA | 14 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0183others(11): Show | 14 | HG01993.hp1 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-487_-127-483d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | |||||
| chr2:33514505
|
C | CAAAAAA | 9 | a0001c0001t0001g0082a0001c0001t0003g0011a0001c0001t0003g0103others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-488_-127-483d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | |||||
| chr2:33514615
|
G | T | 1 | a0001c0001t0035g0348 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-127-395G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514615 | ||||||
| chr2:33514634
|
G | A | 1 | a0001c0001t0032g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-127-376G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514634 | ||||||
| chr2:33514677
|
A | G | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-127-333A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514677 | ||||||
| chr2:33514711
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-127-299A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514711 | ||||||
| chr2:33514725
|
A | T | 120 | a0001c0001t0001g0060a0001c0001t0001g0100a0001c0001t0001g0227others(117): Show | 120 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.-127-285A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514725 | ||||||
| chr2:33515211
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18961.hp2 | splice_region_variant&intron_variant | LOW | c.70+5G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515211 | ||||||
| chr2:33515259
|
T | G | 1 | a0001c0004t0019g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70+53T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515259 | ||||||
| chr2:33515322
|
G | T | 14 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+116G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515322 | ||||||
| chr2:33515351
|
C | G | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.70+145C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515351 | ||||||
| chr2:33515388
|
G | T | 3 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172 | 3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.70+182G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515388 | ||||||
| chr2:33515435
|
A | G | 1 | a0001c0001t0012g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70+229A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515435 | ||||||
| chr2:33515473
|
A | T | 2 | a0001c0001t0001g0045a0005c0014t0001g0007 | 2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.70+267A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515473 | ||||||
| chr2:33515662
|
T | C | 126 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0048others(123): Show | 126 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.70+456T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515662 | ||||||
| chr2:33515788
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.70+582C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515788 | ||||||
| chr2:33515921
|
T | A | 299 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(296): Show | 299 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.71-621T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515921 | ||||||
| chr2:33515941
|
A | T | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.71-601A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515941 | ||||||
| chr2:33516012
|
T | A | 1 | a0001c0004t0019g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71-530T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516012 | ||||||
| chr2:33516148
|
G | A | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71-394G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516148 | ||||||
| chr2:33516184
|
C | T | 48 | a0001c0001t0001g0060a0001c0001t0001g0227a0001c0001t0001g0269others(45): Show | 48 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.71-358C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516184 | ||||||
| chr2:33516225
|
T | C | 14 | a0001c0001t0001g0353a0001c0001t0002g0126a0001c0001t0002g0190others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-317T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516225 | ||||||
| chr2:33516268
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.71-274C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516268 | ||||||
| chr2:33516306
|
G | A | 1 | a0001c0004t0019g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71-236G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516306 | ||||||
| chr2:33516403
|
T | C | 34 | a0001c0001t0001g0030a0001c0001t0001g0183a0001c0001t0002g0037others(31): Show | 34 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-139T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516403 | ||||||
| chr2:33516469
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.71-73G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516469 | ||||||
| chr2:33516773
|
A | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+129A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516773 | ||||||
| chr2:33516893
|
G | C | 2 | a0001c0001t0004g0143a0001c0001t0058g0124 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173+249G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516893 | ||||||
| chr2:33516932
|
T | G | 1 | a0001c0001t0003g0304 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.173+288T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516932 | ||||||
| chr2:33517075
|
A | G | 3 | a0001c0001t0002g0190a0001c0001t0008g0180a0001c0001t0032g0235 | 3 | HG02698.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.173+431A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517075 | ||||||
| chr2:33517217
|
G | A | 285 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0100others(282): Show | 285 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.173+573G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517217 | ||||||
| chr2:33517435
|
G | T | 6 | a0001c0001t0003g0211a0001c0002t0004g0229a0001c0002t0004g0230others(3): Show | 6 | HG02071.hp2 HG02083.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.173+791G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517435 | ||||||
| chr2:33517925
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.173+1281C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517925 | ||||||
| chr2:33518109
|
G | A | 3 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172 | 3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.173+1465G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518109 | ||||||
| chr2:33518114
|
A | G | 169 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(166): Show | 169 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.173+1470A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518114 | ||||||
| chr2:33518261
|
C | T | 6 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.173+1617C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518261 | ||||||
| chr2:33518314
|
C | A | 11 | a0001c0001t0001g0353a0001c0001t0002g0126a0001c0001t0003g0015others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.174-1638C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518314 | ||||||
| chr2:33518612
|
C | G | 1 | a0001c0001t0002g0222 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.174-1340C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518612 | ||||||
| chr2:33518709
|
A | AT | 8 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.174-1232dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 33518709 | |||||
| chr2:33518738
|
C | T | 281 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0100others(278): Show | 281 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.174-1214C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518738 | ||||||
| chr2:33518743
|
A | G | 3 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172 | 3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.174-1209A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518743 | ||||||
| chr2:33518880
|
G | GTCA | 143 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(140): Show | 143 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.174-1069_174-1067d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 33518880 | |||||
| chr2:33518912
|
G | C | 12 | a0001c0001t0001g0353a0001c0001t0002g0190a0001c0001t0003g0015others(9): Show | 12 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-1040G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518912 | ||||||
| chr2:33519094
|
A | G | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-858A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519094 | ||||||
| chr2:33519113
|
T | G | 6 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.174-839T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519113 | ||||||
| chr2:33519171
|
T | A | 1 | a0001c0002t0006g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.174-781T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519171 | ||||||
| chr2:33519245
|
T | C | 1 | a0001c0002t0037g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.174-707T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519245 | ||||||
| chr2:33519248
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0327 | 2 | NA19005.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.174-704A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519248 | ||||||
| chr2:33519345
|
G | A | 2 | a0001c0001t0041g0322a0001c0001t0042g0122 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.174-607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519345 | ||||||
| chr2:33519355
|
A | G | 1 | a0001c0001t0008g0180 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.174-597A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519355 | ||||||
| chr2:33519383
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.174-569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519383 | ||||||
| chr2:33519413
|
A | G | 119 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0028others(116): Show | 119 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.174-539A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519413 | ||||||
| chr2:33519427
|
T | C | 7 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-525T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519427 | ||||||
| chr2:33519548
|
A | C | 16 | a0001c0001t0013g0301a0001c0002t0006g0134a0001c0002t0006g0139others(13): Show | 16 | HG00738.hp1 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.174-404A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519548 | ||||||
| chr2:33519621
|
T | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-331T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519621 | ||||||
| chr2:33519636
|
A | G | 1 | a0001c0002t0003g0291 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.174-316A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519636 | ||||||
| chr2:33519717
|
C | A | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.174-235C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519717 | ||||||
| chr2:33519735
|
T | G | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-217T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519735 | ||||||
| chr2:33519749
|
A | G | 14 | a0001c0001t0003g0302a0001c0001t0005g0177a0001c0001t0013g0121others(11): Show | 14 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.174-203A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519749 | ||||||
| chr2:33519853
|
A | C | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.174-99A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519853 | ||||||
| chr2:33519891
|
C | T | 142 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0100others(139): Show | 142 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.174-61C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519891 | ||||||
| chr2:33519905
|
T | C | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-47T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519905 | ||||||
| chr2:33519929
|
T | A | 1 | a0001c0001t0025g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.174-23T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519929 | ||||||
| chr2:33520043
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.236+29G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520043 | ||||||
| chr2:33520111
|
A | G | 8 | a0001c0001t0001g0044a0001c0001t0001g0234a0001c0001t0001g0262others(5): Show | 8 | HG01192.hp1 HG02015.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+97A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520111 | ||||||
| chr2:33520141
|
T | C | 144 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0061others(141): Show | 144 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.236+127T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520141 | ||||||
| chr2:33520224
|
C | T | 1 | a0001c0002t0001g0029 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.236+210C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520224 | ||||||
| chr2:33520269
|
T | C | 303 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(300): Show | 303 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.236+255T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520269 | ||||||
| chr2:33520335
|
A | G | 121 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(118): Show | 121 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.237-218A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520335 | ||||||
| chr2:33520341
|
G | C | 3 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172 | 3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.237-212G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520341 | ||||||
| chr2:33520420
|
A | T | 6 | a0001c0001t0002g0245a0001c0001t0003g0298a0001c0001t0003g0363others(3): Show | 6 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-133A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520420 | ||||||
| chr2:33520483
|
C | T | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.237-70C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520483 | ||||||
| chr2:33520824
|
C | T | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.368+140C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33520824 | ||||||
| chr2:33520918
|
C | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+234C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33520918 | ||||||
| chr2:33521099
|
A | G | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+415A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521099 | ||||||
| chr2:33521175
|
A | G | 1 | a0001c0002t0017g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.368+491A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521175 | ||||||
| chr2:33521266
|
C | T | 162 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0213others(159): Show | 162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.368+582C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521266 | ||||||
| chr2:33521276
|
AG | A | 3 | a0001c0001t0005g0177a0001c0001t0019g0311a0001c0004t0019g0118 | 3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.368+594delG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 33521276 | |||||
| chr2:33521407
|
C | T | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.369-548C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521407 | ||||||
| chr2:33521429
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.369-526C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521429 | ||||||
| chr2:33521739
|
T | A | 298 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0061others(295): Show | 298 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.369-216T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521739 | ||||||
| chr2:33521752
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369-203C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521752 | ||||||
| chr2:33521754
|
A | G | 2 | a0001c0001t0004g0145a0001c0001t0008g0185 | 2 | HG00639.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.369-201A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521754 | ||||||
| chr2:33521775
|
G | C | 117 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(114): Show | 117 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.369-180G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521775 | ||||||
| chr2:33521790
|
G | T | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.369-165G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521790 | ||||||
| chr2:33521934
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.369-21G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521934 | ||||||
| chr2:33522218
|
G | A | 298 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(295): Show | 298 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.516+116G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522218 | ||||||
| chr2:33522389
|
G | C | 1 | a0001c0001t0061g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.516+287G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522389 | ||||||
| chr2:33522470
|
G | A | 15 | a0001c0001t0001g0268a0001c0001t0001g0353a0001c0001t0002g0190others(12): Show | 15 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+368G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522470 | ||||||
| chr2:33522498
|
A | G | 301 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0060others(298): Show | 301 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.516+396A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522498 | ||||||
| chr2:33522519
|
T | C | 114 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(111): Show | 114 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.516+417T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522519 | ||||||
| chr2:33522571
|
A | T | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.516+469A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522571 | ||||||
| chr2:33522677
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0003g0242a0001c0001t0018g0249 | 3 | NA18946.hp2 NA18954.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.516+575T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522677 | ||||||
| chr2:33522685
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+583C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522685 | ||||||
| chr2:33522709
|
T | C | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.516+607T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522709 | ||||||
| chr2:33522744
|
G | T | 2 | a0001c0001t0001g0353a0008c0010t0008g0319 | 2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.516+642G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522744 | ||||||
| chr2:33522762
|
C | T | 1 | a0001c0001t0038g0282 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.516+660C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522762 | ||||||
| chr2:33522801
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.516+699C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522801 | ||||||
| chr2:33522925
|
C | T | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.516+823C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522925 | ||||||
| chr2:33522927
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+825C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522927 | ||||||
| chr2:33523105
|
T | C | 1 | a0001c0001t0054g0036 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-774T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523105 | ||||||
| chr2:33523132
|
G | A | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-747G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523132 | ||||||
| chr2:33523195
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.517-684C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523195 | ||||||
| chr2:33523245
|
T | C | 1 | a0001c0001t0048g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.517-634T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523245 | ||||||
| chr2:33523281
|
G | A | 106 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.517-598G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523281 | ||||||
| chr2:33523319
|
G | T | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-560G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523319 | ||||||
| chr2:33523429
|
C | T | 1 | a0001c0001t0057g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.517-450C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523429 | ||||||
| chr2:33523449
|
G | A | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.517-430G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523449 | ||||||
| chr2:33523450
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.517-429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523450 | ||||||
| chr2:33523461
|
TA | T | 94 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0268others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.517-402delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 33523461 | |||||
| chr2:33523461
|
TAA | T | 110 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(107): Show | 110 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.517-403_517-402del others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 33523461 | |||||
| chr2:33523649
|
G | A | 87 | a0001c0001t0001g0183a0001c0001t0001g0268a0001c0001t0001g0353others(84): Show | 87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.517-230G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523649 | ||||||
| chr2:33523771
|
A | G | 112 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(109): Show | 112 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.517-108A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523771 | ||||||
| chr2:33523784
|
C | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0250a0001c0001t0002g0355 | 3 | NA18612.hp1 NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.517-95C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523784 | ||||||
| chr2:33523834
|
A | G | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.517-45A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523834 | ||||||
| chr2:33523846
|
A | G | 18 | a0001c0001t0001g0030a0001c0001t0002g0037a0001c0001t0005g0177others(15): Show | 18 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.517-33A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523846 | ||||||
| chr2:33524078
|
C | G | 8 | a0001c0001t0005g0177a0001c0001t0009g0215a0001c0001t0013g0121others(5): Show | 8 | HG02280.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+26C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524078 | ||||||
| chr2:33524147
|
G | A | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+95G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524147 | ||||||
| chr2:33524390
|
A | G | 5 | a0001c0001t0013g0121a0001c0001t0013g0166a0001c0001t0013g0240others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-42A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524390 | ||||||
| chr2:33524693
|
A | T | 1 | a0001c0001t0007g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.807+145A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33524693 | ||||||
| chr2:33525080
|
C | CA | 10 | a0001c0001t0001g0059a0001c0001t0001g0333a0001c0001t0001g0334others(7): Show | 10 | HG02451.hp2 HG03041.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.807+545dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525080 | |||||
| chr2:33525095
|
C | CA | 14 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0115others(11): Show | 14 | HG02257.hp1 HG02280.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+564dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525095 | |||||
| chr2:33525106
|
A | T | 189 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(186): Show | 189 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.807+558A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525106 | ||||||
| chr2:33525341
|
A | AAT | 162 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0082others(159): Show | 162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.807+808_807+809dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525341 | |||||
| chr2:33525388
|
G | A | 100 | a0001c0001t0001g0100a0001c0001t0001g0227a0001c0001t0001g0266others(97): Show | 100 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.807+840G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525388 | ||||||
| chr2:33525571
|
A | G | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807+1023A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525571 | ||||||
| chr2:33525578
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | NA18945.hp2 NA18989.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+1030G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525578 | ||||||
| chr2:33525699
|
C | CA | 33 | a0001c0001t0001g0044a0001c0001t0001g0052a0001c0001t0001g0059others(30): Show | 33 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.807+1179dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
C | CAA | 48 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0082others(45): Show | 48 | HG00323.hp2 HG00423.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.807+1178_807+1179d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
C | CAAA | 42 | a0001c0001t0001g0030a0001c0001t0001g0083a0001c0001t0001g0183others(39): Show | 42 | HG00438.hp1 HG01175.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+1177_807+1179d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
C | CAAAA | 7 | a0001c0001t0003g0302a0001c0001t0023g0138a0001c0001t0032g0316others(4): Show | 7 | HG01109.hp1 HG01256.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+1176_807+1179d others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
CA | C | 45 | a0001c0001t0001g0227a0001c0001t0001g0266a0001c0001t0002g0013others(42): Show | 45 | HG00438.hp2 HG00642.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.807+1179delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
CAA | C | 60 | a0001c0001t0001g0100a0001c0001t0001g0345a0001c0001t0002g0006others(57): Show | 60 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+1178_807+1179d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525699
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0016g0369a0001c0001t0030g0051a0001c0001t0030g0362 | 3 | HG02074.hp2 HG03669.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.807+1170_807+1179d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | |||||
| chr2:33525726
|
A | AAC | 30 | a0001c0001t0001g0014a0001c0001t0001g0318a0001c0001t0022g0259others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.807+1179_807+1180d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525726 | |||||
| chr2:33525726
|
A | AC | 37 | a0001c0001t0001g0213a0001c0001t0022g0260a0001c0002t0001g0003others(34): Show | 37 | HG00609.hp1 HG01255.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.807+1178_807+1179i others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525726 | ||||||
| chr2:33525726
|
A | C | 4 | a0001c0001t0016g0369a0001c0001t0030g0051a0001c0001t0030g0362others(1): Show | 4 | HG02074.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+1178A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525726 | ||||||
| chr2:33525737
|
T | TGTGGCA | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.807+1193_807+1198d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525737 | |||||
| chr2:33525804
|
G | C | 1 | a0001c0001t0065g0357 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.807+1256G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525804 | ||||||
| chr2:33525920
|
C | T | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.808-1217C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525920 | ||||||
| chr2:33525995
|
A | G | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.808-1142A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525995 | ||||||
| chr2:33526105
|
G | A | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.808-1032G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526105 | ||||||
| chr2:33526151
|
A | G | 1 | a0003c0009t0049g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.808-986A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526151 | ||||||
| chr2:33526276
|
A | G | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.808-861A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526276 | ||||||
| chr2:33526348
|
C | T | 1 | a0001c0001t0024g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-789C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526348 | ||||||
| chr2:33526414
|
G | A | 123 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(120): Show | 123 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.808-723G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526414 | ||||||
| chr2:33526553
|
T | C | 1 | a0001c0001t0007g0076 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.808-584T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526553 | ||||||
| chr2:33526597
|
C | T | 58 | a0001c0001t0001g0183a0001c0001t0003g0011a0001c0001t0003g0012others(55): Show | 58 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.808-540C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526597 | ||||||
| chr2:33526783
|
C | A | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.808-354C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526783 | ||||||
| chr2:33526810
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.808-327C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526810 | ||||||
| chr2:33526866
|
A | G | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.808-271A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526866 | ||||||
| chr2:33527062
|
GC | G | 58 | a0001c0001t0001g0183a0001c0001t0003g0011a0001c0001t0003g0012others(55): Show | 58 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.808-73delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33527062 | |||||
| chr2:33527085
|
G | T | 3 | a0001c0001t0002g0037a0001c0001t0032g0316a0001c0001t0033g0280 | 3 | HG01175.hp1 HG01256.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.808-52G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33527085 | ||||||
| chr2:33528012
|
T | G | 8 | a0001c0001t0001g0030a0001c0001t0002g0037a0001c0001t0032g0316others(5): Show | 8 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+600T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528012 | ||||||
| chr2:33528112
|
T | A | 367 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0022others(364): Show | 367 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(364): Show |
intron_variant | MODIFIER | c.1083+700T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528112 | ||||||
| chr2:33528143
|
C | T | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+731C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528143 | ||||||
| chr2:33528187
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1083+775G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528187 | ||||||
| chr2:33528196
|
C | T | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1083+784C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528196 | ||||||
| chr2:33528299
|
G | A | 176 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0001t0001g0179others(173): Show | 176 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.1083+887G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528299 | ||||||
| chr2:33528306
|
C | A | 1 | a0001c0003t0005g0241 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1083+894C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528306 | ||||||
| chr2:33528330
|
T | C | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1083+918T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528330 | ||||||
| chr2:33528545
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1083+1133A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528545 | ||||||
| chr2:33528670
|
T | C | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1083+1258T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528670 | ||||||
| chr2:33528971
|
G | A | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1083+1559G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528971 | ||||||
| chr2:33529027
|
A | G | 1 | a0001c0001t0019g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1083+1615A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529027 | ||||||
| chr2:33529054
|
C | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+1642C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529054 | ||||||
| chr2:33529115
|
G | C | 1 | a0001c0001t0032g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1083+1703G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529115 | ||||||
| chr2:33529215
|
C | T | 1 | a0001c0001t0019g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1083+1803C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529215 | ||||||
| chr2:33529222
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1083+1810T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529222 | ||||||
| chr2:33529232
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0334 | 2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1820A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529232 | ||||||
| chr2:33529240
|
A | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0334 | 2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1828A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529240 | ||||||
| chr2:33529241
|
T | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0334 | 2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1829T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529241 | ||||||
| chr2:33529242
|
T | C | 1 | a0001c0001t0021g0336 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1083+1830T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529242 | ||||||
| chr2:33529261
|
A | G | 302 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0061others(299): Show | 302 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.1083+1849A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529261 | ||||||
| chr2:33529269
|
C | A | 71 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0002g0037others(68): Show | 71 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1083+1857C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529269 | ||||||
| chr2:33529318
|
C | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0353others(81): Show | 84 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1083+1906C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529318 | ||||||
| chr2:33529319
|
G | C | 114 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(111): Show | 114 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1083+1907G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529319 | ||||||
| chr2:33529474
|
C | G | 1 | a0001c0002t0003g0075 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1083+2062C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529474 | ||||||
| chr2:33529487
|
C | CAAAAAAA others(8): Show |
10 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0058others(7): Show | 10 | HG01993.hp2 NA18942.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(19): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(9): Show |
72 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0001t0001g0184others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(10): Show |
76 | a0001c0001t0001g0318a0001c0001t0001g0345a0001c0001t0002g0066others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(11): Show |
61 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0213others(58): Show | 61 | HG01081.hp2 HG01192.hp2 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(12): Show |
21 | a0001c0001t0002g0367a0001c0001t0003g0103a0001c0001t0003g0304others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(13): Show |
11 | a0001c0001t0002g0037a0001c0001t0003g0062a0001c0001t0015g0219others(8): Show | 11 | HG00323.hp2 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0020g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0003g0302a0001c0001t0027g0199 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0027g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(27): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0026g0196a0001c0001t0044g0172 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(28): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(18): Show |
6 | a0001c0001t0008g0035a0001c0001t0008g0180a0001c0001t0013g0121others(3): Show | 6 | HG02280.hp1 HG02698.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(29): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(19): Show |
6 | a0001c0001t0009g0215a0001c0001t0013g0166a0001c0001t0013g0300others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(30): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(31): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(21): Show |
7 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0185others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(32): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(22): Show |
3 | a0001c0001t0001g0268a0001c0001t0008g0034a0001c0004t0019g0042 | 3 | HG03579.hp2 NA18949.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0001g0353a0001c0004t0043g0201 | 2 | HG00544.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(34): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529487
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(36): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | |||||
| chr2:33529802
|
C | A | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+2390C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529802 | ||||||
| chr2:33529859
|
CA | C | 71 | a0001c0001t0001g0213a0001c0001t0001g0318a0001c0001t0001g0345others(68): Show | 71 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1083+2449delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529859 | |||||
| chr2:33530014
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1083+2602A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530014 | ||||||
| chr2:33530083
|
C | T | 6 | a0001c0001t0004g0145a0001c0001t0008g0034a0001c0001t0008g0185others(3): Show | 6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2671C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530083 | ||||||
| chr2:33530110
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1083+2698C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530110 | ||||||
| chr2:33530214
|
T | A | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083+2802T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530214 | ||||||
| chr2:33530235
|
T | G | 8 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+2823T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530235 | ||||||
| chr2:33530271
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1083+2859A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530271 | ||||||
| chr2:33530338
|
C | G | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1083+2926C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530338 | ||||||
| chr2:33530358
|
G | A | 7 | a0001c0001t0011g0077a0001c0001t0011g0080a0001c0001t0011g0204others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+2946G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530358 | ||||||
| chr2:33530393
|
GTTTTCAC others(5): Show |
G | 17 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1083+2990_1083+300 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530393 | |||||
| chr2:33530489
|
G | A | 2 | a0001c0001t0026g0196a0003c0009t0049g0070 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+3077G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530489 | ||||||
| chr2:33530497
|
C | CT | 12 | a0001c0001t0001g0100a0001c0001t0002g0066a0001c0001t0002g0315others(9): Show | 12 | HG01109.hp1 HG01255.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+3109dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | |||||
| chr2:33530497
|
CT | C | 87 | a0001c0001t0001g0045a0001c0001t0001g0179a0001c0001t0001g0183others(84): Show | 87 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1083+3109delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | |||||
| chr2:33530497
|
CTT | C | 16 | a0001c0001t0003g0062a0001c0001t0003g0302a0001c0001t0012g0123others(13): Show | 16 | HG00323.hp2 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1083+3108_1083+310 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | |||||
| chr2:33530564
|
A | C | 3 | a0001c0001t0051g0299a0001c0004t0019g0042a0001c0004t0043g0201 | 3 | HG03130.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1083+3152A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530564 | ||||||
| chr2:33530702
|
A | T | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1083+3290A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530702 | ||||||
| chr2:33530740
|
G | A | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+3328G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530740 | ||||||
| chr2:33530792
|
C | G | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1083+3380C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530792 | ||||||
| chr2:33530852
|
CT | C | 196 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(193): Show | 196 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1083+3442delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530852 | |||||
| chr2:33530930
|
T | C | 290 | a0001c0001t0001g0100a0001c0001t0001g0179a0001c0001t0001g0183others(287): Show | 290 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.1084-3393T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530930 | ||||||
| chr2:33531083
|
G | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1084-3240G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531083 | ||||||
| chr2:33531159
|
A | G | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1084-3164A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531159 | ||||||
| chr2:33531164
|
G | A | 2 | a0001c0001t0042g0122a0003c0011t0046g0202 | 2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1084-3159G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531164 | ||||||
| chr2:33531248
|
C | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1084-3075C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531248 | ||||||
| chr2:33531316
|
T | C | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-3007T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531316 | ||||||
| chr2:33531341
|
C | A | 272 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0179others(269): Show | 272 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.1084-2982C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531341 | ||||||
| chr2:33531421
|
G | A | 16 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(13): Show | 16 | HG00639.hp2 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-2902G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531421 | ||||||
| chr2:33531453
|
C | T | 66 | a0001c0001t0001g0183a0001c0001t0002g0037a0001c0001t0003g0011others(63): Show | 66 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1084-2870C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531453 | ||||||
| chr2:33531511
|
T | C | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-2812T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531511 | ||||||
| chr2:33531665
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0003g0062 | 2 | HG00323.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1084-2658T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531665 | ||||||
| chr2:33531683
|
T | C | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2640T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531683 | ||||||
| chr2:33531909
|
G | GTCAGGAG others(50): Show |
3 | a0001c0004t0019g0042a0001c0004t0019g0118a0001c0004t0043g0201 | 3 | HG01884.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-2374_1084-237 others(61): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531909 | |||||
| chr2:33531995
|
CTCTT | C | 11 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(8): Show | 11 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-2326_1084-232 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531995 | |||||
| chr2:33531997
|
C | CTTTA | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2320_1084-231 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531997 | |||||
| chr2:33532048
|
A | G | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1084-2275A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532048 | ||||||
| chr2:33532148
|
C | T | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1084-2175C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532148 | ||||||
| chr2:33532168
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0059 | 2 | NA18945.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1084-2155G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532168 | ||||||
| chr2:33532270
|
A | G | 1 | a0003c0011t0046g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1084-2053A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532270 | ||||||
| chr2:33532401
|
C | A | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-1922C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532401 | ||||||
| chr2:33532426
|
C | T | 1 | a0001c0001t0020g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1084-1897C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532426 | ||||||
| chr2:33532487
|
C | A | 166 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(163): Show | 166 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1084-1836C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532487 | ||||||
| chr2:33532575
|
G | A | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1748G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532575 | ||||||
| chr2:33532653
|
C | G | 4 | a0001c0001t0023g0138a0001c0001t0023g0154a0001c0001t0044g0172others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1670C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532653 | ||||||
| chr2:33532718
|
G | A | 189 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(186): Show | 189 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1084-1605G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532718 | ||||||
| chr2:33532746
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1084-1577T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532746 | ||||||
| chr2:33532771
|
C | T | 2 | a0001c0001t0008g0035a0001c0002t0001g0116 | 2 | HG04228.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1084-1552C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532771 | ||||||
| chr2:33532908
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1084-1415G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532908 | ||||||
| chr2:33532909
|
A | T | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1084-1414A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532909 | ||||||
| chr2:33533270
|
T | C | 6 | a0001c0001t0004g0145a0001c0001t0008g0034a0001c0001t0008g0185others(3): Show | 6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-1053T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533270 | ||||||
| chr2:33533272
|
T | C | 14 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(11): Show | 14 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1084-1051T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533272 | ||||||
| chr2:33533281
|
C | T | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-1042C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533281 | ||||||
| chr2:33533388
|
C | T | 10 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-935C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533388 | ||||||
| chr2:33533389
|
G | A | 103 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0001t0001g0184others(100): Show | 103 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1084-934G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533389 | ||||||
| chr2:33533463
|
A | G | 1 | a0001c0001t0040g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1084-860A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533463 | ||||||
| chr2:33533626
|
G | A | 17 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1084-697G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533626 | ||||||
| chr2:33533670
|
C | T | 5 | a0001c0001t0002g0046a0001c0001t0002g0073a0001c0001t0002g0163others(2): Show | 5 | HG01109.hp2 HG01123.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084-653C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533670 | ||||||
| chr2:33533731
|
C | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0339a0009c0015t0002g0038 | 3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1084-592C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533731 | ||||||
| chr2:33533989
|
A | G | 7 | a0001c0001t0011g0077a0001c0001t0011g0080a0001c0001t0011g0204others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-334A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533989 | ||||||
| chr2:33533997
|
T | C | 1 | a0001c0002t0004g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1084-326T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533997 | ||||||
| chr2:33534062
|
A | C | 6 | a0001c0001t0044g0172a0001c0001t0057g0079a0001c0004t0019g0042others(3): Show | 6 | HG01884.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-261A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534062 | ||||||
| chr2:33534119
|
C | T | 1 | a0006c0013t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1084-204C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534119 | ||||||
| chr2:33534224
|
A | G | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1084-99A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534224 | ||||||
| chr2:33534291
|
C | T | 1 | a0001c0001t0024g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1084-32C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534291 | ||||||
| chr2:33534303
|
C | G | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1084-20C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534303 | ||||||
| chr2:33534496
|
G | A | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+96G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534496 | ||||||
| chr2:33534534
|
T | C | 18 | a0001c0001t0052g0303a0001c0003t0005g0040a0001c0003t0005g0119others(15): Show | 18 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+134T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534534 | ||||||
| chr2:33534644
|
T | C | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1161+244T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534644 | ||||||
| chr2:33534671
|
G | A | 7 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(4): Show | 7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+271G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534671 | ||||||
| chr2:33534676
|
A | G | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1161+276A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534676 | ||||||
| chr2:33534694
|
A | AT | 93 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0083others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1161+314dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | |||||
| chr2:33534694
|
A | ATT | 18 | a0001c0001t0001g0213a0001c0001t0003g0041a0001c0001t0003g0211others(15): Show | 18 | HG01496.hp1 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+313_1161+314d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | |||||
| chr2:33534694
|
A | ATTT | 6 | a0001c0003t0005g0119a0001c0003t0005g0175a0001c0003t0005g0176others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+312_1161+314d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | |||||
| chr2:33534694
|
AT | A | 19 | a0001c0001t0001g0061a0001c0001t0001g0161a0001c0001t0002g0111others(16): Show | 19 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+314delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | |||||
| chr2:33534740
|
C | A | 15 | a0001c0001t0052g0303a0001c0003t0005g0040a0001c0003t0005g0119others(12): Show | 15 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161+340C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534740 | ||||||
| chr2:33534754
|
C | T | 72 | a0001c0001t0001g0345a0001c0001t0017g0120a0001c0001t0017g0238others(69): Show | 72 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1161+354C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534754 | ||||||
| chr2:33534755
|
G | A | 18 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(15): Show | 18 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+355G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534755 | ||||||
| chr2:33534765
|
G | A | 1 | a0001c0001t0013g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1161+365G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534765 | ||||||
| chr2:33534792
|
C | T | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1161+392C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534792 | ||||||
| chr2:33534836
|
C | T | 8 | a0001c0001t0002g0349a0001c0001t0005g0177a0001c0001t0013g0121others(5): Show | 8 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+436C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534836 | ||||||
| chr2:33535051
|
T | C | 1 | a0001c0001t0045g0106 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1161+651T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535051 | ||||||
| chr2:33535099
|
A | G | 1 | a0001c0002t0006g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1161+699A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535099 | ||||||
| chr2:33535124
|
A | G | 3 | a0001c0001t0004g0089a0001c0001t0004g0150a0002c0007t0008g0081 | 3 | HG03831.hp1 HG03942.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1161+724A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535124 | ||||||
| chr2:33535186
|
G | A | 2 | a0001c0001t0042g0122a0003c0011t0046g0202 | 2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1161+786G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535186 | ||||||
| chr2:33535209
|
G | A | 270 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(267): Show | 270 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.1161+809G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535209 | ||||||
| chr2:33535265
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1161+865T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535265 | ||||||
| chr2:33535295
|
T | C | 1 | a0001c0001t0012g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1161+895T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535295 | ||||||
| chr2:33535348
|
T | G | 1 | a0001c0001t0045g0106 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1161+948T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535348 | ||||||
| chr2:33535368
|
G | A | 1 | a0001c0002t0001g0343 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1161+968G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535368 | ||||||
| chr2:33535426
|
C | A | 1 | a0001c0002t0001g0236 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1161+1026C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535426 | ||||||
| chr2:33535531
|
G | A | 3 | a0001c0001t0002g0108a0001c0001t0002g0339a0009c0015t0002g0038 | 3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1161+1131G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535531 | ||||||
| chr2:33535555
|
G | GC | 4 | a0001c0001t0001g0030a0001c0001t0042g0122a0003c0011t0046g0202others(1): Show | 4 | HG02300.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+1157dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33535555 | |||||
| chr2:33535558
|
G | A | 1 | a0001c0001t0036g0274 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1161+1158G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535558 | ||||||
| chr2:33535698
|
C | A | 2 | a0001c0001t0007g0064a0001c0001t0007g0068 | 2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1161+1298C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535698 | ||||||
| chr2:33535752
|
C | T | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1161+1352C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535752 | ||||||
| chr2:33535793
|
A | G | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1161+1393A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535793 | ||||||
| chr2:33535826
|
G | T | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+1426G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535826 | ||||||
| chr2:33535943
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0020g0142a0001c0001t0020g0148others(6): Show | 9 | HG01496.hp1 HG02300.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161+1543T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535943 | ||||||
| chr2:33535944
|
C | T | 196 | a0001c0001t0001g0030a0001c0001t0001g0100a0001c0001t0001g0183others(193): Show | 196 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1161+1544C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535944 | ||||||
| chr2:33536038
|
C | T | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1161+1638C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536038 | ||||||
| chr2:33536068
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1161+1668C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536068 | ||||||
| chr2:33536148
|
A | G | 2 | a0001c0001t0044g0172a0001c0001t0057g0079 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1161+1748A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536148 | ||||||
| chr2:33536159
|
G | A | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1161+1759G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536159 | ||||||
| chr2:33536207
|
C | T | 100 | a0001c0001t0001g0100a0001c0001t0001g0227a0001c0001t0001g0266others(97): Show | 100 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1161+1807C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536207 | ||||||
| chr2:33536267
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1161+1867A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536267 | ||||||
| chr2:33536312
|
A | T | 1 | a0001c0003t0005g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1161+1912A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536312 | ||||||
| chr2:33536322
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1161+1922G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536322 | ||||||
| chr2:33536322
|
G | GA | 136 | a0001c0001t0001g0014a0001c0001t0001g0065a0001c0001t0001g0082others(133): Show | 136 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1161+1937dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33536322 | |||||
| chr2:33536322
|
GA | G | 105 | a0001c0001t0001g0100a0001c0001t0001g0227a0001c0001t0001g0266others(102): Show | 105 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.1161+1937delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33536322 | |||||
| chr2:33536337
|
A | G | 1 | a0001c0001t0002g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1161+1937A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536337 | ||||||
| chr2:33536339
|
G | A | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1161+1939G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536339 | ||||||
| chr2:33536392
|
C | T | 1 | a0002c0007t0008g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1161+1992C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536392 | ||||||
| chr2:33536393
|
G | A | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+1993G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536393 | ||||||
| chr2:33536474
|
C | T | 5 | a0001c0001t0017g0120a0001c0001t0017g0238a0001c0001t0023g0138others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+2074C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536474 | ||||||
| chr2:33536490
|
T | C | 6 | a0001c0001t0016g0369a0001c0001t0030g0051a0001c0001t0030g0362others(3): Show | 6 | HG02074.hp2 HG02132.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2090T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536490 | ||||||
| chr2:33536526
|
G | A | 48 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(45): Show | 48 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1161+2126G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536526 | ||||||
| chr2:33536528
|
G | A | 48 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(45): Show | 48 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1161+2128G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536528 | ||||||
| chr2:33536851
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1162-2243C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536851 | ||||||
| chr2:33536857
|
G | T | 1 | a0001c0001t0003g0363 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1162-2237G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536857 | ||||||
| chr2:33536952
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1162-2142G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536952 | ||||||
| chr2:33536970
|
T | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0345a0001c0001t0016g0369others(54): Show | 57 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1162-2124T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536970 | ||||||
| chr2:33537192
|
G | GAT | 60 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(57): Show | 60 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1162-1885_1162-188 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537192 | |||||
| chr2:33537265
|
A | T | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1162-1829A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537265 | ||||||
| chr2:33537305
|
T | TAC | 6 | a0001c0001t0008g0180a0001c0001t0008g0220a0001c0001t0008g0244others(3): Show | 6 | HG01070.hp1 HG02698.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1774_1162-177 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537305 | |||||
| chr2:33537305
|
T | TACAC | 11 | a0001c0001t0002g0006a0001c0001t0002g0108a0001c0001t0002g0250others(8): Show | 11 | HG03130.hp1 HG03195.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162-1776_1162-177 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537305 | |||||
| chr2:33537318
|
A | C | 2 | a0001c0001t0024g0074a0001c0001t0040g0128 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-1776A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537318 | ||||||
| chr2:33537320
|
A | ACACACAC | 9 | a0001c0001t0007g0056a0001c0001t0007g0068a0001c0001t0007g0104others(6): Show | 9 | HG01168.hp2 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACACC | 4 | a0001c0001t0013g0121a0001c0001t0013g0166a0001c0001t0013g0300others(1): Show | 4 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACACCA others(3): Show |
2 | a0001c0001t0002g0245a0001c0002t0001g0350 | 2 | HG00544.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACACCA others(5): Show |
1 | a0001c0002t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1162-1773_1162-177 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACACCC | 21 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0046others(18): Show | 21 | HG01074.hp2 HG01123.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACACCC others(1): Show |
12 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0102others(9): Show | 12 | HG00323.hp1 HG00642.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACACCC | 4 | a0001c0001t0008g0185a0001c0001t0022g0259a0001c0001t0022g0260others(1): Show | 4 | HG01109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACCAC | 6 | a0001c0001t0002g0126a0001c0001t0002g0224a0001c0001t0010g0019others(3): Show | 6 | HG00438.hp2 HG02451.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACCACC | 12 | a0001c0001t0001g0227a0001c0001t0001g0263a0001c0001t0002g0187others(9): Show | 12 | HG01192.hp2 HG02027.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACCACCC | 30 | a0001c0001t0001g0061a0001c0001t0001g0161a0001c0001t0001g0162others(27): Show | 30 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | ACCACCCC | 5 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0003g0164others(2): Show | 5 | HG03017.hp1 HG03710.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | |||||
| chr2:33537320
|
A | C | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-1774A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537320 | ||||||
| chr2:33537321
|
C | CA | 3 | a0001c0001t0002g0190a0001c0001t0008g0034a0001c0001t0008g0035 | 3 | HG03834.hp2 HG04228.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | ||||||
| chr2:33537321
|
C | CACA | 46 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | ||||||
| chr2:33537321
|
C | CACACA | 6 | a0001c0001t0011g0077a0001c0001t0011g0080a0001c0001t0011g0204others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | ||||||
| chr2:33537322
|
C | A | 28 | a0001c0001t0005g0177a0001c0001t0012g0123a0001c0001t0012g0127others(25): Show | 28 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.1162-1772C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537322 | ||||||
| chr2:33537323
|
G | A | 6 | a0001c0001t0002g0347a0001c0001t0003g0363a0001c0001t0011g0077others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1771G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537323 | ||||||
| chr2:33537323
|
G | C | 297 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0061others(294): Show | 297 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.1162-1771G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537323 | ||||||
| chr2:33537326
|
C | CA | 4 | a0001c0002t0001g0112a0001c0002t0001g0207a0001c0002t0001g0354others(1): Show | 4 | NA18993.hp2 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-1768_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537326 | ||||||
| chr2:33537328
|
C | A | 4 | a0001c0002t0001g0112a0001c0002t0001g0207a0001c0002t0001g0354others(1): Show | 4 | NA18993.hp2 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-1766C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | ||||||
| chr2:33537328
|
C | CA | 44 | a0001c0001t0001g0345a0001c0001t0016g0369a0001c0001t0030g0051others(41): Show | 44 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1162-1766_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | ||||||
| chr2:33537328
|
C | CACA | 3 | a0001c0002t0001g0223a0001c0002t0001g0361a0001c0002t0016g0205 | 3 | HG02132.hp2 NA19060.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1162-1766_1162-176 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | ||||||
| chr2:33537330
|
C | A | 108 | a0001c0001t0001g0100a0001c0001t0001g0345a0001c0001t0002g0025others(105): Show | 108 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1162-1764C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | ||||||
| chr2:33537330
|
C | CA | 15 | a0001c0002t0004g0090a0001c0002t0006g0134a0001c0002t0006g0139others(12): Show | 15 | HG00738.hp1 HG01255.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | ||||||
| chr2:33537330
|
C | CAACACA | 49 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(46): Show | 49 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | ||||||
| chr2:33537330
|
C | CACA | 12 | a0001c0001t0002g0006a0001c0001t0002g0108a0001c0001t0002g0250others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | ||||||
| chr2:33537330
|
C | CCCCACA | 15 | a0001c0001t0005g0177a0001c0001t0019g0311a0001c0001t0052g0303others(12): Show | 15 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-1763_1162-176 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537330 | |||||
| chr2:33537330
|
C | CCCCCAAC others(3): Show |
1 | a0001c0002t0003g0075 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1162-1763_1162-176 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537330 | |||||
| chr2:33537332
|
A | C | 69 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1162-1762A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537332 | ||||||
| chr2:33537334
|
A | C | 6 | a0001c0001t0001g0268a0001c0001t0004g0129a0001c0001t0004g0143others(3): Show | 6 | HG00639.hp2 HG02055.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1760A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537334 | ||||||
| chr2:33537367
|
A | AT | 68 | a0001c0001t0001g0345a0001c0001t0016g0369a0001c0001t0030g0051others(65): Show | 68 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1716dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537367 | |||||
| chr2:33537395
|
G | A | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1162-1699G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537395 | ||||||
| chr2:33537416
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1162-1678C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537416 | ||||||
| chr2:33537417
|
G | A | 72 | a0001c0001t0001g0030a0001c0001t0001g0345a0001c0001t0009g0215others(69): Show | 72 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1162-1677G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537417 | ||||||
| chr2:33537519
|
C | T | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1162-1575C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537519 | ||||||
| chr2:33537586
|
C | G | 1 | a0001c0008t0033g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1162-1508C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537586 | ||||||
| chr2:33537588
|
T | C | 1 | a0001c0001t0002g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-1506T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537588 | ||||||
| chr2:33537589
|
G | T | 1 | a0001c0001t0002g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-1505G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537589 | ||||||
| chr2:33537591
|
C | T | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1162-1503C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537591 | ||||||
| chr2:33537625
|
T | C | 7 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(4): Show | 7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-1469T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537625 | ||||||
| chr2:33537648
|
A | G | 1 | a0001c0002t0015g0278 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1162-1446A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537648 | ||||||
| chr2:33537896
|
A | G | 59 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(56): Show | 59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1162-1198A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537896 | ||||||
| chr2:33537933
|
G | A | 8 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162-1161G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537933 | ||||||
| chr2:33537966
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1162-1128C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537966 | ||||||
| chr2:33538212
|
T | C | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-882T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538212 | ||||||
| chr2:33538300
|
C | G | 2 | a0001c0001t0002g0330a0001c0001t0002g0332 | 2 | NA18963.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1162-794C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538300 | ||||||
| chr2:33538362
|
G | A | 1 | a0001c0001t0007g0335 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1162-732G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538362 | ||||||
| chr2:33538430
|
G | C | 4 | a0001c0001t0042g0122a0003c0009t0049g0070a0003c0011t0046g0202others(1): Show | 4 | HG03041.hp1 HG03139.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-664G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538430 | ||||||
| chr2:33538452
|
G | A | 2 | a0001c0001t0042g0122a0003c0011t0046g0202 | 2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1162-642G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538452 | ||||||
| chr2:33538503
|
A | AAAATAAA others(1): Show |
20 | a0001c0001t0044g0172a0001c0001t0052g0303a0001c0001t0057g0079others(17): Show | 20 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-572_1162-565d others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33538503 | |||||
| chr2:33538509
|
A | AATAAATA others(1): Show |
18 | a0001c0001t0001g0268a0001c0001t0002g0190a0001c0001t0004g0145others(15): Show | 18 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1162-578_1162-577i others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33538509 | |||||
| chr2:33538519
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1162-575T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538519 | ||||||
| chr2:33538676
|
T | A | 7 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(4): Show | 7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-418T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538676 | ||||||
| chr2:33538836
|
A | G | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1162-258A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538836 | ||||||
| chr2:33538880
|
T | A | 221 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(218): Show | 221 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.1162-214T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538880 | ||||||
| chr2:33538933
|
G | C | 5 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-161G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538933 | ||||||
| chr2:33539074
|
G | GT | 14 | a0001c0001t0001g0268a0001c0001t0002g0340a0001c0001t0004g0145others(11): Show | 14 | HG00639.hp2 HG01070.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-10dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33539074 | |||||
| chr2:33539219
|
T | C | 131 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(128): Show | 131 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1278+9T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539219 | ||||||
| chr2:33539317
|
C | G | 2 | a0001c0001t0007g0056a0001c0001t0007g0261 | 2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1278+107C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539317 | ||||||
| chr2:33539434
|
T | C | 109 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(106): Show | 109 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1278+224T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539434 | ||||||
| chr2:33539436
|
C | G | 109 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(106): Show | 109 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1278+226C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539436 | ||||||
| chr2:33539475
|
T | C | 5 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+265T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539475 | ||||||
| chr2:33539482
|
CAACAGCT others(6): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1278+274_1278+286d others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539482 | |||||
| chr2:33539533
|
G | T | 108 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(105): Show | 108 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1278+323G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539533 | ||||||
| chr2:33539642
|
C | G | 108 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(105): Show | 108 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1278+432C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539642 | ||||||
| chr2:33539650
|
C | T | 280 | a0001c0001t0001g0100a0001c0001t0001g0179a0001c0001t0001g0183others(277): Show | 280 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.1278+440C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539650 | ||||||
| chr2:33539730
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0107 | 3 | NA18994.hp2 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1278+520G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539730 | ||||||
| chr2:33539797
|
G | A | 206 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(203): Show | 206 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1278+587G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539797 | ||||||
| chr2:33539888
|
A | T | 286 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(283): Show | 286 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1278+678A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539888 | ||||||
| chr2:33539987
|
G | GA | 10 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0115others(7): Show | 10 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1278+790dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539987 | |||||
| chr2:33539987
|
GAAAAA | G | 46 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1278+786_1278+790d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539987 | |||||
| chr2:33539996
|
AAAAAG | A | 136 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(133): Show | 136 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.1278+806_1278+810d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539996 | |||||
| chr2:33539996
|
AAAAAGAA others(3): Show |
A | 20 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0005g0177others(17): Show | 20 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1278+801_1278+810d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539996 | |||||
| chr2:33540001
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1278+791G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540001 | ||||||
| chr2:33540006
|
GAAAAGAA others(4): Show |
G | 1 | a0001c0001t0008g0034 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+801_1278+811d others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540006 | |||||
| chr2:33540199
|
G | A | 1 | a0001c0001t0007g0338 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1278+989G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540199 | ||||||
| chr2:33540209
|
T | G | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1278+999T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540209 | ||||||
| chr2:33540233
|
G | A | 1 | a0001c0001t0058g0124 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1278+1023G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540233 | ||||||
| chr2:33540439
|
T | C | 19 | a0001c0001t0044g0172a0001c0001t0057g0079a0001c0003t0005g0040others(16): Show | 19 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1278+1229T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540439 | ||||||
| chr2:33540543
|
C | G | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(5): Show | 8 | HG03130.hp1 HG03927.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1278+1333C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540543 | ||||||
| chr2:33540543
|
CTGTGTGT others(22): Show |
C | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1278+1345_1278+137 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540543 | |||||
| chr2:33540545
|
G | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0269a0001c0001t0001g0333others(7): Show | 10 | HG02615.hp1 HG02886.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1278+1335G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540545 | ||||||
| chr2:33540553
|
GTT | G | 12 | a0001c0001t0001g0179a0001c0001t0056g0248a0001c0002t0001g0094others(9): Show | 12 | HG00609.hp2 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+1346_1278+134 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540553 | |||||
| chr2:33540554
|
T | TTG | 9 | a0001c0001t0002g0347a0001c0002t0001g0085a0001c0002t0001g0113others(6): Show | 9 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1345_1278+134 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTG | T | 28 | a0001c0001t0016g0369a0001c0001t0027g0194a0001c0001t0030g0051others(25): Show | 28 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1278+1346_1278+134 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTG | T | 9 | a0001c0001t0001g0345a0001c0002t0001g0003a0001c0002t0001g0029others(6): Show | 9 | HG00609.hp1 HG02071.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTGT others(1): Show |
T | 9 | a0001c0001t0013g0301a0001c0001t0027g0199a0001c0002t0001g0295others(6): Show | 9 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTGT others(3): Show |
T | 6 | a0001c0001t0013g0121a0001c0001t0013g0166a0001c0001t0013g0240others(3): Show | 6 | HG02074.hp2 HG02280.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTGT others(7): Show |
T | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTGT others(9): Show |
T | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1278+1346_1278+136 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540554
|
TTTTGTGT others(15): Show |
T | 1 | a0001c0002t0006g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1278+1346_1278+136 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | |||||
| chr2:33540555
|
T | G | 4 | a0001c0001t0001g0031a0001c0001t0002g0066a0001c0001t0042g0122others(1): Show | 4 | HG03041.hp1 HG03139.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+1345T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540555 | ||||||
| chr2:33540556
|
T | G | 214 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(211): Show | 214 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.1278+1346T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540556 | ||||||
| chr2:33540556
|
T | TTG | 9 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0115others(6): Show | 9 | HG00673.hp1 HG01109.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1394_1278+139 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | |||||
| chr2:33540556
|
T | TTGTG | 7 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0048others(4): Show | 7 | HG02155.hp2 NA18944.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278+1392_1278+139 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | |||||
| chr2:33540556
|
TTG | T | 19 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0213others(16): Show | 19 | HG00544.hp1 HG00558.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1278+1394_1278+139 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | |||||
| chr2:33540556
|
TTGTG | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0329others(2): Show | 5 | HG02074.hp1 HG02572.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+1392_1278+139 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | |||||
| chr2:33540556
|
TTGTGTG | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0162a0001c0001t0004g0191others(1): Show | 4 | HG01175.hp2 HG03704.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1390_1278+139 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | |||||
| chr2:33540559
|
TGTGTGTG others(2): Show |
T | 9 | a0001c0001t0011g0195a0001c0001t0012g0123a0001c0001t0012g0127others(6): Show | 9 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1350_1278+135 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(4): Show |
T | 6 | a0001c0001t0003g0062a0001c0001t0003g0211a0001c0001t0014g0130others(3): Show | 6 | HG00323.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(6): Show |
T | 36 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(33): Show | 36 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(8): Show |
T | 22 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0052g0303others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(19): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(10): Show |
T | 2 | a0001c0001t0002g0297a0001c0001t0003g0041 | 2 | HG01993.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(12): Show |
T | 102 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(99): Show | 102 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540559
|
TGTGTGTG others(14): Show |
T | 1 | a0001c0001t0004g0033 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278+1350_1278+137 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | ||||||
| chr2:33540561
|
TGTGTG | T | 4 | a0001c0001t0008g0185a0001c0001t0020g0142a0001c0001t0020g0148others(1): Show | 4 | HG01496.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1352_1278+135 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | ||||||
| chr2:33540561
|
TGTGTGTG others(2): Show |
T | 8 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1352_1278+136 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | ||||||
| chr2:33540561
|
TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1278+1352_1278+136 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | ||||||
| chr2:33540561
|
TGTGTGTG others(6): Show |
T | 2 | a0001c0001t0042g0122a0003c0011t0046g0202 | 2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1278+1352_1278+136 others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | ||||||
| chr2:33540561
|
TGTGTGTG others(12): Show |
T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1278+1352_1278+137 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | ||||||
| chr2:33540562
|
G | T | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1278+1352G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540562 | ||||||
| chr2:33540572
|
G | T | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1278+1362G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540572 | ||||||
| chr2:33540576
|
G | T | 6 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0042g0122others(3): Show | 6 | HG01884.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278+1366G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540576 | ||||||
| chr2:33540615
|
T | C | 3 | a0001c0001t0003g0015a0001c0001t0003g0225a0001c0001t0003g0304 | 3 | HG01496.hp2 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1278+1405T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540615 | ||||||
| chr2:33540615
|
T | TTC | 92 | a0001c0001t0001g0054a0001c0001t0001g0179a0001c0001t0001g0345others(89): Show | 92 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1278+1429_1278+143 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | |||||
| chr2:33540615
|
T | TTCTC | 6 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155others(3): Show | 6 | HG01496.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+1427_1278+143 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | |||||
| chr2:33540615
|
TTCTC | T | 106 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1278+1427_1278+143 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | |||||
| chr2:33540746
|
G | A | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1278+1536G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540746 | ||||||
| chr2:33540861
|
T | TA | 8 | a0001c0001t0004g0145a0001c0001t0008g0035a0001c0001t0008g0180others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1662dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540861 | |||||
| chr2:33540861
|
TA | T | 67 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0002g0006others(64): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1278+1662delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540861 | |||||
| chr2:33540868
|
A | G | 8 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(5): Show | 8 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1658A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540868 | ||||||
| chr2:33540888
|
T | C | 108 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(105): Show | 108 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1278+1678T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540888 | ||||||
| chr2:33540937
|
A | T | 1 | a0001c0001t0008g0034 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+1727A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540937 | ||||||
| chr2:33540966
|
A | T | 1 | a0001c0001t0008g0034 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+1756A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540966 | ||||||
| chr2:33541061
|
A | C | 4 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0116others(1): Show | 4 | HG00558.hp1 NA18954.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1851A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541061 | ||||||
| chr2:33541151
|
G | A | 4 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0014g0133others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1941G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541151 | ||||||
| chr2:33541188
|
A | G | 1 | a0001c0001t0010g0009 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1278+1978A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541188 | ||||||
| chr2:33541391
|
G | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0263a0001c0001t0001g0345others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1279-2121G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541391 | ||||||
| chr2:33541512
|
C | T | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1279-2000C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541512 | ||||||
| chr2:33541726
|
C | T | 1 | a0001c0001t0019g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279-1786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541726 | ||||||
| chr2:33541741
|
G | T | 100 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(97): Show | 100 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1279-1771G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541741 | ||||||
| chr2:33542099
|
C | A | 1 | a0001c0001t0001g0268 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1279-1413C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542099 | ||||||
| chr2:33542299
|
T | A | 12 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-1213T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542299 | ||||||
| chr2:33542348
|
T | C | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1279-1164T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542348 | ||||||
| chr2:33542370
|
C | T | 12 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-1142C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542370 | ||||||
| chr2:33542525
|
A | G | 2 | a0001c0001t0002g0245a0001c0001t0045g0106 | 2 | HG00642.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1279-987A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542525 | ||||||
| chr2:33542583
|
A | T | 14 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(11): Show | 14 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1279-929A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542583 | ||||||
| chr2:33542601
|
G | A | 20 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0002g0006others(17): Show | 20 | HG01433.hp2 HG01928.hp2 NA18612.hp1 others(17): Show |
intron_variant | MODIFIER | c.1279-911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542601 | ||||||
| chr2:33542628
|
A | G | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1279-884A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542628 | ||||||
| chr2:33542657
|
T | TC | 17 | a0001c0001t0002g0013a0001c0001t0002g0058a0001c0001t0002g0111others(14): Show | 17 | HG00438.hp2 HG02818.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.1279-846dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33542657 | |||||
| chr2:33542663
|
C | A | 2 | a0001c0001t0022g0259a0001c0001t0022g0260 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1279-849C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542663 | ||||||
| chr2:33542819
|
G | C | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-693G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542819 | ||||||
| chr2:33542850
|
A | T | 2 | a0001c0001t0003g0302a0001c0001t0050g0313 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1279-662A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542850 | ||||||
| chr2:33542956
|
G | T | 1 | a0001c0002t0001g0214 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1279-556G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542956 | ||||||
| chr2:33542982
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1279-530C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542982 | ||||||
| chr2:33543006
|
T | C | 1 | a0001c0002t0034g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1279-506T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543006 | ||||||
| chr2:33543049
|
G | T | 22 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0005g0177others(19): Show | 22 | HG00639.hp2 HG01070.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279-463G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543049 | ||||||
| chr2:33543088
|
A | G | 2 | a0001c0001t0004g0191a0001c0001t0004g0197 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1279-424A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543088 | ||||||
| chr2:33543202
|
A | C | 1 | a0001c0002t0038g0346 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1279-310A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543202 | ||||||
| chr2:33543230
|
G | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0339a0009c0015t0002g0038 | 3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1279-282G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543230 | ||||||
| chr2:33543250
|
A | G | 1 | a0001c0001t0008g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1279-262A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543250 | ||||||
| chr2:33543280
|
C | G | 3 | a0001c0001t0042g0122a0003c0009t0049g0070a0003c0011t0046g0202 | 3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1279-232C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543280 | ||||||
| chr2:33543391
|
T | C | 1 | a0001c0003t0005g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1279-121T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543391 | ||||||
| chr2:33543441
|
G | A | 1 | a0001c0001t0010g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1279-71G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543441 | ||||||
| chr2:33543664
|
C | G | 1 | a0001c0001t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1394+37C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543664 | ||||||
| chr2:33543698
|
G | A | 1 | a0001c0002t0006g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1394+71G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543698 | ||||||
| chr2:33543901
|
C | G | 217 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0001t0001g0183others(214): Show | 217 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.1394+274C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543901 | ||||||
| chr2:33544126
|
C | G | 1 | a0001c0001t0040g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1394+499C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544126 | ||||||
| chr2:33544181
|
G | A | 10 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+554G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544181 | ||||||
| chr2:33544230
|
C | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1394+603C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544230 | ||||||
| chr2:33544520
|
G | GA | 107 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0171others(104): Show | 107 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1394+903dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33544520 | |||||
| chr2:33544708
|
T | C | 8 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+1081T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544708 | ||||||
| chr2:33544747
|
C | T | 10 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+1120C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544747 | ||||||
| chr2:33544835
|
AT | A | 9 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(6): Show | 9 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1394+1217delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33544835 | |||||
| chr2:33545133
|
A | T | 23 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0005g0177others(20): Show | 23 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+1506A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545133 | ||||||
| chr2:33545200
|
T | C | 1 | a0006c0013t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1394+1573T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545200 | ||||||
| chr2:33545336
|
G | A | 3 | a0001c0001t0042g0122a0003c0009t0049g0070a0003c0011t0046g0202 | 3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+1709G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545336 | ||||||
| chr2:33545661
|
T | C | 289 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(286): Show | 289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.1394+2034T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545661 | ||||||
| chr2:33545793
|
CTAT | C | 288 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(285): Show | 288 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.1394+2184_1394+218 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33545793 | |||||
| chr2:33545910
|
T | A | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1394+2283T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545910 | ||||||
| chr2:33545915
|
A | C | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1394+2288A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545915 | ||||||
| chr2:33546107
|
G | A | 17 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394+2480G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546107 | ||||||
| chr2:33546150
|
G | A | 102 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(99): Show | 102 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1394+2523G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546150 | ||||||
| chr2:33546240
|
G | C | 1 | a0001c0001t0002g0111 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1394+2613G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546240 | ||||||
| chr2:33546315
|
C | T | 94 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(91): Show | 94 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1394+2688C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546315 | ||||||
| chr2:33546340
|
A | G | 289 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(286): Show | 289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.1394+2713A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546340 | ||||||
| chr2:33546347
|
C | G | 3 | a0001c0001t0042g0122a0003c0009t0049g0070a0003c0011t0046g0202 | 3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+2720C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546347 | ||||||
| chr2:33546348
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0277others(2): Show | 5 | HG00621.hp2 NA18944.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+2721G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546348 | ||||||
| chr2:33546355
|
G | A | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1394+2728G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546355 | ||||||
| chr2:33546402
|
G | C | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1394+2775G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546402 | ||||||
| chr2:33546422
|
C | CA | 17 | a0001c0001t0003g0302a0001c0001t0005g0177a0001c0001t0013g0121others(14): Show | 17 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394+2811dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33546422 | |||||
| chr2:33546422
|
CA | C | 23 | a0001c0001t0001g0045a0001c0001t0001g0115a0001c0001t0001g0268others(20): Show | 23 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+2811delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33546422 | |||||
| chr2:33546473
|
C | T | 3 | a0001c0001t0042g0122a0003c0009t0049g0070a0003c0011t0046g0202 | 3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+2846C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546473 | ||||||
| chr2:33546626
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0107 | 3 | NA18994.hp2 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1395-2978T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546626 | ||||||
| chr2:33546739
|
TACATATA others(1333): Show |
T | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-2864_1395-152 others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546739 | ||||||
| chr2:33546892
|
C | A | 1 | a0001c0001t0007g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1395-2712C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546892 | ||||||
| chr2:33546942
|
C | G | 56 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(53): Show | 56 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1395-2662C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546942 | ||||||
| chr2:33547053
|
G | GA | 99 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0100others(96): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1395-2530dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
G | GAA | 9 | a0001c0001t0001g0183a0001c0001t0002g0013a0001c0001t0002g0058others(6): Show | 9 | HG02965.hp2 NA18941.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395-2531_1395-253 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
GA | G | 18 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0115others(15): Show | 18 | HG01496.hp1 HG02015.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395-2530delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
GAA | G | 45 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(42): Show | 45 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1395-2531_1395-253 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
GAAAAAA | G | 22 | a0001c0001t0004g0129a0001c0001t0004g0143a0001c0001t0042g0122others(19): Show | 22 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-2535_1395-253 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
GAAAAAAA | G | 6 | a0001c0001t0017g0120a0001c0001t0017g0238a0001c0001t0023g0138others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-2536_1395-253 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547053
|
GAAAAAAA others(2): Show |
G | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-2538_1395-253 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | |||||
| chr2:33547054
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1395-2550A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547054 | ||||||
| chr2:33547073
|
A | G | 32 | a0001c0001t0003g0015a0001c0001t0003g0225a0001c0001t0003g0304others(29): Show | 32 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1395-2531A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547073 | ||||||
| chr2:33547074
|
AGAG | A | 6 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(3): Show | 6 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2529_1395-252 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547074 | ||||||
| chr2:33547087
|
G | A | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395-2517G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547087 | ||||||
| chr2:33547342
|
C | CT | 20 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0059others(17): Show | 20 | HG00597.hp2 HG01175.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1395-2233dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT | 8 | a0001c0001t0003g0012a0001c0001t0003g0225a0001c0001t0003g0302others(5): Show | 8 | HG01358.hp2 HG02602.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-2239_1395-223 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(1): Show |
13 | a0001c0001t0003g0011a0001c0001t0003g0015a0001c0001t0003g0062others(10): Show | 13 | HG00323.hp2 HG01081.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1395-2240_1395-223 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0002g0037a0001c0001t0003g0041a0001c0001t0003g0140others(9): Show | 12 | HG01175.hp1 HG01496.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1395-2241_1395-223 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0149a0001c0001t0003g0304a0001c0001t0014g0130others(3): Show | 6 | HG01952.hp1 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2242_1395-223 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0012g0186a0001c0001t0014g0131a0001c0001t0014g0193others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-2243_1395-223 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(9): Show |
1 | a0001c0002t0001g0350 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1395-2248_1395-223 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(15): Show |
1 | a0002c0005t0003g0216 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1395-2254_1395-223 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(16): Show |
1 | a0002c0005t0003g0206 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1395-2255_1395-223 others(27): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(17): Show |
3 | a0001c0002t0001g0223a0001c0002t0001g0368a0001c0002t0004g0090 | 3 | HG02132.hp2 HG03704.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1395-2256_1395-223 others(28): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(18): Show |
4 | a0001c0002t0001g0361a0001c0002t0006g0139a0001c0002t0006g0189others(1): Show | 4 | HG01255.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-2257_1395-223 others(29): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(19): Show |
3 | a0001c0002t0006g0158a0001c0002t0006g0168a0001c0002t0016g0205 | 3 | HG02886.hp1 HG03486.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1395-2258_1395-223 others(30): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(20): Show |
2 | a0001c0002t0001g0275a0001c0002t0006g0188 | 2 | HG00738.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1395-2259_1395-223 others(31): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(21): Show |
1 | a0001c0002t0006g0157 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1395-2260_1395-223 others(32): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(22): Show |
1 | a0001c0002t0006g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1395-2261_1395-223 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(23): Show |
1 | a0001c0002t0006g0174 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1395-2233_1395-223 others(34): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
C | CTTTTTTT others(24): Show |
1 | a0001c0002t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1395-2233_1395-223 others(35): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CT | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0045a0001c0001t0001g0052others(18): Show | 21 | HG00423.hp1 HG00639.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1395-2233delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTT | C | 6 | a0001c0001t0040g0128a0001c0002t0001g0343a0001c0002t0006g0134others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2235_1395-223 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTT | C | 14 | a0001c0001t0005g0177a0001c0001t0017g0238a0001c0001t0019g0311others(11): Show | 14 | HG00621.hp1 HG00673.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395-2236_1395-223 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTT | C | 22 | a0001c0001t0017g0120a0001c0001t0022g0259a0001c0001t0022g0260others(19): Show | 22 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-2237_1395-223 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTTTT others(1): Show |
C | 15 | a0001c0001t0002g0046a0001c0001t0002g0073a0001c0001t0002g0108others(12): Show | 15 | HG00597.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1395-2240_1395-223 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTTTT others(2): Show |
C | 80 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0183others(77): Show | 80 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1395-2241_1395-223 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0002g0102a0001c0001t0002g0245a0001c0001t0002g0290others(3): Show | 6 | HG00642.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2242_1395-223 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0003t0005g0119a0001c0003t0005g0192a0001c0003t0005g0241others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395-2243_1395-223 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547342
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0012g0123a0001c0001t0052g0303a0001c0003t0005g0040others(12): Show | 15 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1395-2244_1395-223 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | |||||
| chr2:33547458
|
G | A | 157 | a0001c0001t0001g0179a0001c0001t0002g0037a0001c0001t0002g0190others(154): Show | 157 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1395-2146G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547458 | ||||||
| chr2:33547470
|
G | C | 1 | a0001c0001t0004g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1395-2134G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547470 | ||||||
| chr2:33547483
|
G | A | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1395-2121G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547483 | ||||||
| chr2:33547574
|
G | A | 10 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0008g0034others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-2030G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547574 | ||||||
| chr2:33547586
|
G | A | 5 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395-2018G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547586 | ||||||
| chr2:33547680
|
A | C | 2 | a0002c0005t0003g0206a0002c0005t0003g0216 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1395-1924A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547680 | ||||||
| chr2:33547888
|
G | C | 8 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-1716G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547888 | ||||||
| chr2:33547919
|
G | A | 3 | a0001c0001t0016g0369a0001c0001t0030g0051a0001c0001t0030g0362 | 3 | HG02074.hp2 HG03669.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1395-1685G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547919 | ||||||
| chr2:33547934
|
A | G | 1 | a0001c0001t0025g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1395-1670A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547934 | ||||||
| chr2:33548072
|
G | C | 2 | a0001c0001t0003g0103a0001c0001t0003g0210 | 2 | HG00423.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1395-1532G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548072 | ||||||
| chr2:33548083
|
T | C | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-1521T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548083 | ||||||
| chr2:33548106
|
A | T | 2 | a0001c0001t0024g0074a0001c0001t0058g0124 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1395-1498A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548106 | ||||||
| chr2:33548167
|
T | A | 2 | a0001c0001t0001g0317a0001c0001t0038g0282 | 2 | NA19010.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1395-1437T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548167 | ||||||
| chr2:33548233
|
C | T | 91 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(88): Show | 91 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1395-1371C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548233 | ||||||
| chr2:33548336
|
A | C | 1 | a0001c0001t0041g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1395-1268A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548336 | ||||||
| chr2:33548360
|
C | CA | 31 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0098others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1395-1221dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | |||||
| chr2:33548360
|
CA | C | 22 | a0001c0001t0002g0073a0001c0001t0002g0163a0001c0001t0002g0222others(19): Show | 22 | HG01109.hp2 HG01123.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-1221delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | |||||
| chr2:33548360
|
CAA | C | 104 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(101): Show | 104 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1395-1222_1395-122 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | |||||
| chr2:33548381
|
A | AAAAAAG | 8 | a0001c0001t0003g0041a0001c0001t0011g0195a0001c0001t0014g0130others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-1221_1395-122 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548381 | |||||
| chr2:33548381
|
A | AAAAAG | 49 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1395-1221_1395-122 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548381 | |||||
| chr2:33548409
|
T | TG | 15 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(12): Show | 15 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1395-1193dupG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548409 | |||||
| chr2:33548469
|
T | C | 58 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(55): Show | 58 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1395-1135T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548469 | ||||||
| chr2:33548479
|
G | A | 1 | a0003c0011t0046g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1395-1125G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548479 | ||||||
| chr2:33548672
|
A | T | 91 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(88): Show | 91 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1395-932A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548672 | ||||||
| chr2:33548698
|
A | AATTATT | 7 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155others(4): Show | 7 | HG01496.hp1 HG02922.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395-890_1395-885d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548698 | |||||
| chr2:33548714
|
A | T | 1 | a0001c0001t0009g0010 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1395-890A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548714 | ||||||
| chr2:33548717
|
A | T | 99 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(96): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1395-887A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548717 | ||||||
| chr2:33548762
|
A | G | 47 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(44): Show | 47 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1395-842A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548762 | ||||||
| chr2:33548842
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1395-762C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548842 | ||||||
| chr2:33548920
|
C | T | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1395-684C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548920 | ||||||
| chr2:33549085
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1395-519C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549085 | ||||||
| chr2:33549155
|
C | G | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395-449C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549155 | ||||||
| chr2:33549303
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1395-301A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549303 | ||||||
| chr2:33549311
|
G | A | 5 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395-293G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549311 | ||||||
| chr2:33549339
|
CAT | C | 93 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(90): Show | 93 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1395-264_1395-263d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549339 | ||||||
| chr2:33549383
|
C | T | 6 | a0001c0001t0027g0194a0001c0001t0027g0199a0001c0001t0050g0313others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-221C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549383 | ||||||
| chr2:33549384
|
G | A | 10 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(7): Show | 10 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-220G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549384 | ||||||
| chr2:33549537
|
A | G | 2 | a0001c0001t0008g0035a0001c0001t0008g0180 | 2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1395-67A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549537 | ||||||
| chr2:33549794
|
G | A | 3 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0040g0128 | 3 | HG01884.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542+43G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33549794 | ||||||
| chr2:33549950
|
G | A | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1542+199G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33549950 | ||||||
| chr2:33550092
|
C | T | 2 | a0001c0002t0006g0168a0001c0002t0006g0174 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1542+341C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550092 | ||||||
| chr2:33550119
|
G | T | 3 | a0001c0001t0050g0313a0001c0001t0051g0299a0001c0004t0019g0118 | 3 | HG01884.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542+368G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550119 | ||||||
| chr2:33550141
|
G | A | 11 | a0001c0001t0001g0268a0001c0001t0002g0190a0001c0001t0004g0145others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+390G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550141 | ||||||
| chr2:33550149
|
A | G | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+398A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550149 | ||||||
| chr2:33550152
|
G | C | 2 | a0002c0005t0003g0206a0002c0005t0003g0216 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1542+401G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550152 | ||||||
| chr2:33550216
|
T | A | 53 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(50): Show | 53 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1542+465T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550216 | ||||||
| chr2:33550358
|
C | T | 2 | a0001c0001t0017g0120a0001c0001t0017g0238 | 2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1542+607C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550358 | ||||||
| chr2:33550484
|
C | G | 59 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(56): Show | 59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1542+733C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550484 | ||||||
| chr2:33550544
|
C | T | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1542+793C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550544 | ||||||
| chr2:33550598
|
T | G | 1 | a0006c0013t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1542+847T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550598 | ||||||
| chr2:33550741
|
G | A | 3 | a0001c0001t0024g0074a0001c0001t0040g0128a0001c0001t0058g0124 | 3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1542+990G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550741 | ||||||
| chr2:33550849
|
TG | T | 5 | a0001c0001t0017g0120a0001c0001t0017g0238a0001c0001t0023g0138others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+1101delG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33550849 | |||||
| chr2:33551040
|
C | T | 7 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(4): Show | 7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542+1289C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551040 | ||||||
| chr2:33551248
|
G | C | 42 | a0001c0001t0002g0190a0001c0001t0004g0145a0001c0001t0005g0177others(39): Show | 42 | HG00639.hp2 HG01070.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1542+1497G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551248 | ||||||
| chr2:33551252
|
G | A | 1 | a0001c0001t0009g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1542+1501G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551252 | ||||||
| chr2:33551284
|
G | T | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+1533G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551284 | ||||||
| chr2:33551376
|
C | T | 72 | a0001c0001t0001g0345a0001c0001t0039g0146a0001c0001t0040g0128others(69): Show | 72 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1542+1625C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551376 | ||||||
| chr2:33551421
|
G | A | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542+1670G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551421 | ||||||
| chr2:33551424
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0333 | 2 | NA19012.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1542+1673C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551424 | ||||||
| chr2:33551613
|
T | G | 211 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(208): Show | 211 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1542+1862T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551613 | ||||||
| chr2:33551676
|
A | G | 52 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(49): Show | 52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542+1925A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551676 | ||||||
| chr2:33551678
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1542+1927C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551678 | ||||||
| chr2:33551697
|
A | T | 51 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(48): Show | 51 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1542+1946A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551697 | ||||||
| chr2:33551721
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1542+1970C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551721 | ||||||
| chr2:33551821
|
G | T | 2 | a0001c0004t0019g0042a0001c0004t0043g0201 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1542+2070G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551821 | ||||||
| chr2:33551898
|
C | A | 5 | a0001c0001t0013g0121a0001c0001t0013g0166a0001c0001t0013g0240others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+2147C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551898 | ||||||
| chr2:33551925
|
G | A | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+2174G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551925 | ||||||
| chr2:33551972
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0140 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1542+2221G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551972 | ||||||
| chr2:33551994
|
A | AAAAC | 56 | a0001c0001t0001g0345a0001c0001t0039g0146a0001c0001t0040g0128others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1542+2273_1542+227 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33551994 | |||||
| chr2:33551994
|
AAAAC | A | 3 | a0001c0001t0002g0305a0001c0001t0009g0039a0001c0001t0032g0316 | 3 | HG00642.hp1 HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1542+2273_1542+227 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33551994 | |||||
| chr2:33552010
|
CAAACAAA others(10): Show |
C | 1 | a0001c0001t0013g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1542+2260_1542+227 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552010 | ||||||
| chr2:33552022
|
CAAACA | C | 52 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(49): Show | 52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542+2272_1542+227 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552022 | ||||||
| chr2:33552026
|
CA | C | 32 | a0001c0001t0004g0145a0001c0001t0008g0035a0001c0001t0008g0180others(29): Show | 32 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.1542+2276delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552026 | ||||||
| chr2:33552027
|
A | AAAC | 15 | a0001c0001t0005g0177a0001c0001t0008g0034a0001c0001t0013g0121others(12): Show | 15 | HG02056.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542+2276_1542+227 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552027 | ||||||
| chr2:33552027
|
A | T | 1 | a0003c0011t0046g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1542+2276A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552027 | ||||||
| chr2:33552054
|
C | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0143 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1542+2303C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552054 | ||||||
| chr2:33552055
|
G | A | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+2304G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552055 | ||||||
| chr2:33552183
|
A | G | 2 | a0001c0001t0008g0035a0001c0001t0008g0180 | 2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1542+2432A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552183 | ||||||
| chr2:33552277
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1542+2526G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552277 | ||||||
| chr2:33552476
|
G | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2725G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552476 | ||||||
| chr2:33552482
|
A | T | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2731A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552482 | ||||||
| chr2:33552549
|
T | C | 2 | a0001c0001t0050g0313a0001c0001t0051g0299 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542+2798T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552549 | ||||||
| chr2:33552568
|
A | ATAAC | 24 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(21): Show | 24 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1542+2820_1542+282 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33552568 | |||||
| chr2:33552590
|
G | C | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2839G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552590 | ||||||
| chr2:33552744
|
T | TTTGTAGA others(5): Show |
1 | a0001c0001t0050g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2787_1543-278 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552744 | ||||||
| chr2:33552745
|
C | T | 1 | a0001c0001t0050g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552745 | ||||||
| chr2:33552746
|
C | A | 1 | a0001c0001t0050g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2785C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552746 | ||||||
| chr2:33552747
|
C | G | 1 | a0001c0001t0050g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2784C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552747 | ||||||
| chr2:33552856
|
C | G | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-2675C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552856 | ||||||
| chr2:33552869
|
G | A | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1543-2662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552869 | ||||||
| chr2:33552924
|
G | A | 1 | a0001c0001t0051g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1543-2607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552924 | ||||||
| chr2:33552996
|
C | T | 1 | a0003c0011t0046g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1543-2535C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552996 | ||||||
| chr2:33553102
|
C | T | 2 | a0001c0001t0007g0064a0001c0001t0007g0068 | 2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1543-2429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553102 | ||||||
| chr2:33553267
|
T | G | 1 | a0003c0011t0046g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1543-2264T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553267 | ||||||
| chr2:33553429
|
G | C | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1543-2102G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553429 | ||||||
| chr2:33553457
|
T | C | 2 | a0001c0001t0044g0172a0001c0001t0057g0079 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1543-2074T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553457 | ||||||
| chr2:33553468
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1543-2063T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553468 | ||||||
| chr2:33553516
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0002g0102 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1543-2015T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553516 | ||||||
| chr2:33553662
|
C | G | 4 | a0001c0003t0005g0175a0001c0003t0005g0176a0001c0003t0005g0253others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-1869C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553662 | ||||||
| chr2:33553995
|
C | T | 52 | a0001c0001t0002g0037a0001c0001t0003g0011a0001c0001t0003g0012others(49): Show | 52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1543-1536C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553995 | ||||||
| chr2:33554040
|
A | G | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-1491A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554040 | ||||||
| chr2:33554153
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1543-1378T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554153 | ||||||
| chr2:33554170
|
C | T | 1 | a0001c0002t0063g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1543-1361C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554170 | ||||||
| chr2:33554207
|
G | C | 2 | a0001c0001t0050g0313a0001c0001t0051g0299 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-1324G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554207 | ||||||
| chr2:33554267
|
C | T | 71 | a0001c0001t0001g0345a0001c0001t0039g0146a0001c0001t0040g0128others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1543-1264C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554267 | ||||||
| chr2:33554269
|
G | T | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-1262G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554269 | ||||||
| chr2:33554542
|
A | G | 59 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(56): Show | 59 | HG00323.hp2 HG00423.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1543-989A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554542 | ||||||
| chr2:33554783
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1543-748C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554783 | ||||||
| chr2:33554801
|
G | C | 2 | a0001c0001t0003g0298a0001c0001t0003g0363 | 2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1543-730G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554801 | ||||||
| chr2:33554812
|
G | A | 10 | a0001c0001t0005g0177a0001c0001t0013g0121a0001c0001t0013g0166others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543-719G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554812 | ||||||
| chr2:33554839
|
T | C | 110 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(107): Show | 110 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1543-692T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554839 | ||||||
| chr2:33554850
|
C | T | 58 | a0001c0001t0001g0179a0001c0001t0001g0345a0001c0001t0039g0146others(55): Show | 58 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1543-681C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554850 | ||||||
| chr2:33554869
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1543-662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554869 | ||||||
| chr2:33554886
|
C | T | 1 | a0001c0001t0007g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1543-645C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554886 | ||||||
| chr2:33555069
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1543-462C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555069 | ||||||
| chr2:33555112
|
A | G | 2 | a0001c0001t0050g0313a0001c0001t0052g0303 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-419A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555112 | ||||||
| chr2:33555164
|
G | A | 92 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(89): Show | 92 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1543-367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555164 | ||||||
| chr2:33555219
|
G | A | 1 | a0001c0002t0006g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1543-312G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555219 | ||||||
| chr2:33555252
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1543-279G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555252 | ||||||
| chr2:33555259
|
G | A | 3 | a0001c0001t0050g0313a0001c0001t0051g0299a0001c0001t0052g0303 | 3 | HG02922.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-272G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555259 | ||||||
| chr2:33555276
|
C | G | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0295others(1): Show | 4 | HG00621.hp1 HG00673.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-255C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555276 | ||||||
| chr2:33555286
|
T | C | 2 | a0003c0009t0049g0070a0003c0011t0046g0202 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1543-245T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555286 | ||||||
| chr2:33555334
|
G | C | 17 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-197G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555334 | ||||||
| chr2:33555369
|
G | A | 1 | a0001c0001t0013g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1543-162G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555369 | ||||||
| chr2:33555377
|
G | A | 1 | a0001c0003t0005g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1543-154G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555377 | ||||||
| chr2:33555634
|
G | C | 83 | a0001c0001t0001g0179a0001c0001t0001g0345a0001c0001t0016g0369others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1579+67G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555634 | ||||||
| chr2:33555766
|
AC | A | 5 | a0001c0001t0017g0120a0001c0001t0017g0238a0001c0001t0023g0138others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+200delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555766 | ||||||
| chr2:33555864
|
C | T | 2 | a0001c0001t0017g0120a0001c0001t0017g0238 | 2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1579+297C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555864 | ||||||
| chr2:33555898
|
AC | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0048others(7): Show | 10 | HG00621.hp2 HG02132.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1579+333delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33555898 | |||||
| chr2:33555992
|
C | T | 1 | a0001c0004t0043g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1579+425C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555992 | ||||||
| chr2:33556041
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1579+474C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556041 | ||||||
| chr2:33556095
|
C | G | 66 | a0001c0001t0001g0179a0001c0001t0001g0345a0001c0001t0016g0369others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1579+528C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556095 | ||||||
| chr2:33556190
|
G | A | 100 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(97): Show | 100 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1579+623G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556190 | ||||||
| chr2:33556218
|
TTCTTCTA others(321): Show |
T | 107 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(104): Show | 107 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1579+667_1579+994d others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556218 | |||||
| chr2:33556231
|
C | CT | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0171others(15): Show | 18 | HG00544.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579+691dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(2): Show |
8 | a0001c0002t0006g0134a0001c0002t0006g0157a0001c0002t0006g0158others(5): Show | 8 | HG00738.hp1 HG01255.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579+683_1579+691d others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(3): Show |
6 | a0001c0002t0006g0139a0001c0002t0006g0153a0001c0002t0006g0156others(3): Show | 6 | HG01891.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+682_1579+691d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0001g0295 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1579+681_1579+691d others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(5): Show |
15 | a0001c0001t0001g0345a0001c0001t0016g0369a0001c0001t0039g0146others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1579+680_1579+691d others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(6): Show |
23 | a0001c0001t0001g0179a0001c0001t0030g0051a0001c0001t0030g0362others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1579+679_1579+691d others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(7): Show |
13 | a0001c0001t0040g0128a0001c0002t0001g0021a0001c0002t0001g0047others(10): Show | 13 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1579+678_1579+691d others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(8): Show |
6 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0113others(3): Show | 6 | HG00621.hp1 HG00673.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+677_1579+691d others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0034g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1579+673_1579+691d others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556231
|
CTTTTTTT | C | 97 | a0001c0001t0001g0183a0001c0001t0001g0227a0001c0001t0001g0266others(94): Show | 97 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1579+685_1579+691d others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | |||||
| chr2:33556271
|
C | T | 2 | a0001c0001t0024g0074a0001c0001t0058g0124 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1579+704C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556271 | ||||||
| chr2:33556364
|
C | T | 2 | a0001c0001t0044g0172a0001c0002t0017g0147 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1579+797C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556364 | ||||||
| chr2:33556408
|
C | T | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1579+841C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556408 | ||||||
| chr2:33556768
|
C | T | 39 | a0001c0001t0001g0162a0001c0001t0001g0227a0001c0001t0001g0266others(36): Show | 39 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1579+1201C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556768 | ||||||
| chr2:33556839
|
C | A | 1 | a0001c0001t0026g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1579+1272C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556839 | ||||||
| chr2:33556890
|
T | TAC | 6 | a0001c0001t0001g0061a0001c0001t0001g0337a0001c0001t0002g0290others(3): Show | 6 | HG01081.hp1 HG01515.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1284_1580-128 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACAC | 13 | a0001c0001t0002g0066a0001c0001t0002g0073a0001c0001t0002g0108others(10): Show | 13 | HG01168.hp2 HG01358.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1580-1286_1580-128 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACAC | 12 | a0001c0001t0009g0010a0001c0001t0009g0016a0001c0001t0009g0017others(9): Show | 12 | HG01074.hp2 HG01192.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580-1288_1580-128 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACACA others(1): Show |
35 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0183others(32): Show | 35 | HG00597.hp1 HG01071.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1580-1290_1580-128 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACACA others(3): Show |
15 | a0001c0001t0002g0027a0001c0001t0002g0126a0001c0001t0002g0144others(12): Show | 15 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1580-1292_1580-128 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACACA others(5): Show |
24 | a0001c0001t0001g0227a0001c0001t0001g0266a0001c0001t0002g0046others(21): Show | 24 | HG00438.hp2 HG00642.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1580-1294_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACACA others(7): Show |
6 | a0001c0001t0002g0013a0001c0001t0002g0231a0001c0001t0002g0360others(3): Show | 6 | HG03579.hp1 NA18941.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1296_1580-128 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
T | TACACACA others(9): Show |
1 | a0001c0001t0004g0096 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1580-1298_1580-128 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
TAC | T | 127 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0028others(124): Show | 127 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1580-1284_1580-128 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
TACAC | T | 4 | a0001c0001t0001g0318a0001c0002t0001g0343a0002c0005t0003g0206others(1): Show | 4 | HG01516.hp2 HG01517.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-1286_1580-128 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556890
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0044g0172a0001c0002t0017g0147 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1580-1294_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | |||||
| chr2:33556928
|
C | CACACACA others(15): Show |
1 | a0001c0001t0011g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1580-1283_1580-128 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACACA others(13): Show |
1 | a0001c0001t0013g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-1283_1580-128 others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACACA others(11): Show |
7 | a0001c0001t0013g0121a0001c0001t0013g0240a0001c0001t0013g0301others(4): Show | 7 | HG01496.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACACA others(9): Show |
6 | a0001c0001t0009g0215a0001c0001t0011g0312a0001c0001t0013g0300others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACACA others(7): Show |
5 | a0001c0001t0003g0164a0001c0001t0003g0363a0001c0001t0015g0050others(2): Show | 5 | HG01358.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACACA others(5): Show |
46 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACACATA others(3): Show |
7 | a0001c0001t0002g0190a0001c0001t0005g0177a0001c0001t0011g0077others(4): Show | 7 | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CACATACA others(1): Show |
13 | a0001c0001t0008g0035a0001c0001t0008g0180a0001c0001t0012g0123others(10): Show | 13 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | CATACAT | 14 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(11): Show | 14 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33556928
|
C | T | 4 | a0001c0003t0005g0257a0001c0004t0019g0042a0001c0004t0019g0118others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-1283C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | ||||||
| chr2:33557001
|
GA | G | 9 | a0001c0001t0012g0123a0001c0001t0012g0127a0001c0001t0012g0132others(6): Show | 9 | HG01168.hp2 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1580-1200delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557001 | |||||
| chr2:33557145
|
C | T | 17 | a0001c0003t0005g0040a0001c0003t0005g0119a0001c0003t0005g0175others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1580-1066C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557145 | ||||||
| chr2:33557268
|
C | G | 2 | a0001c0001t0005g0177a0001c0001t0019g0311 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1580-943C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557268 | ||||||
| chr2:33557289
|
C | T | 5 | a0001c0001t0017g0120a0001c0001t0017g0238a0001c0001t0023g0138others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-922C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557289 | ||||||
| chr2:33557635
|
G | A | 59 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(56): Show | 59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1580-576G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557635 | ||||||
| chr2:33557642
|
G | A | 1 | a0001c0002t0063g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1580-569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557642 | ||||||
| chr2:33557661
|
G | A | 1 | a0001c0001t0004g0151 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1580-550G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557661 | ||||||
| chr2:33557710
|
G | GA | 16 | a0001c0001t0001g0325a0001c0001t0002g0190a0001c0001t0002g0305others(13): Show | 16 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1580-485dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557710 | |||||
| chr2:33557710
|
GA | G | 20 | a0001c0001t0040g0128a0001c0001t0044g0172a0001c0001t0052g0303others(17): Show | 20 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-485delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557710 | |||||
| chr2:33557775
|
G | A | 4 | a0001c0001t0022g0259a0001c0001t0022g0260a0001c0001t0024g0074others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-436G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557775 | ||||||
| chr2:33557782
|
G | T | 1 | a0001c0003t0005g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-429G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557782 | ||||||
| chr2:33557808
|
T | G | 1 | a0001c0001t0024g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1580-403T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557808 | ||||||
| chr2:33557844
|
G | A | 75 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(72): Show | 75 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.1580-367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557844 | ||||||
| chr2:33557873
|
C | A | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1580-338C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557873 | ||||||
| chr2:33557881
|
T | A | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1580-330T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557881 | ||||||
| chr2:33557954
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0036g0218 | 3 | HG01070.hp2 HG01071.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1580-257T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557954 | ||||||
| chr2:33558006
|
G | A | 3 | a0001c0001t0020g0142a0001c0001t0020g0148a0001c0001t0020g0155 | 3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-205G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33558006 | ||||||
| chr2:33558014
|
G | A | 6 | a0001c0001t0004g0145a0001c0001t0008g0034a0001c0001t0008g0185others(3): Show | 6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-197G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33558014 | ||||||
| chr2:33558425
|
G | A | 1 | a0001c0001t0010g0344 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1705+89G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558425 | ||||||
| chr2:33558425
|
G | T | 2 | a0003c0009t0049g0070a0003c0011t0046g0202 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1705+89G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558425 | ||||||
| chr2:33558563
|
C | T | 1 | a0001c0004t0019g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1706-109C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558563 | ||||||
| chr2:33558594
|
G | A | 1 | a0001c0002t0003g0294 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1706-78G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558594 | ||||||
| chr2:33559068
|
A | G | 50 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(47): Show | 50 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2064+38A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559068 | ||||||
| chr2:33559094
|
G | A | 93 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(90): Show | 93 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2064+64G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559094 | ||||||
| chr2:33559293
|
C | T | 2 | a0001c0001t0017g0120a0001c0001t0017g0238 | 2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2064+263C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559293 | ||||||
| chr2:33559304
|
G | A | 58 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(55): Show | 58 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.2064+274G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559304 | ||||||
| chr2:33559433
|
G | A | 93 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0227others(90): Show | 93 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2064+403G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559433 | ||||||
| chr2:33559468
|
C | A | 1 | a0001c0002t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2064+438C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559468 | ||||||
| chr2:33559550
|
C | T | 3 | a0001c0001t0003g0015a0001c0001t0003g0225a0001c0001t0003g0304 | 3 | HG01496.hp2 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2064+520C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559550 | ||||||
| chr2:33559629
|
G | A | 9 | a0001c0001t0004g0145a0001c0001t0008g0034a0001c0001t0008g0035others(6): Show | 9 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064+599G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559629 | ||||||
| chr2:33559665
|
A | G | 2 | a0001c0001t0007g0064a0001c0001t0007g0068 | 2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2064+635A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559665 | ||||||
| chr2:33559734
|
G | A | 61 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2064+704G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559734 | ||||||
| chr2:33559972
|
C | A | 1 | a0002c0007t0008g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2064+942C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559972 | ||||||
| chr2:33560009
|
T | C | 2 | a0001c0001t0050g0313a0001c0001t0051g0299 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2064+979T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560009 | ||||||
| chr2:33560055
|
G | T | 1 | a0001c0002t0063g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2064+1025G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560055 | ||||||
| chr2:33560079
|
A | G | 3 | a0001c0001t0044g0172a0001c0001t0057g0079a0001c0002t0017g0147 | 3 | HG02451.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2064+1049A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560079 | ||||||
| chr2:33560119
|
T | G | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2064+1089T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560119 | ||||||
| chr2:33560370
|
C | T | 1 | a0001c0001t0009g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2064+1340C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560370 | ||||||
| chr2:33560666
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0334 | 2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2064+1636G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560666 | ||||||
| chr2:33560989
|
T | A | 1 | a0001c0001t0038g0282 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2065-1740T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560989 | ||||||
| chr2:33561060
|
T | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0115others(2): Show | 5 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2065-1669T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561060 | ||||||
| chr2:33561094
|
T | A | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2065-1635T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561094 | ||||||
| chr2:33561097
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2065-1632C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561097 | ||||||
| chr2:33561157
|
C | G | 1 | a0001c0001t0010g0344 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2065-1572C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561157 | ||||||
| chr2:33561192
|
A | G | 180 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(177): Show | 180 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.2065-1537A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561192 | ||||||
| chr2:33561288
|
A | T | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2065-1441A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561288 | ||||||
| chr2:33561322
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2065-1407C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561322 | ||||||
| chr2:33561354
|
A | G | 1 | a0001c0001t0002g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2065-1375A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561354 | ||||||
| chr2:33561445
|
C | A | 105 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(102): Show | 105 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.2065-1284C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561445 | ||||||
| chr2:33561471
|
A | G | 3 | a0001c0001t0050g0313a0001c0001t0051g0299a0001c0001t0052g0303 | 3 | HG02922.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2065-1258A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561471 | ||||||
| chr2:33561552
|
A | G | 2 | a0001c0001t0044g0172a0001c0001t0057g0079 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2065-1177A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561552 | ||||||
| chr2:33561755
|
T | C | 1 | a0001c0002t0017g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2065-974T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561755 | ||||||
| chr2:33561850
|
A | G | 2 | a0001c0001t0027g0194a0001c0001t0027g0199 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2065-879A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561850 | ||||||
| chr2:33561968
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2065-761C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561968 | ||||||
| chr2:33562115
|
A | C | 1 | a0001c0001t0011g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2065-614A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562115 | ||||||
| chr2:33562245
|
G | C | 107 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0171others(104): Show | 107 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.2065-484G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562245 | ||||||
| chr2:33562267
|
C | CT | 170 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(167): Show | 170 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2065-444dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562267 | |||||
| chr2:33562267
|
CT | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0179a0001c0001t0001g0279others(7): Show | 10 | HG01256.hp1 HG02155.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2065-444delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562267 | |||||
| chr2:33562352
|
C | T | 1 | a0001c0003t0028g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2065-377C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562352 | ||||||
| chr2:33562641
|
A | AAAG | 13 | a0001c0001t0002g0037a0001c0001t0002g0111a0001c0001t0002g0126others(10): Show | 13 | HG00438.hp2 HG00642.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2065-87_2065-85dup others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562641 | |||||
| chr2:33562677
|
T | C | 2 | a0001c0001t0003g0041a0001c0001t0003g0140 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2065-52T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562677 | ||||||
| chr2:33562706
|
A | G | 17 | a0001c0001t0002g0037a0001c0001t0002g0111a0001c0001t0002g0126others(14): Show | 17 | HG00438.hp2 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2065-23A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562706 |