Item | Value |
---|---|
geneid | 25780 |
ensemblid | ENSG00000152689.18 |
hgncid | 14545 |
symbol | RASGRP3 |
name | RAS guanyl releasing protein 3 |
refseq_nuc | NM_001139488.2 |
refseq_prot | NP_001132960.1 |
ensembl_nuc | ENST00000403687.8 |
ensembl_prot | ENSP00000384192.3 |
mane_status | MANE Select |
chr | chr2 |
start | 33476649 |
end | 33564731 |
strand | + |
ver | v1.2 |
region | chr2:33476649-33564731 |
region5000 | chr2:33471649-33569731 |
regionname0 | RASGRP3_chr2_33476649_33564731 |
regionname5000 | RASGRP3_chr2_33471649_33569731 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 690 | 359 | 90 | 46 | 184 | 9 | 28 | 142 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0002 | 0/0 | 690 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0003 | 0/0 | 690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0004 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0005 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0006 | 0/0 | 690 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0007 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0008 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
a0009 | 0/0 | 690 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | MGSSG others(685): Show |
chr2 | 33471649 | 33569731 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2070 | 262 | 57 | 41 | 127 | 9 | 26 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0001c0002 | 0/0 | 2070 | 76 | 13 | 4 | 57 | 0 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0001c0003 | 0/0 | 2070 | 15 | 15 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0001c0004 | 0/0 | 2070 | 3 | 3 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0001c0006 | 0/0 | 2070 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0001c0008 | 0/0 | 2070 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0002c0005 | 0/0 | 2070 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0002c0007 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0003c0009 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0003c0011 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0004c0010 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0005c0014 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0006c0015 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0007c0012 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0008c0016 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 | ||
a0009c0013 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ATGGG others(2065): Show |
chr2 | 33471649 | 33569731 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4382 | 62 | 0 | 6 | 53 | 0 | 3 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0002 | 0/0 | 4379 | 45 | 1 | 12 | 27 | 1 | 4 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0003 | 0/0 | 4375 | 19 | 3 | 5 | 5 | 1 | 5 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0004 | 0/0 | 4380 | 14 | 2 | 2 | 7 | 1 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0005 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0007 | 0/0 | 4375 | 12 | 0 | 3 | 8 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0008 | 0/0 | 4380 | 7 | 0 | 1 | 2 | 0 | 4 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0009 | 0/0 | 4380 | 9 | 2 | 3 | 0 | 2 | 2 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0010 | 0/0 | 4379 | 8 | 0 | 0 | 8 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0011 | 0/0 | 4375 | 7 | 7 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0012 | 0/0 | 4371 | 6 | 6 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4366): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0013 | 0/0 | 4370 | 5 | 5 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4365): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0014 | 0/0 | 4375 | 4 | 4 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0015 | 0/0 | 4375 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0016 | 0/0 | 4382 | 3 | 0 | 0 | 3 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0017 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0018 | 0/0 | 4375 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0019 | 0/0 | 4375 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0020 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0021 | 0/0 | 4381 | 3 | 2 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4376): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0022 | 1/0 | 4386 | 3 | 1 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4381): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0023 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0024 | 0/0 | 4379 | 2 | 1 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0025 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0026 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0027 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0028 | 0/0 | 4379 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0029 | 0/0 | 4380 | 2 | 0 | 0 | 1 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0030 | 0/0 | 4371 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4366): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0031 | 0/0 | 4382 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0032 | 0/0 | 4381 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4376): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0034 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0035 | 0/0 | 4386 | 2 | 0 | 1 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4381): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0037 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0038 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0039 | 0/0 | 4379 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0040 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0041 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0043 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0044 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0046 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4378): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0047 | 0/0 | 4385 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4380): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0049 | 0/1 | 4377 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4372): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0050 | 0/0 | 4376 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4371): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0051 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0052 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0053 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0054 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0056 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0057 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0058 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0059 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0060 | 0/0 | 4377 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4372): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0061 | 0/0 | 4381 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4376): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0065 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0001t0066 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0001 | 0/0 | 4382 | 41 | 0 | 1 | 39 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0003 | 0/0 | 4375 | 6 | 0 | 0 | 6 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0004 | 0/0 | 4380 | 4 | 0 | 0 | 3 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0006 | 0/0 | 4379 | 13 | 11 | 2 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0015 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0016 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0017 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0018 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0033 | 0/0 | 4382 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0036 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4381): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0037 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0055 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4369): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0063 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0001c0002t0064 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4381): Show |
chr2 | 33471649 | 33569731 |
a0001c0003t0005 | 0/0 | 4375 | 12 | 12 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0003t0018 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0003t0019 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0003t0026 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0004t0020 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0004t0042 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0006t0005 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0001c0008t0032 | 0/0 | 4381 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4376): Show |
chr2 | 33471649 | 33569731 |
a0002c0005t0003 | 0/0 | 4375 | 2 | 0 | 0 | 0 | 2 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0002c0007t0008 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0003c0009t0048 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0003c0011t0045 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0004c0010t0008 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0005c0014t0001 | 0/0 | 4382 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4377): Show |
chr2 | 33471649 | 33569731 |
a0006c0015t0002 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
a0007c0012t0015 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4370): Show |
chr2 | 33471649 | 33569731 |
a0008c0016t0062 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4375): Show |
chr2 | 33471649 | 33569731 |
a0009c0013t0002 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | ACTTG others(4374): Show |
chr2 | 33471649 | 33569731 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0009g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0010g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0013g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0015g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0016g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0018g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0019g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0019g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0020g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0021g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0021g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0021g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0022g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0022g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0022g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0023g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0023g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0024g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0024g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0025g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0025g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0026g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0027g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0027g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0028g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0028g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0029g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0029g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0030g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0030g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0031g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0031g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0032g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0034g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0034g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0035g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0035g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0037g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0038g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0038g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0039g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0040g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0041g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0043g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0044g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0046g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0047g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0049g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0050g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0051g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0052g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0053g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0054g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0056g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0057g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0058g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0059g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0060g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0061g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0065g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0001t0066g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0015g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0033g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0033g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0036g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0036g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0037g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0055g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0063g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0002t0064g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0019g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0003t0026g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0004t0020g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0004t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0004t0042g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0006t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0006t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0001c0008t0032g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0002c0005t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0002c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0002c0007t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0003c0009t0048g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0003c0011t0045g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0004c0010t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0005c0014t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0006c0015t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0007c0012t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0008c0016t0062g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
a0009c0013t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0053 | g0090 | EUR | FIN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | FIN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00438 | hp1 | a0001 | c0002 | t0033 | g0150 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00558 | hp2 | a0001 | c0001 | t0038 | g0262 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00597 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00609 | hp2 | a0001 | c0002 | t0064 | g0215 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00639 | hp1 | a0001 | c0002 | t0055 | g0059 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | CHS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00738 | hp1 | a0001 | c0002 | t0006 | g0186 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01070 | hp1 | a0001 | c0001 | t0008 | g0242 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01074 | hp1 | a0001 | c0001 | t0009 | g0110 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01074 | hp2 | a0001 | c0001 | t0009 | g0073 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01099 | hp1 | a0001 | c0001 | t0054 | g0038 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01099 | hp2 | a0001 | c0001 | t0035 | g0272 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01109 | hp1 | a0001 | c0001 | t0024 | g0136 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01168 | hp2 | a0001 | c0001 | t0046 | g0105 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01192 | hp2 | a0001 | c0001 | t0009 | g0018 | AMR | PUR | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01255 | hp1 | a0001 | c0008 | t0032 | g0065 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01255 | hp2 | a0001 | c0002 | t0006 | g0187 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01256 | hp2 | a0001 | c0001 | t0032 | g0278 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01361 | hp1 | a0001 | c0001 | t0047 | g0089 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01361 | hp2 | a0001 | c0001 | t0031 | g0314 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01433 | hp1 | a0001 | c0001 | t0056 | g0246 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01496 | hp1 | a0001 | c0001 | t0021 | g0140 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01515 | hp1 | a0001 | c0001 | t0022 | g0334 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01515 | hp2 | a0001 | c0001 | t0028 | g0306 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0019 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01516 | hp2 | a0002 | c0005 | t0003 | g0204 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01517 | hp1 | a0002 | c0005 | t0003 | g0214 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01517 | hp2 | a0001 | c0001 | t0028 | g0305 | EUR | IBS | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01884 | hp1 | a0001 | c0001 | t0039 | g0128 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01884 | hp2 | a0001 | c0004 | t0020 | g0118 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0154 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0191 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0095 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02015 | hp1 | a0001 | c0001 | t0034 | g0274 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02027 | hp2 | a0001 | c0001 | t0066 | g0003 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02055 | hp2 | a0001 | c0003 | t0005 | g0250 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02056 | hp1 | a0004 | c0010 | t0008 | g0317 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02071 | hp2 | a0001 | c0002 | t0063 | g0286 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02074 | hp2 | a0001 | c0001 | t0029 | g0361 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02080 | hp2 | a0001 | c0001 | t0038 | g0144 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02083 | hp1 | a0001 | c0002 | t0037 | g0344 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02083 | hp2 | a0001 | c0002 | t0033 | g0074 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0045 | EAS | CDX | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02257 | hp1 | a0001 | c0001 | t0027 | g0192 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0308 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02258 | hp1 | a0001 | c0002 | t0006 | g0155 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02258 | hp2 | a0001 | c0001 | t0022 | g0109 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0121 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02280 | hp2 | a0001 | c0002 | t0018 | g0135 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02451 | hp1 | a0001 | c0003 | t0005 | g0042 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02451 | hp2 | a0001 | c0002 | t0017 | g0145 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02523 | hp2 | a0005 | c0014 | t0001 | g0010 | EAS | KHV | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0236 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02572 | hp2 | a0001 | c0001 | t0014 | g0133 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02615 | hp1 | a0001 | c0002 | t0006 | g0172 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02622 | hp1 | a0001 | c0001 | t0012 | g0184 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0079 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02630 | hp1 | a0001 | c0003 | t0019 | g0176 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0132 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0178 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02698 | hp2 | a0001 | c0001 | t0009 | g0304 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0123 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0299 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0321 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02735 | hp1 | a0001 | c0001 | t0035 | g0216 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02809 | hp1 | a0001 | c0003 | t0005 | g0190 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0130 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02818 | hp1 | a0001 | c0001 | t0030 | g0125 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02818 | hp2 | a0001 | c0001 | t0057 | g0081 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0166 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02886 | hp2 | a0001 | c0001 | t0027 | g0197 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0137 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02895 | hp2 | a0001 | c0006 | t0005 | g0253 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02896 | hp1 | a0001 | c0001 | t0012 | g0127 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02896 | hp2 | a0001 | c0001 | t0023 | g0258 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02897 | hp1 | a0001 | c0001 | t0023 | g0257 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02897 | hp2 | a0001 | c0006 | t0005 | g0252 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02922 | hp1 | a0001 | c0001 | t0052 | g0301 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0193 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0173 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02970 | hp2 | a0001 | c0001 | t0043 | g0170 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0165 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02976 | hp2 | a0001 | c0003 | t0005 | g0174 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0333 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03041 | hp1 | a0003 | c0011 | t0045 | g0200 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03041 | hp2 | a0001 | c0003 | t0005 | g0119 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0151 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03098 | hp2 | a0001 | c0002 | t0006 | g0237 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03130 | hp2 | a0001 | c0001 | t0051 | g0297 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03139 | hp1 | a0001 | c0001 | t0041 | g0122 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03139 | hp2 | a0001 | c0001 | t0058 | g0124 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03195 | hp1 | a0001 | c0001 | t0040 | g0320 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03195 | hp2 | a0001 | c0001 | t0050 | g0311 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0157 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0082 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03225 | hp2 | a0001 | c0003 | t0005 | g0239 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0298 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0310 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0156 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03486 | hp2 | a0001 | c0003 | t0005 | g0251 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0219 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03491 | hp2 | a0006 | c0015 | t0002 | g0040 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03516 | hp1 | a0001 | c0003 | t0005 | g0255 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0309 | AFR | ESN | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03540 | hp2 | a0001 | c0001 | t0021 | g0153 | AFR | GWD | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03579 | hp1 | a0001 | c0001 | t0026 | g0194 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03579 | hp2 | a0001 | c0004 | t0020 | g0044 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03669 | hp1 | a0001 | c0001 | t0029 | g0053 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0337 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0092 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0148 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03831 | hp2 | a0001 | c0001 | t0060 | g0022 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03927 | hp1 | a0001 | c0001 | t0018 | g0180 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03927 | hp2 | a0001 | c0001 | t0031 | g0233 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03942 | hp1 | a0002 | c0007 | t0008 | g0083 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | STU | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG04228 | hp2 | a0001 | c0001 | t0008 | g0037 | SAS | STU | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0202 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | CHB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18906 | hp1 | a0001 | c0003 | t0026 | g0163 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0164 | AFR | YRI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18943 | hp2 | a0001 | c0001 | t0010 | g0021 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18946 | hp1 | a0001 | c0001 | t0019 | g0279 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18947 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18950 | hp1 | a0001 | c0002 | t0036 | g0269 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18951 | hp1 | a0001 | c0001 | t0061 | g0097 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18954 | hp2 | a0001 | c0001 | t0019 | g0247 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18956 | hp2 | a0001 | c0002 | t0015 | g0276 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18960 | hp2 | a0001 | c0001 | t0010 | g0167 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18962 | hp1 | a0001 | c0001 | t0034 | g0346 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0292 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18964 | hp2 | a0001 | c0001 | t0044 | g0106 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18968 | hp1 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18969 | hp2 | a0001 | c0002 | t0004 | g0228 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18971 | hp1 | a0001 | c0002 | t0036 | g0270 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0227 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18980 | hp1 | a0001 | c0001 | t0010 | g0307 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18981 | hp1 | a0001 | c0001 | t0010 | g0342 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18984 | hp1 | a0001 | c0001 | t0016 | g0367 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18988 | hp2 | a0001 | c0001 | t0007 | g0336 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18998 | hp1 | a0001 | c0001 | t0015 | g0052 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18998 | hp2 | a0001 | c0001 | t0065 | g0355 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18999 | hp1 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19002 | hp1 | a0007 | c0012 | t0015 | g0117 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19003 | hp2 | a0001 | c0001 | t0007 | g0318 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19004 | hp2 | a0001 | c0001 | t0015 | g0218 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19011 | hp1 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19030 | hp1 | a0001 | c0001 | t0024 | g0152 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0254 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19043 | hp1 | a0001 | c0003 | t0018 | g0171 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0238 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19055 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19063 | hp1 | a0001 | c0001 | t0010 | g0324 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19083 | hp2 | a0001 | c0001 | t0037 | g0280 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19085 | hp1 | a0001 | c0002 | t0016 | g0203 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19087 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA19091 | hp2 | a0008 | c0016 | t0062 | g0027 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20752 | hp1 | a0009 | c0013 | t0002 | g0071 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0142 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0091 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20805 | hp2 | a0001 | c0001 | t0009 | g0012 | EUR | TSI | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0217 | SAS | GIH | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0183 | SAS | GIH | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02109 | hp1 | a0001 | c0001 | t0059 | g0201 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02486 | hp2 | a0001 | c0003 | t0005 | g0196 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02559 | hp1 | a0001 | c0001 | t0030 | g0139 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG02559 | hp2 | a0001 | c0003 | t0005 | g0256 | AFR | ACB | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03471 | hp1 | a0001 | c0001 | t0021 | g0146 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG03471 | hp2 | a0001 | c0004 | t0042 | g0199 | AFR | MSL | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
HG06807 | hp2 | a0001 | c0002 | t0006 | g0198 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20300 | hp1 | a0001 | c0002 | t0006 | g0134 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA20300 | hp2 | a0001 | c0001 | t0017 | g0120 | AFR | USA | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA21309 | hp1 | a0001 | c0001 | t0025 | g0076 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
NA21309 | hp2 | a0003 | c0009 | t0048 | g0072 | AFR | LWK | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
homoSapiens | chm13v2 | a0001 | c0001 | t0049 | g0168 | REF | REF | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
homoSapiens | grch38p0 | a0001 | c0001 | t0022 | g0263 | REF | REF | RASGRP3_chr2_33471649_33569731 | RASGRP3 | chr2 | 33471649 | 33569731 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33516634 | C | T | 1 | a0008 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.163C>T | p.Leu55Phe | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/18 | 482/4386 | 163/2073 | 55/690 | chr2 | 33516634 | |||
chr2:33524042 | A | G | 1 | a0006 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.680A>G | p.Asn227Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/18 | 999/4386 | 680/2073 | 227/690 | chr2 | 33524042 | |||
chr2:33527152 | A | G | 1 | a0005 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.823A>G | p.Thr275Ala | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1142/4386 | 823/2073 | 275/690 | chr2 | 33527152 | |||
chr2:33527173 | G | A | 1 | a0002 | 3 | HG01516.hp2 HG01517.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.844G>A | p.Gly282Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1163/4386 | 844/2073 | 282/690 | chr2 | 33527173 | |||
chr2:33539109 | A | G | 1 | a0009 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1177A>G | p.Thr393Ala | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/18 | 1496/4386 | 1177/2073 | 393/690 | chr2 | 33539109 | |||
chr2:33558303 | G | A | 1 | a0004 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1672G>A | p.Gly558Arg | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/18 | 1991/4386 | 1672/2073 | 558/690 | chr2 | 33558303 | |||
chr2:33558682 | G | C | 1 | a0003 | 2 | HG03041.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1716G>C | p.Glu572Asp | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/18 | 2035/4386 | 1716/2073 | 572/690 | chr2 | 33558682 | |||
chr2:33559021 | G | T | 1 | a0007 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.2055G>T | p.Gln685His | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/18 | 2374/4386 | 2055/2073 | 685/690 | chr2 | 33559021 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33527232 | C | A | 1 | a0001c0008 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.903C>A | p.Ile301Ile | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/18 | 1222/4386 | 903/2073 | 301/690 | chr2 | 33527232 | |||
chr2:33534328 | C | T | 1 | a0001c0004 | 3 | HG01884.hp2 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1089C>T | p.Ser363Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/18 | 1408/4386 | 1089/2073 | 363/690 | chr2 | 33534328 | |||
chr2:33549694 | T | C | 4 | a0001c0002 a0001c0006 a0002c0005 others(1): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
synonymous_variant | LOW | c.1485T>C | p.His495His | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/18 | 1804/4386 | 1485/2073 | 495/690 | chr2 | 33549694 | |||
chr2:33558326 | G | A | 2 | a0001c0003 a0001c0006 |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
synonymous_variant | LOW | c.1695G>A | p.Ser565Ser | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/18 | 2014/4386 | 1695/2073 | 565/690 | chr2 | 33558326 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33511727 | T | A | 7 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0023 others(4): Show |
16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-243T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/18 | 3410 | chr2 | 33511727 | ||||||
chr2:33511790 | G | A | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(83): Show |
366 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(363): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/18 | 3347 | chr2 | 33511790 | ||||||
chr2:33515057 | A | G | 1 | a0001c0001t0038 | 2 | HG00558.hp2 HG02080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 80 | chr2 | 33515057 | ||||||
chr2:33515058 | T | G | 2 | a0001c0001t0024 a0001c0001t0043 |
3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 79 | chr2 | 33515058 | ||||||
chr2:33515122 | A | G | 3 | a0001c0001t0037 a0001c0001t0066 a0001c0002t0037 |
3 | HG02027.hp2 HG02083.hp1 NA19083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-15A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/18 | 15 | chr2 | 33515122 | ||||||
chr2:33562748 | C | T | 1 | a0001c0001t0065 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 11 | chr2 | 33562748 | ||||||
chr2:33562801 | T | A | 1 | a0001c0001t0044 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 64 | chr2 | 33562801 | ||||||
chr2:33562811 | T | G | 1 | a0001c0001t0039 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 74 | chr2 | 33562811 | ||||||
chr2:33562909 | CCTAA | C | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
347 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*184_*187delACTA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 184 | INFO_REALIGN_3_PRIME | chr2 | 33562909 | |||||
chr2:33562993 | CTT | C | 65 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(62): Show |
236 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*261_*262delTT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 261 | INFO_REALIGN_3_PRIME | chr2 | 33562993 | |||||
chr2:33563038 | A | G | 6 | a0001c0001t0011 a0001c0001t0043 a0001c0001t0056 others(3): Show |
12 | HG01433.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 301 | chr2 | 33563038 | ||||||
chr2:33563065 | TACTC | T | 3 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0030 |
13 | HG02280.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*330_*333delCTCA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 330 | INFO_REALIGN_3_PRIME | chr2 | 33563065 | |||||
chr2:33563089 | C | T | 18 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(15): Show |
73 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 352 | chr2 | 33563089 | ||||||
chr2:33563137 | T | G | 1 | a0003c0011t0045 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 400 | chr2 | 33563137 | ||||||
chr2:33563163 | A | G | 1 | a0003c0011t0045 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 426 | chr2 | 33563163 | ||||||
chr2:33563203 | CTTGTT | C | 67 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(64): Show |
212 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*487_*491delTTGTT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 487 | INFO_REALIGN_3_PRIME | chr2 | 33563203 | |||||
chr2:33563399 | G | A | 1 | a0001c0002t0033 | 2 | HG00438.hp1 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 662 | chr2 | 33563399 | ||||||
chr2:33563520 | G | C | 1 | a0001c0001t0025 | 2 | HG03209.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 783 | chr2 | 33563520 | ||||||
chr2:33563548 | G | C | 1 | a0003c0009t0048 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 811 | chr2 | 33563548 | ||||||
chr2:33563588 | C | T | 30 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(27): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 851 | chr2 | 33563588 | ||||||
chr2:33563592 | T | TAACA | 12 | a0001c0001t0002 a0001c0001t0028 a0001c0001t0032 others(9): Show |
58 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*859dupAACA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 860 | INFO_REALIGN_3_PRIME | chr2 | 33563592 | |||||
chr2:33563680 | G | GA | 7 | a0001c0001t0008 a0001c0001t0021 a0001c0001t0031 others(4): Show |
16 | HG01070.hp1 HG01361.hp2 HG01496.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*953dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 954 | INFO_REALIGN_3_PRIME | chr2 | 33563680 | |||||
chr2:33563680 | GA | G | 3 | a0001c0001t0013 a0001c0002t0055 a0008c0016t0062 |
7 | HG00639.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*953delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 953 | INFO_REALIGN_3_PRIME | chr2 | 33563680 | |||||
chr2:33563965 | A | G | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(6): Show |
44 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1228 | chr2 | 33563965 | ||||||
chr2:33564001 | C | G | 38 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(35): Show |
128 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1264C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1264 | chr2 | 33564001 | ||||||
chr2:33564002 | G | A | 1 | a0001c0001t0051 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1265 | chr2 | 33564002 | ||||||
chr2:33564032 | G | T | 5 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0052 others(2): Show |
18 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1295G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1295 | chr2 | 33564032 | ||||||
chr2:33564082 | G | A | 1 | a0001c0001t0053 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1345 | chr2 | 33564082 | ||||||
chr2:33564138 | T | C | 2 | a0001c0001t0052 a0003c0009t0048 |
2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1401T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1401 | chr2 | 33564138 | ||||||
chr2:33564178 | A | AAGTT | 7 | a0001c0001t0010 a0001c0001t0044 a0001c0001t0061 others(4): Show |
15 | HG00597.hp1 HG00609.hp2 HG02027.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1443_*1446dupGTTA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1447 | INFO_REALIGN_3_PRIME | chr2 | 33564178 | |||||
chr2:33564316 | A | C | 2 | a0001c0001t0052 a0003c0009t0048 |
2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1579A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1579 | chr2 | 33564316 | ||||||
chr2:33564335 | T | TATCA | 4 | a0001c0001t0008 a0001c0001t0031 a0002c0007t0008 others(1): Show |
11 | HG01070.hp1 HG01361.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1599_*1602dupATCA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1603 | INFO_REALIGN_3_PRIME | chr2 | 33564335 | |||||
chr2:33564344 | G | A | 2 | a0001c0001t0017 a0001c0002t0017 |
3 | HG02451.hp2 HG02572.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1607 | chr2 | 33564344 | ||||||
chr2:33564426 | T | C | 2 | a0001c0001t0052 a0003c0009t0048 |
2 | HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1689 | chr2 | 33564426 | ||||||
chr2:33564467 | A | G | 40 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(37): Show |
132 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1730A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1730 | chr2 | 33564467 | ||||||
chr2:33564650 | A | G | 1 | a0001c0002t0063 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1913A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1913 | chr2 | 33564650 | ||||||
chr2:33564723 | A | G | 1 | a0001c0001t0054 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1986A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 18/18 | 1986 | chr2 | 33564723 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33476728 | C | CCT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(132): Show |
137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-261+36_-261+37dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476728 | ||||||
chr2:33476757 | C | CCGTG | 9 | a0001c0001t0001g0115 a0001c0001t0002g0108 a0001c0001t0002g0111 others(6): Show |
9 | HG00558.hp1 HG01074.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+51_-261+54dup others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476757 | ||||||
chr2:33476758 | C | CGT | 19 | a0001c0001t0002g0241 a0001c0001t0002g0243 a0001c0001t0002g0245 others(16): Show |
19 | HG00642.hp2 HG01070.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+88_-261+89dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGCGT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0101 others(17): Show |
21 | HG00323.hp1 HG00423.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGCGTG others(1): Show |
49 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(46): Show |
49 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGCGTG others(3): Show |
22 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0030 others(19): Show |
22 | HG01099.hp1 HG01175.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGCGTG others(5): Show |
14 | a0001c0001t0001g0016 a0001c0001t0002g0008 a0001c0001t0002g0015 others(11): Show |
14 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+54_-261+55ins others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGCGTG others(7): Show |
1 | a0001c0001t0066g0003 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+54_-261+55ins others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGT | 5 | a0001c0001t0003g0235 a0001c0001t0013g0238 a0001c0001t0017g0236 others(2): Show |
5 | HG01993.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+86_-261+89dup others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGT | 25 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0225 others(22): Show |
25 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-261+84_-261+89dup others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(1): Show |
15 | a0001c0001t0002g0207 a0001c0001t0003g0208 a0001c0001t0003g0209 others(12): Show |
15 | HG01516.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+82_-261+89dup others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(3): Show |
8 | a0001c0001t0004g0195 a0001c0001t0011g0193 a0001c0001t0012g0123 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-261+80_-261+89dup others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(5): Show |
6 | a0001c0001t0002g0185 a0001c0001t0002g0188 a0001c0001t0004g0189 others(3): Show |
6 | HG00738.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+78_-261+89dup others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(7): Show |
14 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0182 others(11): Show |
14 | HG01071.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+76_-261+89dup others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(9): Show |
8 | a0001c0001t0001g0169 a0001c0001t0010g0167 a0001c0001t0013g0121 others(5): Show |
8 | HG01070.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-261+74_-261+89dup others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(11): Show |
13 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0161 others(10): Show |
13 | HG01891.hp1 HG02258.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.-261+72_-261+89dup others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(13): Show |
7 | a0001c0001t0003g0147 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
7 | HG00438.hp1 HG01952.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+70_-261+89dup others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(15): Show |
6 | a0001c0001t0002g0142 a0001c0001t0004g0141 a0001c0001t0004g0143 others(3): Show |
6 | HG00639.hp2 HG01496.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+68_-261+89dup others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(17): Show |
3 | a0001c0001t0003g0138 a0001c0001t0024g0136 a0001c0002t0006g0137 |
3 | HG01109.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+66_-261+89dup others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | C | CGTGTGTG others(19): Show |
1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-261+64_-261+89dup others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | CGT | C | 9 | a0001c0001t0009g0304 a0001c0001t0010g0307 a0001c0001t0011g0308 others(6): Show |
9 | HG01515.hp2 HG01517.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+88_-261+89del others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | CGTGT | C | 9 | a0001c0001t0004g0129 a0001c0001t0011g0310 a0001c0001t0012g0002 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+86_-261+89del others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0002g0313 others(3): Show |
6 | HG01361.hp2 HG03195.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+82_-261+89del others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476758 | CGTGTGTG others(3): Show |
C | 52 | a0001c0001t0001g0319 a0001c0001t0001g0322 a0001c0001t0001g0323 others(49): Show |
52 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-261+80_-261+89del others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476758 | ||||||
chr2:33476764 | T | C | 1 | a0007c0012t0015g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-261+57T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476764 | |||||||
chr2:33476823 | T | C | 40 | a0001c0001t0001g0319 a0001c0001t0001g0322 a0001c0001t0001g0323 others(37): Show |
40 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-261+116T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476823 | |||||||
chr2:33476846 | G | A | 1 | a0001c0001t0047g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-261+139G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33476846 | |||||||
chr2:33476930 | C | CG | 139 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(136): Show |
141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-261+224dupG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33476930 | ||||||
chr2:33477035 | T | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(139): Show |
144 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-261+328T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477035 | |||||||
chr2:33477050 | G | GA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(136): Show |
141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-261+343_-261+344i others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477050 | |||||||
chr2:33477059 | A | G | 3 | a0001c0001t0012g0184 a0001c0001t0043g0170 a0001c0003t0005g0190 |
3 | HG02622.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-261+352A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477059 | |||||||
chr2:33477136 | C | T | 38 | a0001c0001t0001g0319 a0001c0001t0001g0322 a0001c0001t0001g0323 others(35): Show |
38 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-261+429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477136 | |||||||
chr2:33477308 | C | T | 4 | a0001c0001t0012g0123 a0001c0001t0030g0125 a0001c0001t0041g0122 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+601C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477308 | |||||||
chr2:33477339 | T | A | 6 | a0001c0001t0013g0164 a0001c0001t0021g0153 a0001c0002t0006g0137 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+632T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477339 | |||||||
chr2:33477344 | T | C | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-261+637T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477344 | |||||||
chr2:33477366 | C | T | 5 | a0001c0001t0021g0146 a0001c0001t0024g0136 a0001c0001t0024g0152 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+659C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477366 | |||||||
chr2:33477419 | C | G | 86 | a0001c0001t0001g0107 a0001c0001t0001g0159 a0001c0001t0001g0160 others(83): Show |
86 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-261+712C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477419 | |||||||
chr2:33477439 | G | T | 30 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0232 others(27): Show |
30 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261+732G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477439 | |||||||
chr2:33477448 | C | A | 1 | a0001c0001t0007g0259 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-261+741C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477448 | |||||||
chr2:33477612 | G | A | 3 | a0001c0001t0004g0141 a0001c0001t0021g0140 a0001c0002t0006g0165 |
3 | HG01496.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-261+905G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477612 | |||||||
chr2:33477612 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(134): Show |
139 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-261+905G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477612 | |||||||
chr2:33477795 | C | G | 1 | a0001c0002t0018g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-261+1088C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477795 | |||||||
chr2:33477835 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(256): Show |
261 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.-261+1128C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477835 | |||||||
chr2:33477838 | G | A | 6 | a0001c0001t0013g0164 a0001c0001t0021g0153 a0001c0002t0006g0137 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+1131G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477838 | |||||||
chr2:33477878 | T | C | 15 | a0001c0001t0004g0129 a0001c0001t0012g0002 a0001c0001t0012g0127 others(12): Show |
16 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-261+1171T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477878 | |||||||
chr2:33477936 | C | T | 90 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(87): Show |
90 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-261+1229C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477936 | |||||||
chr2:33477986 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0011g0202 a0001c0001t0026g0194 others(2): Show |
5 | HG02109.hp1 HG02129.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+1279C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33477986 | |||||||
chr2:33478013 | C | T | 1 | a0002c0007t0008g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-261+1306C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478013 | |||||||
chr2:33478142 | G | A | 4 | a0001c0001t0005g0175 a0001c0003t0005g0173 a0001c0003t0005g0174 others(1): Show |
4 | HG02630.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+1435G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478142 | |||||||
chr2:33478150 | C | G | 23 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0169 others(20): Show |
23 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-261+1443C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478150 | |||||||
chr2:33478322 | G | A | 54 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0225 others(51): Show |
54 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-261+1615G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478322 | |||||||
chr2:33478472 | C | T | 34 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(31): Show |
34 | HG01358.hp2 HG02071.hp2 HG02074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-261+1765C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478472 | |||||||
chr2:33478490 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(197): Show |
202 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.-261+1783C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478490 | |||||||
chr2:33478536 | G | A | 1 | a0001c0002t0001g0352 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-261+1829G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478536 | |||||||
chr2:33478644 | C | T | 1 | a0001c0001t0002g0015 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-261+1937C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478644 | |||||||
chr2:33478682 | A | G | 1 | a0001c0002t0001g0234 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-261+1975A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478682 | |||||||
chr2:33478708 | G | A | 3 | a0001c0001t0030g0139 a0001c0002t0006g0186 a0001c0003t0018g0171 |
3 | HG00738.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-261+2001G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478708 | |||||||
chr2:33478721 | C | T | 27 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0169 others(24): Show |
27 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.-261+2014C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478721 | |||||||
chr2:33478788 | C | T | 55 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(52): Show |
56 | HG01358.hp2 HG01884.hp1 HG02071.hp2 others(53): Show |
intron_variant | MODIFIER | c.-261+2081C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478788 | |||||||
chr2:33478829 | A | C | 3 | a0001c0001t0012g0184 a0001c0001t0043g0170 a0001c0003t0005g0190 |
3 | HG02622.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-261+2122A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478829 | |||||||
chr2:33478833 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-261+2126T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478833 | |||||||
chr2:33478863 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(138): Show |
142 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-261+2156G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33478863 | |||||||
chr2:33479056 | A | G | 45 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0225 others(42): Show |
45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-261+2349A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479056 | |||||||
chr2:33479206 | C | A | 4 | a0001c0001t0012g0123 a0001c0001t0021g0153 a0001c0001t0030g0125 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+2499C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479206 | |||||||
chr2:33479253 | G | T | 5 | a0001c0001t0005g0175 a0001c0002t0006g0166 a0001c0003t0005g0173 others(2): Show |
5 | HG02886.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+2546G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479253 | |||||||
chr2:33479363 | G | A | 1 | a0004c0010t0008g0317 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-261+2656G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479363 | |||||||
chr2:33479411 | A | ACTC | 52 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0115 others(49): Show |
53 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-261+2706_-261+270 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33479411 | ||||||
chr2:33479417 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-261+2710C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479417 | |||||||
chr2:33479551 | G | A | 4 | a0001c0001t0014g0191 a0001c0001t0027g0192 a0001c0001t0027g0197 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+2844G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479551 | |||||||
chr2:33479665 | T | C | 1 | a0001c0001t0022g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-261+2958T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479665 | |||||||
chr2:33479694 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0211 a0001c0001t0001g0232 others(12): Show |
15 | HG00544.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+2987A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479694 | |||||||
chr2:33479718 | C | A | 93 | a0001c0001t0001g0020 a0001c0001t0001g0260 a0001c0001t0001g0261 others(90): Show |
94 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.-261+3011C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479718 | |||||||
chr2:33479782 | C | G | 1 | a0001c0001t0030g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-261+3075C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479782 | |||||||
chr2:33479874 | A | ATTACAT | 4 | a0001c0001t0009g0213 a0001c0001t0011g0082 a0001c0001t0043g0170 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+3167_-261+316 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479874 | |||||||
chr2:33479875 | G | A | 4 | a0001c0001t0009g0213 a0001c0001t0011g0082 a0001c0001t0043g0170 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+3168G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479875 | |||||||
chr2:33479883 | T | C | 24 | a0001c0001t0001g0115 a0001c0001t0001g0260 a0001c0001t0001g0332 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-261+3176T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479883 | |||||||
chr2:33479902 | A | G | 42 | a0001c0001t0001g0115 a0001c0001t0001g0260 a0001c0001t0001g0332 others(39): Show |
42 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-261+3195A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479902 | |||||||
chr2:33479909 | T | G | 9 | a0001c0001t0004g0141 a0001c0001t0023g0257 a0001c0001t0023g0258 others(6): Show |
9 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+3202T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33479909 | |||||||
chr2:33480042 | A | AT | 92 | a0001c0001t0001g0016 a0001c0001t0001g0084 a0001c0001t0001g0085 others(89): Show |
92 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-261+3355dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | ||||||
chr2:33480042 | A | ATT | 46 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0159 others(43): Show |
46 | HG00323.hp1 HG00423.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+3354_-261+335 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | ||||||
chr2:33480042 | AT | A | 12 | a0001c0001t0001g0331 a0001c0001t0004g0141 a0001c0001t0009g0304 others(9): Show |
12 | HG01168.hp2 HG01256.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+3355delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | ||||||
chr2:33480042 | ATTT | A | 28 | a0001c0001t0001g0115 a0001c0001t0001g0332 a0001c0001t0002g0142 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-261+3353_-261+335 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33480042 | ||||||
chr2:33480074 | G | A | 1 | a0001c0001t0004g0091 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-261+3367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480074 | |||||||
chr2:33480105 | A | C | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+3398A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480105 | |||||||
chr2:33480108 | T | A | 1 | a0001c0002t0006g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-261+3401T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480108 | |||||||
chr2:33480128 | C | T | 3 | a0001c0001t0005g0175 a0001c0001t0011g0193 a0001c0001t0020g0309 |
3 | HG02965.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-261+3421C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480128 | |||||||
chr2:33480167 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0332 others(67): Show |
71 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-261+3460T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480167 | |||||||
chr2:33480188 | G | A | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+3481G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480188 | |||||||
chr2:33480199 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-261+3492T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480199 | |||||||
chr2:33480318 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0035g0272 |
2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-261+3611C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480318 | |||||||
chr2:33480322 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(43): Show |
47 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-261+3615C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480322 | |||||||
chr2:33480376 | A | T | 1 | a0001c0001t0007g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-261+3669A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480376 | |||||||
chr2:33480436 | A | G | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+3729A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480436 | |||||||
chr2:33480497 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(47): Show |
51 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-261+3790T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480497 | |||||||
chr2:33480513 | G | C | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+3806G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480513 | |||||||
chr2:33480524 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-261+3817G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480524 | |||||||
chr2:33480531 | G | A | 1 | a0001c0002t0001g0350 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-261+3824G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480531 | |||||||
chr2:33480538 | G | A | 1 | a0001c0001t0021g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-261+3831G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480538 | |||||||
chr2:33480565 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+3858A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480565 | |||||||
chr2:33480638 | A | G | 1 | a0001c0001t0066g0003 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+3931A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480638 | |||||||
chr2:33480853 | T | C | 1 | a0001c0001t0002g0358 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-261+4146T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480853 | |||||||
chr2:33480923 | G | A | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+4216G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480923 | |||||||
chr2:33480931 | G | C | 9 | a0001c0001t0004g0141 a0001c0001t0011g0082 a0001c0001t0043g0170 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+4224G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480931 | |||||||
chr2:33480944 | T | A | 21 | a0001c0001t0003g0043 a0001c0001t0003g0138 a0001c0001t0009g0110 others(18): Show |
21 | HG01074.hp1 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+4237T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33480944 | |||||||
chr2:33481019 | T | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4312T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481019 | |||||||
chr2:33481041 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0004g0357 others(2): Show |
5 | NA18944.hp2 NA18945.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+4334C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481041 | |||||||
chr2:33481075 | G | C | 1 | a0001c0001t0041g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-261+4368G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481075 | |||||||
chr2:33481247 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-261+4540C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481247 | |||||||
chr2:33481254 | C | T | 1 | a0001c0001t0030g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-261+4547C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481254 | |||||||
chr2:33481299 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4592C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481299 | |||||||
chr2:33481452 | C | T | 1 | a0009c0013t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-261+4745C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481452 | |||||||
chr2:33481519 | C | T | 1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+4812C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481519 | |||||||
chr2:33481588 | G | A | 4 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0001c0004t0020g0044 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+4881G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481588 | |||||||
chr2:33481611 | C | T | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+4904C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481611 | |||||||
chr2:33481682 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-261+4975C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481682 | |||||||
chr2:33481894 | G | A | 1 | a0001c0002t0006g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-261+5187G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481894 | |||||||
chr2:33481896 | T | C | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+5189T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481896 | |||||||
chr2:33481923 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0011g0310 a0001c0002t0018g0135 |
3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-261+5216C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33481923 | |||||||
chr2:33482017 | AT | A | 12 | a0001c0001t0004g0141 a0001c0001t0011g0082 a0001c0001t0027g0192 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+5324delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33482017 | ||||||
chr2:33482087 | C | T | 1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+5380C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482087 | |||||||
chr2:33482114 | T | A | 9 | a0001c0001t0004g0141 a0001c0001t0011g0082 a0001c0001t0043g0170 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+5407T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482114 | |||||||
chr2:33482114 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(63): Show |
67 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-261+5407T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482114 | |||||||
chr2:33482158 | C | T | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+5451C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482158 | |||||||
chr2:33482289 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(70): Show |
74 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-261+5582G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482289 | |||||||
chr2:33482307 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+5600C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482307 | |||||||
chr2:33482314 | G | T | 1 | a0001c0001t0011g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-261+5607G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482314 | |||||||
chr2:33482332 | T | C | 16 | a0001c0001t0003g0138 a0001c0001t0009g0110 a0001c0001t0011g0079 others(13): Show |
16 | HG01074.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-261+5625T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482332 | |||||||
chr2:33482416 | G | A | 1 | a0001c0001t0011g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+5709G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482416 | |||||||
chr2:33482419 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0004g0091 a0001c0001t0009g0012 others(2): Show |
5 | HG01515.hp1 HG02258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+5712A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482419 | |||||||
chr2:33482557 | G | T | 10 | a0001c0001t0002g0207 a0001c0001t0002g0226 a0001c0001t0002g0229 others(7): Show |
10 | HG02132.hp2 NA18747.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+5850G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482557 | |||||||
chr2:33482608 | C | A | 1 | a0001c0002t0001g0113 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-261+5901C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482608 | |||||||
chr2:33482667 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(43): Show |
47 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-261+5960T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482667 | |||||||
chr2:33482717 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-261+6010G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482717 | |||||||
chr2:33482778 | A | T | 1 | a0001c0001t0041g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-261+6071A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33482778 | |||||||
chr2:33483013 | G | A | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+6306G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483013 | |||||||
chr2:33483034 | A | AT | 15 | a0001c0001t0003g0138 a0001c0001t0009g0110 a0001c0001t0011g0079 others(12): Show |
15 | HG01074.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+6329dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483034 | ||||||
chr2:33483036 | TA | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(82): Show |
86 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.-261+6341delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483036 | ||||||
chr2:33483038 | A | T | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+6331A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483038 | |||||||
chr2:33483273 | G | A | 1 | a0001c0001t0059g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-261+6566G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483273 | |||||||
chr2:33483347 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(50): Show |
54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+6640T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483347 | |||||||
chr2:33483424 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(75): Show |
79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-261+6717A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483424 | |||||||
chr2:33483475 | T | C | 15 | a0001c0001t0003g0138 a0001c0001t0009g0110 a0001c0001t0011g0079 others(12): Show |
15 | HG01074.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+6768T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483475 | |||||||
chr2:33483486 | A | AT | 137 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0024 others(134): Show |
138 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-261+6799dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483486 | A | ATT | 50 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0169 others(47): Show |
50 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-261+6798_-261+679 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483486 | A | ATTT | 8 | a0001c0001t0001g0069 a0001c0001t0002g0068 a0001c0001t0002g0313 others(5): Show |
8 | HG02132.hp1 HG03516.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.-261+6797_-261+679 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483486 | AT | A | 23 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0335 others(20): Show |
23 | HG00323.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-261+6799delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483486 | ATTTTTT | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(41): Show |
45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-261+6794_-261+679 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483486 | ATTTTTTT | A | 6 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(3): Show |
6 | HG01884.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+6793_-261+679 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483486 | ||||||
chr2:33483511 | C | T | 2 | a0001c0001t0016g0367 a0001c0001t0060g0022 |
2 | HG03831.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-261+6804C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483511 | |||||||
chr2:33483582 | G | A | 2 | a0001c0001t0041g0122 a0001c0002t0001g0359 |
2 | HG03139.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-261+6875G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483582 | |||||||
chr2:33483583 | G | C | 1 | a0001c0001t0038g0262 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-261+6876G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483583 | |||||||
chr2:33483586 | T | TC | 53 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(50): Show |
54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+6880dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33483586 | ||||||
chr2:33483591 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(66): Show |
70 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-261+6884T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483591 | |||||||
chr2:33483611 | C | G | 1 | a0001c0001t0014g0191 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-261+6904C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483611 | |||||||
chr2:33483682 | T | C | 1 | a0001c0001t0011g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+6975T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483682 | |||||||
chr2:33483696 | T | A | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+6989T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483696 | |||||||
chr2:33483793 | C | G | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+7086C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483793 | |||||||
chr2:33483891 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-261+7184G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33483891 | |||||||
chr2:33484131 | C | A | 1 | a0001c0001t0011g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-261+7424C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484131 | |||||||
chr2:33484160 | C | A | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+7453C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484160 | |||||||
chr2:33484219 | G | A | 1 | a0001c0001t0037g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-261+7512G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484219 | |||||||
chr2:33484280 | G | T | 1 | a0001c0001t0037g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-261+7573G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484280 | |||||||
chr2:33484376 | A | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+7669A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484376 | |||||||
chr2:33484509 | A | G | 1 | a0001c0004t0020g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+7802A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484509 | |||||||
chr2:33484536 | A | AT | 17 | a0001c0001t0002g0248 a0001c0001t0003g0138 a0001c0001t0009g0110 others(14): Show |
17 | HG01074.hp1 HG02257.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-261+7841dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33484536 | ||||||
chr2:33484713 | C | T | 1 | a0001c0002t0001g0364 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-261+8006C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484713 | |||||||
chr2:33484730 | C | T | 4 | a0001c0001t0001g0101 a0001c0001t0002g0102 a0001c0002t0001g0100 others(1): Show |
4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+8023C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484730 | |||||||
chr2:33484822 | A | G | 37 | a0001c0001t0001g0061 a0001c0001t0001g0107 a0001c0001t0001g0177 others(34): Show |
37 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.-261+8115A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484822 | |||||||
chr2:33484894 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(52): Show |
56 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-261+8187T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484894 | |||||||
chr2:33484973 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(156): Show |
160 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.-261+8266T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484973 | |||||||
chr2:33484975 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(52): Show |
56 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-261+8268G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33484975 | |||||||
chr2:33485158 | A | G | 2 | a0001c0001t0002g0220 a0001c0001t0003g0296 |
2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-261+8451A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485158 | |||||||
chr2:33485222 | A | C | 38 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0050 others(35): Show |
38 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-261+8515A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485222 | |||||||
chr2:33485356 | G | A | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+8649G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485356 | |||||||
chr2:33485493 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+8786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485493 | |||||||
chr2:33485510 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(114): Show |
118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.-261+8803G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485510 | |||||||
chr2:33485530 | G | C | 3 | a0001c0001t0001g0264 a0001c0002t0001g0265 a0001c0002t0001g0350 |
3 | HG00423.hp2 NA18948.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-261+8823G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485530 | |||||||
chr2:33485761 | T | C | 3 | a0001c0001t0011g0082 a0001c0001t0043g0170 a0001c0004t0042g0199 |
3 | HG02970.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-261+9054T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485761 | |||||||
chr2:33485768 | A | G | 2 | a0001c0001t0003g0138 a0001c0002t0006g0165 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+9061A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485768 | |||||||
chr2:33485796 | G | A | 2 | a0001c0001t0052g0301 a0001c0002t0006g0151 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-261+9089G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33485796 | |||||||
chr2:33486042 | C | T | 5 | a0001c0001t0001g0319 a0001c0001t0002g0029 a0001c0001t0010g0011 others(2): Show |
5 | NA18952.hp1 NA18998.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+9335C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486042 | |||||||
chr2:33486120 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-261+9413C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486120 | |||||||
chr2:33486164 | AT | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(244): Show |
249 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.-261+9471delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | ||||||
chr2:33486164 | ATT | A | 28 | a0001c0001t0002g0111 a0001c0001t0002g0231 a0001c0001t0003g0138 others(25): Show |
28 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-261+9470_-261+947 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | ||||||
chr2:33486164 | ATTT | A | 23 | a0001c0001t0001g0061 a0001c0001t0001g0181 a0001c0001t0001g0260 others(20): Show |
23 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.-261+9469_-261+947 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486164 | ||||||
chr2:33486166 | T | A | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+9459T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486166 | |||||||
chr2:33486169 | T | A | 7 | a0001c0001t0001g0266 a0001c0001t0001g0316 a0001c0001t0002g0285 others(4): Show |
7 | HG00423.hp1 NA18949.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+9462T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486169 | |||||||
chr2:33486170 | T | A | 10 | a0001c0001t0012g0123 a0001c0001t0013g0298 a0001c0001t0025g0157 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+9463T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486170 | |||||||
chr2:33486178 | T | TGA | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | NA18945.hp2 NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-261+9483_-261+948 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486178 | ||||||
chr2:33486222 | T | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | NA18956.hp1 NA18960.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+9515T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486222 | |||||||
chr2:33486310 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+9603C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486310 | |||||||
chr2:33486318 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(47): Show |
51 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-261+9611C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486318 | |||||||
chr2:33486327 | C | T | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+9620C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486327 | |||||||
chr2:33486492 | C | CT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(69): Show |
73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-261+9788dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33486492 | ||||||
chr2:33486552 | G | T | 1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+9845G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486552 | |||||||
chr2:33486698 | G | A | 2 | a0001c0001t0050g0311 a0001c0001t0060g0022 |
2 | HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-261+9991G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486698 | |||||||
chr2:33486716 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(45): Show |
49 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-261+10009G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486716 | |||||||
chr2:33486852 | C | T | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10145C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486852 | |||||||
chr2:33486854 | G | A | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-261+10147G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486854 | |||||||
chr2:33486900 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(103): Show |
107 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-261+10193T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486900 | |||||||
chr2:33486922 | C | T | 10 | a0001c0001t0012g0123 a0001c0001t0013g0298 a0001c0001t0025g0157 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+10215C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486922 | |||||||
chr2:33486939 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-261+10232G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486939 | |||||||
chr2:33486964 | A | G | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10257A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486964 | |||||||
chr2:33486990 | A | T | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+10283A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33486990 | |||||||
chr2:33487002 | C | A | 1 | a0001c0001t0002g0358 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-261+10295C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487002 | |||||||
chr2:33487048 | T | C | 1 | a0001c0002t0033g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-261+10341T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487048 | |||||||
chr2:33487069 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0003g0302 |
2 | HG00642.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-261+10362G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487069 | |||||||
chr2:33487118 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+10411A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487118 | |||||||
chr2:33487144 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+10437A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487144 | |||||||
chr2:33487175 | A | G | 1 | a0001c0001t0013g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-261+10468A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487175 | |||||||
chr2:33487271 | A | T | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+10564A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487271 | |||||||
chr2:33487336 | C | T | 1 | a0001c0001t0060g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-261+10629C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487336 | |||||||
chr2:33487346 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-261+10639C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487346 | |||||||
chr2:33487387 | G | C | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+10680G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487387 | |||||||
chr2:33487418 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0275 a0001c0001t0002g0068 others(2): Show |
5 | HG02132.hp1 NA18991.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+10711A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487418 | |||||||
chr2:33487580 | A | G | 1 | a0001c0001t0010g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-261+10873A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487580 | |||||||
chr2:33487602 | C | A | 3 | a0001c0002t0006g0166 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+10895C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487602 | |||||||
chr2:33487898 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0030 others(237): Show |
242 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(239): Show |
intron_variant | MODIFIER | c.-261+11191T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487898 | |||||||
chr2:33487962 | G | A | 2 | a0001c0001t0015g0052 a0007c0012t0015g0117 |
2 | NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-261+11255G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487962 | |||||||
chr2:33487968 | A | C | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+11261A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33487968 | |||||||
chr2:33488080 | A | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(39): Show |
43 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-261+11373A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488080 | |||||||
chr2:33488083 | C | G | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+11376C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488083 | |||||||
chr2:33488142 | A | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11435A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488142 | |||||||
chr2:33488242 | T | A | 1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-261+11535T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488242 | |||||||
chr2:33488352 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11645C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488352 | |||||||
chr2:33488392 | T | C | 1 | a0001c0002t0006g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-261+11685T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488392 | |||||||
chr2:33488398 | A | C | 2 | a0001c0001t0011g0082 a0001c0004t0020g0044 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-261+11691A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488398 | |||||||
chr2:33488460 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0345 |
2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-261+11753G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488460 | |||||||
chr2:33488493 | G | A | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11786G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488493 | |||||||
chr2:33488581 | C | A | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+11874C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488581 | |||||||
chr2:33488669 | G | A | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11962G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488669 | |||||||
chr2:33488670 | C | A | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+11963C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488670 | |||||||
chr2:33488678 | C | T | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-261+11971C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488678 | |||||||
chr2:33488719 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-261+12012C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488719 | |||||||
chr2:33488734 | A | T | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+12027A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488734 | |||||||
chr2:33488740 | G | A | 2 | a0001c0002t0017g0145 a0003c0009t0048g0072 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+12033G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33488740 | |||||||
chr2:33488954 | A | AT | 38 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(35): Show |
38 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(35): Show |
intron_variant | MODIFIER | c.-261+12259dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33488954 | ||||||
chr2:33488954 | AT | A | 9 | a0001c0001t0007g0095 a0001c0001t0009g0019 a0001c0001t0009g0213 others(6): Show |
9 | HG01361.hp1 HG01516.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+12259delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33488954 | ||||||
chr2:33489038 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(42): Show |
46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+12331G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489038 | |||||||
chr2:33489097 | G | C | 1 | a0001c0001t0011g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-261+12390G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489097 | |||||||
chr2:33489129 | A | G | 2 | a0001c0001t0043g0170 a0001c0004t0042g0199 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-261+12422A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489129 | |||||||
chr2:33489171 | A | G | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+12464A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489171 | |||||||
chr2:33489227 | A | T | 14 | a0001c0001t0003g0138 a0001c0001t0009g0110 a0001c0001t0011g0079 others(11): Show |
14 | HG01074.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-261+12520A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489227 | |||||||
chr2:33489280 | A | G | 1 | a0001c0002t0006g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-261+12573A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489280 | |||||||
chr2:33489333 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-261+12626A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489333 | |||||||
chr2:33489336 | G | T | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+12629G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489336 | |||||||
chr2:33489367 | C | T | 3 | a0001c0001t0002g0347 a0001c0001t0043g0170 a0001c0004t0042g0199 |
3 | HG02970.hp2 HG03471.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-261+12660C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489367 | |||||||
chr2:33489489 | C | G | 1 | a0001c0003t0005g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-261+12782C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489489 | |||||||
chr2:33489531 | T | G | 2 | a0001c0001t0019g0279 a0001c0002t0001g0025 |
2 | NA18946.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-261+12824T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489531 | |||||||
chr2:33489542 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(55): Show |
59 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-261+12835T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489542 | |||||||
chr2:33489602 | A | G | 35 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
35 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.-261+12895A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489602 | |||||||
chr2:33489796 | C | G | 1 | a0001c0002t0006g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+13089C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489796 | |||||||
chr2:33489952 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0004g0091 a0001c0001t0009g0012 others(2): Show |
5 | HG01515.hp1 HG02258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+13245A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33489952 | |||||||
chr2:33490000 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13293C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490000 | |||||||
chr2:33490021 | CT | C | 32 | a0001c0001t0001g0061 a0001c0001t0001g0177 a0001c0001t0001g0181 others(29): Show |
32 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.-261+13315delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490021 | |||||||
chr2:33490203 | T | G | 6 | a0001c0001t0011g0202 a0001c0001t0013g0121 a0001c0001t0058g0124 others(3): Show |
6 | HG01255.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13496T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490203 | |||||||
chr2:33490360 | G | A | 2 | a0001c0001t0050g0311 a0001c0001t0060g0022 |
2 | HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-261+13653G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490360 | |||||||
chr2:33490365 | C | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13658C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490365 | |||||||
chr2:33490549 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-261+13842C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490549 | |||||||
chr2:33490610 | C | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(41): Show |
44 | HG01074.hp1 HG01255.hp1 HG01358.hp2 others(41): Show |
intron_variant | MODIFIER | c.-261+13903C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490610 | |||||||
chr2:33490675 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(155): Show |
159 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-261+13968T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490675 | |||||||
chr2:33490718 | G | A | 2 | a0001c0001t0024g0136 a0001c0001t0024g0152 |
2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-261+14011G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490718 | |||||||
chr2:33490721 | G | A | 1 | a0001c0001t0002g0241 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-261+14014G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490721 | |||||||
chr2:33490861 | G | A | 2 | a0001c0001t0038g0144 a0001c0002t0033g0150 |
2 | HG00438.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-261+14154G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490861 | |||||||
chr2:33490878 | C | T | 3 | a0001c0001t0005g0175 a0001c0001t0011g0193 a0001c0001t0020g0309 |
3 | HG02965.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-261+14171C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33490878 | |||||||
chr2:33491043 | C | T | 2 | a0001c0001t0004g0189 a0001c0001t0004g0195 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-261+14336C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491043 | |||||||
chr2:33491066 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0026g0194 a0001c0001t0039g0128 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+14359A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491066 | |||||||
chr2:33491105 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+14398C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491105 | |||||||
chr2:33491172 | T | TGGGTGTG others(8238): Show |
1 | a0001c0002t0016g0203 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-261+14467_-261+14 others(8251): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33491172 | ||||||
chr2:33491399 | A | G | 6 | a0001c0001t0001g0319 a0001c0001t0002g0029 a0001c0001t0010g0011 others(3): Show |
6 | HG02027.hp2 NA18952.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+14692A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491399 | |||||||
chr2:33491438 | ATTAATAC | A | 11 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-261+14737_-261+14 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33491438 | ||||||
chr2:33491630 | A | G | 19 | a0001c0001t0003g0138 a0001c0001t0004g0141 a0001c0001t0009g0110 others(16): Show |
19 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+14923A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491630 | |||||||
chr2:33491642 | G | A | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-261+14935G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491642 | |||||||
chr2:33491778 | C | T | 1 | a0001c0002t0006g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+15071C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491778 | |||||||
chr2:33491851 | G | A | 2 | a0001c0001t0013g0298 a0001c0001t0025g0157 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-261+15144G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33491851 | |||||||
chr2:33492362 | A | G | 1 | a0001c0001t0007g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-261+15655A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492362 | |||||||
chr2:33492368 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(42): Show |
46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+15661A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492368 | |||||||
chr2:33492474 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-261+15767C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492474 | |||||||
chr2:33492488 | C | G | 2 | a0001c0001t0004g0189 a0001c0001t0004g0195 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-261+15781C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492488 | |||||||
chr2:33492616 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(146): Show |
150 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.-261+15909G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492616 | |||||||
chr2:33492724 | T | A | 10 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+16017T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492724 | |||||||
chr2:33492879 | A | C | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+16172A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492879 | |||||||
chr2:33492919 | C | T | 3 | a0001c0001t0003g0138 a0001c0001t0051g0297 a0001c0002t0006g0166 |
3 | HG02886.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-261+16212C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492919 | |||||||
chr2:33492922 | A | G | 2 | a0001c0001t0024g0136 a0001c0001t0024g0152 |
2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-261+16215A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492922 | |||||||
chr2:33492996 | A | T | 43 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(40): Show |
43 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(40): Show |
intron_variant | MODIFIER | c.-261+16289A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33492996 | |||||||
chr2:33493046 | T | C | 2 | a0001c0002t0017g0145 a0003c0009t0048g0072 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+16339T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493046 | |||||||
chr2:33493065 | A | G | 1 | a0001c0002t0006g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-261+16358A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493065 | |||||||
chr2:33493188 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(131): Show |
135 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.-261+16481T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493188 | |||||||
chr2:33493189 | G | A | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+16482G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493189 | |||||||
chr2:33493251 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(38): Show |
42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-261+16544C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493251 | |||||||
chr2:33493259 | C | T | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-261+16552C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493259 | |||||||
chr2:33493264 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(38): Show |
42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-261+16557C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493264 | |||||||
chr2:33493456 | T | C | 1 | a0001c0004t0020g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+16749T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493456 | |||||||
chr2:33493550 | A | C | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+16843A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493550 | |||||||
chr2:33493592 | T | C | 14 | a0001c0001t0004g0129 a0001c0001t0012g0123 a0001c0003t0005g0042 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+16885T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493592 | |||||||
chr2:33493605 | G | GA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(161): Show |
165 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-261+16898_-261+16 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493605 | |||||||
chr2:33493612 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(46): Show |
50 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-261+16905C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493612 | |||||||
chr2:33493682 | G | A | 6 | a0001c0001t0002g0161 a0001c0001t0003g0162 a0001c0001t0009g0018 others(3): Show |
6 | HG01192.hp2 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+16975G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493682 | |||||||
chr2:33493756 | TA | T | 7 | a0001c0001t0009g0110 a0001c0001t0011g0079 a0001c0001t0030g0125 others(4): Show |
7 | HG01074.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+17060delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33493756 | ||||||
chr2:33493789 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(63): Show |
67 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-261+17082T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493789 | |||||||
chr2:33493874 | A | G | 1 | a0001c0001t0016g0367 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-261+17167A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493874 | |||||||
chr2:33493975 | G | A | 33 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(30): Show |
33 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(30): Show |
intron_variant | MODIFIER | c.-261+17268G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493975 | |||||||
chr2:33493998 | A | G | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-261+17291A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33493998 | |||||||
chr2:33494042 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(50): Show |
54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-261+17335A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494042 | |||||||
chr2:33494156 | C | A | 33 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(30): Show |
33 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(30): Show |
intron_variant | MODIFIER | c.-261+17449C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494156 | |||||||
chr2:33494301 | G | T | 1 | a0001c0002t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-260-17409G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494301 | |||||||
chr2:33494406 | C | T | 14 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-17304C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494406 | |||||||
chr2:33494407 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-260-17303G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494407 | |||||||
chr2:33494584 | A | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-17126A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494584 | |||||||
chr2:33494772 | A | T | 2 | a0001c0001t0004g0189 a0001c0001t0004g0195 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-260-16938A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494772 | |||||||
chr2:33494908 | A | T | 6 | a0001c0001t0038g0144 a0001c0001t0038g0262 a0001c0001t0044g0106 others(3): Show |
6 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-16802A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494908 | |||||||
chr2:33494942 | T | C | 14 | a0001c0001t0001g0266 a0001c0001t0001g0316 a0001c0001t0003g0043 others(11): Show |
14 | HG00738.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-16768T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33494942 | |||||||
chr2:33495067 | C | A | 8 | a0001c0001t0001g0290 a0001c0001t0003g0147 a0001c0002t0001g0293 others(5): Show |
8 | HG01952.hp1 NA18944.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-16643C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495067 | |||||||
chr2:33495091 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-260-16619A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495091 | |||||||
chr2:33495217 | A | G | 1 | a0001c0001t0030g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-260-16493A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495217 | |||||||
chr2:33495287 | T | C | 2 | a0001c0001t0013g0299 a0001c0003t0005g0119 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-260-16423T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495287 | |||||||
chr2:33495289 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(38): Show |
42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-260-16421G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495289 | |||||||
chr2:33495292 | G | A | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-260-16418G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495292 | |||||||
chr2:33495463 | C | T | 1 | a0001c0002t0006g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-16247C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495463 | |||||||
chr2:33495508 | A | ACCAGGCC others(5): Show |
4 | a0001c0001t0009g0213 a0001c0001t0011g0082 a0001c0001t0043g0170 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-16196_-260-16 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33495508 | ||||||
chr2:33495567 | A | G | 21 | a0001c0001t0001g0266 a0001c0001t0001g0281 a0001c0001t0001g0316 others(18): Show |
21 | HG00738.hp1 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-260-16143A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495567 | |||||||
chr2:33495568 | T | C | 2 | a0001c0001t0013g0164 a0001c0001t0057g0081 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-260-16142T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495568 | |||||||
chr2:33495613 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-260-16097G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495613 | |||||||
chr2:33495671 | T | A | 1 | a0001c0001t0009g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-260-16039T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495671 | |||||||
chr2:33495727 | T | TA | 14 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-15979dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33495727 | ||||||
chr2:33495742 | A | G | 21 | a0001c0001t0011g0202 a0001c0001t0011g0308 a0001c0001t0012g0002 others(18): Show |
22 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-260-15968A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495742 | |||||||
chr2:33495746 | T | C | 1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-260-15964T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495746 | |||||||
chr2:33495935 | C | G | 1 | a0001c0001t0034g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-260-15775C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33495935 | |||||||
chr2:33496101 | T | C | 1 | a0001c0002t0006g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-260-15609T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496101 | |||||||
chr2:33496180 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-260-15530A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496180 | |||||||
chr2:33496248 | G | C | 32 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0055 others(29): Show |
32 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-260-15462G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496248 | |||||||
chr2:33496264 | A | G | 1 | a0001c0003t0005g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-260-15446A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496264 | |||||||
chr2:33496276 | G | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(34): Show |
38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-260-15434G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496276 | |||||||
chr2:33496390 | A | T | 6 | a0001c0001t0001g0283 a0001c0001t0002g0245 a0001c0001t0002g0248 others(3): Show |
6 | HG01192.hp1 HG01433.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-15320A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496390 | |||||||
chr2:33496429 | A | G | 26 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0275 others(23): Show |
26 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-260-15281A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496429 | |||||||
chr2:33496479 | T | A | 84 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0069 others(81): Show |
84 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.-260-15231T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496479 | |||||||
chr2:33496538 | T | G | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-15172T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496538 | |||||||
chr2:33496683 | C | T | 1 | a0001c0001t0038g0262 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-260-15027C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496683 | |||||||
chr2:33496718 | G | A | 26 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0275 others(23): Show |
26 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-260-14992G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496718 | |||||||
chr2:33496722 | C | T | 1 | a0001c0001t0031g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-260-14988C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496722 | |||||||
chr2:33496799 | G | A | 23 | a0001c0001t0001g0266 a0001c0001t0001g0316 a0001c0001t0002g0185 others(20): Show |
23 | HG00738.hp1 HG01496.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-14911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496799 | |||||||
chr2:33496851 | T | C | 6 | a0001c0001t0009g0110 a0001c0001t0011g0079 a0001c0001t0023g0257 others(3): Show |
6 | HG01074.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-14859T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496851 | |||||||
chr2:33496862 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(133): Show |
137 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.-260-14848G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496862 | |||||||
chr2:33496896 | C | G | 41 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(38): Show |
41 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(38): Show |
intron_variant | MODIFIER | c.-260-14814C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496896 | |||||||
chr2:33496936 | G | A | 4 | a0001c0001t0001g0101 a0001c0001t0002g0102 a0001c0002t0001g0100 others(1): Show |
4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-14774G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496936 | |||||||
chr2:33496948 | G | C | 2 | a0001c0001t0002g0337 a0001c0001t0018g0180 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-260-14762G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496948 | |||||||
chr2:33496978 | C | T | 36 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(33): Show |
36 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.-260-14732C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33496978 | |||||||
chr2:33497003 | T | C | 1 | a0001c0001t0002g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-260-14707T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497003 | |||||||
chr2:33497033 | T | C | 73 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(70): Show |
73 | HG01074.hp1 HG01255.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-14677T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497033 | |||||||
chr2:33497085 | C | G | 1 | a0001c0001t0008g0242 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-260-14625C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497085 | |||||||
chr2:33497225 | A | G | 1 | a0001c0001t0004g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-260-14485A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497225 | |||||||
chr2:33497402 | T | C | 1 | a0001c0002t0001g0368 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-260-14308T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497402 | |||||||
chr2:33497498 | A | T | 48 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0085 others(45): Show |
48 | HG01255.hp1 HG01358.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-260-14212A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497498 | |||||||
chr2:33497610 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-260-14100T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497610 | |||||||
chr2:33497745 | T | C | 1 | a0001c0001t0015g0218 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-260-13965T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497745 | |||||||
chr2:33497787 | A | G | 67 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0169 others(64): Show |
67 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-260-13923A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497787 | |||||||
chr2:33497790 | G | C | 1 | a0001c0002t0003g0289 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-260-13920G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497790 | |||||||
chr2:33497849 | G | C | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-13861G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497849 | |||||||
chr2:33497912 | G | A | 1 | a0001c0002t0001g0005 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-260-13798G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497912 | |||||||
chr2:33497950 | G | A | 27 | a0001c0001t0001g0061 a0001c0001t0001g0177 a0001c0001t0001g0181 others(24): Show |
27 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.-260-13760G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33497950 | |||||||
chr2:33497973 | C | CCCTTTCT others(13): Show |
37 | a0001c0001t0001g0061 a0001c0001t0001g0177 a0001c0001t0001g0181 others(34): Show |
37 | HG01255.hp1 HG01358.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.-260-13707_-260-13 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33497973 | ||||||
chr2:33498081 | C | A | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-260-13629C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498081 | |||||||
chr2:33498117 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0067 others(120): Show |
124 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-260-13593A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498117 | |||||||
chr2:33498126 | C | T | 1 | a0001c0002t0006g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-13584C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498126 | |||||||
chr2:33498127 | T | C | 5 | a0001c0001t0001g0281 a0001c0001t0002g0075 a0001c0001t0008g0178 others(2): Show |
5 | HG01099.hp1 HG01358.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-13583T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498127 | |||||||
chr2:33498190 | G | A | 1 | a0001c0001t0004g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-260-13520G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498190 | |||||||
chr2:33498443 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(32): Show |
36 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-260-13267C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498443 | |||||||
chr2:33498498 | G | C | 1 | a0001c0001t0009g0018 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-260-13212G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498498 | |||||||
chr2:33498566 | T | A | 4 | a0001c0001t0001g0101 a0001c0001t0002g0102 a0001c0002t0001g0100 others(1): Show |
4 | NA18978.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-13144T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498566 | |||||||
chr2:33498624 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(75): Show |
79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-260-13086C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498624 | |||||||
chr2:33498699 | C | T | 1 | a0001c0001t0031g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-260-13011C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498699 | |||||||
chr2:33498873 | T | A | 1 | a0001c0002t0001g0363 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-260-12837T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33498873 | |||||||
chr2:33499275 | C | A | 3 | a0001c0001t0025g0076 a0001c0002t0017g0145 a0003c0009t0048g0072 |
3 | HG02451.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-260-12435C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499275 | |||||||
chr2:33499452 | G | A | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-12258G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499452 | |||||||
chr2:33499527 | C | T | 5 | a0001c0001t0011g0193 a0001c0001t0027g0192 a0001c0001t0050g0311 others(2): Show |
5 | HG02257.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-12183C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499527 | |||||||
chr2:33499539 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-260-12171C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499539 | |||||||
chr2:33499706 | T | G | 12 | a0001c0001t0001g0061 a0001c0001t0001g0260 a0001c0001t0001g0315 others(9): Show |
12 | HG00544.hp2 HG02074.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-260-12004T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499706 | |||||||
chr2:33499744 | C | G | 1 | a0001c0002t0001g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-260-11966C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499744 | |||||||
chr2:33499763 | C | CA | 34 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(31): Show |
35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-11936dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499763 | ||||||
chr2:33499773 | A | AAAGAG | 13 | a0001c0001t0003g0138 a0001c0001t0004g0141 a0001c0001t0013g0238 others(10): Show |
13 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-11936_-260-11 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499773 | ||||||
chr2:33499773 | A | AAGAG | 23 | a0001c0001t0004g0129 a0001c0001t0009g0213 a0001c0001t0011g0082 others(20): Show |
23 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-11934_-260-11 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499773 | ||||||
chr2:33499776 | A | AGAGG | 50 | a0001c0001t0001g0067 a0001c0001t0001g0169 a0001c0001t0001g0182 others(47): Show |
50 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-260-11933_-260-11 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33499776 | ||||||
chr2:33499815 | A | G | 1 | a0001c0001t0061g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-260-11895A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499815 | |||||||
chr2:33499862 | G | A | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-11848G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499862 | |||||||
chr2:33499949 | G | A | 1 | a0001c0004t0042g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-260-11761G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33499949 | |||||||
chr2:33500030 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0067 others(118): Show |
122 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.-260-11680A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500030 | |||||||
chr2:33500212 | T | C | 6 | a0001c0001t0002g0161 a0001c0001t0002g0231 a0001c0001t0003g0162 others(3): Show |
6 | HG01109.hp2 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-11498T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500212 | |||||||
chr2:33500381 | T | C | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-11329T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500381 | |||||||
chr2:33500385 | A | T | 1 | a0007c0012t0015g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-260-11325A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500385 | |||||||
chr2:33500419 | G | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-11291G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500419 | |||||||
chr2:33500630 | T | C | 1 | a0001c0001t0010g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-260-11080T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500630 | |||||||
chr2:33500639 | A | T | 3 | a0001c0001t0009g0012 a0001c0001t0022g0109 a0001c0001t0022g0334 |
3 | HG01515.hp1 HG02258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-260-11071A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500639 | |||||||
chr2:33500679 | T | C | 3 | a0001c0001t0028g0305 a0001c0001t0028g0306 a0001c0001t0032g0278 |
3 | HG01256.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-260-11031T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500679 | |||||||
chr2:33500709 | G | A | 5 | a0001c0001t0011g0193 a0001c0001t0027g0192 a0001c0001t0050g0311 others(2): Show |
5 | HG02257.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-11001G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500709 | |||||||
chr2:33500788 | G | A | 2 | a0002c0005t0003g0204 a0002c0005t0003g0214 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-260-10922G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500788 | |||||||
chr2:33500802 | C | T | 1 | a0001c0002t0001g0005 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-260-10908C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500802 | |||||||
chr2:33500866 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(31): Show |
35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-10844G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500866 | |||||||
chr2:33500875 | A | G | 23 | a0001c0001t0003g0138 a0001c0001t0004g0141 a0001c0001t0009g0110 others(20): Show |
23 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-10835A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500875 | |||||||
chr2:33500910 | G | A | 2 | a0001c0002t0001g0359 a0001c0002t0006g0198 |
2 | HG06807.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-260-10800G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500910 | |||||||
chr2:33500927 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-260-10783C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33500927 | |||||||
chr2:33500936 | AAAAT | A | 4 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 others(1): Show |
4 | HG00738.hp1 HG01496.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-10762_-260-10 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33500936 | ||||||
chr2:33501136 | C | T | 5 | a0001c0001t0025g0076 a0001c0001t0052g0301 a0001c0002t0006g0151 others(2): Show |
5 | HG02451.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-10574C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501136 | |||||||
chr2:33501299 | A | G | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-10411A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501299 | |||||||
chr2:33501391 | C | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(31): Show |
35 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-10319C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501391 | |||||||
chr2:33501393 | A | G | 4 | a0001c0001t0002g0303 a0001c0001t0003g0302 a0001c0001t0009g0073 others(1): Show |
4 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-10317A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501393 | |||||||
chr2:33501403 | G | A | 1 | a0001c0001t0024g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-260-10307G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501403 | |||||||
chr2:33501543 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(87): Show |
91 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.-260-10167C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501543 | |||||||
chr2:33501546 | C | T | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-260-10164C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501546 | |||||||
chr2:33501577 | C | T | 1 | a0001c0001t0007g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-260-10133C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501577 | |||||||
chr2:33501657 | G | A | 3 | a0001c0001t0001g0343 a0001c0002t0001g0005 a0001c0002t0001g0006 |
3 | HG00597.hp2 HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-260-10053G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501657 | |||||||
chr2:33501692 | C | T | 1 | a0001c0002t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-260-10018C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501692 | |||||||
chr2:33501799 | C | T | 1 | a0001c0002t0006g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-260-9911C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33501799 | |||||||
chr2:33502059 | G | T | 1 | a0001c0001t0002g0288 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-260-9651G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502059 | |||||||
chr2:33502246 | C | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-9464C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502246 | |||||||
chr2:33502310 | G | T | 1 | a0001c0002t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-260-9400G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502310 | |||||||
chr2:33502443 | A | T | 1 | a0001c0001t0027g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-260-9267A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502443 | |||||||
chr2:33502501 | C | CT | 89 | a0001c0001t0001g0063 a0001c0001t0001g0115 a0001c0001t0001g0159 others(86): Show |
89 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.-260-9195dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33502501 | ||||||
chr2:33502501 | C | CTT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0275 others(26): Show |
30 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.-260-9196_-260-919 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33502501 | ||||||
chr2:33502542 | T | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0067 others(117): Show |
121 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.-260-9168T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502542 | |||||||
chr2:33502555 | G | C | 4 | a0001c0001t0011g0193 a0001c0001t0030g0139 a0001c0001t0050g0311 others(1): Show |
4 | HG02559.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-9155G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502555 | |||||||
chr2:33502584 | C | G | 1 | a0001c0001t0034g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-260-9126C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502584 | |||||||
chr2:33502599 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-260-9111G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502599 | |||||||
chr2:33502604 | C | T | 6 | a0001c0001t0011g0202 a0001c0001t0013g0121 a0001c0001t0058g0124 others(3): Show |
6 | HG01255.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-9106C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502604 | |||||||
chr2:33502606 | G | A | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-260-9104G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502606 | |||||||
chr2:33502621 | T | C | 1 | a0001c0002t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-260-9089T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502621 | |||||||
chr2:33502671 | C | A | 2 | a0001c0001t0001g0107 a0001c0002t0001g0360 |
2 | NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-260-9039C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502671 | |||||||
chr2:33502784 | G | A | 27 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0177 others(24): Show |
27 | HG00544.hp2 HG01255.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-8926G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502784 | |||||||
chr2:33502913 | A | T | 64 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0033 others(61): Show |
64 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.-260-8797A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33502913 | |||||||
chr2:33503048 | T | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(39): Show |
43 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-260-8662T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503048 | |||||||
chr2:33503108 | A | G | 3 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0063g0286 |
3 | HG00621.hp1 HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.-260-8602A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503108 | |||||||
chr2:33503138 | G | C | 2 | a0001c0001t0011g0082 a0001c0001t0043g0170 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-8572G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503138 | |||||||
chr2:33503371 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-260-8339C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503371 | |||||||
chr2:33503419 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0224 others(6): Show |
9 | HG02129.hp1 HG02523.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-8291A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503419 | |||||||
chr2:33503499 | A | G | 35 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0177 others(32): Show |
35 | HG00544.hp2 HG01255.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.-260-8211A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503499 | |||||||
chr2:33503526 | G | T | 2 | a0001c0001t0003g0103 a0001c0001t0003g0208 |
2 | HG00423.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-260-8184G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503526 | |||||||
chr2:33503541 | G | A | 2 | a0001c0001t0027g0192 a0001c0004t0020g0044 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-260-8169G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503541 | |||||||
chr2:33503587 | A | T | 13 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-8123A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503587 | |||||||
chr2:33503592 | C | CT | 49 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(46): Show |
49 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.-260-8108dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33503592 | ||||||
chr2:33503592 | C | CTT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(42): Show |
46 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-260-8109_-260-810 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33503592 | ||||||
chr2:33503612 | A | G | 2 | a0001c0001t0052g0301 a0001c0002t0006g0151 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-260-8098A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503612 | |||||||
chr2:33503832 | C | T | 2 | a0001c0001t0011g0082 a0001c0001t0043g0170 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-7878C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33503832 | |||||||
chr2:33504093 | G | A | 9 | a0001c0001t0004g0141 a0001c0001t0013g0238 a0001c0001t0017g0236 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-260-7617G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504093 | |||||||
chr2:33504188 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-260-7522C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504188 | |||||||
chr2:33504391 | C | T | 1 | a0003c0009t0048g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-7319C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504391 | |||||||
chr2:33504555 | T | C | 1 | a0001c0001t0024g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-260-7155T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504555 | |||||||
chr2:33504607 | T | C | 1 | a0001c0002t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-260-7103T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504607 | |||||||
chr2:33504722 | C | G | 1 | a0001c0001t0010g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-260-6988C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504722 | |||||||
chr2:33504745 | T | C | 54 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0084 others(51): Show |
54 | HG00423.hp1 HG00544.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.-260-6965T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504745 | |||||||
chr2:33504793 | A | T | 6 | a0001c0001t0004g0141 a0001c0002t0006g0137 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-6917A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33504793 | |||||||
chr2:33505119 | C | T | 19 | a0001c0001t0004g0129 a0001c0001t0005g0175 a0001c0001t0012g0123 others(16): Show |
19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6591C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505119 | |||||||
chr2:33505153 | T | TCAC | 50 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(47): Show |
51 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-260-6533_-260-653 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | ||||||
chr2:33505153 | T | TCACCAC | 10 | a0001c0001t0004g0129 a0001c0001t0012g0123 a0001c0003t0005g0042 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-260-6536_-260-653 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | ||||||
chr2:33505153 | T | TCACCACC others(14): Show |
4 | a0001c0003t0005g0173 a0001c0003t0005g0174 a0001c0003t0005g0251 others(1): Show |
4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-6551_-260-653 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | ||||||
chr2:33505153 | T | TCATCAC | 14 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0211 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-6555_-260-655 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505153 | ||||||
chr2:33505224 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(43): Show |
47 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-260-6486A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505224 | |||||||
chr2:33505291 | C | T | 19 | a0001c0001t0004g0129 a0001c0001t0005g0175 a0001c0001t0012g0123 others(16): Show |
19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6419C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505291 | |||||||
chr2:33505299 | A | AT | 40 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0084 others(37): Show |
40 | HG00423.hp1 HG00544.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.-260-6395dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | ||||||
chr2:33505299 | AT | A | 19 | a0001c0001t0001g0169 a0001c0001t0002g0345 a0001c0001t0003g0138 others(16): Show |
19 | HG00738.hp2 HG01070.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6395delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | ||||||
chr2:33505299 | ATT | A | 19 | a0001c0001t0004g0129 a0001c0001t0005g0175 a0001c0001t0012g0123 others(16): Show |
19 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-6396_-260-639 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33505299 | ||||||
chr2:33505364 | G | A | 8 | a0001c0001t0011g0193 a0001c0001t0023g0257 a0001c0001t0023g0258 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-6346G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505364 | |||||||
chr2:33505395 | C | T | 2 | a0001c0001t0011g0082 a0001c0001t0043g0170 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-260-6315C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505395 | |||||||
chr2:33505436 | G | C | 1 | a0001c0001t0007g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-260-6274G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505436 | |||||||
chr2:33505558 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0046 others(229): Show |
233 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-260-6152T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505558 | |||||||
chr2:33505606 | C | T | 3 | a0001c0001t0013g0238 a0001c0001t0017g0236 a0001c0002t0006g0237 |
3 | HG02572.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-260-6104C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505606 | |||||||
chr2:33505633 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0115 others(34): Show |
38 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-260-6077G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505633 | |||||||
chr2:33505730 | C | T | 4 | a0001c0001t0011g0193 a0001c0001t0030g0139 a0001c0001t0050g0311 others(1): Show |
4 | HG02559.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-5980C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505730 | |||||||
chr2:33505873 | A | G | 1 | a0001c0001t0004g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-260-5837A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33505873 | |||||||
chr2:33506173 | A | G | 55 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0177 others(52): Show |
55 | HG00423.hp1 HG00544.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.-260-5537A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506173 | |||||||
chr2:33506175 | C | A | 1 | a0001c0001t0004g0189 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-260-5535C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506175 | |||||||
chr2:33506367 | T | A | 2 | a0001c0002t0006g0166 a0001c0002t0006g0172 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-260-5343T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506367 | |||||||
chr2:33506494 | A | G | 18 | a0001c0001t0003g0138 a0001c0001t0009g0110 a0001c0001t0011g0079 others(15): Show |
18 | HG01074.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-260-5216A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506494 | |||||||
chr2:33506574 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(142): Show |
146 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-260-5136G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506574 | |||||||
chr2:33506655 | A | G | 3 | a0001c0001t0003g0043 a0001c0001t0011g0310 a0001c0002t0018g0135 |
3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-260-5055A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506655 | |||||||
chr2:33506718 | T | C | 1 | a0001c0001t0008g0219 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-260-4992T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506718 | |||||||
chr2:33506879 | G | A | 5 | a0001c0001t0011g0193 a0001c0001t0027g0192 a0001c0001t0030g0139 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-4831G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506879 | |||||||
chr2:33506901 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-260-4809A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506901 | |||||||
chr2:33506928 | G | C | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-260-4782G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506928 | |||||||
chr2:33506936 | G | C | 1 | a0003c0009t0048g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-4774G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506936 | |||||||
chr2:33506937 | T | C | 1 | a0001c0001t0060g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-260-4773T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33506937 | |||||||
chr2:33507019 | C | A | 1 | a0001c0002t0006g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-260-4691C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507019 | |||||||
chr2:33507143 | T | C | 1 | a0009c0013t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-260-4567T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507143 | |||||||
chr2:33507193 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-260-4517C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507193 | |||||||
chr2:33507198 | C | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0226 |
2 | NA18984.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-260-4512C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507198 | |||||||
chr2:33507211 | A | G | 1 | a0001c0001t0015g0218 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-260-4499A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507211 | |||||||
chr2:33507282 | G | C | 4 | a0001c0002t0001g0234 a0001c0002t0036g0269 a0001c0002t0036g0270 others(1): Show |
4 | HG00639.hp1 HG01928.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-4428G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507282 | |||||||
chr2:33507379 | A | G | 12 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0001t0001g0281 others(9): Show |
12 | HG01175.hp1 HG01358.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-260-4331A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507379 | |||||||
chr2:33507571 | G | A | 2 | a0001c0002t0006g0165 a0001c0004t0042g0199 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-260-4139G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507571 | |||||||
chr2:33507573 | A | T | 26 | a0001c0001t0001g0055 a0001c0001t0001g0264 a0001c0001t0001g0322 others(23): Show |
27 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-4137A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507573 | |||||||
chr2:33507595 | G | T | 22 | a0001c0001t0004g0129 a0001c0001t0011g0082 a0001c0001t0011g0308 others(19): Show |
22 | HG01255.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-260-4115G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507595 | |||||||
chr2:33507629 | G | A | 1 | a0001c0001t0002g0365 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-260-4081G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507629 | |||||||
chr2:33507714 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0007g0318 |
2 | NA18993.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-260-3996T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507714 | |||||||
chr2:33507715 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0007g0318 |
2 | NA18993.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-260-3995G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507715 | |||||||
chr2:33507741 | G | C | 17 | a0001c0001t0004g0141 a0001c0001t0009g0110 a0001c0001t0011g0079 others(14): Show |
17 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-260-3969G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507741 | |||||||
chr2:33507748 | A | G | 3 | a0001c0001t0003g0300 a0001c0001t0009g0213 a0001c0001t0051g0297 |
3 | HG02615.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-260-3962A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507748 | |||||||
chr2:33507751 | C | A | 1 | a0001c0003t0026g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-260-3959C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507751 | |||||||
chr2:33507805 | C | T | 27 | a0001c0001t0003g0043 a0001c0001t0004g0129 a0001c0001t0011g0082 others(24): Show |
27 | HG01255.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-3905C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507805 | |||||||
chr2:33507860 | A | G | 4 | a0001c0001t0009g0110 a0001c0001t0011g0079 a0001c0001t0011g0193 others(1): Show |
4 | HG01074.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-3850A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507860 | |||||||
chr2:33507877 | G | A | 1 | a0001c0003t0005g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-260-3833G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33507877 | |||||||
chr2:33508031 | G | T | 1 | a0001c0001t0034g0346 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-260-3679G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508031 | |||||||
chr2:33508042 | C | T | 4 | a0001c0001t0009g0019 a0001c0001t0021g0140 a0001c0001t0021g0146 others(1): Show |
4 | HG01496.hp1 HG01516.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-3668C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508042 | |||||||
chr2:33508117 | G | A | 1 | a0001c0001t0009g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-260-3593G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508117 | |||||||
chr2:33508129 | C | T | 1 | a0001c0003t0005g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-260-3581C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508129 | |||||||
chr2:33508354 | C | A | 25 | a0001c0001t0001g0055 a0001c0001t0002g0039 a0001c0001t0003g0013 others(22): Show |
25 | HG00323.hp2 HG00423.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.-260-3356C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508354 | |||||||
chr2:33508447 | C | T | 23 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(20): Show |
23 | HG00323.hp2 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-3263C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508447 | |||||||
chr2:33508480 | G | A | 1 | a0001c0003t0005g0255 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-3230G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508480 | |||||||
chr2:33508487 | T | C | 111 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0050 others(108): Show |
111 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.-260-3223T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508487 | |||||||
chr2:33508528 | T | C | 1 | a0001c0002t0006g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-260-3182T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508528 | |||||||
chr2:33508546 | T | C | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-260-3164T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508546 | |||||||
chr2:33508652 | C | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0030 others(294): Show |
299 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.-260-3058C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508652 | |||||||
chr2:33508660 | G | A | 1 | a0001c0001t0025g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-260-3050G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508660 | |||||||
chr2:33508686 | T | G | 15 | a0001c0001t0001g0351 a0001c0001t0002g0126 a0001c0001t0002g0188 others(12): Show |
15 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.-260-3024T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508686 | |||||||
chr2:33508756 | C | A | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-260-2954C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508756 | |||||||
chr2:33508850 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-260-2860A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508850 | |||||||
chr2:33508893 | G | A | 1 | a0001c0001t0018g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-260-2817G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508893 | |||||||
chr2:33508920 | A | G | 2 | a0001c0002t0017g0145 a0003c0011t0045g0200 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-260-2790A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508920 | |||||||
chr2:33508942 | T | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0232 |
3 | HG02015.hp2 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-260-2768T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508942 | |||||||
chr2:33508976 | G | A | 2 | a0001c0002t0017g0145 a0003c0011t0045g0200 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-260-2734G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508976 | |||||||
chr2:33508995 | G | A | 15 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-2715G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33508995 | |||||||
chr2:33509055 | G | C | 14 | a0001c0002t0001g0023 a0001c0002t0001g0031 a0001c0002t0001g0049 others(11): Show |
14 | HG00558.hp1 HG00639.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-2655G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509055 | |||||||
chr2:33509059 | T | G | 16 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0003g0300 others(13): Show |
16 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-2651T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509059 | |||||||
chr2:33509141 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-260-2569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509141 | |||||||
chr2:33509230 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0232 others(6): Show |
9 | HG02015.hp2 HG02129.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-2480C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509230 | |||||||
chr2:33509399 | C | CA | 47 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(44): Show |
47 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-260-2299dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33509399 | ||||||
chr2:33509425 | A | C | 1 | a0001c0002t0006g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-260-2285A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509425 | |||||||
chr2:33509452 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-260-2258T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509452 | |||||||
chr2:33509560 | C | G | 2 | a0001c0001t0040g0320 a0001c0001t0041g0122 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-260-2150C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509560 | |||||||
chr2:33509762 | C | G | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0009g0110 others(1): Show |
4 | HG01074.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-1948C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509762 | |||||||
chr2:33509815 | G | A | 283 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0084 others(280): Show |
284 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.-260-1895G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509815 | |||||||
chr2:33509840 | A | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-1870A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509840 | |||||||
chr2:33509899 | A | G | 5 | a0001c0001t0002g0142 a0001c0001t0002g0230 a0001c0001t0002g0303 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-1811A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33509899 | |||||||
chr2:33510179 | T | G | 1 | a0003c0009t0048g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-1531T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510179 | |||||||
chr2:33510216 | A | T | 4 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-1494A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510216 | |||||||
chr2:33510243 | C | G | 15 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-1467C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510243 | |||||||
chr2:33510284 | C | CA | 6 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(3): Show |
6 | HG01109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-1422dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 33510284 | ||||||
chr2:33510324 | C | T | 6 | a0001c0001t0009g0012 a0001c0001t0009g0041 a0001c0001t0009g0073 others(3): Show |
6 | HG01074.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-1386C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510324 | |||||||
chr2:33510345 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0017g0120 a0001c0001t0025g0157 others(1): Show |
4 | HG03130.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-1365A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510345 | |||||||
chr2:33510394 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-260-1316G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510394 | |||||||
chr2:33510426 | G | C | 1 | a0001c0002t0001g0364 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-260-1284G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510426 | |||||||
chr2:33510490 | G | C | 9 | a0001c0001t0003g0043 a0001c0001t0003g0138 a0001c0001t0011g0082 others(6): Show |
9 | HG01256.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-1220G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510490 | |||||||
chr2:33510493 | C | T | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-260-1217C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510493 | |||||||
chr2:33510970 | T | C | 1 | a0001c0001t0003g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-260-740T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33510970 | |||||||
chr2:33511009 | C | A | 1 | a0001c0001t0052g0301 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-260-701C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511009 | |||||||
chr2:33511010 | G | A | 100 | a0001c0001t0001g0069 a0001c0001t0001g0177 a0001c0001t0001g0211 others(97): Show |
100 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-260-700G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511010 | |||||||
chr2:33511214 | C | T | 278 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0101 others(275): Show |
279 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-260-496C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511214 | |||||||
chr2:33511289 | T | G | 15 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-260-421T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511289 | |||||||
chr2:33511321 | T | A | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-260-389T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511321 | |||||||
chr2:33511644 | A | G | 5 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(2): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-66A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511644 | |||||||
chr2:33511656 | T | C | 15 | a0001c0001t0001g0351 a0001c0001t0002g0126 a0001c0001t0002g0188 others(12): Show |
15 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.-260-54T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511656 | |||||||
chr2:33511686 | G | A | 1 | a0001c0002t0006g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-260-24G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 1/17 | chr2 | 33511686 | |||||||
chr2:33511922 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-128+80C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33511922 | |||||||
chr2:33512022 | G | A | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128+180G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512022 | |||||||
chr2:33512039 | C | T | 27 | a0001c0001t0001g0351 a0001c0001t0002g0188 a0001c0001t0003g0017 others(24): Show |
28 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-128+197C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512039 | |||||||
chr2:33512177 | G | A | 127 | a0001c0001t0001g0069 a0001c0001t0001g0177 a0001c0001t0001g0181 others(124): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-128+335G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512177 | |||||||
chr2:33512347 | G | T | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+505G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512347 | |||||||
chr2:33512364 | C | G | 1 | a0001c0004t0042g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-128+522C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512364 | |||||||
chr2:33512561 | C | G | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+719C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512561 | |||||||
chr2:33512633 | C | T | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-128+791C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512633 | |||||||
chr2:33512753 | G | A | 2 | a0001c0001t0040g0320 a0001c0001t0041g0122 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-128+911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512753 | |||||||
chr2:33512820 | T | A | 159 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(156): Show |
160 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-128+978T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512820 | |||||||
chr2:33512884 | A | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128+1042A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512884 | |||||||
chr2:33512902 | A | G | 120 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(117): Show |
120 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.-128+1060A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512902 | |||||||
chr2:33512977 | A | G | 16 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(13): Show |
17 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.-128+1135A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33512977 | |||||||
chr2:33513224 | C | T | 1 | a0001c0002t0033g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-128+1382C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513224 | |||||||
chr2:33513382 | C | T | 6 | a0001c0001t0003g0300 a0001c0001t0017g0120 a0001c0001t0030g0125 others(3): Show |
6 | HG02559.hp1 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128+1540C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513382 | |||||||
chr2:33513483 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-127-1527T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513483 | |||||||
chr2:33513546 | C | T | 102 | a0001c0001t0001g0062 a0001c0001t0001g0101 a0001c0001t0001g0225 others(99): Show |
102 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.-127-1464C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33513546 | |||||||
chr2:33514032 | A | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-978A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514032 | |||||||
chr2:33514230 | T | G | 126 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(123): Show |
126 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.-127-780T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514230 | |||||||
chr2:33514245 | A | C | 13 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-765A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514245 | |||||||
chr2:33514294 | A | T | 5 | a0001c0001t0003g0300 a0001c0001t0017g0120 a0001c0001t0030g0125 others(2): Show |
5 | HG02559.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-716A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514294 | |||||||
chr2:33514333 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-127-677G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514333 | |||||||
chr2:33514489 | T | C | 157 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(154): Show |
158 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.-127-521T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514489 | |||||||
chr2:33514505 | C | CA | 93 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0062 others(90): Show |
93 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.-127-483dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | ||||||
chr2:33514505 | C | CAA | 116 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(113): Show |
116 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-127-484_-127-483d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | ||||||
chr2:33514505 | C | CAAA | 42 | a0001c0001t0001g0101 a0001c0001t0001g0211 a0001c0001t0001g0315 others(39): Show |
42 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-127-485_-127-483d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | ||||||
chr2:33514505 | C | CAAAAA | 14 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0181 others(11): Show |
14 | HG01993.hp1 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-487_-127-483d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | ||||||
chr2:33514505 | C | CAAAAAA | 9 | a0001c0001t0001g0084 a0001c0001t0003g0013 a0001c0001t0003g0103 others(6): Show |
9 | HG00423.hp1 HG00438.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-488_-127-483d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 33514505 | ||||||
chr2:33514615 | G | T | 1 | a0001c0001t0034g0346 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-127-395G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514615 | |||||||
chr2:33514634 | G | A | 1 | a0001c0001t0031g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-127-376G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514634 | |||||||
chr2:33514677 | A | G | 1 | a0001c0001t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-127-333A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514677 | |||||||
chr2:33514711 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-127-299A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514711 | |||||||
chr2:33514725 | A | T | 119 | a0001c0001t0001g0062 a0001c0001t0001g0101 a0001c0001t0001g0225 others(116): Show |
119 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.-127-285A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 2/17 | chr2 | 33514725 | |||||||
chr2:33515211 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | splice_region_variant&intron_variant | LOW | c.70+5G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515211 | |||||||
chr2:33515259 | T | G | 1 | a0001c0004t0020g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70+53T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515259 | |||||||
chr2:33515322 | G | T | 13 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+116G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515322 | |||||||
chr2:33515351 | C | G | 1 | a0001c0001t0009g0018 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.70+145C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515351 | |||||||
chr2:33515388 | G | T | 3 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 |
3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.70+182G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515388 | |||||||
chr2:33515435 | A | G | 1 | a0001c0001t0012g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70+229A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515435 | |||||||
chr2:33515473 | A | T | 2 | a0001c0001t0001g0047 a0005c0014t0001g0010 |
2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.70+267A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515473 | |||||||
chr2:33515662 | T | C | 126 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0050 others(123): Show |
126 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.70+456T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515662 | |||||||
chr2:33515788 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.70+582C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515788 | |||||||
chr2:33515921 | T | A | 297 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(294): Show |
298 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.71-621T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515921 | |||||||
chr2:33515941 | A | T | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.71-601A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33515941 | |||||||
chr2:33516012 | T | A | 1 | a0001c0004t0020g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71-530T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516012 | |||||||
chr2:33516148 | G | A | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71-394G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516148 | |||||||
chr2:33516184 | C | T | 48 | a0001c0001t0001g0062 a0001c0001t0001g0225 a0001c0001t0001g0267 others(45): Show |
48 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.71-358C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516184 | |||||||
chr2:33516225 | T | C | 14 | a0001c0001t0001g0351 a0001c0001t0002g0126 a0001c0001t0002g0188 others(11): Show |
14 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-317T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516225 | |||||||
chr2:33516268 | C | T | 1 | a0001c0002t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.71-274C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516268 | |||||||
chr2:33516306 | G | A | 1 | a0001c0004t0020g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71-236G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516306 | |||||||
chr2:33516403 | T | C | 34 | a0001c0001t0001g0032 a0001c0001t0001g0181 a0001c0001t0002g0039 others(31): Show |
34 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-139T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516403 | |||||||
chr2:33516469 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.71-73G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 3/17 | chr2 | 33516469 | |||||||
chr2:33516773 | A | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+129A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516773 | |||||||
chr2:33516893 | G | C | 2 | a0001c0001t0004g0141 a0001c0001t0058g0124 |
2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173+249G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516893 | |||||||
chr2:33516932 | T | G | 1 | a0001c0001t0003g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.173+288T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33516932 | |||||||
chr2:33517075 | A | G | 3 | a0001c0001t0002g0188 a0001c0001t0008g0178 a0001c0001t0031g0233 |
3 | HG02698.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.173+431A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517075 | |||||||
chr2:33517217 | G | A | 283 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0101 others(280): Show |
284 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.173+573G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517217 | |||||||
chr2:33517435 | G | T | 6 | a0001c0001t0003g0209 a0001c0002t0004g0227 a0001c0002t0004g0228 others(3): Show |
6 | HG02071.hp2 HG02083.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.173+791G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517435 | |||||||
chr2:33517925 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.173+1281C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33517925 | |||||||
chr2:33518109 | G | A | 3 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 |
3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.173+1465G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518109 | |||||||
chr2:33518114 | A | G | 167 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(164): Show |
168 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.173+1470A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518114 | |||||||
chr2:33518261 | C | T | 5 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(2): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.173+1617C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518261 | |||||||
chr2:33518314 | C | A | 11 | a0001c0001t0001g0351 a0001c0001t0002g0126 a0001c0001t0003g0017 others(8): Show |
11 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.174-1638C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518314 | |||||||
chr2:33518612 | C | G | 1 | a0001c0001t0002g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.174-1340C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518612 | |||||||
chr2:33518709 | A | AT | 8 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.174-1232dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 33518709 | ||||||
chr2:33518738 | C | T | 279 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0101 others(276): Show |
280 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.174-1214C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518738 | |||||||
chr2:33518743 | A | G | 3 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 |
3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.174-1209A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518743 | |||||||
chr2:33518880 | G | GTCA | 141 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(138): Show |
142 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.174-1069_174-1067d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 33518880 | ||||||
chr2:33518912 | G | C | 12 | a0001c0001t0001g0351 a0001c0001t0002g0188 a0001c0001t0003g0017 others(9): Show |
12 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-1040G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33518912 | |||||||
chr2:33519094 | A | G | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-858A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519094 | |||||||
chr2:33519113 | T | G | 5 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(2): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.174-839T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519113 | |||||||
chr2:33519171 | T | A | 1 | a0001c0002t0006g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.174-781T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519171 | |||||||
chr2:33519245 | T | C | 1 | a0001c0002t0036g0269 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.174-707T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519245 | |||||||
chr2:33519248 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0325 |
2 | NA19005.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.174-704A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519248 | |||||||
chr2:33519345 | G | A | 2 | a0001c0001t0040g0320 a0001c0001t0041g0122 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.174-607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519345 | |||||||
chr2:33519355 | A | G | 1 | a0001c0001t0008g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.174-597A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519355 | |||||||
chr2:33519383 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.174-569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519383 | |||||||
chr2:33519413 | A | G | 119 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0030 others(116): Show |
119 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.174-539A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519413 | |||||||
chr2:33519427 | T | C | 7 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-525T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519427 | |||||||
chr2:33519548 | A | C | 16 | a0001c0001t0013g0299 a0001c0002t0006g0134 a0001c0002t0006g0137 others(13): Show |
16 | HG00738.hp1 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.174-404A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519548 | |||||||
chr2:33519621 | T | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-331T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519621 | |||||||
chr2:33519636 | A | G | 1 | a0001c0002t0003g0289 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.174-316A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519636 | |||||||
chr2:33519717 | C | A | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.174-235C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519717 | |||||||
chr2:33519735 | T | G | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-217T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519735 | |||||||
chr2:33519749 | A | G | 14 | a0001c0001t0003g0300 a0001c0001t0005g0175 a0001c0001t0013g0121 others(11): Show |
14 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.174-203A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519749 | |||||||
chr2:33519853 | A | C | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.174-99A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519853 | |||||||
chr2:33519891 | C | T | 141 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0101 others(138): Show |
141 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.174-61C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519891 | |||||||
chr2:33519905 | T | C | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174-47T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519905 | |||||||
chr2:33519929 | T | A | 1 | a0001c0001t0018g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.174-23T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 4/17 | chr2 | 33519929 | |||||||
chr2:33520043 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.236+29G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520043 | |||||||
chr2:33520111 | A | G | 8 | a0001c0001t0001g0046 a0001c0001t0001g0232 a0001c0001t0001g0260 others(5): Show |
8 | HG01192.hp1 HG02015.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+97A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520111 | |||||||
chr2:33520141 | T | C | 143 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(140): Show |
143 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.236+127T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520141 | |||||||
chr2:33520224 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.236+210C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520224 | |||||||
chr2:33520269 | T | C | 301 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(298): Show |
302 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.236+255T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520269 | |||||||
chr2:33520335 | A | G | 120 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(117): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.237-218A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520335 | |||||||
chr2:33520341 | G | C | 3 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 |
3 | HG01109.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.237-212G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520341 | |||||||
chr2:33520420 | A | T | 6 | a0001c0001t0002g0243 a0001c0001t0003g0296 a0001c0001t0003g0362 others(3): Show |
6 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-133A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520420 | |||||||
chr2:33520483 | C | T | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.237-70C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 5/17 | chr2 | 33520483 | |||||||
chr2:33520824 | C | T | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.368+140C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33520824 | |||||||
chr2:33520918 | C | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+234C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33520918 | |||||||
chr2:33521099 | A | G | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+415A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521099 | |||||||
chr2:33521175 | A | G | 1 | a0001c0002t0017g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.368+491A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521175 | |||||||
chr2:33521266 | C | T | 161 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0211 others(158): Show |
162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.368+582C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521266 | |||||||
chr2:33521276 | AG | A | 3 | a0001c0001t0005g0175 a0001c0001t0020g0309 a0001c0004t0020g0118 |
3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.368+594delG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 33521276 | ||||||
chr2:33521407 | C | T | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.369-548C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521407 | |||||||
chr2:33521429 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.369-526C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521429 | |||||||
chr2:33521739 | T | A | 296 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(293): Show |
297 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.369-216T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521739 | |||||||
chr2:33521752 | C | T | 1 | a0001c0001t0039g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369-203C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521752 | |||||||
chr2:33521754 | A | G | 2 | a0001c0001t0004g0143 a0001c0001t0008g0183 |
2 | HG00639.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.369-201A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521754 | |||||||
chr2:33521775 | G | C | 116 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(113): Show |
116 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.369-180G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521775 | |||||||
chr2:33521790 | G | T | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.369-165G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521790 | |||||||
chr2:33521934 | G | A | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.369-21G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 6/17 | chr2 | 33521934 | |||||||
chr2:33522218 | G | A | 296 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0063 others(293): Show |
297 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.516+116G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522218 | |||||||
chr2:33522389 | G | C | 1 | a0001c0001t0061g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.516+287G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522389 | |||||||
chr2:33522470 | G | A | 15 | a0001c0001t0001g0266 a0001c0001t0001g0351 a0001c0001t0002g0188 others(12): Show |
15 | HG00544.hp1 HG00639.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+368G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522470 | |||||||
chr2:33522498 | A | G | 299 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0062 others(296): Show |
300 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.516+396A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522498 | |||||||
chr2:33522519 | T | C | 113 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(110): Show |
113 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.516+417T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522519 | |||||||
chr2:33522571 | A | T | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.516+469A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522571 | |||||||
chr2:33522677 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0003g0240 a0001c0001t0019g0247 |
3 | NA18946.hp2 NA18954.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.516+575T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522677 | |||||||
chr2:33522685 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+583C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522685 | |||||||
chr2:33522709 | T | C | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.516+607T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522709 | |||||||
chr2:33522744 | G | T | 2 | a0001c0001t0001g0351 a0004c0010t0008g0317 |
2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.516+642G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522744 | |||||||
chr2:33522762 | C | T | 1 | a0001c0001t0037g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.516+660C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522762 | |||||||
chr2:33522801 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.516+699C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522801 | |||||||
chr2:33522925 | C | T | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.516+823C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522925 | |||||||
chr2:33522927 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+825C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33522927 | |||||||
chr2:33523105 | T | C | 1 | a0001c0001t0054g0038 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-774T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523105 | |||||||
chr2:33523132 | G | A | 5 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-747G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523132 | |||||||
chr2:33523195 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.517-684C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523195 | |||||||
chr2:33523245 | T | C | 1 | a0001c0001t0047g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.517-634T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523245 | |||||||
chr2:33523281 | G | A | 105 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(102): Show |
105 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.517-598G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523281 | |||||||
chr2:33523319 | G | T | 5 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-560G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523319 | |||||||
chr2:33523429 | C | T | 1 | a0001c0001t0057g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.517-450C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523429 | |||||||
chr2:33523449 | G | A | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.517-430G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523449 | |||||||
chr2:33523450 | C | T | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.517-429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523450 | |||||||
chr2:33523461 | TA | T | 93 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0266 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.517-402delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 33523461 | ||||||
chr2:33523461 | TAA | T | 109 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(106): Show |
109 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.517-403_517-402del others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 33523461 | ||||||
chr2:33523649 | G | A | 86 | a0001c0001t0001g0181 a0001c0001t0001g0266 a0001c0001t0001g0351 others(83): Show |
87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.517-230G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523649 | |||||||
chr2:33523771 | A | G | 111 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(108): Show |
111 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.517-108A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523771 | |||||||
chr2:33523784 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0248 a0001c0001t0002g0353 |
3 | NA18612.hp1 NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.517-95C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523784 | |||||||
chr2:33523834 | A | G | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.517-45A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523834 | |||||||
chr2:33523846 | A | G | 18 | a0001c0001t0001g0032 a0001c0001t0002g0039 a0001c0001t0005g0175 others(15): Show |
18 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.517-33A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 7/17 | chr2 | 33523846 | |||||||
chr2:33524078 | C | G | 8 | a0001c0001t0005g0175 a0001c0001t0009g0213 a0001c0001t0013g0121 others(5): Show |
8 | HG02280.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+26C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524078 | |||||||
chr2:33524147 | G | A | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+95G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524147 | |||||||
chr2:33524390 | A | G | 5 | a0001c0001t0013g0121 a0001c0001t0013g0164 a0001c0001t0013g0238 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-42A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 8/17 | chr2 | 33524390 | |||||||
chr2:33524693 | A | T | 1 | a0001c0001t0007g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.807+145A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33524693 | |||||||
chr2:33525080 | C | CA | 10 | a0001c0001t0001g0061 a0001c0001t0001g0331 a0001c0001t0001g0332 others(7): Show |
10 | HG02451.hp2 HG03041.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.807+545dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525080 | ||||||
chr2:33525095 | C | CA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0268 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+564dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525095 | ||||||
chr2:33525106 | A | T | 188 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(185): Show |
188 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.807+558A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525106 | |||||||
chr2:33525341 | A | AAT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0032 others(157): Show |
162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.807+808_807+809dup others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525341 | ||||||
chr2:33525388 | G | A | 99 | a0001c0001t0001g0101 a0001c0001t0001g0225 a0001c0001t0001g0264 others(96): Show |
99 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.807+840G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525388 | |||||||
chr2:33525571 | A | G | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807+1023A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525571 | |||||||
chr2:33525578 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18945.hp2 NA18989.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+1030G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525578 | |||||||
chr2:33525699 | C | CA | 33 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0061 others(30): Show |
33 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.807+1179dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | C | CAA | 47 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0084 others(44): Show |
48 | HG00323.hp2 HG00423.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.807+1178_807+1179d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | C | CAAA | 42 | a0001c0001t0001g0032 a0001c0001t0001g0085 a0001c0001t0001g0181 others(39): Show |
42 | HG00438.hp1 HG01175.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+1177_807+1179d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | C | CAAAA | 7 | a0001c0001t0003g0300 a0001c0001t0024g0136 a0001c0001t0031g0314 others(4): Show |
7 | HG01109.hp1 HG01256.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+1176_807+1179d others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | CA | C | 45 | a0001c0001t0001g0225 a0001c0001t0001g0264 a0001c0001t0002g0015 others(42): Show |
45 | HG00438.hp2 HG00642.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.807+1179delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | CAA | C | 59 | a0001c0001t0001g0101 a0001c0001t0001g0343 a0001c0001t0002g0008 others(56): Show |
59 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.807+1178_807+1179d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525699 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0016g0367 a0001c0001t0029g0053 a0001c0001t0029g0361 |
3 | HG02074.hp2 HG03669.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.807+1170_807+1179d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525699 | ||||||
chr2:33525726 | A | AAC | 30 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0023g0257 others(27): Show |
30 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.807+1179_807+1180d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525726 | ||||||
chr2:33525726 | A | AC | 37 | a0001c0001t0001g0211 a0001c0001t0023g0258 a0001c0002t0001g0005 others(34): Show |
37 | HG00609.hp1 HG01255.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.807+1178_807+1179i others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525726 | |||||||
chr2:33525726 | A | C | 4 | a0001c0001t0016g0367 a0001c0001t0029g0053 a0001c0001t0029g0361 others(1): Show |
4 | HG02074.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+1178A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525726 | |||||||
chr2:33525737 | T | TGTGGCA | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.807+1193_807+1198d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33525737 | ||||||
chr2:33525804 | G | C | 1 | a0001c0001t0065g0355 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.807+1256G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525804 | |||||||
chr2:33525920 | C | T | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.808-1217C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525920 | |||||||
chr2:33525995 | A | G | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.808-1142A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33525995 | |||||||
chr2:33526105 | G | A | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.808-1032G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526105 | |||||||
chr2:33526151 | A | G | 1 | a0003c0009t0048g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.808-986A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526151 | |||||||
chr2:33526276 | A | G | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.808-861A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526276 | |||||||
chr2:33526348 | C | T | 1 | a0001c0001t0025g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-789C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526348 | |||||||
chr2:33526414 | G | A | 122 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(119): Show |
122 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.808-723G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526414 | |||||||
chr2:33526553 | T | C | 1 | a0001c0001t0007g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.808-584T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526553 | |||||||
chr2:33526597 | C | T | 57 | a0001c0001t0001g0181 a0001c0001t0003g0013 a0001c0001t0003g0014 others(54): Show |
58 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.808-540C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526597 | |||||||
chr2:33526783 | C | A | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.808-354C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526783 | |||||||
chr2:33526810 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.808-327C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526810 | |||||||
chr2:33526866 | A | G | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.808-271A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33526866 | |||||||
chr2:33527062 | GC | G | 57 | a0001c0001t0001g0181 a0001c0001t0003g0013 a0001c0001t0003g0014 others(54): Show |
58 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.808-73delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 33527062 | ||||||
chr2:33527085 | G | T | 3 | a0001c0001t0002g0039 a0001c0001t0031g0314 a0001c0001t0032g0278 |
3 | HG01175.hp1 HG01256.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.808-52G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 9/17 | chr2 | 33527085 | |||||||
chr2:33528012 | T | G | 8 | a0001c0001t0001g0032 a0001c0001t0002g0039 a0001c0001t0031g0314 others(5): Show |
8 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+600T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528012 | |||||||
chr2:33528112 | T | A | 364 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(361): Show |
366 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(363): Show |
intron_variant | MODIFIER | c.1083+700T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528112 | |||||||
chr2:33528143 | C | T | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+731C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528143 | |||||||
chr2:33528187 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1083+775G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528187 | |||||||
chr2:33528196 | C | T | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1083+784C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528196 | |||||||
chr2:33528299 | G | A | 175 | a0001c0001t0001g0101 a0001c0001t0001g0169 a0001c0001t0001g0177 others(172): Show |
175 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1083+887G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528299 | |||||||
chr2:33528306 | C | A | 1 | a0001c0003t0005g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1083+894C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528306 | |||||||
chr2:33528330 | T | C | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1083+918T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528330 | |||||||
chr2:33528545 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1083+1133A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528545 | |||||||
chr2:33528670 | T | C | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1083+1258T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528670 | |||||||
chr2:33528971 | G | A | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1083+1559G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33528971 | |||||||
chr2:33529027 | A | G | 1 | a0001c0001t0020g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1083+1615A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529027 | |||||||
chr2:33529054 | C | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+1642C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529054 | |||||||
chr2:33529115 | G | C | 1 | a0001c0001t0031g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1083+1703G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529115 | |||||||
chr2:33529215 | C | T | 1 | a0001c0001t0020g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1083+1803C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529215 | |||||||
chr2:33529222 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1083+1810T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529222 | |||||||
chr2:33529232 | A | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0332 |
2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1820A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529232 | |||||||
chr2:33529240 | A | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0332 |
2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1828A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529240 | |||||||
chr2:33529241 | T | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0332 |
2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1083+1829T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529241 | |||||||
chr2:33529242 | T | C | 1 | a0001c0001t0022g0334 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1083+1830T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529242 | |||||||
chr2:33529261 | A | G | 300 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(297): Show |
301 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1083+1849A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529261 | |||||||
chr2:33529269 | C | A | 70 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0002g0039 others(67): Show |
71 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1083+1857C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529269 | |||||||
chr2:33529318 | C | T | 83 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0351 others(80): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1083+1906C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529318 | |||||||
chr2:33529319 | G | C | 113 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(110): Show |
113 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1083+1907G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529319 | |||||||
chr2:33529474 | C | G | 1 | a0001c0002t0003g0077 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1083+2062C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529474 | |||||||
chr2:33529487 | C | CAAAAAAA others(8): Show |
10 | a0001c0001t0002g0026 a0001c0001t0002g0029 a0001c0001t0002g0060 others(7): Show |
10 | HG01993.hp2 NA18942.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(19): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(9): Show |
71 | a0001c0001t0001g0101 a0001c0001t0001g0169 a0001c0001t0001g0182 others(68): Show |
71 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(10): Show |
76 | a0001c0001t0001g0316 a0001c0001t0001g0343 a0001c0001t0002g0068 others(73): Show |
76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(11): Show |
60 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0211 others(57): Show |
61 | HG01081.hp2 HG01192.hp2 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(12): Show |
21 | a0001c0001t0002g0365 a0001c0001t0003g0103 a0001c0001t0003g0302 others(18): Show |
21 | HG00423.hp1 HG00438.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(13): Show |
11 | a0001c0001t0002g0039 a0001c0001t0003g0064 a0001c0001t0015g0218 others(8): Show |
11 | HG00323.hp2 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0021g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0003g0300 a0001c0001t0027g0197 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0027g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(27): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0026g0194 a0001c0001t0043g0170 |
2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(28): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(18): Show |
6 | a0001c0001t0008g0037 a0001c0001t0008g0178 a0001c0001t0013g0121 others(3): Show |
6 | HG02280.hp1 HG02698.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(29): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(19): Show |
6 | a0001c0001t0009g0213 a0001c0001t0013g0164 a0001c0001t0013g0298 others(3): Show |
6 | HG01109.hp1 HG02615.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(30): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(20): Show |
2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(31): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(21): Show |
7 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0183 others(4): Show |
7 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(32): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(22): Show |
3 | a0001c0001t0001g0266 a0001c0001t0008g0036 a0001c0004t0020g0044 |
3 | HG03579.hp2 NA18949.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0001g0351 a0001c0004t0042g0199 |
2 | HG00544.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1083+2088_1083+208 others(34): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529487 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+2088_1083+208 others(36): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529487 | ||||||
chr2:33529802 | C | A | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083+2390C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33529802 | |||||||
chr2:33529859 | CA | C | 71 | a0001c0001t0001g0211 a0001c0001t0001g0316 a0001c0001t0001g0343 others(68): Show |
71 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1083+2449delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33529859 | ||||||
chr2:33530014 | A | G | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1083+2602A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530014 | |||||||
chr2:33530083 | C | T | 6 | a0001c0001t0004g0143 a0001c0001t0008g0036 a0001c0001t0008g0183 others(3): Show |
6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+2671C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530083 | |||||||
chr2:33530110 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1083+2698C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530110 | |||||||
chr2:33530214 | T | A | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083+2802T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530214 | |||||||
chr2:33530235 | T | G | 7 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+2823T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530235 | |||||||
chr2:33530271 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1083+2859A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530271 | |||||||
chr2:33530338 | C | G | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1083+2926C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530338 | |||||||
chr2:33530358 | G | A | 7 | a0001c0001t0011g0079 a0001c0001t0011g0082 a0001c0001t0011g0202 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+2946G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530358 | |||||||
chr2:33530393 | GTTTTCAC others(5): Show |
G | 17 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1083+2990_1083+300 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530393 | ||||||
chr2:33530489 | G | A | 2 | a0001c0001t0026g0194 a0003c0009t0048g0072 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+3077G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530489 | |||||||
chr2:33530497 | C | CT | 12 | a0001c0001t0001g0101 a0001c0001t0002g0068 a0001c0001t0002g0313 others(9): Show |
12 | HG01109.hp1 HG01255.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+3109dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | ||||||
chr2:33530497 | CT | C | 87 | a0001c0001t0001g0047 a0001c0001t0001g0177 a0001c0001t0001g0181 others(84): Show |
87 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1083+3109delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | ||||||
chr2:33530497 | CTT | C | 15 | a0001c0001t0003g0064 a0001c0001t0003g0300 a0001c0001t0012g0002 others(12): Show |
16 | HG00323.hp2 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1083+3108_1083+310 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530497 | ||||||
chr2:33530564 | A | C | 3 | a0001c0001t0051g0297 a0001c0004t0020g0044 a0001c0004t0042g0199 |
3 | HG03130.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1083+3152A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530564 | |||||||
chr2:33530702 | A | T | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1083+3290A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530702 | |||||||
chr2:33530740 | G | A | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+3328G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530740 | |||||||
chr2:33530792 | C | G | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1083+3380C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530792 | |||||||
chr2:33530852 | CT | C | 194 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(191): Show |
195 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1083+3442delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33530852 | ||||||
chr2:33530930 | T | C | 288 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0181 others(285): Show |
289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.1084-3393T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33530930 | |||||||
chr2:33531083 | G | C | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1084-3240G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531083 | |||||||
chr2:33531159 | A | G | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1084-3164A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531159 | |||||||
chr2:33531164 | G | A | 2 | a0001c0001t0041g0122 a0003c0011t0045g0200 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1084-3159G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531164 | |||||||
chr2:33531248 | C | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1084-3075C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531248 | |||||||
chr2:33531316 | T | C | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-3007T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531316 | |||||||
chr2:33531341 | C | A | 270 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0001g0177 others(267): Show |
271 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1084-2982C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531341 | |||||||
chr2:33531421 | G | A | 16 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(13): Show |
16 | HG00639.hp2 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-2902G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531421 | |||||||
chr2:33531453 | C | T | 65 | a0001c0001t0001g0181 a0001c0001t0002g0039 a0001c0001t0003g0013 others(62): Show |
66 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1084-2870C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531453 | |||||||
chr2:33531511 | T | C | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-2812T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531511 | |||||||
chr2:33531665 | T | C | 2 | a0001c0001t0002g0039 a0001c0001t0003g0064 |
2 | HG00323.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1084-2658T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531665 | |||||||
chr2:33531683 | T | C | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2640T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33531683 | |||||||
chr2:33531909 | G | GTCAGGAG others(50): Show |
3 | a0001c0004t0020g0044 a0001c0004t0020g0118 a0001c0004t0042g0199 |
3 | HG01884.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-2374_1084-237 others(61): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531909 | ||||||
chr2:33531995 | CTCTT | C | 11 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0007 others(8): Show |
11 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-2326_1084-232 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531995 | ||||||
chr2:33531997 | C | CTTTA | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2320_1084-231 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 33531997 | ||||||
chr2:33532048 | A | G | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1084-2275A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532048 | |||||||
chr2:33532148 | C | T | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1084-2175C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532148 | |||||||
chr2:33532168 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0061 |
2 | NA18945.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1084-2155G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532168 | |||||||
chr2:33532270 | A | G | 1 | a0003c0011t0045g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1084-2053A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532270 | |||||||
chr2:33532401 | C | A | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-1922C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532401 | |||||||
chr2:33532426 | C | T | 1 | a0001c0001t0021g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1084-1897C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532426 | |||||||
chr2:33532487 | C | A | 164 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(161): Show |
165 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1084-1836C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532487 | |||||||
chr2:33532575 | G | A | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1748G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532575 | |||||||
chr2:33532653 | C | G | 4 | a0001c0001t0024g0136 a0001c0001t0024g0152 a0001c0001t0043g0170 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1670C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532653 | |||||||
chr2:33532718 | G | A | 187 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(184): Show |
188 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1084-1605G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532718 | |||||||
chr2:33532746 | T | C | 1 | a0001c0002t0001g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1084-1577T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532746 | |||||||
chr2:33532771 | C | T | 2 | a0001c0001t0008g0037 a0001c0002t0001g0116 |
2 | HG04228.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1084-1552C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532771 | |||||||
chr2:33532908 | G | A | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1084-1415G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532908 | |||||||
chr2:33532909 | A | T | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1084-1414A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33532909 | |||||||
chr2:33533270 | T | C | 6 | a0001c0001t0004g0143 a0001c0001t0008g0036 a0001c0001t0008g0183 others(3): Show |
6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-1053T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533270 | |||||||
chr2:33533272 | T | C | 14 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(11): Show |
14 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1084-1051T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533272 | |||||||
chr2:33533281 | C | T | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-1042C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533281 | |||||||
chr2:33533388 | C | T | 10 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-935C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533388 | |||||||
chr2:33533389 | G | A | 102 | a0001c0001t0001g0101 a0001c0001t0001g0169 a0001c0001t0001g0182 others(99): Show |
102 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1084-934G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533389 | |||||||
chr2:33533463 | A | G | 1 | a0001c0001t0039g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1084-860A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533463 | |||||||
chr2:33533626 | G | A | 17 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1084-697G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533626 | |||||||
chr2:33533670 | C | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0075 a0001c0001t0002g0161 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084-653C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533670 | |||||||
chr2:33533731 | C | T | 3 | a0001c0001t0002g0108 a0001c0001t0002g0337 a0006c0015t0002g0040 |
3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1084-592C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533731 | |||||||
chr2:33533989 | A | G | 7 | a0001c0001t0011g0079 a0001c0001t0011g0082 a0001c0001t0011g0202 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-334A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533989 | |||||||
chr2:33533997 | T | C | 1 | a0001c0002t0004g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1084-326T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33533997 | |||||||
chr2:33534062 | A | C | 6 | a0001c0001t0043g0170 a0001c0001t0057g0081 a0001c0004t0020g0044 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-261A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534062 | |||||||
chr2:33534119 | C | T | 1 | a0009c0013t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1084-204C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534119 | |||||||
chr2:33534224 | A | G | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1084-99A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534224 | |||||||
chr2:33534291 | C | T | 1 | a0001c0001t0025g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1084-32C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534291 | |||||||
chr2:33534303 | C | G | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1084-20C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 10/17 | chr2 | 33534303 | |||||||
chr2:33534496 | G | A | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+96G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534496 | |||||||
chr2:33534534 | T | C | 18 | a0001c0001t0052g0301 a0001c0003t0005g0042 a0001c0003t0005g0119 others(15): Show |
18 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+134T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534534 | |||||||
chr2:33534644 | T | C | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1161+244T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534644 | |||||||
chr2:33534671 | G | A | 7 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(4): Show |
7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+271G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534671 | |||||||
chr2:33534676 | A | G | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1161+276A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534676 | |||||||
chr2:33534694 | A | AT | 92 | a0001c0001t0001g0032 a0001c0001t0001g0084 a0001c0001t0001g0085 others(89): Show |
93 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1161+314dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | ||||||
chr2:33534694 | A | ATT | 18 | a0001c0001t0001g0211 a0001c0001t0003g0043 a0001c0001t0003g0209 others(15): Show |
18 | HG01496.hp1 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+313_1161+314d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | ||||||
chr2:33534694 | A | ATTT | 6 | a0001c0003t0005g0119 a0001c0003t0005g0173 a0001c0003t0005g0174 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+312_1161+314d others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | ||||||
chr2:33534694 | AT | A | 19 | a0001c0001t0001g0063 a0001c0001t0001g0159 a0001c0001t0002g0111 others(16): Show |
19 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+314delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33534694 | ||||||
chr2:33534740 | C | A | 15 | a0001c0001t0052g0301 a0001c0003t0005g0042 a0001c0003t0005g0119 others(12): Show |
15 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161+340C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534740 | |||||||
chr2:33534754 | C | T | 72 | a0001c0001t0001g0343 a0001c0001t0017g0120 a0001c0001t0017g0236 others(69): Show |
72 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1161+354C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534754 | |||||||
chr2:33534755 | G | A | 18 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(15): Show |
18 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+355G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534755 | |||||||
chr2:33534765 | G | A | 1 | a0001c0001t0013g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1161+365G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534765 | |||||||
chr2:33534792 | C | T | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1161+392C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534792 | |||||||
chr2:33534836 | C | T | 8 | a0001c0001t0002g0347 a0001c0001t0005g0175 a0001c0001t0013g0121 others(5): Show |
8 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+436C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33534836 | |||||||
chr2:33535051 | T | C | 1 | a0001c0001t0044g0106 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1161+651T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535051 | |||||||
chr2:33535099 | A | G | 1 | a0001c0002t0006g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1161+699A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535099 | |||||||
chr2:33535124 | A | G | 3 | a0001c0001t0004g0091 a0001c0001t0004g0148 a0002c0007t0008g0083 |
3 | HG03831.hp1 HG03942.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1161+724A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535124 | |||||||
chr2:33535186 | G | A | 2 | a0001c0001t0041g0122 a0003c0011t0045g0200 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1161+786G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535186 | |||||||
chr2:33535209 | G | A | 268 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(265): Show |
269 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.1161+809G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535209 | |||||||
chr2:33535265 | T | C | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1161+865T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535265 | |||||||
chr2:33535295 | T | C | 1 | a0001c0001t0012g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1161+895T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535295 | |||||||
chr2:33535348 | T | G | 1 | a0001c0001t0044g0106 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1161+948T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535348 | |||||||
chr2:33535368 | G | A | 1 | a0001c0002t0001g0341 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1161+968G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535368 | |||||||
chr2:33535426 | C | A | 1 | a0001c0002t0001g0234 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1161+1026C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535426 | |||||||
chr2:33535531 | G | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0337 a0006c0015t0002g0040 |
3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1161+1131G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535531 | |||||||
chr2:33535555 | G | GC | 4 | a0001c0001t0001g0032 a0001c0001t0041g0122 a0003c0011t0045g0200 others(1): Show |
4 | HG02300.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+1157dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33535555 | ||||||
chr2:33535558 | G | A | 1 | a0001c0001t0035g0272 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1161+1158G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535558 | |||||||
chr2:33535698 | C | A | 2 | a0001c0001t0007g0066 a0001c0001t0007g0070 |
2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1161+1298C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535698 | |||||||
chr2:33535752 | C | T | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1161+1352C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535752 | |||||||
chr2:33535793 | A | G | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1161+1393A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535793 | |||||||
chr2:33535826 | G | T | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+1426G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535826 | |||||||
chr2:33535943 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0021g0140 a0001c0001t0021g0146 others(6): Show |
9 | HG01496.hp1 HG02300.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161+1543T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535943 | |||||||
chr2:33535944 | C | T | 194 | a0001c0001t0001g0032 a0001c0001t0001g0101 a0001c0001t0001g0181 others(191): Show |
195 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1161+1544C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33535944 | |||||||
chr2:33536038 | C | T | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1161+1638C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536038 | |||||||
chr2:33536068 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1161+1668C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536068 | |||||||
chr2:33536148 | A | G | 2 | a0001c0001t0043g0170 a0001c0001t0057g0081 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1161+1748A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536148 | |||||||
chr2:33536159 | G | A | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1161+1759G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536159 | |||||||
chr2:33536207 | C | T | 99 | a0001c0001t0001g0101 a0001c0001t0001g0225 a0001c0001t0001g0264 others(96): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1161+1807C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536207 | |||||||
chr2:33536267 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1161+1867A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536267 | |||||||
chr2:33536312 | A | T | 1 | a0001c0003t0005g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1161+1912A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536312 | |||||||
chr2:33536322 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1161+1922G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536322 | |||||||
chr2:33536322 | G | GA | 135 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0084 others(132): Show |
136 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1161+1937dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33536322 | ||||||
chr2:33536322 | GA | G | 104 | a0001c0001t0001g0101 a0001c0001t0001g0225 a0001c0001t0001g0264 others(101): Show |
104 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1161+1937delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33536322 | ||||||
chr2:33536337 | A | G | 1 | a0001c0001t0002g0338 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1161+1937A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536337 | |||||||
chr2:33536339 | G | A | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1161+1939G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536339 | |||||||
chr2:33536392 | C | T | 1 | a0002c0007t0008g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1161+1992C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536392 | |||||||
chr2:33536393 | G | A | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+1993G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536393 | |||||||
chr2:33536474 | C | T | 5 | a0001c0001t0017g0120 a0001c0001t0017g0236 a0001c0001t0024g0136 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+2074C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536474 | |||||||
chr2:33536490 | T | C | 6 | a0001c0001t0016g0367 a0001c0001t0029g0053 a0001c0001t0029g0361 others(3): Show |
6 | HG02074.hp2 HG02132.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2090T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536490 | |||||||
chr2:33536526 | G | A | 48 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(45): Show |
48 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1161+2126G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536526 | |||||||
chr2:33536528 | G | A | 48 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(45): Show |
48 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1161+2128G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536528 | |||||||
chr2:33536851 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1162-2243C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536851 | |||||||
chr2:33536857 | G | T | 1 | a0001c0001t0003g0362 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1162-2237G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536857 | |||||||
chr2:33536952 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1162-2142G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536952 | |||||||
chr2:33536970 | T | C | 57 | a0001c0001t0001g0016 a0001c0001t0001g0343 a0001c0001t0016g0367 others(54): Show |
57 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1162-2124T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33536970 | |||||||
chr2:33537192 | G | GAT | 59 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(56): Show |
60 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1162-1885_1162-188 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537192 | ||||||
chr2:33537265 | A | T | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1162-1829A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537265 | |||||||
chr2:33537305 | T | TAC | 6 | a0001c0001t0008g0178 a0001c0001t0008g0219 a0001c0001t0008g0242 others(3): Show |
6 | HG01070.hp1 HG02698.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1774_1162-177 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537305 | ||||||
chr2:33537305 | T | TACAC | 11 | a0001c0001t0002g0008 a0001c0001t0002g0108 a0001c0001t0002g0248 others(8): Show |
11 | HG03130.hp1 HG03195.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162-1776_1162-177 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537305 | ||||||
chr2:33537318 | A | C | 2 | a0001c0001t0025g0076 a0001c0001t0039g0128 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-1776A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537318 | |||||||
chr2:33537320 | A | ACACACAC | 8 | a0001c0001t0007g0058 a0001c0001t0007g0070 a0001c0001t0007g0104 others(5): Show |
8 | HG01168.hp2 HG01255.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACACC | 4 | a0001c0001t0013g0121 a0001c0001t0013g0164 a0001c0001t0013g0298 others(1): Show |
4 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACACCA others(3): Show |
2 | a0001c0001t0002g0243 a0001c0002t0001g0348 |
2 | HG00544.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACACCA others(5): Show |
1 | a0001c0002t0001g0350 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1162-1773_1162-177 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACACCC | 21 | a0001c0001t0002g0026 a0001c0001t0002g0029 a0001c0001t0002g0048 others(18): Show |
21 | HG01074.hp2 HG01123.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACACCC others(1): Show |
12 | a0001c0001t0002g0060 a0001c0001t0002g0068 a0001c0001t0002g0102 others(9): Show |
12 | HG00323.hp1 HG00642.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACACCC | 4 | a0001c0001t0008g0183 a0001c0001t0023g0257 a0001c0001t0023g0258 others(1): Show |
4 | HG01109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACCAC | 6 | a0001c0001t0002g0126 a0001c0001t0002g0222 a0001c0001t0010g0021 others(3): Show |
6 | HG00438.hp2 HG02451.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACCACC | 12 | a0001c0001t0001g0225 a0001c0001t0001g0261 a0001c0001t0002g0185 others(9): Show |
12 | HG01192.hp2 HG02027.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACCACCC | 30 | a0001c0001t0001g0063 a0001c0001t0001g0159 a0001c0001t0001g0160 others(27): Show |
30 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | ACCACCCC | 5 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0003g0162 others(2): Show |
5 | HG03017.hp1 HG03710.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-1772_1162-177 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537320 | ||||||
chr2:33537320 | A | C | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-1774A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537320 | |||||||
chr2:33537321 | C | CA | 3 | a0001c0001t0002g0188 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG03834.hp2 HG04228.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | |||||||
chr2:33537321 | C | CACA | 46 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(43): Show |
46 | HG00323.hp2 HG00423.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | |||||||
chr2:33537321 | C | CACACA | 6 | a0001c0001t0011g0079 a0001c0001t0011g0082 a0001c0001t0011g0202 others(3): Show |
6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1773_1162-177 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537321 | |||||||
chr2:33537322 | C | A | 27 | a0001c0001t0005g0175 a0001c0001t0012g0002 a0001c0001t0012g0123 others(24): Show |
28 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.1162-1772C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537322 | |||||||
chr2:33537323 | G | A | 6 | a0001c0001t0002g0345 a0001c0001t0003g0362 a0001c0001t0011g0079 others(3): Show |
6 | HG00738.hp2 HG01099.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1771G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537323 | |||||||
chr2:33537323 | G | C | 295 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(292): Show |
296 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(293): Show |
intron_variant | MODIFIER | c.1162-1771G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537323 | |||||||
chr2:33537326 | C | CA | 4 | a0001c0002t0001g0112 a0001c0002t0001g0205 a0001c0002t0001g0352 others(1): Show |
4 | NA18993.hp2 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-1768_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537326 | |||||||
chr2:33537328 | C | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0205 a0001c0002t0001g0352 others(1): Show |
4 | NA18993.hp2 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-1766C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | |||||||
chr2:33537328 | C | CA | 44 | a0001c0001t0001g0343 a0001c0001t0016g0367 a0001c0001t0029g0053 others(41): Show |
44 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1162-1766_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | |||||||
chr2:33537328 | C | CACA | 3 | a0001c0002t0001g0221 a0001c0002t0001g0359 a0001c0002t0016g0203 |
3 | HG02132.hp2 NA19060.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1162-1766_1162-176 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537328 | |||||||
chr2:33537330 | C | A | 107 | a0001c0001t0001g0101 a0001c0001t0001g0343 a0001c0001t0002g0026 others(104): Show |
107 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1162-1764C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | |||||||
chr2:33537330 | C | CA | 15 | a0001c0002t0004g0092 a0001c0002t0006g0134 a0001c0002t0006g0137 others(12): Show |
15 | HG00738.hp1 HG01255.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(5): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | |||||||
chr2:33537330 | C | CAACACA | 49 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(46): Show |
49 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | |||||||
chr2:33537330 | C | CACA | 12 | a0001c0001t0002g0008 a0001c0001t0002g0108 a0001c0001t0002g0248 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162-1764_1162-176 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537330 | |||||||
chr2:33537330 | C | CCCCACA | 15 | a0001c0001t0005g0175 a0001c0001t0020g0309 a0001c0001t0052g0301 others(12): Show |
15 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-1763_1162-176 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537330 | ||||||
chr2:33537330 | C | CCCCCAAC others(3): Show |
1 | a0001c0002t0003g0077 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1162-1763_1162-176 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537330 | ||||||
chr2:33537332 | A | C | 69 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(66): Show |
69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1162-1762A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537332 | |||||||
chr2:33537334 | A | C | 6 | a0001c0001t0001g0266 a0001c0001t0004g0129 a0001c0001t0004g0141 others(3): Show |
6 | HG00639.hp2 HG02055.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1760A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537334 | |||||||
chr2:33537367 | A | AT | 68 | a0001c0001t0001g0343 a0001c0001t0016g0367 a0001c0001t0029g0053 others(65): Show |
68 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1716dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33537367 | ||||||
chr2:33537395 | G | A | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1162-1699G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537395 | |||||||
chr2:33537416 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1162-1678C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537416 | |||||||
chr2:33537417 | G | A | 72 | a0001c0001t0001g0032 a0001c0001t0001g0343 a0001c0001t0009g0213 others(69): Show |
72 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1162-1677G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537417 | |||||||
chr2:33537519 | C | T | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1162-1575C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537519 | |||||||
chr2:33537586 | C | G | 1 | a0001c0008t0032g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1162-1508C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537586 | |||||||
chr2:33537588 | T | C | 1 | a0001c0001t0002g0338 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-1506T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537588 | |||||||
chr2:33537589 | G | T | 1 | a0001c0001t0002g0338 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-1505G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537589 | |||||||
chr2:33537591 | C | T | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1162-1503C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537591 | |||||||
chr2:33537625 | T | C | 7 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(4): Show |
7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-1469T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537625 | |||||||
chr2:33537648 | A | G | 1 | a0001c0002t0015g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1162-1446A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537648 | |||||||
chr2:33537896 | A | G | 58 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(55): Show |
59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1162-1198A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537896 | |||||||
chr2:33537933 | G | A | 7 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162-1161G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537933 | |||||||
chr2:33537966 | C | T | 1 | a0001c0002t0001g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1162-1128C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33537966 | |||||||
chr2:33538212 | T | C | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1162-882T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538212 | |||||||
chr2:33538300 | C | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0330 |
2 | NA18963.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1162-794C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538300 | |||||||
chr2:33538362 | G | A | 1 | a0001c0001t0007g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1162-732G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538362 | |||||||
chr2:33538430 | G | C | 4 | a0001c0001t0041g0122 a0003c0009t0048g0072 a0003c0011t0045g0200 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-664G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538430 | |||||||
chr2:33538452 | G | A | 2 | a0001c0001t0041g0122 a0003c0011t0045g0200 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1162-642G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538452 | |||||||
chr2:33538503 | A | AAAATAAA others(1): Show |
20 | a0001c0001t0043g0170 a0001c0001t0052g0301 a0001c0001t0057g0081 others(17): Show |
20 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-572_1162-565d others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33538503 | ||||||
chr2:33538509 | A | AATAAATA others(1): Show |
18 | a0001c0001t0001g0266 a0001c0001t0002g0188 a0001c0001t0004g0143 others(15): Show |
18 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1162-578_1162-577i others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33538509 | ||||||
chr2:33538519 | T | C | 1 | a0001c0001t0002g0015 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1162-575T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538519 | |||||||
chr2:33538676 | T | A | 7 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(4): Show |
7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-418T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538676 | |||||||
chr2:33538836 | A | G | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1162-258A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538836 | |||||||
chr2:33538880 | T | A | 219 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(216): Show |
220 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.1162-214T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538880 | |||||||
chr2:33538933 | G | C | 5 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-161G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | chr2 | 33538933 | |||||||
chr2:33539074 | G | GT | 14 | a0001c0001t0001g0266 a0001c0001t0002g0338 a0001c0001t0004g0143 others(11): Show |
14 | HG00639.hp2 HG01070.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-10dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 33539074 | ||||||
chr2:33539219 | T | C | 130 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(127): Show |
130 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1278+9T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539219 | |||||||
chr2:33539317 | C | G | 2 | a0001c0001t0007g0058 a0001c0001t0007g0259 |
2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1278+107C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539317 | |||||||
chr2:33539434 | T | C | 108 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(105): Show |
108 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1278+224T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539434 | |||||||
chr2:33539436 | C | G | 108 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(105): Show |
108 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1278+226C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539436 | |||||||
chr2:33539475 | T | C | 5 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+265T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539475 | |||||||
chr2:33539482 | CAACAGCT others(6): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1278+274_1278+286d others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539482 | ||||||
chr2:33539533 | G | T | 107 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(104): Show |
107 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1278+323G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539533 | |||||||
chr2:33539642 | C | G | 107 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(104): Show |
107 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1278+432C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539642 | |||||||
chr2:33539650 | C | T | 278 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0181 others(275): Show |
279 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.1278+440C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539650 | |||||||
chr2:33539730 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0107 |
3 | NA18994.hp2 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1278+520G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539730 | |||||||
chr2:33539797 | G | A | 204 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(201): Show |
205 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1278+587G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539797 | |||||||
chr2:33539888 | A | T | 284 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(281): Show |
285 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.1278+678A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33539888 | |||||||
chr2:33539987 | G | GA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0267 others(6): Show |
10 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1278+790dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539987 | ||||||
chr2:33539987 | GAAAAA | G | 45 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(42): Show |
46 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1278+786_1278+790d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539987 | ||||||
chr2:33539996 | AAAAAG | A | 135 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(132): Show |
135 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.1278+806_1278+810d others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539996 | ||||||
chr2:33539996 | AAAAAGAA others(3): Show |
A | 20 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0005g0175 others(17): Show |
20 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1278+801_1278+810d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33539996 | ||||||
chr2:33540001 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1278+791G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540001 | |||||||
chr2:33540006 | GAAAAGAA others(4): Show |
G | 1 | a0001c0001t0008g0036 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+801_1278+811d others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540006 | ||||||
chr2:33540199 | G | A | 1 | a0001c0001t0007g0336 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1278+989G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540199 | |||||||
chr2:33540209 | T | G | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1278+999T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540209 | |||||||
chr2:33540233 | G | A | 1 | a0001c0001t0058g0124 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1278+1023G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540233 | |||||||
chr2:33540439 | T | C | 19 | a0001c0001t0043g0170 a0001c0001t0057g0081 a0001c0003t0005g0042 others(16): Show |
19 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1278+1229T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540439 | |||||||
chr2:33540543 | C | G | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(5): Show |
8 | HG03130.hp1 HG03927.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1278+1333C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540543 | |||||||
chr2:33540543 | CTGTGTGT others(22): Show |
C | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1278+1345_1278+137 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540543 | ||||||
chr2:33540545 | G | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0267 a0001c0001t0001g0331 others(7): Show |
10 | HG02615.hp1 HG02886.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1278+1335G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540545 | |||||||
chr2:33540553 | GTT | G | 12 | a0001c0001t0001g0177 a0001c0001t0056g0246 a0001c0002t0001g0096 others(9): Show |
12 | HG00609.hp2 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+1346_1278+134 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540553 | ||||||
chr2:33540554 | T | TTG | 9 | a0001c0001t0002g0345 a0001c0002t0001g0087 a0001c0002t0001g0113 others(6): Show |
9 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1345_1278+134 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTG | T | 28 | a0001c0001t0016g0367 a0001c0001t0027g0192 a0001c0001t0029g0053 others(25): Show |
28 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1278+1346_1278+134 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTG | T | 9 | a0001c0001t0001g0343 a0001c0002t0001g0005 a0001c0002t0001g0031 others(6): Show |
9 | HG00609.hp1 HG02071.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTGT others(1): Show |
T | 9 | a0001c0001t0013g0299 a0001c0001t0027g0197 a0001c0002t0001g0293 others(6): Show |
9 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTGT others(3): Show |
T | 6 | a0001c0001t0013g0121 a0001c0001t0013g0164 a0001c0001t0013g0238 others(3): Show |
6 | HG02074.hp2 HG02280.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTGT others(7): Show |
T | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1278+1346_1278+135 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTGT others(9): Show |
T | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1278+1346_1278+136 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540554 | TTTTGTGT others(15): Show |
T | 1 | a0001c0002t0006g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1278+1346_1278+136 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540554 | ||||||
chr2:33540555 | T | G | 4 | a0001c0001t0001g0033 a0001c0001t0002g0068 a0001c0001t0041g0122 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+1345T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540555 | |||||||
chr2:33540556 | T | G | 212 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(209): Show |
213 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1278+1346T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540556 | |||||||
chr2:33540556 | T | TTG | 9 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0115 others(6): Show |
9 | HG00673.hp1 HG01109.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1394_1278+139 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | ||||||
chr2:33540556 | T | TTGTG | 7 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0050 others(4): Show |
7 | HG02155.hp2 NA18944.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278+1392_1278+139 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | ||||||
chr2:33540556 | TTG | T | 19 | a0001c0001t0001g0032 a0001c0001t0001g0055 a0001c0001t0001g0211 others(16): Show |
19 | HG00544.hp1 HG00558.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1278+1394_1278+139 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | ||||||
chr2:33540556 | TTGTG | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0327 others(2): Show |
5 | HG02074.hp1 HG02572.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+1392_1278+139 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | ||||||
chr2:33540556 | TTGTGTG | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0160 a0001c0001t0004g0189 others(1): Show |
4 | HG01175.hp2 HG03704.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1390_1278+139 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540556 | ||||||
chr2:33540559 | TGTGTGTG others(2): Show |
T | 8 | a0001c0001t0011g0193 a0001c0001t0012g0002 a0001c0001t0012g0123 others(5): Show |
9 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+1350_1278+135 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(4): Show |
T | 6 | a0001c0001t0003g0064 a0001c0001t0003g0209 a0001c0001t0014g0130 others(3): Show |
6 | HG00323.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(6): Show |
T | 36 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(33): Show |
36 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(8): Show |
T | 22 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0052g0301 others(19): Show |
22 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(19): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(10): Show |
T | 2 | a0001c0001t0002g0295 a0001c0001t0003g0043 |
2 | HG01993.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(12): Show |
T | 101 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(98): Show |
101 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1278+1350_1278+136 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540559 | TGTGTGTG others(14): Show |
T | 1 | a0001c0001t0004g0035 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278+1350_1278+137 others(25): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540559 | |||||||
chr2:33540561 | TGTGTG | T | 4 | a0001c0001t0008g0183 a0001c0001t0021g0140 a0001c0001t0021g0146 others(1): Show |
4 | HG01496.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1352_1278+135 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | |||||||
chr2:33540561 | TGTGTGTG others(2): Show |
T | 8 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(5): Show |
8 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1352_1278+136 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | |||||||
chr2:33540561 | TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1278+1352_1278+136 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | |||||||
chr2:33540561 | TGTGTGTG others(6): Show |
T | 2 | a0001c0001t0041g0122 a0003c0011t0045g0200 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1278+1352_1278+136 others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | |||||||
chr2:33540561 | TGTGTGTG others(12): Show |
T | 1 | a0001c0001t0002g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1278+1352_1278+137 others(23): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540561 | |||||||
chr2:33540562 | G | T | 1 | a0001c0001t0001g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1278+1352G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540562 | |||||||
chr2:33540572 | G | T | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1278+1362G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540572 | |||||||
chr2:33540576 | G | T | 6 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0041g0122 others(3): Show |
6 | HG01884.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278+1366G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540576 | |||||||
chr2:33540615 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0223 a0001c0001t0003g0302 |
3 | HG01496.hp2 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1278+1405T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540615 | |||||||
chr2:33540615 | T | TTC | 92 | a0001c0001t0001g0056 a0001c0001t0001g0177 a0001c0001t0001g0343 others(89): Show |
92 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1278+1429_1278+143 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | ||||||
chr2:33540615 | T | TTCTC | 6 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 others(3): Show |
6 | HG01496.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+1427_1278+143 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | ||||||
chr2:33540615 | TTCTC | T | 105 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(102): Show |
105 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1278+1427_1278+143 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540615 | ||||||
chr2:33540746 | G | A | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1278+1536G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540746 | |||||||
chr2:33540861 | T | TA | 8 | a0001c0001t0004g0143 a0001c0001t0008g0037 a0001c0001t0008g0178 others(5): Show |
8 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1662dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540861 | ||||||
chr2:33540861 | TA | T | 66 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0002g0008 others(63): Show |
66 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1278+1662delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33540861 | ||||||
chr2:33540868 | A | G | 8 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(5): Show |
8 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278+1658A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540868 | |||||||
chr2:33540888 | T | C | 107 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(104): Show |
107 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1278+1678T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540888 | |||||||
chr2:33540937 | A | T | 1 | a0001c0001t0008g0036 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+1727A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540937 | |||||||
chr2:33540966 | A | T | 1 | a0001c0001t0008g0036 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1278+1756A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33540966 | |||||||
chr2:33541061 | A | C | 4 | a0001c0002t0001g0113 a0001c0002t0001g0114 a0001c0002t0001g0116 others(1): Show |
4 | HG00558.hp1 NA18954.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1851A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541061 | |||||||
chr2:33541151 | G | A | 4 | a0001c0001t0014g0130 a0001c0001t0014g0131 a0001c0001t0014g0133 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1941G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541151 | |||||||
chr2:33541188 | A | G | 1 | a0001c0001t0010g0011 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1278+1978A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541188 | |||||||
chr2:33541391 | G | A | 81 | a0001c0001t0001g0177 a0001c0001t0001g0261 a0001c0001t0001g0343 others(78): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1279-2121G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541391 | |||||||
chr2:33541512 | C | T | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1279-2000C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541512 | |||||||
chr2:33541726 | C | T | 1 | a0001c0001t0020g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279-1786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541726 | |||||||
chr2:33541741 | G | T | 99 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(96): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1279-1771G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33541741 | |||||||
chr2:33542099 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1279-1413C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542099 | |||||||
chr2:33542299 | T | A | 12 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-1213T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542299 | |||||||
chr2:33542348 | T | C | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1279-1164T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542348 | |||||||
chr2:33542370 | C | T | 12 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-1142C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542370 | |||||||
chr2:33542525 | A | G | 2 | a0001c0001t0002g0243 a0001c0001t0044g0106 |
2 | HG00642.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1279-987A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542525 | |||||||
chr2:33542583 | A | T | 14 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(11): Show |
14 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1279-929A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542583 | |||||||
chr2:33542601 | G | A | 20 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0002g0008 others(17): Show |
20 | HG01433.hp2 HG01928.hp2 NA18612.hp1 others(17): Show |
intron_variant | MODIFIER | c.1279-911G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542601 | |||||||
chr2:33542628 | A | G | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1279-884A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542628 | |||||||
chr2:33542657 | T | TC | 17 | a0001c0001t0002g0015 a0001c0001t0002g0060 a0001c0001t0002g0111 others(14): Show |
17 | HG00438.hp2 HG02818.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.1279-846dupC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 33542657 | ||||||
chr2:33542663 | C | A | 2 | a0001c0001t0023g0257 a0001c0001t0023g0258 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1279-849C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542663 | |||||||
chr2:33542819 | G | C | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-693G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542819 | |||||||
chr2:33542850 | A | T | 2 | a0001c0001t0003g0300 a0001c0001t0050g0311 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1279-662A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542850 | |||||||
chr2:33542956 | G | T | 1 | a0001c0002t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1279-556G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542956 | |||||||
chr2:33542982 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1279-530C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33542982 | |||||||
chr2:33543006 | T | C | 1 | a0001c0002t0033g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1279-506T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543006 | |||||||
chr2:33543049 | G | T | 22 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0005g0175 others(19): Show |
22 | HG00639.hp2 HG01070.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279-463G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543049 | |||||||
chr2:33543088 | A | G | 2 | a0001c0001t0004g0189 a0001c0001t0004g0195 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1279-424A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543088 | |||||||
chr2:33543202 | A | C | 1 | a0001c0002t0037g0344 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1279-310A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543202 | |||||||
chr2:33543230 | G | T | 3 | a0001c0001t0002g0108 a0001c0001t0002g0337 a0006c0015t0002g0040 |
3 | HG03491.hp2 HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1279-282G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543230 | |||||||
chr2:33543250 | A | G | 1 | a0001c0001t0008g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1279-262A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543250 | |||||||
chr2:33543280 | C | G | 3 | a0001c0001t0041g0122 a0003c0009t0048g0072 a0003c0011t0045g0200 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1279-232C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543280 | |||||||
chr2:33543391 | T | C | 1 | a0001c0003t0005g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1279-121T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543391 | |||||||
chr2:33543441 | G | A | 1 | a0001c0001t0010g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1279-71G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 12/17 | chr2 | 33543441 | |||||||
chr2:33543664 | C | G | 1 | a0001c0001t0002g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1394+37C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543664 | |||||||
chr2:33543698 | G | A | 1 | a0001c0002t0006g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1394+71G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543698 | |||||||
chr2:33543901 | C | G | 216 | a0001c0001t0001g0101 a0001c0001t0001g0169 a0001c0001t0001g0181 others(213): Show |
216 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.1394+274C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33543901 | |||||||
chr2:33544126 | C | G | 1 | a0001c0001t0039g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1394+499C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544126 | |||||||
chr2:33544181 | G | A | 10 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+554G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544181 | |||||||
chr2:33544230 | C | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1394+603C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544230 | |||||||
chr2:33544520 | G | GA | 106 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0001g0169 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1394+903dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33544520 | ||||||
chr2:33544708 | T | C | 7 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+1081T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544708 | |||||||
chr2:33544747 | C | T | 10 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+1120C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33544747 | |||||||
chr2:33544835 | AT | A | 8 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(5): Show |
9 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1394+1217delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33544835 | ||||||
chr2:33545133 | A | T | 23 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0005g0175 others(20): Show |
23 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+1506A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545133 | |||||||
chr2:33545200 | T | C | 1 | a0009c0013t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1394+1573T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545200 | |||||||
chr2:33545336 | G | A | 3 | a0001c0001t0041g0122 a0003c0009t0048g0072 a0003c0011t0045g0200 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+1709G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545336 | |||||||
chr2:33545661 | T | C | 287 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(284): Show |
288 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.1394+2034T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545661 | |||||||
chr2:33545793 | CTAT | C | 286 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(283): Show |
287 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.1394+2184_1394+218 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33545793 | ||||||
chr2:33545910 | T | A | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1394+2283T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545910 | |||||||
chr2:33545915 | A | C | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1394+2288A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33545915 | |||||||
chr2:33546107 | G | A | 17 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394+2480G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546107 | |||||||
chr2:33546150 | G | A | 101 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(98): Show |
101 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1394+2523G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546150 | |||||||
chr2:33546240 | G | C | 1 | a0001c0001t0002g0111 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1394+2613G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546240 | |||||||
chr2:33546315 | C | T | 93 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(90): Show |
93 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1394+2688C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546315 | |||||||
chr2:33546340 | A | G | 287 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(284): Show |
288 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.1394+2713A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546340 | |||||||
chr2:33546347 | C | G | 3 | a0001c0001t0041g0122 a0003c0009t0048g0072 a0003c0011t0045g0200 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+2720C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546347 | |||||||
chr2:33546348 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0275 others(2): Show |
5 | HG00621.hp2 NA18944.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+2721G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546348 | |||||||
chr2:33546355 | G | A | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1394+2728G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546355 | |||||||
chr2:33546402 | G | C | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1394+2775G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546402 | |||||||
chr2:33546422 | C | CA | 17 | a0001c0001t0003g0300 a0001c0001t0005g0175 a0001c0001t0013g0121 others(14): Show |
17 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394+2811dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33546422 | ||||||
chr2:33546422 | CA | C | 23 | a0001c0001t0001g0047 a0001c0001t0001g0115 a0001c0001t0001g0266 others(20): Show |
23 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+2811delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33546422 | ||||||
chr2:33546473 | C | T | 3 | a0001c0001t0041g0122 a0003c0009t0048g0072 a0003c0011t0045g0200 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1394+2846C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546473 | |||||||
chr2:33546626 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0107 |
3 | NA18994.hp2 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1395-2978T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546626 | |||||||
chr2:33546739 | TACATATA others(1333): Show |
T | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-2864_1395-152 others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546739 | |||||||
chr2:33546892 | C | A | 1 | a0001c0001t0007g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1395-2712C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546892 | |||||||
chr2:33546942 | C | G | 55 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(52): Show |
56 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1395-2662C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33546942 | |||||||
chr2:33547053 | G | GA | 98 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0101 others(95): Show |
98 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1395-2530dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | G | GAA | 9 | a0001c0001t0001g0181 a0001c0001t0002g0015 a0001c0001t0002g0060 others(6): Show |
9 | HG02965.hp2 NA18941.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395-2531_1395-253 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | GA | G | 17 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0115 others(14): Show |
18 | HG01496.hp1 HG02015.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395-2530delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | GAA | G | 45 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(42): Show |
45 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1395-2531_1395-253 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | GAAAAAA | G | 22 | a0001c0001t0004g0129 a0001c0001t0004g0141 a0001c0001t0041g0122 others(19): Show |
22 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-2535_1395-253 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | GAAAAAAA | G | 6 | a0001c0001t0017g0120 a0001c0001t0017g0236 a0001c0001t0024g0136 others(3): Show |
6 | HG01109.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-2536_1395-253 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547053 | GAAAAAAA others(2): Show |
G | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-2538_1395-253 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547053 | ||||||
chr2:33547054 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1395-2550A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547054 | |||||||
chr2:33547073 | A | G | 32 | a0001c0001t0003g0017 a0001c0001t0003g0223 a0001c0001t0003g0302 others(29): Show |
32 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1395-2531A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547073 | |||||||
chr2:33547074 | AGAG | A | 6 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(3): Show |
6 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2529_1395-252 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547074 | |||||||
chr2:33547087 | G | A | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395-2517G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547087 | |||||||
chr2:33547342 | C | CT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0055 others(17): Show |
20 | HG00597.hp2 HG01175.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1395-2233dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT | 8 | a0001c0001t0003g0014 a0001c0001t0003g0223 a0001c0001t0003g0300 others(5): Show |
8 | HG01358.hp2 HG02602.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-2239_1395-223 others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0003g0013 a0001c0001t0003g0017 a0001c0001t0003g0064 others(10): Show |
13 | HG00323.hp2 HG01081.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1395-2240_1395-223 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0002g0039 a0001c0001t0003g0043 a0001c0001t0003g0138 others(9): Show |
12 | HG01175.hp1 HG01496.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1395-2241_1395-223 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0147 a0001c0001t0003g0302 a0001c0001t0014g0130 others(3): Show |
6 | HG01952.hp1 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2242_1395-223 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0012g0184 a0001c0001t0014g0131 a0001c0001t0014g0191 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-2243_1395-223 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(9): Show |
1 | a0001c0002t0001g0348 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1395-2248_1395-223 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(15): Show |
1 | a0002c0005t0003g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1395-2254_1395-223 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(16): Show |
1 | a0002c0005t0003g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1395-2255_1395-223 others(27): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(17): Show |
3 | a0001c0002t0001g0221 a0001c0002t0001g0366 a0001c0002t0004g0092 |
3 | HG02132.hp2 HG03704.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1395-2256_1395-223 others(28): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(18): Show |
4 | a0001c0002t0001g0359 a0001c0002t0006g0137 a0001c0002t0006g0187 others(1): Show |
4 | HG01255.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-2257_1395-223 others(29): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(19): Show |
3 | a0001c0002t0006g0156 a0001c0002t0006g0166 a0001c0002t0016g0203 |
3 | HG02886.hp1 HG03486.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1395-2258_1395-223 others(30): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(20): Show |
2 | a0001c0002t0001g0273 a0001c0002t0006g0186 |
2 | HG00738.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1395-2259_1395-223 others(31): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(21): Show |
1 | a0001c0002t0006g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1395-2260_1395-223 others(32): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(22): Show |
1 | a0001c0002t0006g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1395-2261_1395-223 others(33): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(23): Show |
1 | a0001c0002t0006g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1395-2233_1395-223 others(34): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | C | CTTTTTTT others(24): Show |
1 | a0001c0002t0001g0350 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1395-2233_1395-223 others(35): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CT | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0054 others(18): Show |
21 | HG00423.hp1 HG00639.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1395-2233delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTT | C | 6 | a0001c0001t0039g0128 a0001c0002t0001g0341 a0001c0002t0006g0134 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2235_1395-223 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTT | C | 14 | a0001c0001t0005g0175 a0001c0001t0017g0236 a0001c0001t0020g0309 others(11): Show |
14 | HG00621.hp1 HG00673.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395-2236_1395-223 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTT | C | 22 | a0001c0001t0017g0120 a0001c0001t0023g0257 a0001c0001t0023g0258 others(19): Show |
22 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-2237_1395-223 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0002g0048 a0001c0001t0002g0075 a0001c0001t0002g0108 others(11): Show |
14 | HG00597.hp1 HG01109.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395-2240_1395-223 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTTTT others(2): Show |
C | 80 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0001g0181 others(77): Show |
80 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1395-2241_1395-223 others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0002g0102 a0001c0001t0002g0243 a0001c0001t0002g0288 others(3): Show |
6 | HG00642.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-2242_1395-223 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTTTT others(4): Show |
C | 4 | a0001c0003t0005g0119 a0001c0003t0005g0190 a0001c0003t0005g0239 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395-2243_1395-223 others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547342 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0012g0123 a0001c0001t0052g0301 a0001c0003t0005g0042 others(12): Show |
15 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1395-2244_1395-223 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33547342 | ||||||
chr2:33547458 | G | A | 156 | a0001c0001t0001g0177 a0001c0001t0002g0039 a0001c0001t0002g0188 others(153): Show |
157 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1395-2146G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547458 | |||||||
chr2:33547470 | G | C | 1 | a0001c0001t0004g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1395-2134G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547470 | |||||||
chr2:33547483 | G | A | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1395-2121G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547483 | |||||||
chr2:33547574 | G | A | 10 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0008g0036 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-2030G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547574 | |||||||
chr2:33547586 | G | A | 5 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395-2018G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547586 | |||||||
chr2:33547680 | A | C | 2 | a0002c0005t0003g0204 a0002c0005t0003g0214 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1395-1924A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547680 | |||||||
chr2:33547888 | G | C | 7 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-1716G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547888 | |||||||
chr2:33547919 | G | A | 3 | a0001c0001t0016g0367 a0001c0001t0029g0053 a0001c0001t0029g0361 |
3 | HG02074.hp2 HG03669.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1395-1685G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547919 | |||||||
chr2:33547934 | A | G | 1 | a0001c0001t0018g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1395-1670A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33547934 | |||||||
chr2:33548072 | G | C | 2 | a0001c0001t0003g0103 a0001c0001t0003g0208 |
2 | HG00423.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1395-1532G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548072 | |||||||
chr2:33548083 | T | C | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-1521T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548083 | |||||||
chr2:33548106 | A | T | 2 | a0001c0001t0025g0076 a0001c0001t0058g0124 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1395-1498A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548106 | |||||||
chr2:33548167 | T | A | 2 | a0001c0001t0001g0315 a0001c0001t0037g0280 |
2 | NA19010.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1395-1437T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548167 | |||||||
chr2:33548233 | C | T | 90 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(87): Show |
90 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1395-1371C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548233 | |||||||
chr2:33548336 | A | C | 1 | a0001c0001t0040g0320 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1395-1268A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548336 | |||||||
chr2:33548360 | C | CA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0067 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1395-1221dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | ||||||
chr2:33548360 | CA | C | 22 | a0001c0001t0002g0075 a0001c0001t0002g0161 a0001c0001t0002g0220 others(19): Show |
22 | HG01109.hp2 HG01123.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395-1221delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | ||||||
chr2:33548360 | CAA | C | 103 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(100): Show |
103 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1395-1222_1395-122 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548360 | ||||||
chr2:33548381 | A | AAAAAAG | 8 | a0001c0001t0003g0043 a0001c0001t0011g0193 a0001c0001t0014g0130 others(5): Show |
8 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-1221_1395-122 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548381 | ||||||
chr2:33548381 | A | AAAAAG | 48 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(45): Show |
49 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1395-1221_1395-122 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548381 | ||||||
chr2:33548409 | T | TG | 15 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(12): Show |
15 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1395-1193dupG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548409 | ||||||
chr2:33548469 | T | C | 57 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(54): Show |
58 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1395-1135T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548469 | |||||||
chr2:33548479 | G | A | 1 | a0003c0011t0045g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1395-1125G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548479 | |||||||
chr2:33548672 | A | T | 90 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(87): Show |
90 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1395-932A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548672 | |||||||
chr2:33548698 | A | AATTATT | 7 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 others(4): Show |
7 | HG01496.hp1 HG02922.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395-890_1395-885d others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 33548698 | ||||||
chr2:33548714 | A | T | 1 | a0001c0001t0009g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1395-890A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548714 | |||||||
chr2:33548717 | A | T | 98 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(95): Show |
98 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1395-887A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548717 | |||||||
chr2:33548762 | A | G | 47 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(44): Show |
47 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1395-842A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548762 | |||||||
chr2:33548842 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1395-762C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548842 | |||||||
chr2:33548920 | C | T | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1395-684C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33548920 | |||||||
chr2:33549085 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1395-519C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549085 | |||||||
chr2:33549155 | C | G | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395-449C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549155 | |||||||
chr2:33549303 | A | C | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1395-301A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549303 | |||||||
chr2:33549311 | G | A | 5 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395-293G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549311 | |||||||
chr2:33549339 | CAT | C | 92 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1395-264_1395-263d others(4): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549339 | |||||||
chr2:33549383 | C | T | 6 | a0001c0001t0027g0192 a0001c0001t0027g0197 a0001c0001t0050g0311 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-221C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549383 | |||||||
chr2:33549384 | G | A | 10 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(7): Show |
10 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-220G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549384 | |||||||
chr2:33549537 | A | G | 2 | a0001c0001t0008g0037 a0001c0001t0008g0178 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1395-67A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 13/17 | chr2 | 33549537 | |||||||
chr2:33549794 | G | A | 3 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0039g0128 |
3 | HG01884.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542+43G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33549794 | |||||||
chr2:33549950 | G | A | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1542+199G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33549950 | |||||||
chr2:33550092 | C | T | 2 | a0001c0002t0006g0166 a0001c0002t0006g0172 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1542+341C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550092 | |||||||
chr2:33550119 | G | T | 3 | a0001c0001t0050g0311 a0001c0001t0051g0297 a0001c0004t0020g0118 |
3 | HG01884.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542+368G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550119 | |||||||
chr2:33550141 | G | A | 11 | a0001c0001t0001g0266 a0001c0001t0002g0188 a0001c0001t0004g0143 others(8): Show |
11 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+390G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550141 | |||||||
chr2:33550149 | A | G | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+398A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550149 | |||||||
chr2:33550152 | G | C | 2 | a0002c0005t0003g0204 a0002c0005t0003g0214 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1542+401G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550152 | |||||||
chr2:33550216 | T | A | 52 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(49): Show |
53 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1542+465T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550216 | |||||||
chr2:33550358 | C | T | 2 | a0001c0001t0017g0120 a0001c0001t0017g0236 |
2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1542+607C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550358 | |||||||
chr2:33550484 | C | G | 58 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(55): Show |
59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1542+733C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550484 | |||||||
chr2:33550544 | C | T | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1542+793C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550544 | |||||||
chr2:33550598 | T | G | 1 | a0009c0013t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1542+847T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550598 | |||||||
chr2:33550741 | G | A | 3 | a0001c0001t0025g0076 a0001c0001t0039g0128 a0001c0001t0058g0124 |
3 | HG01884.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1542+990G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33550741 | |||||||
chr2:33550849 | TG | T | 5 | a0001c0001t0017g0120 a0001c0001t0017g0236 a0001c0001t0024g0136 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+1101delG | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33550849 | ||||||
chr2:33551040 | C | T | 7 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(4): Show |
7 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542+1289C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551040 | |||||||
chr2:33551248 | G | C | 42 | a0001c0001t0002g0188 a0001c0001t0004g0143 a0001c0001t0005g0175 others(39): Show |
42 | HG00639.hp2 HG01070.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1542+1497G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551248 | |||||||
chr2:33551252 | G | A | 1 | a0001c0001t0009g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1542+1501G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551252 | |||||||
chr2:33551284 | G | T | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+1533G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551284 | |||||||
chr2:33551376 | C | T | 72 | a0001c0001t0001g0343 a0001c0001t0038g0144 a0001c0001t0039g0128 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1542+1625C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551376 | |||||||
chr2:33551421 | G | A | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542+1670G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551421 | |||||||
chr2:33551424 | C | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0331 |
2 | NA19012.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1542+1673C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551424 | |||||||
chr2:33551613 | T | G | 209 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(206): Show |
210 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.1542+1862T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551613 | |||||||
chr2:33551676 | A | G | 51 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(48): Show |
52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542+1925A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551676 | |||||||
chr2:33551678 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1542+1927C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551678 | |||||||
chr2:33551697 | A | T | 50 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(47): Show |
51 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1542+1946A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551697 | |||||||
chr2:33551721 | C | T | 1 | a0001c0002t0001g0265 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1542+1970C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551721 | |||||||
chr2:33551821 | G | T | 2 | a0001c0004t0020g0044 a0001c0004t0042g0199 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1542+2070G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551821 | |||||||
chr2:33551898 | C | A | 5 | a0001c0001t0013g0121 a0001c0001t0013g0164 a0001c0001t0013g0238 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+2147C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551898 | |||||||
chr2:33551925 | G | A | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+2174G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551925 | |||||||
chr2:33551972 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0138 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1542+2221G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33551972 | |||||||
chr2:33551994 | A | AAAAC | 56 | a0001c0001t0001g0343 a0001c0001t0038g0144 a0001c0001t0039g0128 others(53): Show |
56 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1542+2273_1542+227 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33551994 | ||||||
chr2:33551994 | AAAAC | A | 3 | a0001c0001t0002g0303 a0001c0001t0009g0041 a0001c0001t0031g0314 |
3 | HG00642.hp1 HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1542+2273_1542+227 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33551994 | ||||||
chr2:33552010 | CAAACAAA others(10): Show |
C | 1 | a0001c0001t0013g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1542+2260_1542+227 others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552010 | |||||||
chr2:33552022 | CAAACA | C | 51 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(48): Show |
52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542+2272_1542+227 others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552022 | |||||||
chr2:33552026 | CA | C | 32 | a0001c0001t0004g0143 a0001c0001t0008g0037 a0001c0001t0008g0178 others(29): Show |
32 | HG00639.hp2 HG01070.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.1542+2276delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552026 | |||||||
chr2:33552027 | A | AAAC | 15 | a0001c0001t0005g0175 a0001c0001t0008g0036 a0001c0001t0013g0121 others(12): Show |
15 | HG02056.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542+2276_1542+227 others(7): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552027 | |||||||
chr2:33552027 | A | T | 1 | a0003c0011t0045g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1542+2276A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552027 | |||||||
chr2:33552054 | C | G | 2 | a0001c0001t0004g0129 a0001c0001t0004g0141 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1542+2303C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552054 | |||||||
chr2:33552055 | G | A | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1542+2304G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552055 | |||||||
chr2:33552183 | A | G | 2 | a0001c0001t0008g0037 a0001c0001t0008g0178 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1542+2432A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552183 | |||||||
chr2:33552277 | G | T | 1 | a0001c0001t0002g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1542+2526G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552277 | |||||||
chr2:33552476 | G | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2725G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552476 | |||||||
chr2:33552482 | A | T | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2731A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552482 | |||||||
chr2:33552549 | T | C | 2 | a0001c0001t0050g0311 a0001c0001t0051g0297 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542+2798T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552549 | |||||||
chr2:33552568 | A | ATAAC | 24 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(21): Show |
24 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1542+2820_1542+282 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 33552568 | ||||||
chr2:33552590 | G | C | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+2839G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552590 | |||||||
chr2:33552744 | T | TTTGTAGA others(5): Show |
1 | a0001c0001t0050g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2787_1543-278 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552744 | |||||||
chr2:33552745 | C | T | 1 | a0001c0001t0050g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2786C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552745 | |||||||
chr2:33552746 | C | A | 1 | a0001c0001t0050g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2785C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552746 | |||||||
chr2:33552747 | C | G | 1 | a0001c0001t0050g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1543-2784C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552747 | |||||||
chr2:33552856 | C | G | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-2675C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552856 | |||||||
chr2:33552869 | G | A | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1543-2662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552869 | |||||||
chr2:33552924 | G | A | 1 | a0001c0001t0051g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1543-2607G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552924 | |||||||
chr2:33552996 | C | T | 1 | a0003c0011t0045g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1543-2535C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33552996 | |||||||
chr2:33553102 | C | T | 2 | a0001c0001t0007g0066 a0001c0001t0007g0070 |
2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1543-2429C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553102 | |||||||
chr2:33553267 | T | G | 1 | a0003c0011t0045g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1543-2264T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553267 | |||||||
chr2:33553429 | G | C | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1543-2102G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553429 | |||||||
chr2:33553457 | T | C | 2 | a0001c0001t0043g0170 a0001c0001t0057g0081 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1543-2074T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553457 | |||||||
chr2:33553468 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1543-2063T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553468 | |||||||
chr2:33553516 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0002g0102 |
2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1543-2015T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553516 | |||||||
chr2:33553662 | C | G | 4 | a0001c0003t0005g0173 a0001c0003t0005g0174 a0001c0003t0005g0251 others(1): Show |
4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-1869C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553662 | |||||||
chr2:33553995 | C | T | 51 | a0001c0001t0002g0039 a0001c0001t0003g0013 a0001c0001t0003g0014 others(48): Show |
52 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1543-1536C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33553995 | |||||||
chr2:33554040 | A | G | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-1491A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554040 | |||||||
chr2:33554153 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1543-1378T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554153 | |||||||
chr2:33554170 | C | T | 1 | a0001c0002t0063g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1543-1361C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554170 | |||||||
chr2:33554207 | G | C | 2 | a0001c0001t0050g0311 a0001c0001t0051g0297 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-1324G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554207 | |||||||
chr2:33554267 | C | T | 71 | a0001c0001t0001g0343 a0001c0001t0038g0144 a0001c0001t0039g0128 others(68): Show |
71 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1543-1264C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554267 | |||||||
chr2:33554269 | G | T | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1543-1262G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554269 | |||||||
chr2:33554542 | A | G | 58 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(55): Show |
59 | HG00323.hp2 HG00423.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1543-989A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554542 | |||||||
chr2:33554783 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1543-748C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554783 | |||||||
chr2:33554801 | G | C | 2 | a0001c0001t0003g0296 a0001c0001t0003g0362 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1543-730G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554801 | |||||||
chr2:33554812 | G | A | 10 | a0001c0001t0005g0175 a0001c0001t0013g0121 a0001c0001t0013g0164 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543-719G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554812 | |||||||
chr2:33554839 | T | C | 109 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(106): Show |
110 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1543-692T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554839 | |||||||
chr2:33554850 | C | T | 58 | a0001c0001t0001g0177 a0001c0001t0001g0343 a0001c0001t0038g0144 others(55): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1543-681C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554850 | |||||||
chr2:33554869 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1543-662G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554869 | |||||||
chr2:33554886 | C | T | 1 | a0001c0001t0007g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1543-645C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33554886 | |||||||
chr2:33555069 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1543-462C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555069 | |||||||
chr2:33555112 | A | G | 2 | a0001c0001t0050g0311 a0001c0001t0052g0301 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-419A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555112 | |||||||
chr2:33555164 | G | A | 91 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(88): Show |
92 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1543-367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555164 | |||||||
chr2:33555219 | G | A | 1 | a0001c0002t0006g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1543-312G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555219 | |||||||
chr2:33555252 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1543-279G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555252 | |||||||
chr2:33555259 | G | A | 3 | a0001c0001t0050g0311 a0001c0001t0051g0297 a0001c0001t0052g0301 |
3 | HG02922.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1543-272G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555259 | |||||||
chr2:33555276 | C | G | 4 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0293 others(1): Show |
4 | HG00621.hp1 HG00673.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-255C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555276 | |||||||
chr2:33555286 | T | C | 2 | a0003c0009t0048g0072 a0003c0011t0045g0200 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1543-245T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555286 | |||||||
chr2:33555334 | G | C | 17 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-197G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555334 | |||||||
chr2:33555369 | G | A | 1 | a0001c0001t0013g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1543-162G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555369 | |||||||
chr2:33555377 | G | A | 1 | a0001c0003t0005g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1543-154G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 14/17 | chr2 | 33555377 | |||||||
chr2:33555634 | G | C | 83 | a0001c0001t0001g0177 a0001c0001t0001g0343 a0001c0001t0016g0367 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1579+67G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555634 | |||||||
chr2:33555766 | AC | A | 5 | a0001c0001t0017g0120 a0001c0001t0017g0236 a0001c0001t0024g0136 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+200delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555766 | |||||||
chr2:33555864 | C | T | 2 | a0001c0001t0017g0120 a0001c0001t0017g0236 |
2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1579+297C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555864 | |||||||
chr2:33555898 | AC | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0050 others(7): Show |
10 | HG00621.hp2 HG02132.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1579+333delC | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33555898 | ||||||
chr2:33555992 | C | T | 1 | a0001c0004t0042g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1579+425C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33555992 | |||||||
chr2:33556041 | C | T | 1 | a0001c0001t0010g0009 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1579+474C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556041 | |||||||
chr2:33556095 | C | G | 66 | a0001c0001t0001g0177 a0001c0001t0001g0343 a0001c0001t0016g0367 others(63): Show |
66 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1579+528C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556095 | |||||||
chr2:33556190 | G | A | 99 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(96): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1579+623G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556190 | |||||||
chr2:33556218 | TTCTTCTA others(321): Show |
T | 106 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(103): Show |
107 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1579+667_1579+994d others(2): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556218 | ||||||
chr2:33556231 | C | CT | 18 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0169 others(15): Show |
18 | HG00544.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579+691dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(2): Show |
8 | a0001c0002t0006g0134 a0001c0002t0006g0155 a0001c0002t0006g0156 others(5): Show |
8 | HG00738.hp1 HG01255.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579+683_1579+691d others(11): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(3): Show |
6 | a0001c0002t0006g0137 a0001c0002t0006g0151 a0001c0002t0006g0154 others(3): Show |
6 | HG01891.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+682_1579+691d others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0001g0293 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1579+681_1579+691d others(13): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(5): Show |
15 | a0001c0001t0001g0343 a0001c0001t0016g0367 a0001c0001t0038g0144 others(12): Show |
15 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1579+680_1579+691d others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(6): Show |
23 | a0001c0001t0001g0177 a0001c0001t0029g0053 a0001c0001t0029g0361 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1579+679_1579+691d others(15): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(7): Show |
13 | a0001c0001t0039g0128 a0001c0002t0001g0023 a0001c0002t0001g0049 others(10): Show |
13 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1579+678_1579+691d others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(8): Show |
6 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0113 others(3): Show |
6 | HG00621.hp1 HG00673.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+677_1579+691d others(17): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0033g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1579+673_1579+691d others(21): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556231 | CTTTTTTT | C | 96 | a0001c0001t0001g0181 a0001c0001t0001g0225 a0001c0001t0001g0264 others(93): Show |
96 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1579+685_1579+691d others(9): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556231 | ||||||
chr2:33556271 | C | T | 2 | a0001c0001t0025g0076 a0001c0001t0058g0124 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1579+704C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556271 | |||||||
chr2:33556364 | C | T | 2 | a0001c0001t0043g0170 a0001c0002t0017g0145 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1579+797C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556364 | |||||||
chr2:33556408 | C | T | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1579+841C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556408 | |||||||
chr2:33556768 | C | T | 39 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0001c0001t0001g0264 others(36): Show |
39 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1579+1201C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556768 | |||||||
chr2:33556839 | C | A | 1 | a0001c0001t0026g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1579+1272C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556839 | |||||||
chr2:33556890 | T | TAC | 6 | a0001c0001t0001g0063 a0001c0001t0001g0335 a0001c0001t0002g0288 others(3): Show |
6 | HG01081.hp1 HG01515.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1284_1580-128 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACAC | 12 | a0001c0001t0002g0068 a0001c0001t0002g0075 a0001c0001t0002g0108 others(9): Show |
12 | HG01168.hp2 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580-1286_1580-128 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACAC | 12 | a0001c0001t0009g0012 a0001c0001t0009g0018 a0001c0001t0009g0019 others(9): Show |
12 | HG01074.hp2 HG01192.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580-1288_1580-128 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACACA others(1): Show |
35 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0001g0181 others(32): Show |
35 | HG00597.hp1 HG01071.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1580-1290_1580-128 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACACA others(3): Show |
15 | a0001c0001t0002g0029 a0001c0001t0002g0126 a0001c0001t0002g0142 others(12): Show |
15 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1580-1292_1580-128 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACACA others(5): Show |
24 | a0001c0001t0001g0225 a0001c0001t0001g0264 a0001c0001t0002g0048 others(21): Show |
24 | HG00438.hp2 HG00642.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1580-1294_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACACA others(7): Show |
6 | a0001c0001t0002g0015 a0001c0001t0002g0229 a0001c0001t0002g0358 others(3): Show |
6 | HG03579.hp1 NA18941.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1296_1580-128 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | T | TACACACA others(9): Show |
1 | a0001c0001t0004g0098 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1580-1298_1580-128 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | TAC | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(123): Show |
127 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1580-1284_1580-128 others(6): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | TACAC | T | 4 | a0001c0001t0001g0316 a0001c0002t0001g0341 a0002c0005t0003g0204 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-1286_1580-128 others(8): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556890 | TACACACA others(5): Show |
T | 2 | a0001c0001t0043g0170 a0001c0002t0017g0145 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1580-1294_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33556890 | ||||||
chr2:33556928 | C | CACACACA others(15): Show |
1 | a0001c0001t0011g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1580-1283_1580-128 others(26): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACACA others(13): Show |
1 | a0001c0001t0013g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-1283_1580-128 others(24): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACACA others(11): Show |
7 | a0001c0001t0013g0121 a0001c0001t0013g0238 a0001c0001t0013g0299 others(4): Show |
7 | HG01496.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(22): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACACA others(9): Show |
6 | a0001c0001t0009g0213 a0001c0001t0011g0310 a0001c0001t0013g0298 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(20): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACACA others(7): Show |
5 | a0001c0001t0003g0162 a0001c0001t0003g0362 a0001c0001t0015g0052 others(2): Show |
5 | HG01358.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(18): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACACA others(5): Show |
46 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(43): Show |
46 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(16): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACACATA others(3): Show |
7 | a0001c0001t0002g0188 a0001c0001t0005g0175 a0001c0001t0011g0079 others(4): Show |
7 | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(14): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CACATACA others(1): Show |
12 | a0001c0001t0008g0037 a0001c0001t0008g0178 a0001c0001t0012g0002 others(9): Show |
13 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(12): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | CATACAT | 14 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(11): Show |
14 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580-1283_1580-128 others(10): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33556928 | C | T | 4 | a0001c0003t0005g0255 a0001c0004t0020g0044 a0001c0004t0020g0118 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-1283C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33556928 | |||||||
chr2:33557001 | GA | G | 8 | a0001c0001t0012g0002 a0001c0001t0012g0123 a0001c0001t0012g0127 others(5): Show |
9 | HG01168.hp2 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1580-1200delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557001 | ||||||
chr2:33557145 | C | T | 17 | a0001c0003t0005g0042 a0001c0003t0005g0119 a0001c0003t0005g0173 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1580-1066C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557145 | |||||||
chr2:33557268 | C | G | 2 | a0001c0001t0005g0175 a0001c0001t0020g0309 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1580-943C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557268 | |||||||
chr2:33557289 | C | T | 5 | a0001c0001t0017g0120 a0001c0001t0017g0236 a0001c0001t0024g0136 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-922C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557289 | |||||||
chr2:33557635 | G | A | 58 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(55): Show |
59 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1580-576G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557635 | |||||||
chr2:33557642 | G | A | 1 | a0001c0002t0063g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1580-569G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557642 | |||||||
chr2:33557661 | G | A | 1 | a0001c0001t0004g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1580-550G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557661 | |||||||
chr2:33557710 | G | GA | 16 | a0001c0001t0001g0323 a0001c0001t0002g0188 a0001c0001t0002g0303 others(13): Show |
16 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1580-485dupA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557710 | ||||||
chr2:33557710 | GA | G | 20 | a0001c0001t0039g0128 a0001c0001t0043g0170 a0001c0001t0052g0301 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-485delA | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 33557710 | ||||||
chr2:33557775 | G | A | 4 | a0001c0001t0023g0257 a0001c0001t0023g0258 a0001c0001t0025g0076 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-436G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557775 | |||||||
chr2:33557782 | G | T | 1 | a0001c0003t0005g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-429G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557782 | |||||||
chr2:33557808 | T | G | 1 | a0001c0001t0025g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1580-403T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557808 | |||||||
chr2:33557844 | G | A | 74 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(71): Show |
75 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.1580-367G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557844 | |||||||
chr2:33557873 | C | A | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1580-338C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557873 | |||||||
chr2:33557881 | T | A | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1580-330T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557881 | |||||||
chr2:33557954 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0035g0216 |
3 | HG01070.hp2 HG01071.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1580-257T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33557954 | |||||||
chr2:33558006 | G | A | 3 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0153 |
3 | HG01496.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-205G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33558006 | |||||||
chr2:33558014 | G | A | 6 | a0001c0001t0004g0143 a0001c0001t0008g0036 a0001c0001t0008g0183 others(3): Show |
6 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-197G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 15/17 | chr2 | 33558014 | |||||||
chr2:33558425 | G | A | 1 | a0001c0001t0010g0342 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1705+89G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558425 | |||||||
chr2:33558425 | G | T | 2 | a0003c0009t0048g0072 a0003c0011t0045g0200 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1705+89G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558425 | |||||||
chr2:33558563 | C | T | 1 | a0001c0004t0020g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1706-109C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558563 | |||||||
chr2:33558594 | G | A | 1 | a0001c0002t0003g0292 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1706-78G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 16/17 | chr2 | 33558594 | |||||||
chr2:33559068 | A | G | 50 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(47): Show |
50 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2064+38A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559068 | |||||||
chr2:33559094 | G | A | 92 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2064+64G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559094 | |||||||
chr2:33559293 | C | T | 2 | a0001c0001t0017g0120 a0001c0001t0017g0236 |
2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2064+263C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559293 | |||||||
chr2:33559304 | G | A | 57 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(54): Show |
58 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.2064+274G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559304 | |||||||
chr2:33559433 | G | A | 92 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0001t0001g0225 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2064+403G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559433 | |||||||
chr2:33559468 | C | A | 1 | a0001c0002t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2064+438C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559468 | |||||||
chr2:33559550 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0223 a0001c0001t0003g0302 |
3 | HG01496.hp2 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2064+520C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559550 | |||||||
chr2:33559629 | G | A | 9 | a0001c0001t0004g0143 a0001c0001t0008g0036 a0001c0001t0008g0037 others(6): Show |
9 | HG00639.hp2 HG01070.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064+599G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559629 | |||||||
chr2:33559665 | A | G | 2 | a0001c0001t0007g0066 a0001c0001t0007g0070 |
2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2064+635A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559665 | |||||||
chr2:33559734 | G | A | 60 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(57): Show |
61 | HG00323.hp2 HG00423.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2064+704G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559734 | |||||||
chr2:33559972 | C | A | 1 | a0002c0007t0008g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2064+942C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33559972 | |||||||
chr2:33560009 | T | C | 2 | a0001c0001t0050g0311 a0001c0001t0051g0297 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2064+979T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560009 | |||||||
chr2:33560055 | G | T | 1 | a0001c0002t0063g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2064+1025G>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560055 | |||||||
chr2:33560079 | A | G | 3 | a0001c0001t0043g0170 a0001c0001t0057g0081 a0001c0002t0017g0145 |
3 | HG02451.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2064+1049A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560079 | |||||||
chr2:33560119 | T | G | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2064+1089T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560119 | |||||||
chr2:33560370 | C | T | 1 | a0001c0001t0009g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2064+1340C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560370 | |||||||
chr2:33560666 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0332 |
2 | HG03834.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2064+1636G>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560666 | |||||||
chr2:33560989 | T | A | 1 | a0001c0001t0037g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2065-1740T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33560989 | |||||||
chr2:33561060 | T | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0268 others(1): Show |
5 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2065-1669T>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561060 | |||||||
chr2:33561094 | T | A | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2065-1635T>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561094 | |||||||
chr2:33561097 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2065-1632C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561097 | |||||||
chr2:33561157 | C | G | 1 | a0001c0001t0010g0342 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2065-1572C>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561157 | |||||||
chr2:33561192 | A | G | 178 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(175): Show |
179 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.2065-1537A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561192 | |||||||
chr2:33561288 | A | T | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2065-1441A>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561288 | |||||||
chr2:33561322 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2065-1407C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561322 | |||||||
chr2:33561354 | A | G | 1 | a0001c0001t0002g0338 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2065-1375A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561354 | |||||||
chr2:33561445 | C | A | 104 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(101): Show |
105 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.2065-1284C>A | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561445 | |||||||
chr2:33561471 | A | G | 3 | a0001c0001t0050g0311 a0001c0001t0051g0297 a0001c0001t0052g0301 |
3 | HG02922.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2065-1258A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561471 | |||||||
chr2:33561552 | A | G | 2 | a0001c0001t0043g0170 a0001c0001t0057g0081 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2065-1177A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561552 | |||||||
chr2:33561755 | T | C | 1 | a0001c0002t0017g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2065-974T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561755 | |||||||
chr2:33561850 | A | G | 2 | a0001c0001t0027g0192 a0001c0001t0027g0197 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2065-879A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561850 | |||||||
chr2:33561968 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2065-761C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33561968 | |||||||
chr2:33562115 | A | C | 1 | a0001c0001t0011g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2065-614A>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562115 | |||||||
chr2:33562245 | G | C | 106 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0001g0169 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.2065-484G>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562245 | |||||||
chr2:33562267 | C | CT | 168 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(165): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2065-444dupT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562267 | ||||||
chr2:33562267 | CT | C | 10 | a0001c0001t0001g0046 a0001c0001t0001g0177 a0001c0001t0001g0277 others(7): Show |
10 | HG01256.hp1 HG02155.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2065-444delT | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562267 | ||||||
chr2:33562352 | C | T | 1 | a0001c0003t0018g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2065-377C>T | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562352 | |||||||
chr2:33562641 | A | AAAG | 13 | a0001c0001t0002g0039 a0001c0001t0002g0111 a0001c0001t0002g0126 others(10): Show |
13 | HG00438.hp2 HG00642.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2065-87_2065-85dup others(3): Show |
RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 33562641 | ||||||
chr2:33562677 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0138 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2065-52T>C | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562677 | |||||||
chr2:33562706 | A | G | 17 | a0001c0001t0002g0039 a0001c0001t0002g0111 a0001c0001t0002g0126 others(14): Show |
17 | HG00438.hp2 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2065-23A>G | RASGRP3 | ENSG00000152689.18 | transcript | ENST00000403687.8 | protein_coding | 17/17 | chr2 | 33562706 |