Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10235 |
| ensemblid | ENSG00000068831.19 |
| hgncid | 9879 |
| symbol | RASGRP2 |
| name | RAS guanyl releasing protein 2 |
| refseq_nuc | NM_001098671.2 |
| refseq_prot | NP_001092141.1 |
| ensembl_nuc | ENST00000394432.8 |
| ensembl_prot | ENSP00000377953.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 64726911 |
| end | 64744142 |
| strand | - |
| ver | v1.2 |
| region | chr11:64726911-64744142 |
| region5000 | chr11:64721911-64749142 |
| regionname0 | RASGRP2_chr11_64726911_64744142 |
| regionname5000 | RASGRP2_chr11_64721911_64749142 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 609 | 293 | 88 | 40 | 121 | 10 | 32 | 81 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | MAGTL others(604): Show |
chr11 | 64721911 | 64749142 |
| a0002 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | MAGTL others(604): Show |
chr11 | 64721911 | 64749142 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1827 | 212 | 79 | 26 | 74 | 7 | 24 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0002 | 0/0 | 1827 | 73 | 5 | 13 | 45 | 3 | 7 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0003 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0004 | 0/0 | 1827 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0005 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0007 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0008 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0001c0009 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 | ||
| a0002c0006 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ATGGC others(1822): Show |
chr11 | 64721911 | 64749142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2268 | 211 | 79 | 26 | 73 | 7 | 24 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0001t0002 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0002t0001 | 0/0 | 2268 | 73 | 5 | 13 | 45 | 3 | 7 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0003t0001 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0004t0001 | 0/0 | 2268 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0005t0001 | 0/0 | 2268 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0007t0001 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0008t0001 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0001c0009t0001 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| a0002c0006t0001 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | ACTGC others(2263): Show |
chr11 | 64721911 | 64749142 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 3 | 9 | 15 | 4 | 11 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0003 | 0/0 | 21 | 2 | 0 | 19 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0004 | 1/0 | 12 | 11 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0002 | 0/0 | 30 | 1 | 6 | 21 | 0 | 2 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0004t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0001c0009t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| a0002c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0029 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0029 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ESN | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03927 | hp1 | a0001 | c0005 | t0001 | g0073 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | BEB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18747 | hp2 | a0001 | c0008 | t0001 | g0128 | EAS | CHB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18906 | hp2 | a0001 | c0009 | t0001 | g0130 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19003 | hp1 | a0002 | c0006 | t0001 | g0047 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | LWK | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19079 | hp2 | a0001 | c0007 | t0001 | g0120 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | USA | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0122 | REF | REF | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | RASGRP2_chr11_64721911_64749142 | RASGRP2 | chr11 | 64721911 | 64749142 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:64730129 | C | G | 1 | a0002 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1478G>C | p.Gly493Ala | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 13/17 | 1689/2268 | 1478/1830 | 493/609 | chr11 | 64730129 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:64728885 | G | T | 3 | a0001c0002 a0001c0004 a0002c0006 |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
synonymous_variant | LOW | c.1749C>A | p.Gly583Gly | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/17 | 1960/2268 | 1749/1830 | 583/609 | chr11 | 64728885 | |||
| chr11:64739387 | G | A | 1 | a0001c0007 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.786C>T | p.His262His | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/17 | 997/2268 | 786/1830 | 262/609 | chr11 | 64739387 | |||
| chr11:64741040 | G | A | 1 | a0001c0008 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.279C>T | p.Asn93Asn | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/17 | 490/2268 | 279/1830 | 93/609 | chr11 | 64741040 | |||
| chr11:64742032 | G | A | 1 | a0001c0003 | 2 | HG02922.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.154C>T | p.Leu52Leu | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/17 | 365/2268 | 154/1830 | 52/609 | chr11 | 64742032 | |||
| chr11:64742099 | C | T | 1 | a0001c0005 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.87G>A | p.Lys29Lys | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/17 | 298/2268 | 87/1830 | 29/609 | chr11 | 64742099 | |||
| chr11:64742813 | G | A | 1 | a0001c0009 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.54C>T | p.Arg18Arg | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/17 | 265/2268 | 54/1830 | 18/609 | chr11 | 64742813 | |||
| chr11:64742848 | G | A | 1 | a0001c0004 | 2 | HG01496.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.19C>T | p.Leu7Leu | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/17 | 230/2268 | 19/1830 | 7/609 | chr11 | 64742848 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:64726914 | A | G | 1 | a0001c0001t0002 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 17/17 | 388 | chr11 | 64726914 | ||||||
| chr11:64726915 | G | A | 1 | a0001c0001t0002 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 17/17 | 387 | chr11 | 64726915 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:64727205 | C | G | 3 | a0001c0002t0001g0034 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG01109.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*7-74G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 16/16 | chr11 | 64727205 | |||||||
| chr11:64727250 | C | G | 1 | a0001c0002t0001g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*6+46G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 16/16 | chr11 | 64727250 | |||||||
| chr11:64727504 | C | A | 1 | a0001c0001t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1772-144G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727504 | |||||||
| chr11:64727506 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1772-156_1772-147d others(12): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727506 | |||||||
| chr11:64727506 | AT | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0046 others(29): Show |
74 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1772-147delA | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727506 | |||||||
| chr11:64727506 | ATT | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(61): Show |
148 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1772-148_1772-147d others(4): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727506 | |||||||
| chr11:64727506 | ATTT | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0075 others(10): Show |
13 | HG01261.hp1 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772-149_1772-147d others(5): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727506 | |||||||
| chr11:64727506 | ATTTT | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0069 others(7): Show |
16 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1772-150_1772-147d others(6): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727506 | |||||||
| chr11:64727671 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1772-311G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727671 | |||||||
| chr11:64727783 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1772-423G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727783 | |||||||
| chr11:64727812 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
175 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1772-452G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727812 | |||||||
| chr11:64727996 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1772-636A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64727996 | |||||||
| chr11:64728079 | A | G | 1 | a0001c0005t0001g0073 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1772-719T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728079 | |||||||
| chr11:64728249 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1771+614G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728249 | |||||||
| chr11:64728428 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1771+435A>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728428 | |||||||
| chr11:64728431 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1771+432T>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728431 | |||||||
| chr11:64728577 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1771+286C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728577 | |||||||
| chr11:64728584 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1771+279G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728584 | |||||||
| chr11:64728585 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0121 |
5 | NA18954.hp1 NA18971.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1771+278C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728585 | |||||||
| chr11:64728680 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
8 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1771+183C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728680 | |||||||
| chr11:64728827 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1771+36G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 15/16 | chr11 | 64728827 | |||||||
| chr11:64729045 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0087 others(1): Show |
8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1592-3C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729045 | |||||||
| chr11:64729071 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1592-29T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729071 | |||||||
| chr11:64729115 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
261 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1592-73A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729115 | |||||||
| chr11:64729128 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1592-86C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729128 | |||||||
| chr11:64729130 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1592-88T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729130 | |||||||
| chr11:64729132 | C | A | 1 | a0001c0001t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1592-90G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729132 | |||||||
| chr11:64729272 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0069 others(8): Show |
17 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1592-230G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729272 | |||||||
| chr11:64729273 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG00642.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1592-231C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729273 | |||||||
| chr11:64729333 | G | GT | 4 | a0001c0001t0001g0096 a0001c0001t0001g0112 a0001c0002t0001g0032 others(1): Show |
4 | NA18987.hp2 NA19003.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-292dupA | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729333 | |||||||
| chr11:64729333 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1592-291C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729333 | |||||||
| chr11:64729341 | G | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1592-299C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729341 | |||||||
| chr11:64729344 | G | GT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1592-303dupA | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729344 | |||||||
| chr11:64729344 | G | GTT | 8 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0116 others(5): Show |
9 | HG00621.hp1 HG02129.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1592-304_1592-303d others(4): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729344 | |||||||
| chr11:64729344 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1592-302C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729344 | |||||||
| chr11:64729525 | C | T | 38 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0053 others(35): Show |
84 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1591+237G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729525 | |||||||
| chr11:64729583 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1591+179G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729583 | |||||||
| chr11:64729689 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
279 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1591+73G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729689 | |||||||
| chr11:64729713 | C | CA | 30 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0011 others(27): Show |
75 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1591+48dupT | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729713 | |||||||
| chr11:64729716 | A | AC | 5 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0112 others(2): Show |
5 | HG01934.hp2 HG02109.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1591+45_1591+46ins others(1): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729716 | |||||||
| chr11:64729717 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
170 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1591+45T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729717 | |||||||
| chr11:64729721 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1591+41T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 14/16 | chr11 | 64729721 | |||||||
| chr11:64729864 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1555-66A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 13/16 | chr11 | 64729864 | |||||||
| chr11:64730261 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1413-67G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64730261 | |||||||
| chr11:64730415 | TC | T | 22 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0011 others(19): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1413-222delG | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64730415 | |||||||
| chr11:64730618 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1413-424A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64730618 | |||||||
| chr11:64730757 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1413-563C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64730757 | |||||||
| chr11:64731153 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(61): Show |
143 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1413-959C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64731153 | |||||||
| chr11:64731407 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1413-1213C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64731407 | |||||||
| chr11:64731451 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1413-1257T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64731451 | |||||||
| chr11:64731663 | G | T | 8 | a0001c0002t0001g0019 a0001c0002t0001g0030 a0001c0002t0001g0032 others(5): Show |
9 | HG00609.hp1 HG01109.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1413-1469C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64731663 | |||||||
| chr11:64732004 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1413-1810A>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732004 | |||||||
| chr11:64732010 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(79): Show |
174 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1413-1816A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732010 | |||||||
| chr11:64732035 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1413-1841G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732035 | |||||||
| chr11:64732075 | G | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413-1881C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732075 | |||||||
| chr11:64732255 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1413-2061A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732255 | |||||||
| chr11:64732470 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1413-2276C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732470 | |||||||
| chr11:64732536 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1413-2342C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732536 | |||||||
| chr11:64732636 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(10): Show |
26 | HG01106.hp1 HG01934.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1413-2442G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732636 | |||||||
| chr11:64732939 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
176 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1412+2173T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732939 | |||||||
| chr11:64732961 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
262 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1412+2151C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732961 | |||||||
| chr11:64732982 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1412+2130C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64732982 | |||||||
| chr11:64733146 | AAAAAAAG | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0099 |
5 | HG02818.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412+1959_1412+196 others(11): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733146 | |||||||
| chr11:64733395 | A | AAC | 3 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0089 |
4 | HG02896.hp1 HG03688.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412+1715_1412+171 others(6): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AAC | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(41): Show |
90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1412+1715_1412+171 others(6): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACAC | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(11): Show |
16 | HG00642.hp1 HG00741.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412+1713_1412+171 others(8): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACACAC | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(20): Show |
53 | HG00609.hp2 HG00673.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.1412+1711_1412+171 others(10): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACACACA others(1): Show |
A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
10 | HG02293.hp1 HG02486.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+1709_1412+171 others(12): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACACACA others(3): Show |
A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0083 others(23): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1412+1707_1412+171 others(14): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACACACA others(5): Show |
A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0079 others(3): Show |
10 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+1705_1412+171 others(16): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733395 | AACACACA others(7): Show |
A | 9 | a0001c0002t0001g0019 a0001c0002t0001g0030 a0001c0002t0001g0031 others(6): Show |
10 | HG00609.hp1 HG01109.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+1703_1412+171 others(18): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733395 | |||||||
| chr11:64733849 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1412+1263A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733849 | |||||||
| chr11:64733853 | C | CT | 57 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0024 others(54): Show |
110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1412+1258dupA | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733853 | |||||||
| chr11:64733853 | C | CTT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
148 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1412+1257_1412+125 others(6): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733853 | |||||||
| chr11:64733853 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1412+1259G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733853 | |||||||
| chr11:64733893 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1412+1219G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64733893 | |||||||
| chr11:64734071 | G | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0057 others(4): Show |
11 | HG01106.hp1 HG01243.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+1041C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64734071 | |||||||
| chr11:64734210 | G | T | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1412+902C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64734210 | |||||||
| chr11:64734450 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1412+662C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64734450 | |||||||
| chr11:64734519 | C | T | 38 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0052 others(35): Show |
83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1412+593G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64734519 | |||||||
| chr11:64734933 | C | T | 1 | a0001c0004t0001g0029 | 2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1412+179G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64734933 | |||||||
| chr11:64735047 | C | A | 4 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0068 others(1): Show |
5 | HG01175.hp1 HG01496.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412+65G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64735047 | |||||||
| chr11:64735066 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1412+46C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 12/16 | chr11 | 64735066 | |||||||
| chr11:64735282 | T | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-55A>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 11/16 | chr11 | 64735282 | |||||||
| chr11:64735302 | C | T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0048 a0002c0006t0001g0047 |
6 | HG00597.hp2 HG02523.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-75G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 11/16 | chr11 | 64735302 | |||||||
| chr11:64735374 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0093 others(1): Show |
6 | HG03453.hp1 HG03453.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297-147G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 11/16 | chr11 | 64735374 | |||||||
| chr11:64735402 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0060 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1296+140C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 11/16 | chr11 | 64735402 | |||||||
| chr11:64735707 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
262 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1174-43T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 10/16 | chr11 | 64735707 | |||||||
| chr11:64735721 | G | A | 1 | a0001c0003t0001g0021 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1174-57C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 10/16 | chr11 | 64735721 | |||||||
| chr11:64735891 | G | A | 41 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0046 others(38): Show |
86 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1173+12C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 10/16 | chr11 | 64735891 | |||||||
| chr11:64736024 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
279 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1096-44T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736024 | |||||||
| chr11:64736071 | CT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
176 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1096-92delA | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736071 | |||||||
| chr11:64736188 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1096-208G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736188 | |||||||
| chr11:64736372 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1095+381G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736372 | |||||||
| chr11:64736418 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0060 |
3 | HG01109.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1095+335C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736418 | |||||||
| chr11:64736538 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1095+215G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736538 | |||||||
| chr11:64736689 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1095+64C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 9/16 | chr11 | 64736689 | |||||||
| chr11:64737040 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0081 a0001c0001t0001g0091 others(3): Show |
11 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.814-6C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737040 | |||||||
| chr11:64737181 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0058 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.814-147G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737181 | |||||||
| chr11:64737657 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0103 |
2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.814-623G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737657 | |||||||
| chr11:64737678 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(46): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.814-645delT | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737678 | |||||||
| chr11:64737678 | CAA | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(73): Show |
160 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.814-646_814-645del others(2): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737678 | |||||||
| chr11:64737690 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.814-656T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737690 | |||||||
| chr11:64737907 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.814-873C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64737907 | |||||||
| chr11:64738060 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.814-1026T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738060 | |||||||
| chr11:64738085 | AAAATATT others(6): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.814-1064_814-1052d others(15): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738085 | |||||||
| chr11:64738349 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.813+1011C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738349 | |||||||
| chr11:64738495 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0060 others(1): Show |
4 | HG01109.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+865C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738495 | |||||||
| chr11:64738630 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.813+730C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738630 | |||||||
| chr11:64738822 | G | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+538C>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738822 | |||||||
| chr11:64738837 | C | A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+523G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738837 | |||||||
| chr11:64738841 | T | A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+519A>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738841 | |||||||
| chr11:64738846 | A | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+514T>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738846 | |||||||
| chr11:64738850 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+510T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738850 | |||||||
| chr11:64738851 | C | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+509G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738851 | |||||||
| chr11:64738862 | G | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+498C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738862 | |||||||
| chr11:64738864 | C | A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+496G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738864 | |||||||
| chr11:64738865 | A | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+495T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738865 | |||||||
| chr11:64738881 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.813+479C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738881 | |||||||
| chr11:64738893 | C | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+467G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738893 | |||||||
| chr11:64738894 | A | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+466T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738894 | |||||||
| chr11:64738898 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+462C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738898 | |||||||
| chr11:64738905 | T | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+455A>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738905 | |||||||
| chr11:64738909 | G | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+451C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738909 | |||||||
| chr11:64738911 | C | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+449G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738911 | |||||||
| chr11:64738921 | A | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+439T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738921 | |||||||
| chr11:64738957 | T | TA | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
148 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.813+402dupT | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738957 | |||||||
| chr11:64738960 | A | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+400T>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738960 | |||||||
| chr11:64738966 | A | T | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+394T>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738966 | |||||||
| chr11:64738968 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+392T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738968 | |||||||
| chr11:64738978 | A | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+382T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738978 | |||||||
| chr11:64738979 | T | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+381A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738979 | |||||||
| chr11:64738980 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+380T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738980 | |||||||
| chr11:64738981 | ACAATACA others(6): Show |
A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+366_813+378del others(13): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64738981 | |||||||
| chr11:64739006 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.813+354G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739006 | |||||||
| chr11:64739007 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.813+353C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739007 | |||||||
| chr11:64739016 | T | G | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+344A>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739016 | |||||||
| chr11:64739018 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.813+342C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739018 | |||||||
| chr11:64739067 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(79): Show |
174 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.813+293C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739067 | |||||||
| chr11:64739140 | T | TAA | 2 | a0001c0001t0001g0009 a0001c0001t0001g0063 |
6 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+218_813+219dup others(2): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739140 | |||||||
| chr11:64739140 | TA | T | 11 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0078 others(8): Show |
11 | HG02523.hp2 HG03195.hp2 HG06807.hp1 others(8): Show |
intron_variant | MODIFIER | c.813+219delT | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 8/16 | chr11 | 64739140 | |||||||
| chr11:64739617 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0121 |
3 | NA18954.hp1 NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.696+19C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 7/16 | chr11 | 64739617 | |||||||
| chr11:64739843 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
262 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.523-34A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739843 | |||||||
| chr11:64739844 | G | A | 3 | a0001c0002t0001g0011 a0001c0002t0001g0038 a0001c0002t0001g0039 |
6 | HG00140.hp2 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-35C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739844 | |||||||
| chr11:64739844 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.523-35C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739844 | |||||||
| chr11:64739865 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0060 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.523-56G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739865 | |||||||
| chr11:64739884 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.523-75A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739884 | |||||||
| chr11:64739907 | A | C | 1 | a0001c0002t0001g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.523-98T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64739907 | |||||||
| chr11:64740005 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.522+8C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 6/16 | chr11 | 64740005 | |||||||
| chr11:64740183 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.372-20C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740183 | |||||||
| chr11:64740208 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
263 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.372-45T>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740208 | |||||||
| chr11:64740288 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0125 |
4 | NA18946.hp1 NA18954.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-125C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740288 | |||||||
| chr11:64740326 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.372-163G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740326 | |||||||
| chr11:64740327 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
263 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.372-164C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740327 | |||||||
| chr11:64740345 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.372-182T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740345 | |||||||
| chr11:64740364 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.372-201C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740364 | |||||||
| chr11:64740419 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.372-256G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740419 | |||||||
| chr11:64740558 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+390G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740558 | |||||||
| chr11:64740607 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.371+341G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740607 | |||||||
| chr11:64740668 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.371+280C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 5/16 | chr11 | 64740668 | |||||||
| chr11:64741135 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.240-56G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741135 | |||||||
| chr11:64741194 | C | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.240-115G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741194 | |||||||
| chr11:64741197 | G | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0038 a0001c0002t0001g0039 |
6 | HG00140.hp2 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-118C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741197 | |||||||
| chr11:64741198 | C | T | 3 | a0001c0002t0001g0011 a0001c0002t0001g0038 a0001c0002t0001g0039 |
6 | HG00140.hp2 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-119G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741198 | |||||||
| chr11:64741209 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240-130C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741209 | |||||||
| chr11:64741244 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.240-165G>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741244 | |||||||
| chr11:64741270 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.239+169A>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741270 | |||||||
| chr11:64741285 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239+154C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741285 | |||||||
| chr11:64741319 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.239+120C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 4/16 | chr11 | 64741319 | |||||||
| chr11:64741652 | A | G | 8 | a0001c0002t0001g0019 a0001c0002t0001g0030 a0001c0002t0001g0032 others(5): Show |
9 | HG00609.hp1 HG01109.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.177-151T>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/16 | chr11 | 64741652 | |||||||
| chr11:64741669 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.177-168C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/16 | chr11 | 64741669 | |||||||
| chr11:64741767 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
263 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.176+243G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/16 | chr11 | 64741767 | |||||||
| chr11:64741966 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG01175.hp1 HG01496.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.176+44A>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 3/16 | chr11 | 64741966 | |||||||
| chr11:64742208 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.74-96C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/16 | chr11 | 64742208 | |||||||
| chr11:64742306 | C | T | 1 | a0001c0002t0001g0018 | 2 | HG00735.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.74-194G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/16 | chr11 | 64742306 | |||||||
| chr11:64742695 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.73+99G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/16 | chr11 | 64742695 | |||||||
| chr11:64742778 | C | T | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG01175.hp1 HG01496.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.73+16G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 2/16 | chr11 | 64742778 | |||||||
| chr11:64743284 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(2): Show |
17 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-71-347G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743284 | |||||||
| chr11:64743386 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71-449G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743386 | |||||||
| chr11:64743394 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-457C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743394 | |||||||
| chr11:64743426 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
263 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-71-489G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743426 | |||||||
| chr11:64743443 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-71-506C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743443 | |||||||
| chr11:64743458 | C | T | 1 | a0001c0003t0001g0021 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-71-521G>A | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743458 | |||||||
| chr11:64743494 | C | G | 1 | a0001c0002t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-72+509G>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743494 | |||||||
| chr11:64743578 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(83): Show |
180 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.-72+425C>G | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743578 | |||||||
| chr11:64743748 | C | CGCGCCAA others(20): Show |
1 | a0001c0001t0001g0017 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-72+228_-72+254dup others(27): Show |
RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743748 | |||||||
| chr11:64743850 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
175 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.-72+153A>C | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743850 | |||||||
| chr11:64743920 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-72+83C>T | RASGRP2 | ENSG00000068831.19 | transcript | ENST00000394432.8 | protein_coding | 1/16 | chr11 | 64743920 |