Item | Value |
---|---|
geneid | 22930 |
ensemblid | ENSG00000115839.19 |
hgncid | 17063 |
symbol | RAB3GAP1 |
name | RAB3 GTPase activating protein catalytic subunit 1 |
refseq_nuc | NM_012233.3 |
refseq_prot | NP_036365.1 |
ensembl_nuc | ENST00000264158.13 |
ensembl_prot | ENSP00000264158.8 |
mane_status | MANE Select |
chr | chr2 |
start | 135052292 |
end | 135170710 |
strand | + |
ver | v1.2 |
region | chr2:135052292-135170710 |
region5000 | chr2:135047292-135175710 |
regionname0 | RAB3GAP1_chr2_135052292_135170710 |
regionname5000 | RAB3GAP1_chr2_135047292_135175710 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 981 | 209 | 62 | 38 | 79 | 3 | 25 | 58 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0002 | 0/0 | 981 | 59 | 1 | 8 | 40 | 1 | 9 | 29 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0003 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0004 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0005 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0006 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0007 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
a0008 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | MAADS others(976): Show |
chr2 | 135047292 | 135175710 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2943 | 176 | 51 | 26 | 78 | 1 | 20 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0001c0003 | 1/1 | 2943 | 23 | 2 | 12 | 0 | 2 | 5 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0001c0004 | 0/0 | 2943 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0001c0007 | 0/0 | 2943 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0001c0008 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0001c0009 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0002c0002 | 0/0 | 2943 | 58 | 1 | 7 | 40 | 1 | 9 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0002c0010 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0003c0006 | 0/0 | 2943 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0004c0005 | 0/0 | 2943 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0005c0012 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0006c0011 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0007c0014 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 | ||
a0008c0013 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | ATGGC others(2938): Show |
chr2 | 135047292 | 135175710 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4891 | 42 | 9 | 4 | 26 | 0 | 3 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0002 | 0/0 | 4890 | 68 | 5 | 12 | 39 | 0 | 12 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0003 | 0/0 | 4891 | 19 | 10 | 5 | 3 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0004 | 0/0 | 4891 | 14 | 14 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0005 | 0/0 | 4889 | 8 | 0 | 4 | 3 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4884): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0006 | 0/0 | 4890 | 4 | 2 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0007 | 0/0 | 4891 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0010 | 0/0 | 4889 | 3 | 2 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4884): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0012 | 0/0 | 4892 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4887): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0014 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0015 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0016 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0017 | 0/0 | 4891 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0018 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0020 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0021 | 0/0 | 4890 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0022 | 0/0 | 4890 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0001t0023 | 0/0 | 4890 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0003t0001 | 1/1 | 4891 | 23 | 2 | 12 | 0 | 2 | 5 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0004t0013 | 0/0 | 4892 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4887): Show |
chr2 | 135047292 | 135175710 |
a0001c0004t0026 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0001c0007t0002 | 0/0 | 4890 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0008t0008 | 0/0 | 4890 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0001c0009t0002 | 0/0 | 4890 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0002c0002t0001 | 0/0 | 4891 | 53 | 1 | 7 | 36 | 1 | 8 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0002c0002t0002 | 0/0 | 4890 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0002c0002t0019 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0002c0002t0024 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0002c0010t0001 | 0/0 | 4891 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0003c0006t0002 | 0/0 | 4890 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0003c0006t0009 | 0/0 | 4890 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0004c0005t0011 | 0/0 | 4891 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0004c0005t0025 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0005c0012t0008 | 0/0 | 4890 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0006c0011t0014 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4886): Show |
chr2 | 135047292 | 135175710 |
a0007c0014t0002 | 0/0 | 4890 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4885): Show |
chr2 | 135047292 | 135175710 |
a0008c0013t0005 | 0/0 | 4889 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | CCCGG others(4884): Show |
chr2 | 135047292 | 135175710 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0014g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0016g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0016g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0017g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0018g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0020g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0021g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0022g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0001t0023g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0004t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0004t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0004t0013g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0004t0026g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0007t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0007t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0008t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0008t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0001c0009t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0002t0024g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0002c0010t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0003c0006t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0003c0006t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0003c0006t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0003c0006t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0004c0005t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0004c0005t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0004c0005t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0004c0005t0025g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0005c0012t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0006c0011t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0007c0014t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
a0008c0013t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0005 | g0009 | EUR | FIN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0065 | EUR | FIN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00621 | hp1 | a0001 | c0001 | t0017 | g0224 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0059 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01257 | hp2 | a0002 | c0010 | t0001 | g0124 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01978 | hp1 | a0001 | c0001 | t0021 | g0228 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02132 | hp1 | a0001 | c0009 | t0002 | g0153 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CDX | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02258 | hp2 | a0003 | c0006 | t0009 | g0251 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02280 | hp2 | a0001 | c0007 | t0002 | g0020 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0062 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02451 | hp2 | a0001 | c0008 | t0008 | g0006 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02735 | hp2 | a0002 | c0002 | t0024 | g0117 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02809 | hp1 | a0005 | c0012 | t0008 | g0003 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0253 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02818 | hp1 | a0001 | c0001 | t0020 | g0138 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02895 | hp1 | a0004 | c0005 | t0011 | g0221 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02896 | hp2 | a0001 | c0001 | t0015 | g0272 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02897 | hp1 | a0004 | c0005 | t0011 | g0222 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03017 | hp1 | a0001 | c0001 | t0014 | g0011 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03041 | hp1 | a0001 | c0001 | t0018 | g0074 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03130 | hp1 | a0001 | c0001 | t0012 | g0252 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03130 | hp2 | a0001 | c0004 | t0013 | g0256 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03195 | hp1 | a0004 | c0005 | t0025 | g0220 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0254 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03225 | hp2 | a0004 | c0005 | t0011 | g0219 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0068 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03516 | hp1 | a0003 | c0006 | t0009 | g0250 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03516 | hp2 | a0006 | c0011 | t0014 | g0278 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03579 | hp1 | a0003 | c0006 | t0002 | g0248 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0208 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03688 | hp2 | a0001 | c0001 | t0022 | g0175 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03942 | hp2 | a0001 | c0001 | t0023 | g0201 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0035 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18522 | hp2 | a0001 | c0008 | t0008 | g0005 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | CHB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18906 | hp1 | a0001 | c0001 | t0010 | g0177 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18947 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18954 | hp1 | a0002 | c0002 | t0019 | g0105 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18963 | hp2 | a0007 | c0014 | t0002 | g0202 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19006 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0176 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19030 | hp2 | a0001 | c0004 | t0013 | g0246 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19043 | hp1 | a0003 | c0006 | t0009 | g0249 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19043 | hp2 | a0001 | c0004 | t0026 | g0255 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19058 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19077 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19079 | hp1 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19084 | hp1 | a0001 | c0001 | t0017 | g0226 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA19240 | hp2 | a0001 | c0001 | t0016 | g0235 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20129 | hp2 | a0008 | c0013 | t0005 | g0004 | AFR | ASW | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0115 | EUR | TSI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0114 | EUR | TSI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0023 | SAS | GIH | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | GIH | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0238 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02486 | hp1 | a0001 | c0007 | t0002 | g0018 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
HG03471 | hp2 | a0001 | c0001 | t0015 | g0273 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA20300 | hp2 | a0001 | c0007 | t0002 | g0019 | AFR | USA | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA21309 | hp1 | a0001 | c0004 | t0013 | g0257 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0027 | REF | REF | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0057 | REF | REF | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135120839 | G | T | 1 | a0003 | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.669G>T | p.Leu223Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/24 | 685/4891 | 669/2946 | 223/981 | chr2 | 135120839 | |||
chr2:135126200 | A | G | 1 | a0007 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.850A>G | p.Thr284Ala | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 10/24 | 866/4891 | 850/2946 | 284/981 | chr2 | 135126200 | |||
chr2:135130027 | C | T | 1 | a0008 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1006C>T | p.Arg336Cys | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/24 | 1022/4891 | 1006/2946 | 336/981 | chr2 | 135130027 | |||
chr2:135130711 | C | T | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1226C>T | p.Thr409Ile | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/24 | 1242/4891 | 1226/2946 | 409/981 | chr2 | 135130711 | |||
chr2:135132983 | A | G | 1 | a0004 | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1325A>G | p.Tyr442Cys | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/24 | 1341/4891 | 1325/2946 | 442/981 | chr2 | 135132983 | |||
chr2:135135802 | A | G | 1 | a0002 | 59 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(56): Show |
missense_variant | MODERATE | c.1793A>G | p.Asn598Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/24 | 1809/4891 | 1793/2946 | 598/981 | chr2 | 135135802 | |||
chr2:135168635 | C | T | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2800C>T | p.Pro934Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 2816/4891 | 2800/2946 | 934/981 | chr2 | 135168635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135093688 | A | G | 1 | a0001c0007 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.357A>G | p.Val119Val | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/24 | 373/4891 | 357/2946 | 119/981 | chr2 | 135093688 | |||
chr2:135130062 | A | G | 2 | a0001c0008 a0005c0012 |
3 | HG02451.hp2 HG02809.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1041A>G | p.Arg347Arg | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/24 | 1057/4891 | 1041/2946 | 347/981 | chr2 | 135130062 | |||
chr2:135150437 | G | A | 1 | a0001c0004 | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.1992G>A | p.Ser664Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/24 | 2008/4891 | 1992/2946 | 664/981 | chr2 | 135150437 | |||
chr2:135153852 | T | C | 13 | a0001c0001 a0001c0004 a0001c0007 others(10): Show |
257 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
synonymous_variant | LOW | c.2265T>C | p.Phe755Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/24 | 2281/4891 | 2265/2946 | 755/981 | chr2 | 135153852 | |||
chr2:135162755 | C | T | 1 | a0001c0009 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.2394C>T | p.Leu798Leu | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/24 | 2410/4891 | 2394/2946 | 798/981 | chr2 | 135162755 | |||
chr2:135162824 | C | T | 1 | a0002c0010 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.2463C>T | p.Phe821Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/24 | 2479/4891 | 2463/2946 | 821/981 | chr2 | 135162824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135168916 | C | G | 2 | a0001c0004t0013 a0001c0004t0026 |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*135C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 135 | chr2 | 135168916 | ||||||
chr2:135168918 | G | GA | 1 | a0001c0001t0007 | 3 | NA18947.hp2 NA19058.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 141 | INFO_REALIGN_3_PRIME | chr2 | 135168918 | |||||
chr2:135168951 | C | T | 1 | a0001c0001t0017 | 2 | HG00621.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 170 | chr2 | 135168951 | ||||||
chr2:135168952 | G | A | 6 | a0001c0001t0005 a0001c0001t0014 a0001c0008t0008 others(3): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 171 | chr2 | 135168952 | ||||||
chr2:135169033 | T | G | 1 | a0003c0006t0009 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 252 | chr2 | 135169033 | ||||||
chr2:135169036 | T | TG | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0016 others(4): Show |
33 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*261dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 262 | INFO_REALIGN_3_PRIME | chr2 | 135169036 | |||||
chr2:135169084 | G | A | 1 | a0001c0001t0016 | 2 | HG02109.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 303 | chr2 | 135169084 | ||||||
chr2:135169185 | C | T | 1 | a0002c0002t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 404 | chr2 | 135169185 | ||||||
chr2:135169417 | A | G | 1 | a0001c0001t0023 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 636 | chr2 | 135169417 | ||||||
chr2:135169475 | G | A | 1 | a0001c0001t0015 | 2 | HG02896.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*694G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 694 | chr2 | 135169475 | ||||||
chr2:135169773 | G | A | 1 | a0001c0001t0018 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 992 | chr2 | 135169773 | ||||||
chr2:135169776 | T | C | 1 | a0004c0005t0011 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*995T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 995 | chr2 | 135169776 | ||||||
chr2:135169858 | T | C | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0016 others(1): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1077T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1077 | chr2 | 135169858 | ||||||
chr2:135169974 | TA | T | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(16): Show |
120 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1208 | INFO_REALIGN_3_PRIME | chr2 | 135169974 | |||||
chr2:135169974 | TAA | T | 3 | a0001c0001t0005 a0001c0001t0010 a0008c0013t0005 |
12 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1208delAA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1207 | INFO_REALIGN_3_PRIME | chr2 | 135169974 | |||||
chr2:135170022 | G | T | 1 | a0001c0001t0022 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1241G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1241 | chr2 | 135170022 | ||||||
chr2:135170159 | T | C | 2 | a0001c0001t0004 a0001c0001t0015 |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1378T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1378 | chr2 | 135170159 | ||||||
chr2:135170178 | C | T | 1 | a0001c0001t0021 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1397 | chr2 | 135170178 | ||||||
chr2:135170443 | A | T | 1 | a0001c0001t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1662A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1662 | chr2 | 135170443 | ||||||
chr2:135170607 | G | C | 1 | a0001c0001t0012 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1826G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1826 | chr2 | 135170607 | ||||||
chr2:135170621 | G | A | 1 | a0002c0002t0019 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1840G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1840 | chr2 | 135170621 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135052540 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.74+55C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052540 | |||||||
chr2:135052568 | A | G | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.74+83A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052568 | |||||||
chr2:135052616 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052616 | |||||||
chr2:135052620 | C | T | 3 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0279 |
3 | HG00639.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.74+135C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052620 | |||||||
chr2:135052741 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0006g0274 |
2 | NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.74+256C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052741 | |||||||
chr2:135052779 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+294C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052779 | |||||||
chr2:135052965 | C | T | 44 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(41): Show |
44 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.74+480C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052965 | |||||||
chr2:135053059 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.74+574A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053059 | |||||||
chr2:135053182 | G | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.74+697G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053182 | |||||||
chr2:135053220 | C | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.74+735C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053220 | |||||||
chr2:135053223 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+738C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053223 | |||||||
chr2:135053465 | G | A | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.74+980G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053465 | |||||||
chr2:135053618 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+1133T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053618 | |||||||
chr2:135053621 | G | A | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.74+1136G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053621 | |||||||
chr2:135053759 | T | TA | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+1280dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135053759 | ||||||
chr2:135053950 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+1465G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053950 | |||||||
chr2:135054125 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.74+1640A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054125 | |||||||
chr2:135054291 | TAGAA | T | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.74+1811_74+1814del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135054291 | ||||||
chr2:135054421 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.74+1936A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054421 | |||||||
chr2:135054478 | T | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | HG01993.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.74+1993T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054478 | |||||||
chr2:135054646 | A | G | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.74+2161A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054646 | |||||||
chr2:135054703 | G | C | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.74+2218G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054703 | |||||||
chr2:135055201 | A | G | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.74+2716A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055201 | |||||||
chr2:135055202 | T | C | 3 | a0001c0007t0002g0018 a0001c0007t0002g0019 a0001c0007t0002g0020 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.74+2717T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055202 | |||||||
chr2:135055255 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2756C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055255 | |||||||
chr2:135055288 | A | G | 1 | a0002c0002t0001g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75-2723A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055288 | |||||||
chr2:135055299 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.75-2712C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055299 | |||||||
chr2:135055399 | C | T | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-2612C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055399 | |||||||
chr2:135055404 | A | C | 81 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(78): Show |
81 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.75-2607A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055404 | |||||||
chr2:135055625 | C | G | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-2386C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055625 | |||||||
chr2:135055678 | C | CA | 30 | a0001c0001t0002g0139 a0001c0001t0003g0225 a0001c0001t0003g0227 others(27): Show |
30 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.75-2316dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135055678 | ||||||
chr2:135055714 | G | A | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.75-2297G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055714 | |||||||
chr2:135055748 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.75-2263T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055748 | |||||||
chr2:135055837 | C | CT | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-2165dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135055837 | ||||||
chr2:135055888 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.75-2123G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055888 | |||||||
chr2:135055898 | G | A | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2113G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055898 | |||||||
chr2:135055996 | C | T | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.75-2015C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055996 | |||||||
chr2:135056131 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.75-1880C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056131 | |||||||
chr2:135056135 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-1876C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056135 | |||||||
chr2:135056243 | C | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.75-1768C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056243 | |||||||
chr2:135056295 | T | G | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.75-1716T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056295 | |||||||
chr2:135056451 | G | A | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.75-1560G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056451 | |||||||
chr2:135056467 | T | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-1544T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056467 | |||||||
chr2:135056920 | A | C | 10 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(7): Show |
10 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-1091A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056920 | |||||||
chr2:135057146 | C | T | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-865C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057146 | |||||||
chr2:135057304 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.75-707G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057304 | |||||||
chr2:135057335 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75-676A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057335 | |||||||
chr2:135057465 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-546G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057465 | |||||||
chr2:135057572 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.75-439A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057572 | |||||||
chr2:135057576 | G | T | 1 | a0002c0002t0001g0135 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.75-435G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057576 | |||||||
chr2:135057705 | T | G | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75-306T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057705 | |||||||
chr2:135057793 | A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75-218A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057793 | |||||||
chr2:135058236 | A | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+150A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058236 | |||||||
chr2:135058261 | T | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+175T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058261 | |||||||
chr2:135058266 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+180G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058266 | |||||||
chr2:135058291 | TTA | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+213_150+214del others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135058291 | ||||||
chr2:135058708 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.150+622C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058708 | |||||||
chr2:135058725 | A | G | 10 | a0001c0001t0003g0234 a0001c0001t0003g0236 a0001c0001t0003g0237 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+639A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058725 | |||||||
chr2:135058729 | A | G | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+643A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058729 | |||||||
chr2:135058832 | T | G | 1 | a0001c0001t0002g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+746T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058832 | |||||||
chr2:135058869 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+783A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058869 | |||||||
chr2:135059425 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.150+1339A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135059425 | |||||||
chr2:135059833 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+1747G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135059833 | |||||||
chr2:135060002 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+1916C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060002 | |||||||
chr2:135060190 | T | C | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.150+2104T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060190 | |||||||
chr2:135060256 | A | AT | 9 | a0001c0001t0002g0213 a0001c0001t0003g0234 a0001c0004t0026g0255 others(6): Show |
9 | HG00438.hp2 HG02258.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.150+2191dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | ||||||
chr2:135060256 | A | ATT | 30 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(27): Show |
30 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.150+2190_150+2191d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | ||||||
chr2:135060256 | A | ATTTT | 7 | a0001c0001t0002g0247 a0001c0004t0013g0246 a0004c0005t0011g0219 others(4): Show |
7 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+2188_150+2191d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | ||||||
chr2:135060256 | A | ATTTTT | 10 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0001t0005g0010 others(7): Show |
10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2187_150+2191d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | ||||||
chr2:135060256 | AT | A | 62 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(59): Show |
62 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.150+2191delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | ||||||
chr2:135060344 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.150+2258C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060344 | |||||||
chr2:135060377 | A | G | 4 | a0001c0001t0004g0268 a0001c0001t0004g0269 a0001c0001t0004g0270 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+2291A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060377 | |||||||
chr2:135060394 | C | T | 10 | a0001c0001t0003g0234 a0001c0001t0003g0236 a0001c0001t0003g0237 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2308C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060394 | |||||||
chr2:135060395 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+2309G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060395 | |||||||
chr2:135060420 | T | G | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.150+2334T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060420 | |||||||
chr2:135060424 | T | A | 1 | a0002c0002t0002g0021 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.150+2338T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060424 | |||||||
chr2:135060568 | G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.150+2482G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060568 | |||||||
chr2:135060711 | A | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2625A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060711 | |||||||
chr2:135060907 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.150+2821T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060907 | |||||||
chr2:135060910 | G | C | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.150+2824G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060910 | |||||||
chr2:135060917 | T | C | 16 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(13): Show |
16 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2831T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060917 | |||||||
chr2:135060965 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.150+2879A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060965 | |||||||
chr2:135061003 | C | CT | 207 | a0001c0001t0001g0028 a0001c0001t0001g0078 a0001c0001t0001g0080 others(204): Show |
208 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.150+2936dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135061003 | ||||||
chr2:135061003 | C | CTT | 11 | a0001c0001t0001g0029 a0001c0001t0002g0192 a0001c0001t0003g0243 others(8): Show |
11 | HG02074.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2935_150+2936d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135061003 | ||||||
chr2:135061023 | A | T | 1 | a0001c0009t0002g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.150+2937A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061023 | |||||||
chr2:135061097 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+3011A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061097 | |||||||
chr2:135061223 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3137C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061223 | |||||||
chr2:135061276 | A | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+3190A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061276 | |||||||
chr2:135061337 | C | T | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.150+3251C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061337 | |||||||
chr2:135061443 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3357C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061443 | |||||||
chr2:135061824 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150+3738A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061824 | |||||||
chr2:135061835 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3749T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061835 | |||||||
chr2:135061943 | G | A | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3857G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061943 | |||||||
chr2:135062183 | G | A | 1 | a0001c0001t0018g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150+4097G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062183 | |||||||
chr2:135062210 | G | A | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4124G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062210 | |||||||
chr2:135062261 | A | G | 2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.150+4175A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062261 | |||||||
chr2:135062355 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.150+4269A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062355 | |||||||
chr2:135062885 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+4799G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062885 | |||||||
chr2:135063173 | T | G | 1 | a0002c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.150+5087T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063173 | |||||||
chr2:135063236 | T | TA | 9 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(6): Show |
9 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.150+5151dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135063236 | ||||||
chr2:135063317 | T | G | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+5231T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063317 | |||||||
chr2:135063578 | T | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+5492T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063578 | |||||||
chr2:135063599 | T | C | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+5513T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063599 | |||||||
chr2:135063762 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+5676T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063762 | |||||||
chr2:135063769 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.150+5683T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063769 | |||||||
chr2:135063782 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.150+5696G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063782 | |||||||
chr2:135063863 | A | G | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.150+5777A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063863 | |||||||
chr2:135063900 | T | A | 1 | a0001c0001t0004g0258 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.150+5814T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063900 | |||||||
chr2:135064106 | C | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6020C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064106 | |||||||
chr2:135064234 | C | T | 2 | a0001c0001t0003g0277 a0001c0001t0003g0279 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.150+6148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064234 | |||||||
chr2:135064259 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.150+6173A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064259 | |||||||
chr2:135064392 | G | C | 14 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+6306G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064392 | |||||||
chr2:135064423 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6337C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064423 | |||||||
chr2:135064460 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.150+6374G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064460 | |||||||
chr2:135064728 | C | T | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+6642C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064728 | |||||||
chr2:135064741 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6655T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064741 | |||||||
chr2:135064749 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.150+6663T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064749 | |||||||
chr2:135064755 | G | GT | 86 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0131 others(83): Show |
86 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.150+6684dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064755 | ||||||
chr2:135064755 | G | T | 15 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(12): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.150+6669G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064755 | |||||||
chr2:135064755 | GT | G | 7 | a0001c0001t0003g0225 a0001c0001t0003g0244 a0001c0001t0003g0275 others(4): Show |
7 | HG00558.hp1 HG00621.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+6684delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064755 | ||||||
chr2:135064771 | G | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG00280.hp1 HG01433.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.150+6685G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064771 | |||||||
chr2:135064915 | A | AT | 18 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(15): Show |
18 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.150+6843dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064915 | ||||||
chr2:135064915 | AT | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+6843delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064915 | ||||||
chr2:135064941 | G | A | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+6855G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064941 | |||||||
chr2:135064986 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+6900G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064986 | |||||||
chr2:135065153 | A | G | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+7067A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065153 | |||||||
chr2:135065421 | G | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+7335G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065421 | |||||||
chr2:135065472 | C | G | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.150+7386C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065472 | |||||||
chr2:135065536 | A | G | 1 | a0002c0002t0001g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.150+7450A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065536 | |||||||
chr2:135065694 | C | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.150+7608C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065694 | |||||||
chr2:135065708 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+7622C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065708 | |||||||
chr2:135065748 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.150+7662T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065748 | |||||||
chr2:135065767 | A | AT | 66 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0213 others(63): Show |
66 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.150+7703dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135065767 | ||||||
chr2:135065767 | AT | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0157 a0001c0001t0002g0156 others(2): Show |
5 | HG01255.hp2 HG01346.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+7703delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135065767 | ||||||
chr2:135065880 | C | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+7794C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065880 | |||||||
chr2:135066069 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+7983C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066069 | |||||||
chr2:135066234 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+8148T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066234 | |||||||
chr2:135066264 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+8178A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066264 | |||||||
chr2:135066618 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.150+8532G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066618 | |||||||
chr2:135066627 | C | A | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.150+8541C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066627 | |||||||
chr2:135066644 | C | T | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+8558C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066644 | |||||||
chr2:135066675 | G | T | 1 | a0002c0002t0001g0122 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.150+8589G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066675 | |||||||
chr2:135066704 | A | T | 1 | a0001c0001t0002g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.150+8618A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066704 | |||||||
chr2:135066795 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+8709A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066795 | |||||||
chr2:135066804 | G | T | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.150+8718G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066804 | |||||||
chr2:135066820 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.150+8734C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066820 | |||||||
chr2:135067253 | G | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+9167G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067253 | |||||||
chr2:135067504 | T | C | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.150+9418T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067504 | |||||||
chr2:135067592 | A | G | 8 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(5): Show |
8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+9506A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067592 | |||||||
chr2:135067751 | G | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.150+9665G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067751 | |||||||
chr2:135067799 | T | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+9713T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067799 | |||||||
chr2:135067998 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+9912C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067998 | |||||||
chr2:135068435 | TAGACTAT others(5380): Show |
T | 1 | a0002c0002t0001g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.150+10351_150+1573 others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135068435 | ||||||
chr2:135068437 | G | C | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.150+10351G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068437 | |||||||
chr2:135068482 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0003c0006t0002g0248 others(3): Show |
6 | HG02027.hp2 HG02040.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+10396G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068482 | |||||||
chr2:135068491 | G | A | 1 | a0002c0002t0001g0076 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.150+10405G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068491 | |||||||
chr2:135068491 | G | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+10405G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068491 | |||||||
chr2:135068691 | T | A | 2 | a0001c0001t0001g0078 a0001c0001t0002g0079 |
2 | HG00735.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.150+10605T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068691 | |||||||
chr2:135068738 | G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+10652G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068738 | |||||||
chr2:135068754 | AAAAAC | A | 5 | a0002c0002t0001g0088 a0002c0002t0001g0108 a0002c0002t0001g0109 others(2): Show |
5 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+10686_150+1069 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135068754 | ||||||
chr2:135068893 | C | T | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+10807C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068893 | |||||||
chr2:135068961 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+10875A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068961 | |||||||
chr2:135068966 | T | A | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+10880T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068966 | |||||||
chr2:135069005 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+10919C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069005 | |||||||
chr2:135069066 | A | G | 2 | a0001c0004t0013g0257 a0001c0004t0026g0255 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.150+10980A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069066 | |||||||
chr2:135069249 | C | A | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+11163C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069249 | |||||||
chr2:135069294 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+11208G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069294 | |||||||
chr2:135069341 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.150+11255C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069341 | |||||||
chr2:135069418 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.150+11332T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069418 | |||||||
chr2:135069435 | T | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+11349T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069435 | |||||||
chr2:135069506 | A | G | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.150+11420A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069506 | |||||||
chr2:135069590 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+11504A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069590 | |||||||
chr2:135069838 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+11752A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069838 | |||||||
chr2:135069909 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.150+11823A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069909 | |||||||
chr2:135070052 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+11966G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070052 | |||||||
chr2:135070577 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.150+12491G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070577 | |||||||
chr2:135070668 | C | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0115 |
2 | NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.150+12582C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070668 | |||||||
chr2:135070669 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.150+12583G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070669 | |||||||
chr2:135070741 | G | A | 3 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0002g0210 |
3 | NA18966.hp2 NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.150+12655G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070741 | |||||||
chr2:135070880 | G | A | 2 | a0001c0001t0003g0236 a0001c0001t0003g0241 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.150+12794G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070880 | |||||||
chr2:135070891 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+12805A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070891 | |||||||
chr2:135070896 | T | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+12810T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070896 | |||||||
chr2:135071043 | T | C | 1 | a0001c0001t0006g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.150+12957T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071043 | |||||||
chr2:135071427 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+13341A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071427 | |||||||
chr2:135071474 | C | T | 1 | a0001c0001t0004g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.150+13388C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071474 | |||||||
chr2:135071500 | T | G | 8 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+13414T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071500 | |||||||
chr2:135071532 | T | TAA | 48 | a0001c0001t0002g0247 a0001c0001t0003g0227 a0001c0001t0003g0229 others(45): Show |
48 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.150+13459_150+1346 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135071532 | ||||||
chr2:135071714 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.150+13628A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071714 | |||||||
chr2:135071739 | G | A | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.150+13653G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071739 | |||||||
chr2:135071763 | G | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+13677G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071763 | |||||||
chr2:135071771 | G | A | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.150+13685G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071771 | |||||||
chr2:135071858 | C | G | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.150+13772C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071858 | |||||||
chr2:135071862 | A | G | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.150+13776A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071862 | |||||||
chr2:135071904 | ATCTT | A | 3 | a0001c0001t0010g0176 a0001c0001t0010g0177 a0003c0006t0002g0248 |
3 | HG03579.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.150+13840_150+1384 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135071904 | ||||||
chr2:135071952 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+13866G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071952 | |||||||
chr2:135072022 | C | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0043 others(57): Show |
61 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.150+13936C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072022 | |||||||
chr2:135072077 | T | C | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150+13991T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072077 | |||||||
chr2:135072099 | C | T | 6 | a0001c0001t0001g0082 a0002c0002t0001g0088 a0002c0002t0001g0108 others(3): Show |
6 | HG02027.hp1 HG02055.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+14013C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072099 | |||||||
chr2:135072630 | T | A | 6 | a0001c0001t0001g0102 a0002c0002t0001g0083 a0002c0002t0001g0087 others(3): Show |
6 | HG00738.hp1 NA18967.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+14544T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072630 | |||||||
chr2:135072713 | A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+14627A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072713 | |||||||
chr2:135072766 | A | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+14680A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072766 | |||||||
chr2:135072792 | A | G | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+14706A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072792 | |||||||
chr2:135073037 | G | A | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.150+14951G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073037 | |||||||
chr2:135073047 | G | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+14961G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073047 | |||||||
chr2:135073207 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.150+15121G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073207 | |||||||
chr2:135073235 | G | A | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+15149G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073235 | |||||||
chr2:135073249 | C | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+15163C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073249 | |||||||
chr2:135073524 | G | T | 1 | a0002c0002t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+15438G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073524 | |||||||
chr2:135073690 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.150+15604C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073690 | |||||||
chr2:135073834 | A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+15748A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073834 | |||||||
chr2:135073870 | A | G | 3 | a0001c0001t0007g0151 a0001c0001t0007g0152 a0001c0001t0007g0154 |
3 | NA18947.hp2 NA19058.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.150+15784A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073870 | |||||||
chr2:135073902 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.150+15816C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073902 | |||||||
chr2:135074121 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+16035G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074121 | |||||||
chr2:135074278 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150+16192T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074278 | |||||||
chr2:135074289 | G | A | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+16203G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074289 | |||||||
chr2:135074300 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.150+16214C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074300 | |||||||
chr2:135074444 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+16358T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074444 | |||||||
chr2:135074561 | T | C | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.151-16437T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074561 | |||||||
chr2:135074622 | A | G | 1 | a0001c0001t0006g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151-16376A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074622 | |||||||
chr2:135074624 | A | G | 1 | a0001c0001t0006g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151-16374A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074624 | |||||||
chr2:135074915 | T | C | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.151-16083T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074915 | |||||||
chr2:135074946 | T | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-16052T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074946 | |||||||
chr2:135075151 | G | A | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-15847G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075151 | |||||||
chr2:135075195 | C | T | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-15803C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075195 | |||||||
chr2:135075209 | GTTCT | G | 2 | a0001c0001t0002g0247 a0002c0002t0001g0017 |
2 | HG01243.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.151-15782_151-1577 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075209 | ||||||
chr2:135075265 | C | T | 1 | a0001c0001t0023g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.151-15733C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075265 | |||||||
chr2:135075329 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-15669C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075329 | |||||||
chr2:135075639 | C | CT | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.151-15348dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075639 | ||||||
chr2:135075653 | A | T | 1 | a0002c0002t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.151-15345A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075653 | |||||||
chr2:135075678 | T | G | 1 | a0001c0001t0016g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-15320T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075678 | |||||||
chr2:135075910 | C | CT | 13 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0002g0143 others(10): Show |
13 | HG00438.hp1 HG01175.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.151-15069dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075910 | ||||||
chr2:135075910 | CT | C | 24 | a0001c0001t0002g0156 a0001c0001t0002g0159 a0001c0001t0002g0160 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.151-15069delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075910 | ||||||
chr2:135075920 | T | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-15078T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075920 | |||||||
chr2:135075938 | G | A | 1 | a0004c0005t0011g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151-15060G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075938 | |||||||
chr2:135075951 | G | A | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.151-15047G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075951 | |||||||
chr2:135075951 | G | T | 1 | a0002c0002t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.151-15047G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075951 | |||||||
chr2:135075977 | C | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-15021C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075977 | |||||||
chr2:135076006 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0247 |
2 | HG01243.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.151-14992G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076006 | |||||||
chr2:135076190 | G | A | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0144 others(1): Show |
4 | HG02132.hp1 NA18969.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-14808G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076190 | |||||||
chr2:135076240 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-14758C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076240 | |||||||
chr2:135076401 | A | C | 1 | a0001c0001t0007g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.151-14597A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076401 | |||||||
chr2:135076416 | CATTTTT | C | 11 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(8): Show |
11 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-14577_151-1457 others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135076416 | ||||||
chr2:135077176 | A | T | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-13822A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077176 | |||||||
chr2:135077268 | T | TCAA | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02735.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-13702_151-1370 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135077268 | ||||||
chr2:135077268 | TCAA | T | 109 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(106): Show |
109 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.151-13702_151-1370 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135077268 | ||||||
chr2:135077288 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-13710A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077288 | |||||||
chr2:135077340 | T | C | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-13658T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077340 | |||||||
chr2:135077416 | G | A | 1 | a0001c0001t0005g0014 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.151-13582G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077416 | |||||||
chr2:135077479 | G | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-13519G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077479 | |||||||
chr2:135077938 | G | C | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.151-13060G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077938 | |||||||
chr2:135078456 | T | G | 1 | a0001c0001t0004g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.151-12542T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078456 | |||||||
chr2:135078645 | G | GTCCCC | 34 | a0001c0001t0001g0036 a0001c0001t0003g0225 a0001c0001t0003g0227 others(31): Show |
34 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.151-12311_151-1230 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(3): Show |
8 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0194 others(5): Show |
8 | HG02055.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-12316_151-1230 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(8): Show |
4 | a0001c0001t0003g0276 a0001c0001t0004g0268 a0001c0001t0004g0269 others(1): Show |
4 | HG00639.hp1 HG02109.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-12321_151-1230 others(19): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(43): Show |
2 | a0004c0005t0011g0221 a0004c0005t0011g0222 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-12307_151-1230 others(54): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(103): Show |
1 | a0004c0005t0025g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151-12307_151-1230 others(114): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(118): Show |
1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(129): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(138): Show |
1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(149): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | G | GTCCCCTC others(148): Show |
1 | a0004c0005t0011g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(159): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | GTCCCC | G | 26 | a0001c0001t0001g0070 a0001c0001t0001g0132 a0001c0001t0002g0181 others(23): Show |
26 | HG00280.hp1 HG01070.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151-12311_151-1230 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078645 | GTCCCCTC others(3): Show |
G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-12316_151-1230 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | ||||||
chr2:135078657 | C | CCCCTCCC others(28): Show |
1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.151-12325_151-1229 others(39): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078657 | ||||||
chr2:135078672 | CCCCTCCC others(13): Show |
C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-12310_151-1229 others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078672 | ||||||
chr2:135078692 | G | C | 35 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(32): Show |
35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.151-12306G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078692 | |||||||
chr2:135078707 | C | CCCCTCCC others(198): Show |
1 | a0001c0004t0013g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-12291_151-1229 others(209): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078707 | |||||||
chr2:135078707 | C | CCCCTCCC others(163): Show |
1 | a0001c0004t0026g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151-12291_151-1229 others(174): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078707 | |||||||
chr2:135078708 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-12290T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078708 | |||||||
chr2:135078712 | T | C | 5 | a0001c0001t0002g0247 a0004c0005t0011g0219 a0004c0005t0011g0221 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-12286T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078712 | |||||||
chr2:135078768 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-12230C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078768 | |||||||
chr2:135078821 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151-12177G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078821 | |||||||
chr2:135078873 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-12125T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078873 | |||||||
chr2:135078899 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG00609.hp1 HG02155.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-12099G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078899 | |||||||
chr2:135078906 | C | T | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.151-12092C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078906 | |||||||
chr2:135079016 | C | T | 1 | a0001c0001t0017g0224 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-11982C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079016 | |||||||
chr2:135079028 | C | T | 1 | a0001c0009t0002g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.151-11970C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079028 | |||||||
chr2:135079443 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-11555A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079443 | |||||||
chr2:135079490 | A | G | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-11508A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079490 | |||||||
chr2:135079748 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.151-11250A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079748 | |||||||
chr2:135079895 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11103C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079895 | |||||||
chr2:135079911 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11087C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079911 | |||||||
chr2:135079973 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11025C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079973 | |||||||
chr2:135079990 | G | A | 27 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.151-11008G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079990 | |||||||
chr2:135080022 | C | A | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-10976C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080022 | |||||||
chr2:135080053 | C | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-10945C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080053 | |||||||
chr2:135080116 | C | CA | 109 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(106): Show |
110 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.151-10860dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | ||||||
chr2:135080116 | C | CAA | 22 | a0001c0001t0001g0071 a0001c0001t0002g0247 a0001c0001t0003g0225 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.151-10861_151-1086 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | ||||||
chr2:135080116 | C | CAAAA | 12 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(9): Show |
12 | HG00280.hp1 HG01358.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.151-10863_151-1086 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | ||||||
chr2:135080116 | CA | C | 21 | a0001c0001t0001g0069 a0001c0001t0002g0178 a0001c0001t0002g0188 others(18): Show |
21 | HG00558.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-10860delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | ||||||
chr2:135080336 | C | A | 264 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(261): Show |
265 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.151-10662C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080336 | |||||||
chr2:135080437 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-10561G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080437 | |||||||
chr2:135080524 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10474C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080524 | |||||||
chr2:135080543 | A | G | 5 | a0001c0001t0003g0234 a0001c0004t0013g0246 a0001c0004t0013g0256 others(2): Show |
5 | HG02965.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-10455A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080543 | |||||||
chr2:135080837 | C | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10161C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080837 | |||||||
chr2:135080858 | T | A | 1 | a0002c0002t0001g0039 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151-10140T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080858 | |||||||
chr2:135080889 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.151-10109G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080889 | |||||||
chr2:135081073 | G | GCACACGT others(16): Show |
1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151-9923_151-9922i others(25): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081073 | ||||||
chr2:135081076 | A | C | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151-9922A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081076 | |||||||
chr2:135081083 | A | G | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.151-9915A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081083 | |||||||
chr2:135081100 | A | G | 40 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(37): Show |
40 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.151-9898A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081100 | |||||||
chr2:135081195 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-9803T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081195 | |||||||
chr2:135081255 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151-9743C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081255 | |||||||
chr2:135081263 | C | T | 1 | a0002c0002t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.151-9735C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081263 | |||||||
chr2:135081306 | C | CA | 9 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0203 others(6): Show |
9 | HG00438.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.151-9670dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | ||||||
chr2:135081306 | C | CAA | 10 | a0002c0002t0001g0024 a0002c0002t0001g0039 a0002c0002t0001g0090 others(7): Show |
10 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9671_151-9670d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | ||||||
chr2:135081306 | C | CAAAA | 7 | a0001c0001t0002g0146 a0001c0001t0002g0193 a0001c0001t0003g0227 others(4): Show |
7 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-9673_151-9670d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | ||||||
chr2:135081306 | C | CAAAAAA | 8 | a0001c0001t0003g0225 a0001c0001t0003g0230 a0001c0001t0003g0237 others(5): Show |
8 | HG00621.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.151-9675_151-9670d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | ||||||
chr2:135081306 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.151-9679_151-9670d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | ||||||
chr2:135081319 | A | AATATATA others(3): Show |
1 | a0001c0001t0004g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.151-9678_151-9677i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081319 | ||||||
chr2:135081320 | AAAAAAAA others(8): Show |
A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-9676_151-9662d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081320 | ||||||
chr2:135081321 | A | ATATATAT others(6): Show |
1 | a0003c0006t0009g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151-9677_151-9676i others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081321 | |||||||
chr2:135081321 | A | T | 2 | a0001c0001t0004g0264 a0001c0001t0015g0272 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.151-9677A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081321 | |||||||
chr2:135081321 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.151-9675_151-9664d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081321 | ||||||
chr2:135081323 | A | T | 10 | a0001c0001t0004g0259 a0001c0001t0004g0262 a0001c0001t0004g0264 others(7): Show |
10 | HG02258.hp2 HG02647.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9675A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081323 | |||||||
chr2:135081323 | AAAAAATA others(5): Show |
A | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-9673_151-9662d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081323 | ||||||
chr2:135081323 | AAAAAATA others(7): Show |
A | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-9673_151-9660d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081323 | ||||||
chr2:135081325 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.151-9672_151-9671i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081325 | ||||||
chr2:135081325 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.151-9672_151-9671i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081325 | ||||||
chr2:135081325 | A | T | 21 | a0001c0001t0001g0043 a0001c0001t0001g0073 a0001c0001t0001g0132 others(18): Show |
21 | HG00423.hp1 HG02055.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-9673A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081325 | |||||||
chr2:135081327 | A | AAAAAATA others(3): Show |
2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.151-9670_151-9669i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AAAAAATA others(5): Show |
1 | a0002c0002t0001g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.151-9670_151-9669i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AAAAAATA others(9): Show |
1 | a0002c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.151-9670_151-9669i others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AAAAT | 6 | a0001c0003t0001g0114 a0002c0002t0001g0099 a0002c0002t0001g0101 others(3): Show |
6 | HG02080.hp2 HG02083.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-9670_151-9669i others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AAAATATA others(3): Show |
4 | a0001c0001t0001g0106 a0001c0003t0001g0072 a0002c0002t0001g0112 others(1): Show |
4 | HG01243.hp2 HG03492.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-9670_151-9669i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.151-9645_151-9636d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0136 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02027.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.151-9649_151-9636d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081327 | A | ATAT | 3 | a0001c0001t0001g0040 a0002c0002t0001g0109 a0002c0002t0001g0129 |
3 | HG02129.hp1 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.151-9671_151-9670i others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | |||||||
chr2:135081327 | A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0032 a0002c0002t0001g0047 a0002c0002t0024g0117 |
3 | HG01346.hp1 HG02735.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.151-9671_151-9670i others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | |||||||
chr2:135081327 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0049 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.151-9671_151-9670i others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | |||||||
chr2:135081327 | A | T | 36 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(33): Show |
36 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.151-9671A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | |||||||
chr2:135081327 | AATATATA others(7): Show |
A | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151-9649_151-9636d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | ||||||
chr2:135081328 | AT | A | 19 | a0001c0001t0001g0071 a0001c0001t0002g0148 a0001c0001t0002g0149 others(16): Show |
19 | HG01257.hp1 HG01928.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.151-9669delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATAT | A | 12 | a0001c0001t0002g0141 a0001c0001t0002g0158 a0001c0001t0002g0160 others(9): Show |
12 | HG02559.hp2 HG02818.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.151-9669_151-9667d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATATATAT | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0247 |
3 | HG01243.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9663d others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9669_151-9659d others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0018g0074 a0001c0003t0001g0053 |
2 | HG01928.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9657d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATATATAT others(8): Show |
A | 2 | a0001c0004t0013g0257 a0001c0004t0026g0255 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9655d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081328 | ATATATAT others(50): Show |
A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9669_151-9613d others(59): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | |||||||
chr2:135081329 | T | A | 93 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0157 others(90): Show |
93 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.151-9669T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081329 | |||||||
chr2:135081331 | T | A | 98 | a0001c0001t0001g0071 a0001c0001t0001g0130 a0001c0001t0001g0131 others(95): Show |
98 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.151-9667T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081331 | |||||||
chr2:135081333 | T | A | 100 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0157 others(97): Show |
100 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.151-9665T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081333 | |||||||
chr2:135081335 | T | A | 74 | a0001c0001t0001g0157 a0001c0001t0002g0139 a0001c0001t0002g0140 others(71): Show |
74 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.151-9663T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081335 | |||||||
chr2:135081337 | T | A | 30 | a0001c0001t0001g0030 a0001c0001t0001g0157 a0001c0001t0002g0156 others(27): Show |
30 | HG01070.hp1 HG01192.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-9661T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081337 | |||||||
chr2:135081339 | T | A | 11 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0181 others(8): Show |
11 | HG01070.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-9659T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081339 | |||||||
chr2:135081341 | T | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0247 |
2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.151-9657T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081341 | |||||||
chr2:135081342 | ATATATAT others(31): Show |
A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.151-9644_151-9607d others(40): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081342 | ||||||
chr2:135081343 | T | A | 2 | a0001c0003t0001g0053 a0001c0004t0013g0256 |
2 | HG01928.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-9655T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081343 | |||||||
chr2:135081344 | A | G | 2 | a0001c0001t0012g0253 a0001c0001t0012g0254 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9654A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081344 | |||||||
chr2:135081345 | T | A | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9653T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081345 | |||||||
chr2:135081346 | ATATATAT others(27): Show |
A | 1 | a0002c0010t0001g0124 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.151-9640_151-9607d others(36): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081346 | ||||||
chr2:135081347 | T | A | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9651T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081347 | |||||||
chr2:135081348 | ATATATAT others(25): Show |
A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0071 a0002c0002t0001g0115 |
3 | HG01255.hp1 HG03540.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.151-9638_151-9607d others(34): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081348 | ||||||
chr2:135081350 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0012g0253 a0001c0001t0012g0254 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9646_151-9625d others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081350 | ||||||
chr2:135081350 | ATATATAT others(23): Show |
A | 3 | a0002c0002t0001g0104 a0002c0002t0001g0126 a0002c0002t0001g0127 |
3 | HG01192.hp2 HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.151-9636_151-9607d others(32): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081350 | ||||||
chr2:135081351 | TATATATA others(7): Show |
T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-9645_151-9632d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081351 | ||||||
chr2:135081354 | ATATATAT others(19): Show |
A | 1 | a0002c0002t0001g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.151-9635_151-9610d others(28): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081354 | ||||||
chr2:135081355 | TATATATA others(3): Show |
T | 3 | a0001c0008t0008g0005 a0001c0008t0008g0006 a0005c0012t0008g0003 |
3 | HG02451.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.151-9641_151-9632d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081355 | ||||||
chr2:135081356 | A | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9642A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081356 | |||||||
chr2:135081361 | T | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
11 | HG01255.hp2 HG01346.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-9637T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081361 | |||||||
chr2:135081361 | T | TATATATA others(3): Show |
1 | a0002c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.151-9636_151-9635i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | ||||||
chr2:135081361 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0050 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151-9636_151-9635i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | ||||||
chr2:135081361 | TAC | T | 10 | a0001c0001t0002g0139 a0001c0001t0002g0142 a0001c0001t0002g0143 others(7): Show |
10 | HG01070.hp1 HG01192.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9630_151-9629d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | ||||||
chr2:135081361 | TACAC | T | 46 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0155 others(43): Show |
46 | HG00438.hp1 HG01243.hp1 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.151-9632_151-9629d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | ||||||
chr2:135081362 | ACACACAC others(3): Show |
A | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9635_151-9626d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081362 | |||||||
chr2:135081363 | C | T | 75 | a0001c0001t0001g0102 a0001c0001t0002g0140 a0001c0001t0002g0141 others(72): Show |
75 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.151-9635C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081363 | |||||||
chr2:135081365 | C | T | 76 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 others(73): Show |
76 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.151-9633C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081365 | |||||||
chr2:135081382 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-9616A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081382 | |||||||
chr2:135081382 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9608_151-9599d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081382 | ||||||
chr2:135081387 | T | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9611T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081387 | |||||||
chr2:135081389 | T | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9609T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081389 | |||||||
chr2:135081392 | G | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9606G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081392 | |||||||
chr2:135081521 | T | C | 1 | a0001c0003t0001g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-9477T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081521 | |||||||
chr2:135081686 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.151-9312A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081686 | |||||||
chr2:135081919 | T | A | 1 | a0002c0002t0024g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.151-9079T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081919 | |||||||
chr2:135082068 | G | A | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-8930G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082068 | |||||||
chr2:135082141 | C | CAATGAAT others(1): Show |
3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-8841_151-8834d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | ||||||
chr2:135082141 | C | CAATGAAT others(5): Show |
5 | a0001c0001t0003g0276 a0002c0002t0001g0113 a0004c0005t0011g0219 others(2): Show |
5 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-8845_151-8834d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | ||||||
chr2:135082141 | C | CAATGAAT others(9): Show |
27 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.151-8849_151-8834d others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | ||||||
chr2:135082141 | C | CAATGAAT others(13): Show |
2 | a0001c0001t0002g0247 a0001c0001t0003g0245 |
2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.151-8853_151-8834d others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | ||||||
chr2:135082161 | G | GAATA | 13 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.151-8826_151-8823d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | ||||||
chr2:135082161 | G | GAATGAAT others(5): Show |
15 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(12): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | ||||||
chr2:135082161 | G | GAATGAAT others(9): Show |
71 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0140 others(68): Show |
71 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | ||||||
chr2:135082161 | G | GAATGAAT others(13): Show |
14 | a0001c0001t0002g0139 a0001c0001t0002g0155 a0001c0001t0002g0158 others(11): Show |
14 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | ||||||
chr2:135082161 | G | GAATGAAT others(17): Show |
4 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(26): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | ||||||
chr2:135082235 | C | T | 57 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(54): Show |
57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.151-8763C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082235 | |||||||
chr2:135082386 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.151-8612A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082386 | |||||||
chr2:135082442 | C | CT | 7 | a0001c0001t0003g0240 a0002c0002t0001g0089 a0002c0002t0001g0095 others(4): Show |
7 | HG00621.hp2 HG02258.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-8540dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082442 | ||||||
chr2:135082442 | CT | C | 6 | a0001c0001t0001g0137 a0001c0001t0002g0141 a0001c0001t0002g0247 others(3): Show |
6 | HG01243.hp1 HG02040.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-8540delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082442 | ||||||
chr2:135082722 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151-8276C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082722 | |||||||
chr2:135082912 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.151-8086C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082912 | |||||||
chr2:135083075 | T | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-7923T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083075 | |||||||
chr2:135083110 | CAGTT | C | 3 | a0001c0001t0005g0008 a0001c0001t0005g0012 a0001c0001t0005g0013 |
3 | NA19002.hp1 NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.151-7887_151-7884d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083110 | |||||||
chr2:135083188 | G | C | 14 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-7810G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083188 | |||||||
chr2:135083257 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-7741C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083257 | |||||||
chr2:135083319 | A | G | 1 | a0002c0002t0001g0076 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.151-7679A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083319 | |||||||
chr2:135083507 | C | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.151-7491C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083507 | |||||||
chr2:135083630 | A | T | 29 | a0001c0001t0002g0213 a0001c0001t0003g0225 a0001c0001t0003g0227 others(26): Show |
29 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.151-7368A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083630 | |||||||
chr2:135083631 | T | A | 1 | a0002c0002t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.151-7367T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083631 | |||||||
chr2:135083758 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-7240C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083758 | |||||||
chr2:135083767 | G | GT | 123 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(120): Show |
124 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.151-7207dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | ||||||
chr2:135083767 | G | GTT | 14 | a0001c0001t0001g0043 a0001c0001t0001g0073 a0001c0001t0001g0081 others(11): Show |
14 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-7208_151-7207d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | ||||||
chr2:135083767 | GT | G | 49 | a0001c0001t0002g0168 a0001c0001t0002g0179 a0001c0001t0002g0181 others(46): Show |
49 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.151-7207delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | ||||||
chr2:135083767 | GTT | G | 5 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 others(2): Show |
5 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-7208_151-7207d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | ||||||
chr2:135083906 | A | T | 1 | a0001c0001t0002g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.151-7092A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083906 | |||||||
chr2:135083966 | C | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.151-7032C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083966 | |||||||
chr2:135084193 | C | T | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.151-6805C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084193 | |||||||
chr2:135084207 | T | G | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.151-6791T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084207 | |||||||
chr2:135084264 | T | C | 1 | a0002c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.151-6734T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084264 | |||||||
chr2:135084443 | T | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-6555T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084443 | |||||||
chr2:135084659 | A | AGGAAATA others(8110): Show |
1 | a0001c0003t0001g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-6326_151-6325i others(8119): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135084659 | ||||||
chr2:135084763 | C | T | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151-6235C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084763 | |||||||
chr2:135084881 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG00609.hp1 HG02155.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.151-6117G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084881 | |||||||
chr2:135084998 | G | A | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-6000G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084998 | |||||||
chr2:135085414 | T | A | 1 | a0001c0001t0021g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151-5584T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085414 | |||||||
chr2:135085665 | C | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-5333C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085665 | |||||||
chr2:135085809 | G | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0114 |
2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.151-5189G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085809 | |||||||
chr2:135085828 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5170T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085828 | |||||||
chr2:135085858 | C | G | 4 | a0001c0001t0002g0167 a0001c0001t0002g0171 a0001c0001t0002g0172 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5140C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085858 | |||||||
chr2:135085859 | C | T | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-5139C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085859 | |||||||
chr2:135085886 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-5112G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085886 | |||||||
chr2:135086116 | A | C | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-4882A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086116 | |||||||
chr2:135086250 | AG | A | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-4746delG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086250 | ||||||
chr2:135086383 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.151-4615G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086383 | |||||||
chr2:135086661 | C | CT | 20 | a0001c0001t0001g0042 a0001c0001t0001g0110 a0001c0001t0001g0136 others(17): Show |
20 | HG00280.hp1 HG01433.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.151-4312dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086661 | ||||||
chr2:135086661 | CT | C | 85 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0157 others(82): Show |
85 | HG00438.hp1 HG00609.hp1 HG01433.hp2 others(82): Show |
intron_variant | MODIFIER | c.151-4312delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086661 | ||||||
chr2:135086686 | T | C | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151-4312T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086686 | |||||||
chr2:135086686 | TC | T | 35 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(32): Show |
35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.151-4310delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086686 | ||||||
chr2:135086687 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-4311C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086687 | |||||||
chr2:135087092 | A | G | 1 | a0002c0002t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151-3906A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087092 | |||||||
chr2:135087282 | C | A | 13 | a0001c0001t0001g0043 a0002c0002t0001g0001 a0002c0002t0001g0016 others(10): Show |
14 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-3716C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087282 | |||||||
chr2:135087514 | A | G | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3484A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087514 | |||||||
chr2:135087534 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151-3464T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087534 | |||||||
chr2:135087757 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.151-3241T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087757 | |||||||
chr2:135087820 | T | C | 8 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-3178T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087820 | |||||||
chr2:135088106 | A | C | 1 | a0002c0002t0001g0039 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151-2892A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088106 | |||||||
chr2:135088295 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.151-2703A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088295 | |||||||
chr2:135088333 | T | C | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-2665T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088333 | |||||||
chr2:135088458 | G | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-2540G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088458 | |||||||
chr2:135088478 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-2520C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088478 | |||||||
chr2:135088490 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.151-2508A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088490 | |||||||
chr2:135088544 | C | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-2454C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088544 | |||||||
chr2:135088639 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.151-2359A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088639 | |||||||
chr2:135088688 | C | CA | 25 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
25 | HG01346.hp1 HG01978.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.151-2290dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | ||||||
chr2:135088688 | C | CAA | 40 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(37): Show |
40 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.151-2291_151-2290d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | ||||||
chr2:135088688 | CA | C | 17 | a0001c0001t0001g0080 a0001c0001t0002g0192 a0001c0001t0005g0007 others(14): Show |
17 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.151-2290delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | ||||||
chr2:135089046 | C | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1952C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089046 | |||||||
chr2:135089080 | AAGGGGTC others(389): Show |
A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-1915_151-1520d others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135089080 | ||||||
chr2:135089223 | C | T | 7 | a0001c0001t0002g0139 a0001c0001t0002g0155 a0001c0001t0002g0165 others(4): Show |
7 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-1775C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089223 | |||||||
chr2:135089526 | T | G | 1 | a0001c0001t0002g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.151-1472T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089526 | |||||||
chr2:135089550 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-1448C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089550 | |||||||
chr2:135089565 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-1433C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089565 | |||||||
chr2:135089724 | G | A | 7 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0207 others(4): Show |
7 | NA18952.hp2 NA18966.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-1274G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089724 | |||||||
chr2:135089809 | A | G | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-1189A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089809 | |||||||
chr2:135089831 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.151-1167C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089831 | |||||||
chr2:135089894 | C | T | 20 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(17): Show |
20 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.151-1104C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089894 | |||||||
chr2:135090124 | A | G | 5 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0179 others(2): Show |
5 | NA18939.hp1 NA18959.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-874A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090124 | |||||||
chr2:135090313 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.151-685T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090313 | |||||||
chr2:135090358 | A | G | 29 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(26): Show |
29 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.151-640A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090358 | |||||||
chr2:135090585 | TA | T | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.151-409delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135090585 | ||||||
chr2:135090943 | A | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-55A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090943 | |||||||
chr2:135091205 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0192 |
2 | NA18967.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.283+75G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091205 | |||||||
chr2:135091474 | G | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+344G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091474 | |||||||
chr2:135091496 | A | G | 1 | a0001c0001t0002g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.283+366A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091496 | |||||||
chr2:135091497 | GAGA | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+370_283+372del others(3): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 135091497 | ||||||
chr2:135092043 | G | A | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.283+913G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092043 | |||||||
chr2:135092177 | G | A | 1 | a0001c0003t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.283+1047G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092177 | |||||||
chr2:135092561 | A | G | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.284-1054A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092561 | |||||||
chr2:135092562 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.284-1053A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092562 | |||||||
chr2:135092629 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0002g0216 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.284-986G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092629 | |||||||
chr2:135093042 | A | C | 2 | a0004c0005t0011g0221 a0004c0005t0011g0222 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284-573A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093042 | |||||||
chr2:135093208 | C | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-407C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093208 | |||||||
chr2:135093216 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-399A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093216 | |||||||
chr2:135093380 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-235A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093380 | |||||||
chr2:135093465 | C | G | 5 | a0002c0002t0001g0088 a0002c0002t0001g0108 a0002c0002t0001g0109 others(2): Show |
5 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-150C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093465 | |||||||
chr2:135094166 | G | GA | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+473_362+474ins others(1): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094166 | |||||||
chr2:135094167 | G | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+474G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094167 | |||||||
chr2:135094169 | G | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+476G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094169 | |||||||
chr2:135094371 | G | T | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+678G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094371 | |||||||
chr2:135094393 | G | C | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.362+700G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094393 | |||||||
chr2:135094592 | T | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.362+899T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094592 | |||||||
chr2:135094597 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.362+904A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094597 | |||||||
chr2:135094762 | G | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+1069G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094762 | |||||||
chr2:135095122 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.362+1429C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095122 | |||||||
chr2:135095238 | C | T | 14 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1545C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095238 | |||||||
chr2:135095249 | T | C | 1 | a0002c0002t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.362+1556T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095249 | |||||||
chr2:135095347 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1654C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095347 | |||||||
chr2:135095711 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+2018T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095711 | |||||||
chr2:135095800 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+2107A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095800 | |||||||
chr2:135095817 | C | T | 8 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(5): Show |
8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+2124C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095817 | |||||||
chr2:135095848 | C | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.362+2155C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095848 | |||||||
chr2:135096186 | C | A | 1 | a0001c0001t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.362+2493C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096186 | |||||||
chr2:135096237 | C | T | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.362+2544C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096237 | |||||||
chr2:135096291 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+2598A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096291 | |||||||
chr2:135096330 | G | A | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+2637G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096330 | |||||||
chr2:135096382 | A | C | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362+2689A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096382 | |||||||
chr2:135096498 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+2805A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096498 | |||||||
chr2:135096588 | C | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.362+2895C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096588 | |||||||
chr2:135096641 | C | T | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.362+2948C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096641 | |||||||
chr2:135096799 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+3106C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096799 | |||||||
chr2:135096949 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.362+3256T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096949 | |||||||
chr2:135097115 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+3422A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097115 | |||||||
chr2:135097121 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.362+3428T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097121 | |||||||
chr2:135097137 | C | A | 1 | a0002c0002t0001g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.362+3444C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097137 | |||||||
chr2:135097172 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+3479A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097172 | |||||||
chr2:135097216 | C | CT | 112 | a0001c0001t0001g0031 a0001c0001t0001g0157 a0001c0001t0002g0002 others(109): Show |
112 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.362+3539dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135097216 | ||||||
chr2:135097216 | C | CTT | 39 | a0001c0001t0002g0148 a0001c0001t0002g0193 a0001c0001t0002g0205 others(36): Show |
39 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.362+3538_362+3539d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135097216 | ||||||
chr2:135097242 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.362+3549G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097242 | |||||||
chr2:135097317 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.362+3624G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097317 | |||||||
chr2:135097331 | T | C | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+3638T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097331 | |||||||
chr2:135097387 | G | A | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.362+3694G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097387 | |||||||
chr2:135097462 | C | T | 1 | a0002c0002t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.362+3769C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097462 | |||||||
chr2:135097480 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.362+3787C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097480 | |||||||
chr2:135098328 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02155.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.362+4635G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098328 | |||||||
chr2:135098468 | G | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+4775G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098468 | |||||||
chr2:135098605 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.362+4912T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098605 | |||||||
chr2:135098640 | A | C | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362+4947A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098640 | |||||||
chr2:135098987 | T | A | 1 | a0001c0001t0002g0209 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.362+5294T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098987 | |||||||
chr2:135099096 | T | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+5403T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099096 | |||||||
chr2:135099101 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+5408T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099101 | |||||||
chr2:135099175 | G | A | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.362+5482G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099175 | |||||||
chr2:135099431 | C | CTG | 11 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0098 others(8): Show |
11 | HG00438.hp2 HG00621.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.362+5772_362+5773d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | ||||||
chr2:135099431 | C | CTGTG | 3 | a0001c0001t0001g0055 a0002c0002t0001g0089 a0002c0002t0001g0122 |
3 | HG00423.hp2 NA18967.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.362+5770_362+5773d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | ||||||
chr2:135099431 | C | CTGTGTG | 3 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0046 |
3 | HG03704.hp2 NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.362+5768_362+5773d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | ||||||
chr2:135099431 | CTG | C | 57 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0049 others(54): Show |
57 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.362+5772_362+5773d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | ||||||
chr2:135099431 | CTGTG | C | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0130 others(31): Show |
34 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.362+5770_362+5773d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | ||||||
chr2:135099435 | G | C | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.362+5742G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099435 | |||||||
chr2:135099463 | G | A | 112 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(109): Show |
112 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.362+5770G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099463 | |||||||
chr2:135099463 | G | GTA | 34 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(31): Show |
34 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(31): Show |
intron_variant | MODIFIER | c.362+5771_362+5772i others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099463 | ||||||
chr2:135099463 | G | GTGTA | 6 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0170 others(3): Show |
6 | HG02155.hp2 NA18939.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+5778_362+5781d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099463 | ||||||
chr2:135099655 | AT | A | 19 | a0001c0001t0002g0164 a0001c0001t0002g0198 a0001c0001t0004g0258 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.362+5975delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099655 | ||||||
chr2:135099735 | A | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+6042A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099735 | |||||||
chr2:135099968 | G | T | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.362+6275G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099968 | |||||||
chr2:135100205 | G | T | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.362+6512G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100205 | |||||||
chr2:135100360 | A | G | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.362+6667A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100360 | |||||||
chr2:135100398 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0174 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.362+6705C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100398 | |||||||
chr2:135100629 | A | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+6936A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100629 | |||||||
chr2:135100779 | G | C | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.362+7086G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100779 | |||||||
chr2:135100910 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+7217T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100910 | |||||||
chr2:135101286 | G | A | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362+7593G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101286 | |||||||
chr2:135101587 | A | G | 2 | a0001c0003t0001g0045 a0001c0003t0001g0114 |
2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.362+7894A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101587 | |||||||
chr2:135101686 | A | C | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.362+7993A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101686 | |||||||
chr2:135101795 | T | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.362+8102T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101795 | |||||||
chr2:135101801 | A | T | 225 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(222): Show |
226 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.362+8108A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101801 | |||||||
chr2:135101858 | C | G | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+8165C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101858 | |||||||
chr2:135102257 | G | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+8564G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102257 | |||||||
chr2:135102342 | A | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.362+8649A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102342 | |||||||
chr2:135102350 | A | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+8657A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102350 | |||||||
chr2:135102353 | T | C | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.362+8660T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102353 | |||||||
chr2:135102598 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.362+8905C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102598 | |||||||
chr2:135102735 | T | G | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.362+9042T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102735 | |||||||
chr2:135102777 | A | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+9084A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102777 | |||||||
chr2:135102787 | G | A | 8 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+9094G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102787 | |||||||
chr2:135102872 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.362+9179G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102872 | |||||||
chr2:135102883 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.362+9190C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102883 | |||||||
chr2:135102985 | C | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.362+9292C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102985 | |||||||
chr2:135103006 | G | GA | 104 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0030 others(101): Show |
105 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.362+9330dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | ||||||
chr2:135103006 | G | GAA | 22 | a0001c0001t0001g0029 a0001c0001t0005g0007 a0001c0001t0005g0008 others(19): Show |
22 | HG00280.hp1 HG00423.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.362+9329_362+9330d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | ||||||
chr2:135103006 | G | GAAAAA | 12 | a0001c0001t0003g0233 a0001c0001t0003g0234 a0001c0001t0003g0237 others(9): Show |
12 | HG01175.hp2 HG01261.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.362+9326_362+9330d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | ||||||
chr2:135103006 | G | GAAAAAA | 8 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0236 others(5): Show |
8 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9325_362+9330d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | ||||||
chr2:135103035 | A | AT | 25 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0048 others(22): Show |
25 | HG00609.hp2 HG01070.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+9362dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATT | 5 | a0001c0001t0012g0254 a0002c0002t0001g0095 a0002c0002t0001g0121 others(2): Show |
5 | HG00621.hp2 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+9361_362+9362d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTT | 15 | a0001c0001t0002g0158 a0001c0001t0002g0181 a0001c0001t0002g0183 others(12): Show |
15 | HG01070.hp1 HG02818.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.362+9357_362+9362d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT | 30 | a0001c0001t0002g0002 a0001c0001t0002g0156 a0001c0001t0002g0159 others(27): Show |
30 | HG01192.hp1 HG01433.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.362+9356_362+9362d others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(1): Show |
32 | a0001c0001t0001g0157 a0001c0001t0002g0139 a0001c0001t0002g0142 others(29): Show |
32 | HG00438.hp1 HG01256.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+9355_362+9362d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(2): Show |
17 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0145 others(14): Show |
17 | HG00741.hp2 HG02630.hp2 HG02895.hp2 others(14): Show |
intron_variant | MODIFIER | c.362+9354_362+9362d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(3): Show |
10 | a0001c0001t0002g0194 a0001c0001t0004g0258 a0001c0001t0004g0260 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.362+9353_362+9362d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(4): Show |
6 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(3): Show |
6 | HG01993.hp2 HG02451.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+9352_362+9362d others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(5): Show |
9 | a0001c0001t0003g0242 a0001c0001t0005g0007 a0001c0001t0005g0008 others(6): Show |
9 | HG00280.hp1 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+9351_362+9362d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.362+9350_362+9362d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+9349_362+9362d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(11): Show |
6 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(3): Show |
6 | HG00558.hp1 HG00735.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+9345_362+9362d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(12): Show |
8 | a0001c0001t0003g0227 a0001c0001t0003g0233 a0001c0001t0003g0234 others(5): Show |
8 | HG00621.hp1 HG00639.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9344_362+9362d others(21): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(13): Show |
8 | a0001c0001t0003g0225 a0001c0001t0003g0236 a0001c0001t0003g0237 others(5): Show |
8 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9343_362+9362d others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | A | ATTTTTTT others(14): Show |
3 | a0001c0001t0003g0245 a0001c0001t0003g0276 a0001c0001t0016g0235 |
3 | HG00639.hp1 HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.362+9362_362+9363i others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103035 | AT | A | 6 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0084 others(3): Show |
6 | HG00423.hp2 HG01993.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+9362delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | ||||||
chr2:135103060 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.362+9367C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103060 | |||||||
chr2:135103161 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0106 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.362+9468C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103161 | |||||||
chr2:135103394 | C | T | 1 | a0001c0001t0014g0011 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.362+9701C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103394 | |||||||
chr2:135103468 | G | A | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-9683G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103468 | |||||||
chr2:135103613 | G | A | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.363-9538G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103613 | |||||||
chr2:135103724 | T | TG | 15 | a0001c0001t0003g0277 a0001c0001t0005g0007 a0001c0001t0005g0008 others(12): Show |
15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.363-9425dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103724 | ||||||
chr2:135103726 | G | C | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.363-9425G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103726 | |||||||
chr2:135103727 | C | G | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-9424C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103727 | |||||||
chr2:135103740 | G | A | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.363-9411G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103740 | |||||||
chr2:135103917 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363-9234C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103917 | |||||||
chr2:135103927 | G | C | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.363-9224G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103927 | |||||||
chr2:135104361 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-8790A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104361 | |||||||
chr2:135104539 | T | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-8612T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104539 | |||||||
chr2:135104621 | G | A | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-8530G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104621 | |||||||
chr2:135104639 | G | A | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.363-8512G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104639 | |||||||
chr2:135104652 | A | G | 1 | a0002c0002t0024g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.363-8499A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104652 | |||||||
chr2:135104699 | A | AAAAT | 29 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0054 others(26): Show |
29 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.363-8416_363-8413d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | ||||||
chr2:135104699 | A | AAAATAAA others(1): Show |
8 | a0001c0001t0003g0233 a0001c0001t0003g0234 a0001c0001t0003g0240 others(5): Show |
8 | HG01175.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.363-8420_363-8413d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | ||||||
chr2:135104699 | AAAAT | A | 4 | a0001c0001t0003g0227 a0001c0001t0003g0229 a0001c0001t0003g0230 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-8416_363-8413d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | ||||||
chr2:135104778 | A | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-8373A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104778 | |||||||
chr2:135104831 | G | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-8320G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104831 | |||||||
chr2:135104851 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-8300G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104851 | |||||||
chr2:135104889 | AAAAC | A | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.363-8246_363-8243d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104889 | ||||||
chr2:135104991 | T | C | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363-8160T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104991 | |||||||
chr2:135105174 | G | GCTCTCC | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7957_363-7952d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105174 | ||||||
chr2:135105174 | GCTCTCC | G | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0003g0225 others(27): Show |
30 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.363-7957_363-7952d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105174 | ||||||
chr2:135105213 | C | G | 1 | a0002c0002t0001g0113 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.363-7938C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105213 | |||||||
chr2:135105234 | T | TC | 9 | a0001c0001t0001g0082 a0001c0001t0002g0212 a0001c0001t0003g0245 others(6): Show |
9 | HG00621.hp2 HG01175.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.363-7911dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105234 | ||||||
chr2:135105288 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.363-7863C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105288 | |||||||
chr2:135105384 | A | C | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-7767A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105384 | |||||||
chr2:135105443 | G | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7708G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105443 | |||||||
chr2:135105444 | G | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7707G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105444 | |||||||
chr2:135105445 | G | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7706G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105445 | |||||||
chr2:135105486 | G | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-7665G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105486 | |||||||
chr2:135105522 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-7629G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105522 | |||||||
chr2:135105573 | G | A | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.363-7578G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105573 | |||||||
chr2:135105577 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.363-7574C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105577 | |||||||
chr2:135105578 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.363-7573G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105578 | |||||||
chr2:135105600 | C | T | 2 | a0001c0001t0001g0036 a0001c0008t0008g0005 |
2 | HG03704.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-7551C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105600 | |||||||
chr2:135105616 | C | G | 2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.363-7535C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105616 | |||||||
chr2:135105719 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.363-7432T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105719 | |||||||
chr2:135105750 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363-7401C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105750 | |||||||
chr2:135105821 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-7330G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105821 | |||||||
chr2:135105843 | C | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-7308C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105843 | |||||||
chr2:135105889 | A | G | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-7262A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105889 | |||||||
chr2:135105907 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.363-7244A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105907 | |||||||
chr2:135105946 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7205C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105946 | |||||||
chr2:135106041 | G | A | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.363-7110G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106041 | |||||||
chr2:135106042 | C | T | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363-7109C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106042 | |||||||
chr2:135106121 | C | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-7030C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106121 | |||||||
chr2:135106146 | G | C | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0180 |
3 | HG00438.hp1 NA18954.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.363-7005G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106146 | |||||||
chr2:135106199 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0056 |
2 | NA18992.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.363-6952G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106199 | |||||||
chr2:135106236 | C | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-6915C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106236 | |||||||
chr2:135106240 | A | AC | 35 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0073 others(32): Show |
35 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.363-6907dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106240 | ||||||
chr2:135106265 | A | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6886A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106265 | |||||||
chr2:135106292 | A | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.363-6859A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106292 | |||||||
chr2:135106295 | G | T | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-6856G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106295 | |||||||
chr2:135106441 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6710A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106441 | |||||||
chr2:135106458 | C | G | 1 | a0001c0001t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.363-6693C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106458 | |||||||
chr2:135106464 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6687C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106464 | |||||||
chr2:135106515 | G | A | 2 | a0001c0001t0012g0252 a0001c0001t0012g0253 |
2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.363-6636G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106515 | |||||||
chr2:135106577 | C | T | 6 | a0001c0001t0002g0139 a0001c0001t0002g0155 a0001c0001t0002g0165 others(3): Show |
6 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.363-6574C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106577 | |||||||
chr2:135106693 | A | T | 12 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(9): Show |
12 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-6458A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106693 | |||||||
chr2:135106724 | C | G | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.363-6427C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106724 | |||||||
chr2:135106756 | T | TA | 81 | a0001c0001t0002g0002 a0001c0001t0002g0139 a0001c0001t0002g0140 others(78): Show |
81 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.363-6384dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106756 | ||||||
chr2:135106760 | AAAAAAAA others(1): Show |
A | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-6376_363-6369d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106760 | ||||||
chr2:135106762 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-6389A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106762 | |||||||
chr2:135106767 | AT | A | 3 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363-6383delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106767 | |||||||
chr2:135106771 | A | T | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-6380A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106771 | |||||||
chr2:135106823 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.363-6328A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106823 | |||||||
chr2:135106827 | G | C | 10 | a0001c0001t0003g0234 a0001c0001t0003g0236 a0001c0001t0003g0237 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-6324G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106827 | |||||||
chr2:135107028 | C | G | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-6123C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107028 | |||||||
chr2:135107098 | G | GA | 6 | a0001c0001t0002g0143 a0001c0001t0003g0275 a0001c0003t0001g0058 others(3): Show |
6 | HG01981.hp2 HG02486.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-6038dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | ||||||
chr2:135107098 | GA | G | 7 | a0001c0001t0003g0279 a0001c0001t0005g0013 a0001c0001t0006g0223 others(4): Show |
7 | HG02559.hp1 HG02559.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.363-6038delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | ||||||
chr2:135107098 | GAA | G | 13 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.363-6039_363-6038d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | ||||||
chr2:135107246 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.363-5905G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107246 | |||||||
chr2:135107383 | CAT | C | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-5765_363-5764d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107383 | ||||||
chr2:135107419 | AAAGG | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-5727_363-5724d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107419 | ||||||
chr2:135107587 | T | C | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.363-5564T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107587 | |||||||
chr2:135107644 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.363-5507A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107644 | |||||||
chr2:135107801 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-5350C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107801 | |||||||
chr2:135107953 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0054 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.363-5198C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107953 | |||||||
chr2:135107975 | CA | C | 82 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(79): Show |
83 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.363-5149delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | ||||||
chr2:135107975 | CAA | C | 9 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0002g0079 others(6): Show |
9 | HG00735.hp1 HG01192.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-5150_363-5149d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | ||||||
chr2:135107975 | CAAA | C | 22 | a0001c0001t0002g0139 a0001c0001t0002g0156 a0001c0001t0002g0164 others(19): Show |
22 | HG00438.hp1 HG01070.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.363-5151_363-5149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | ||||||
chr2:135107975 | CAAAA | C | 81 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0140 others(78): Show |
81 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(78): Show |
intron_variant | MODIFIER | c.363-5152_363-5149d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | ||||||
chr2:135107975 | CAAAAA | C | 46 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(43): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.363-5153_363-5149d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | ||||||
chr2:135108002 | A | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-5149A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108002 | |||||||
chr2:135108457 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-4694C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108457 | |||||||
chr2:135108515 | C | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-4636C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108515 | |||||||
chr2:135108515 | C | CT | 38 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(35): Show |
38 | HG00438.hp1 HG01346.hp2 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.363-4622dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135108515 | ||||||
chr2:135108515 | CT | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-4622delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135108515 | ||||||
chr2:135108592 | C | G | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.363-4559C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108592 | |||||||
chr2:135108612 | G | A | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.363-4539G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108612 | |||||||
chr2:135108812 | C | T | 1 | a0002c0002t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.363-4339C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108812 | |||||||
chr2:135108985 | A | G | 5 | a0001c0001t0001g0082 a0004c0005t0011g0219 a0004c0005t0011g0221 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-4166A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108985 | |||||||
chr2:135109036 | AT | A | 3 | a0001c0001t0002g0204 a0001c0001t0002g0211 a0001c0001t0010g0208 |
3 | HG03017.hp2 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.363-4112delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135109036 | ||||||
chr2:135109143 | TTGG | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-4007_363-4005d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109143 | |||||||
chr2:135109180 | A | G | 57 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(54): Show |
57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.363-3971A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109180 | |||||||
chr2:135109209 | C | T | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363-3942C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109209 | |||||||
chr2:135109241 | A | C | 1 | a0001c0001t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.363-3910A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109241 | |||||||
chr2:135109275 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0054 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.363-3876A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109275 | |||||||
chr2:135109513 | C | T | 7 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0262 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.363-3638C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109513 | |||||||
chr2:135109529 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0073 a0001c0001t0001g0218 others(1): Show |
4 | HG00423.hp1 NA18968.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-3622A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109529 | |||||||
chr2:135109574 | T | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-3577T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109574 | |||||||
chr2:135109587 | T | A | 18 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(15): Show |
18 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.363-3564T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109587 | |||||||
chr2:135109776 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363-3375G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109776 | |||||||
chr2:135109803 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-3348C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109803 | |||||||
chr2:135109841 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.363-3310C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109841 | |||||||
chr2:135109878 | G | A | 1 | a0001c0001t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.363-3273G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109878 | |||||||
chr2:135109932 | A | G | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.363-3219A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109932 | |||||||
chr2:135109968 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-3183T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109968 | |||||||
chr2:135109993 | T | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-3158T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109993 | |||||||
chr2:135110063 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-3088A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110063 | |||||||
chr2:135110204 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-2947G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110204 | |||||||
chr2:135110340 | G | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-2811G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110340 | |||||||
chr2:135110448 | AAGAATTT others(6): Show |
A | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363-2701_363-2689d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135110448 | ||||||
chr2:135110729 | C | T | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.363-2422C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110729 | |||||||
chr2:135110975 | GA | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-2169delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135110975 | ||||||
chr2:135111554 | T | C | 1 | a0002c0002t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.363-1597T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111554 | |||||||
chr2:135111560 | G | A | 1 | a0001c0001t0005g0007 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.363-1591G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111560 | |||||||
chr2:135111675 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363-1476A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111675 | |||||||
chr2:135111810 | G | A | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-1341G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111810 | |||||||
chr2:135112003 | G | A | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363-1148G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112003 | |||||||
chr2:135112020 | G | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-1131G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112020 | |||||||
chr2:135112106 | G | A | 1 | a0002c0002t0001g0039 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.363-1045G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112106 | |||||||
chr2:135112166 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-985C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112166 | |||||||
chr2:135112191 | C | T | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-960C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112191 | |||||||
chr2:135112269 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-882G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112269 | |||||||
chr2:135112427 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-724A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112427 | |||||||
chr2:135112573 | C | A | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.363-578C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112573 | |||||||
chr2:135112625 | G | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-526G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112625 | |||||||
chr2:135112746 | C | G | 10 | a0001c0001t0003g0234 a0001c0001t0003g0236 a0001c0001t0003g0237 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-405C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112746 | |||||||
chr2:135112815 | G | GTC | 4 | a0001c0001t0001g0042 a0001c0001t0012g0252 a0001c0001t0012g0253 others(1): Show |
4 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-317_363-316dup others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112815 | ||||||
chr2:135112815 | GTCTCTCT others(1): Show |
G | 5 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0004t0013g0246 others(2): Show |
5 | HG02559.hp1 HG03041.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.363-323_363-316del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112815 | ||||||
chr2:135112824 | TCTCTCTC others(5): Show |
T | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.363-325_363-314del others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112824 | ||||||
chr2:135112826 | TCTCTCTC others(3): Show |
T | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.363-323_363-314del others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112826 | ||||||
chr2:135112828 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-323T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112828 | |||||||
chr2:135112830 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-321T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112830 | |||||||
chr2:135112830 | TCTCTCA | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0006t0002g0248 others(3): Show |
6 | HG02258.hp2 HG02630.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.363-319_363-314del others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112830 | ||||||
chr2:135112830 | TCTCTCAC others(1): Show |
T | 5 | a0001c0001t0002g0247 a0004c0005t0011g0219 a0004c0005t0011g0221 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-319_363-312del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112830 | ||||||
chr2:135112832 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-319T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112832 | |||||||
chr2:135112834 | T | A | 2 | a0001c0001t0003g0276 a0001c0004t0013g0256 |
2 | HG00639.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.363-317T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112834 | |||||||
chr2:135112834 | T | TCA | 14 | a0001c0001t0002g0158 a0001c0001t0002g0199 a0001c0001t0002g0205 others(11): Show |
14 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.363-284_363-283dup others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | T | TCACA | 55 | a0001c0001t0002g0002 a0001c0001t0002g0139 a0001c0001t0002g0140 others(52): Show |
55 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-286_363-283dup others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | T | TCACACA | 6 | a0001c0001t0001g0157 a0001c0001t0002g0144 a0001c0001t0002g0166 others(3): Show |
6 | HG02015.hp2 HG02451.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-288_363-283dup others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | T | TCACACAC others(1): Show |
3 | a0001c0001t0002g0160 a0001c0001t0002g0168 a0001c0001t0002g0216 |
3 | HG02083.hp2 HG04115.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.363-290_363-283dup others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | T | TCTCA | 9 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0149 others(6): Show |
9 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-316_363-315ins others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | TCACA | T | 6 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-286_363-283del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112834 | TCACACAC others(1): Show |
T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-290_363-283del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | ||||||
chr2:135112836 | A | T | 19 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0004g0258 others(16): Show |
19 | HG02055.hp1 HG02056.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.363-315A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112836 | |||||||
chr2:135112838 | A | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-313A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112838 | |||||||
chr2:135112842 | A | T | 2 | a0001c0008t0008g0005 a0001c0008t0008g0006 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-309A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112842 | |||||||
chr2:135112844 | A | T | 13 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.363-307A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112844 | |||||||
chr2:135112877 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.363-274C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112877 | |||||||
chr2:135112971 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.363-180A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112971 | |||||||
chr2:135113392 | T | A | 2 | a0002c0002t0001g0101 a0002c0002t0001g0217 |
2 | HG02083.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.482+122T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113392 | |||||||
chr2:135113418 | C | T | 3 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0279 |
3 | HG00639.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.482+148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113418 | |||||||
chr2:135113494 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.482+224A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113494 | |||||||
chr2:135113568 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482+298C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113568 | |||||||
chr2:135113742 | AT | A | 6 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0003c0006t0002g0248 others(3): Show |
6 | HG02258.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+486delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 135113742 | ||||||
chr2:135113864 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.482+594C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113864 | |||||||
chr2:135113992 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.482+722C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113992 | |||||||
chr2:135114001 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.482+731C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114001 | |||||||
chr2:135114054 | G | A | 150 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(147): Show |
150 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.482+784G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114054 | |||||||
chr2:135114344 | C | T | 99 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(96): Show |
99 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.483-872C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114344 | |||||||
chr2:135114418 | A | G | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.483-798A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114418 | |||||||
chr2:135114528 | C | T | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.483-688C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114528 | |||||||
chr2:135114576 | G | T | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.483-640G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114576 | |||||||
chr2:135114805 | G | A | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-411G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114805 | |||||||
chr2:135115072 | T | A | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-144T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115072 | |||||||
chr2:135115076 | C | A | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.483-140C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115076 | |||||||
chr2:135115153 | T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483-63T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115153 | |||||||
chr2:135115896 | A | G | 2 | a0001c0003t0001g0045 a0001c0003t0001g0114 |
2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.648+515A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135115896 | |||||||
chr2:135116015 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.648+634G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116015 | |||||||
chr2:135116162 | T | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.648+781T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116162 | |||||||
chr2:135116272 | T | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+891T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116272 | |||||||
chr2:135116275 | C | T | 51 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(48): Show |
51 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.648+894C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116275 | |||||||
chr2:135116387 | C | T | 2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.648+1006C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116387 | |||||||
chr2:135116402 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.648+1021T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116402 | |||||||
chr2:135116468 | C | T | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.648+1087C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116468 | |||||||
chr2:135116470 | G | T | 1 | a0007c0014t0002g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.648+1089G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116470 | |||||||
chr2:135116656 | A | G | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.648+1275A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116656 | |||||||
chr2:135117036 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1655T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117036 | |||||||
chr2:135117052 | A | G | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.648+1671A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117052 | |||||||
chr2:135117057 | G | C | 5 | a0001c0001t0003g0234 a0001c0001t0003g0240 a0001c0001t0003g0242 others(2): Show |
5 | HG01175.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+1676G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117057 | |||||||
chr2:135117195 | G | A | 4 | a0001c0001t0003g0245 a0001c0001t0003g0276 a0001c0001t0003g0277 others(1): Show |
4 | HG00639.hp1 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+1814G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117195 | |||||||
chr2:135117409 | T | TTCTTCTT others(13): Show |
1 | a0001c0001t0006g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.648+2029_648+2030i others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTC | 14 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0071 others(11): Show |
14 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+2072_648+2074d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTC | 26 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0050 others(23): Show |
27 | HG00609.hp2 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.648+2069_648+2074d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(2): Show |
26 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0046 others(23): Show |
26 | HG00621.hp2 HG01243.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.648+2066_648+2074d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(5): Show |
31 | a0001c0001t0001g0032 a0001c0001t0001g0110 a0001c0001t0001g0218 others(28): Show |
31 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.648+2063_648+2074d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(8): Show |
27 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0052 others(24): Show |
27 | HG00438.hp2 HG00558.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.648+2060_648+2074d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(11): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0214 others(10): Show |
13 | HG00423.hp1 HG00735.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.648+2057_648+2074d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(14): Show |
12 | a0001c0001t0001g0041 a0001c0001t0001g0054 a0001c0001t0001g0102 others(9): Show |
12 | HG01255.hp1 HG01261.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.648+2054_648+2074d others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | T | TTTCTTCT others(20): Show |
1 | a0001c0001t0003g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.648+2048_648+2074d others(29): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117409 | TTTC | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0098 others(2): Show |
5 | HG02809.hp1 HG02886.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+2072_648+2074d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | ||||||
chr2:135117432 | TCTTCTTC others(17): Show |
T | 1 | a0001c0001t0010g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.648+2057_648+2080d others(26): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117432 | ||||||
chr2:135117435 | TCTTCTTC others(14): Show |
T | 4 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0149 others(1): Show |
4 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2060_648+2080d others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117435 | ||||||
chr2:135117438 | TCTTCTTC others(11): Show |
T | 4 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0022g0175 others(1): Show |
4 | HG03688.hp2 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2063_648+2080d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117438 | ||||||
chr2:135117441 | TCTTCTTC others(8): Show |
T | 58 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(55): Show |
58 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(55): Show |
intron_variant | MODIFIER | c.648+2066_648+2080d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117441 | ||||||
chr2:135117444 | TCTTCTTC others(5): Show |
T | 9 | a0001c0001t0002g0143 a0001c0001t0002g0148 a0001c0001t0002g0155 others(6): Show |
9 | HG01978.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.648+2069_648+2080d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117444 | ||||||
chr2:135117450 | T | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0002g0189 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2069T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117450 | |||||||
chr2:135117450 | T | TCTTCTTC others(11): Show |
1 | a0002c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.648+2074_648+2075i others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117450 | ||||||
chr2:135117450 | TCTTCTG | T | 3 | a0001c0001t0002g0158 a0001c0001t0003g0277 a0001c0004t0013g0246 |
3 | HG02818.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.648+2093_648+2098d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117450 | ||||||
chr2:135117456 | G | T | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0056 others(39): Show |
42 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.648+2075G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117456 | |||||||
chr2:135117462 | G | T | 37 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0229 others(34): Show |
37 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.648+2081G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117462 | |||||||
chr2:135117468 | G | T | 2 | a0001c0001t0003g0231 a0001c0001t0017g0224 |
2 | HG00621.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.648+2087G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117468 | |||||||
chr2:135117474 | G | T | 5 | a0001c0001t0003g0231 a0001c0001t0017g0224 a0004c0005t0011g0221 others(2): Show |
5 | HG00621.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+2093G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117474 | |||||||
chr2:135117477 | T | G | 3 | a0004c0005t0011g0221 a0004c0005t0011g0222 a0004c0005t0025g0220 |
3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.648+2096T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117477 | |||||||
chr2:135117483 | G | T | 7 | a0001c0001t0001g0056 a0001c0001t0002g0189 a0001c0001t0002g0190 others(4): Show |
7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.648+2102G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117483 | |||||||
chr2:135117486 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02896.hp1 HG02897.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.648+2105T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117486 | |||||||
chr2:135117489 | T | G | 3 | a0004c0005t0011g0221 a0004c0005t0011g0222 a0004c0005t0025g0220 |
3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.648+2108T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117489 | |||||||
chr2:135117492 | T | G | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.648+2111T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117492 | |||||||
chr2:135117495 | G | T | 7 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0003g0231 others(4): Show |
7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.648+2114G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117495 | |||||||
chr2:135117495 | GCTT | G | 17 | a0001c0001t0002g0158 a0001c0001t0002g0187 a0001c0001t0005g0007 others(14): Show |
17 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.648+2129_648+2131d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117495 | ||||||
chr2:135117504 | T | G | 6 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0002c0002t0001g0129 others(3): Show |
6 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+2123T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117504 | |||||||
chr2:135117504 | T | TCTTCTTC others(23): Show |
1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.648+2137_648+2138i others(32): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117504 | ||||||
chr2:135117510 | T | G | 22 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(19): Show |
22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2129T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117510 | |||||||
chr2:135117513 | G | T | 23 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(20): Show |
23 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.648+2132G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117513 | |||||||
chr2:135117519 | T | G | 22 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(19): Show |
22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2138T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117519 | |||||||
chr2:135117522 | G | GCTT | 10 | a0001c0001t0003g0231 a0001c0001t0003g0245 a0001c0001t0003g0276 others(7): Show |
10 | HG00621.hp1 HG00639.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+2147_648+2149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117522 | ||||||
chr2:135117522 | G | T | 22 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(19): Show |
22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2141G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117522 | |||||||
chr2:135117522 | GCTT | G | 11 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(8): Show |
11 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.648+2147_648+2149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117522 | ||||||
chr2:135117531 | G | T | 3 | a0001c0001t0002g0185 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2150G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117531 | |||||||
chr2:135117531 | GCTTCTTC others(8): Show |
G | 2 | a0001c0001t0002g0161 a0001c0001t0002g0199 |
2 | HG04228.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.648+2174_648+2188d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117531 | ||||||
chr2:135117534 | T | G | 3 | a0001c0001t0002g0185 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2153T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117534 | |||||||
chr2:135117543 | G | T | 3 | a0001c0001t0002g0185 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2162G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117543 | |||||||
chr2:135117543 | GCTT | G | 75 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(72): Show |
75 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.648+2174_648+2176d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117543 | ||||||
chr2:135117546 | T | G | 35 | a0001c0001t0002g0185 a0001c0001t0002g0189 a0001c0001t0002g0190 others(32): Show |
35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.648+2165T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117546 | |||||||
chr2:135117546 | T | TCTTCTTC others(5): Show |
4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2173_648+2174i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | ||||||
chr2:135117546 | T | TCTTCTTC others(5): Show |
5 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0012g0252 others(2): Show |
5 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+2204_648+2215d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | ||||||
chr2:135117546 | TCTTCTTC others(5): Show |
T | 10 | a0001c0001t0001g0040 a0002c0002t0001g0033 a0002c0002t0001g0075 others(7): Show |
10 | HG01175.hp1 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+2204_648+2215d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | ||||||
chr2:135117555 | T | G | 5 | a0001c0001t0002g0247 a0001c0004t0013g0246 a0001c0004t0013g0256 others(2): Show |
5 | HG01243.hp1 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+2174T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117555 | |||||||
chr2:135117561 | T | TCTTCTTC others(2): Show |
4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2189_648+2197d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117561 | ||||||
chr2:135117573 | TCTTCTTC others(2): Show |
T | 3 | a0001c0001t0002g0144 a0001c0001t0002g0148 a0001c0001t0002g0185 |
3 | HG03834.hp2 NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.648+2201_648+2209d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117573 | ||||||
chr2:135117579 | T | G | 36 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0143 others(33): Show |
36 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.648+2198T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117579 | |||||||
chr2:135117579 | T | TCTG | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2201_648+2203d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117579 | ||||||
chr2:135117582 | G | GCTT | 68 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(65): Show |
68 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.648+2210_648+2212d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | ||||||
chr2:135117582 | G | GCTTCTTC others(5): Show |
2 | a0001c0001t0002g0139 a0001c0001t0002g0174 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.648+2209_648+2210i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | ||||||
chr2:135117582 | G | GCTTCTTC others(8): Show |
27 | a0001c0001t0002g0247 a0001c0001t0004g0258 a0001c0001t0004g0259 others(24): Show |
27 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.648+2215_648+2216i others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | ||||||
chr2:135117582 | G | T | 36 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0143 others(33): Show |
36 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.648+2201G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117582 | |||||||
chr2:135117594 | G | GCTTCTTC others(47): Show |
1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2215_648+2216i others(56): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117594 | ||||||
chr2:135117603 | T | G | 1 | a0001c0001t0010g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.648+2222T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117603 | |||||||
chr2:135117606 | G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2225G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117606 | |||||||
chr2:135117609 | T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2228T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117609 | |||||||
chr2:135117639 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.648+2258T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117639 | |||||||
chr2:135117639 | T | TCTTCTTC others(8): Show |
1 | a0002c0002t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.648+2297_648+2311d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117639 | ||||||
chr2:135117645 | T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2264T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117645 | |||||||
chr2:135117648 | G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2267G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117648 | |||||||
chr2:135117654 | G | T | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.648+2273G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117654 | |||||||
chr2:135117657 | T | TCTGCTTC others(5): Show |
13 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.648+2278_648+2279i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117657 | ||||||
chr2:135117660 | T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2279T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117660 | |||||||
chr2:135117663 | G | GCTT | 13 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.648+2285_648+2287d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | ||||||
chr2:135117663 | G | GCTTCTGC others(2): Show |
30 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(27): Show |
30 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+2294_648+2302d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | ||||||
chr2:135117663 | G | GCTTCTGC others(11): Show |
4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2285_648+2302d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | ||||||
chr2:135117663 | G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2282G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117663 | |||||||
chr2:135117681 | TCTG | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2303_648+2305d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117681 | ||||||
chr2:135117684 | G | T | 3 | a0001c0001t0003g0276 a0001c0001t0003g0279 a0003c0006t0002g0248 |
3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2303G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117684 | |||||||
chr2:135117687 | T | G | 3 | a0001c0001t0003g0276 a0001c0001t0003g0279 a0003c0006t0002g0248 |
3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2306T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117687 | |||||||
chr2:135117690 | T | G | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2309T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117690 | |||||||
chr2:135117693 | T | G | 3 | a0001c0001t0003g0276 a0001c0001t0003g0279 a0003c0006t0002g0248 |
3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2312T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117693 | |||||||
chr2:135117696 | G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2315G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117696 | |||||||
chr2:135117702 | TCTG | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2324_648+2326d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117702 | ||||||
chr2:135117711 | G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2330G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117711 | |||||||
chr2:135117714 | T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2333T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117714 | |||||||
chr2:135117720 | T | G | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2339T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117720 | |||||||
chr2:135117723 | G | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2342G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117723 | |||||||
chr2:135117726 | T | G | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2345T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117726 | |||||||
chr2:135117729 | T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2348T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117729 | |||||||
chr2:135117738 | GCTT | G | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2366_648+2368d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117738 | ||||||
chr2:135117784 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.648+2403C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117784 | |||||||
chr2:135117786 | G | T | 3 | a0001c0001t0004g0266 a0002c0002t0001g0001 a0002c0002t0001g0134 |
4 | HG03540.hp2 NA18952.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2405G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117786 | |||||||
chr2:135117789 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.648+2408T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117789 | |||||||
chr2:135117793 | C | CTTCTTCT others(19): Show |
4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2427_648+2452d others(28): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117793 | ||||||
chr2:135117795 | T | C | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648+2414T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117795 | |||||||
chr2:135117799 | CTTCTTCT others(3): Show |
C | 2 | a0001c0004t0013g0257 a0001c0004t0026g0255 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.648+2440_648+2449d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117799 | ||||||
chr2:135117800 | TTCTTCTT others(15): Show |
T | 1 | a0001c0001t0004g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.648+2421_648+2442d others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117800 | ||||||
chr2:135117803 | TTCTTCTT others(12): Show |
T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.648+2424_648+2442d others(21): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117803 | ||||||
chr2:135117809 | TTTCTTCT others(6): Show |
T | 36 | a0001c0001t0002g0185 a0001c0001t0002g0188 a0001c0001t0002g0247 others(33): Show |
36 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.648+2466_648+2478d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117809 | ||||||
chr2:135117832 | T | TTTC | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2463_648+2465d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117832 | ||||||
chr2:135118044 | G | T | 1 | a0005c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.648+2663G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118044 | |||||||
chr2:135118088 | C | T | 1 | a0001c0001t0012g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648+2707C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118088 | |||||||
chr2:135118278 | TA | T | 16 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(13): Show |
16 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-2531delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135118278 | ||||||
chr2:135118304 | A | G | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-2515A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118304 | |||||||
chr2:135118353 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.649-2466T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118353 | |||||||
chr2:135118413 | C | G | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.649-2406C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118413 | |||||||
chr2:135118550 | T | A | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-2269T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118550 | |||||||
chr2:135118621 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.649-2198T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118621 | |||||||
chr2:135118738 | C | T | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.649-2081C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118738 | |||||||
chr2:135118888 | T | TC | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-1928dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135118888 | ||||||
chr2:135119047 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649-1772T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119047 | |||||||
chr2:135119070 | T | TCCTC | 25 | a0001c0001t0001g0110 a0001c0001t0003g0225 a0001c0001t0003g0227 others(22): Show |
25 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-1725_649-1722d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | ||||||
chr2:135119070 | TCCTC | T | 101 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(98): Show |
101 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.649-1725_649-1722d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | ||||||
chr2:135119070 | TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0003g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.649-1733_649-1722d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | ||||||
chr2:135119094 | C | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.649-1725C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119094 | |||||||
chr2:135119357 | G | A | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-1462G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119357 | |||||||
chr2:135119419 | T | C | 1 | a0004c0005t0011g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.649-1400T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119419 | |||||||
chr2:135119559 | A | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-1260A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119559 | |||||||
chr2:135119563 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-1256G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119563 | |||||||
chr2:135119578 | C | CA | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-1237dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119578 | ||||||
chr2:135119992 | A | G | 224 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0078 others(221): Show |
225 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.649-827A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119992 | |||||||
chr2:135120126 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-693C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120126 | |||||||
chr2:135120504 | G | A | 2 | a0004c0005t0011g0221 a0004c0005t0011g0222 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.649-315G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120504 | |||||||
chr2:135120682 | T | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-137T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120682 | |||||||
chr2:135120703 | TC | T | 5 | a0002c0002t0001g0001 a0002c0002t0001g0090 a0002c0002t0001g0118 others(2): Show |
6 | HG00609.hp2 NA18942.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.649-114delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135120703 | ||||||
chr2:135120737 | A | G | 1 | a0001c0001t0010g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.649-82A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120737 | |||||||
chr2:135121244 | G | A | 153 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(150): Show |
153 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.748+326G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121244 | |||||||
chr2:135121331 | G | C | 1 | a0001c0001t0015g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.748+413G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121331 | |||||||
chr2:135121450 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.748+532T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121450 | |||||||
chr2:135121647 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0070 a0001c0001t0001g0132 |
3 | HG02074.hp2 HG02129.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.748+729A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121647 | |||||||
chr2:135121682 | C | G | 1 | a0002c0002t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.748+764C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121682 | |||||||
chr2:135121688 | C | T | 2 | a0002c0002t0001g0075 a0002c0002t0001g0100 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.748+770C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121688 | |||||||
chr2:135121908 | C | T | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.748+990C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121908 | |||||||
chr2:135121912 | GT | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+995delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121912 | |||||||
chr2:135122049 | C | T | 3 | a0001c0007t0002g0018 a0001c0007t0002g0019 a0001c0007t0002g0020 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.748+1131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122049 | |||||||
chr2:135122083 | A | G | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.748+1165A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122083 | |||||||
chr2:135122092 | C | CA | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.748+1184dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 135122092 | ||||||
chr2:135122379 | TC | T | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.748+1463delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 135122379 | ||||||
chr2:135122443 | G | A | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.748+1525G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122443 | |||||||
chr2:135122495 | A | G | 9 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.748+1577A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122495 | |||||||
chr2:135122611 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.749-1554G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122611 | |||||||
chr2:135122917 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-1248T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122917 | |||||||
chr2:135123114 | T | C | 1 | a0001c0001t0007g0152 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.749-1051T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123114 | |||||||
chr2:135123433 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.749-732T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123433 | |||||||
chr2:135123624 | C | A | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-541C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123624 | |||||||
chr2:135123907 | A | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-258A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123907 | |||||||
chr2:135124086 | T | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.749-79T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135124086 | |||||||
chr2:135124382 | C | T | 2 | a0002c0002t0001g0075 a0002c0002t0001g0100 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.830+136C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124382 | |||||||
chr2:135124418 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.830+172C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124418 | |||||||
chr2:135124519 | A | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.830+273A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124519 | |||||||
chr2:135124589 | C | T | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.830+343C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124589 | |||||||
chr2:135124774 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.830+528A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124774 | |||||||
chr2:135124821 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.830+575T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124821 | |||||||
chr2:135124922 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.830+676G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124922 | |||||||
chr2:135125136 | C | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0193 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.830+890C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125136 | |||||||
chr2:135125383 | T | C | 19 | a0001c0001t0002g0178 a0001c0001t0003g0277 a0001c0001t0003g0279 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.831-798T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125383 | |||||||
chr2:135125898 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-283G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125898 | |||||||
chr2:135125976 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.831-205A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125976 | |||||||
chr2:135126855 | T | C | 1 | a0002c0002t0001g0091 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.973+199T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135126855 | |||||||
chr2:135126917 | G | C | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.973+261G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135126917 | |||||||
chr2:135127088 | G | T | 1 | a0002c0002t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.973+432G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127088 | |||||||
chr2:135127090 | T | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+434T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127090 | |||||||
chr2:135127111 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.973+455G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127111 | |||||||
chr2:135127130 | C | A | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.973+474C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127130 | |||||||
chr2:135127149 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.973+493A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127149 | |||||||
chr2:135127187 | CT | C | 10 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0002g0144 others(7): Show |
10 | HG01192.hp1 HG02293.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+547delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127187 | ||||||
chr2:135127329 | T | TTTTG | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+701_973+704dup others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127329 | ||||||
chr2:135127329 | TTTTG | T | 9 | a0001c0001t0002g0178 a0001c0001t0003g0233 a0001c0001t0004g0268 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.973+701_973+704del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127329 | ||||||
chr2:135127422 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.973+766T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127422 | |||||||
chr2:135127468 | G | T | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0023g0201 |
3 | HG03942.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.973+812G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127468 | |||||||
chr2:135127584 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.973+928C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127584 | |||||||
chr2:135127628 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.973+972C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127628 | |||||||
chr2:135127787 | C | T | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.973+1131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127787 | |||||||
chr2:135127873 | T | A | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.973+1217T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127873 | |||||||
chr2:135127881 | A | G | 5 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0241 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+1225A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127881 | |||||||
chr2:135128013 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.973+1357A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128013 | |||||||
chr2:135128374 | A | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.974-1621A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128374 | |||||||
chr2:135128388 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.974-1607T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128388 | |||||||
chr2:135128494 | C | T | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1501C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128494 | |||||||
chr2:135128627 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.974-1368A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128627 | |||||||
chr2:135128814 | T | G | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.974-1181T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128814 | |||||||
chr2:135128819 | G | C | 1 | a0001c0001t0002g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.974-1176G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128819 | |||||||
chr2:135128839 | C | T | 8 | a0001c0001t0003g0225 a0001c0001t0003g0244 a0001c0001t0003g0275 others(5): Show |
8 | HG00558.hp1 HG00621.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-1156C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128839 | |||||||
chr2:135128893 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.974-1102A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128893 | |||||||
chr2:135128916 | C | T | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-1079C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128916 | |||||||
chr2:135128941 | G | A | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1054G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128941 | |||||||
chr2:135129131 | G | A | 8 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(5): Show |
8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-864G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129131 | |||||||
chr2:135129174 | C | T | 57 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(54): Show |
57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.974-821C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129174 | |||||||
chr2:135129175 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.974-820G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129175 | |||||||
chr2:135129178 | C | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0115 |
2 | NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.974-817C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129178 | |||||||
chr2:135129279 | C | T | 15 | a0001c0001t0002g0145 a0001c0001t0005g0007 a0001c0001t0005g0008 others(12): Show |
15 | HG00280.hp1 HG00741.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-716C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129279 | |||||||
chr2:135129302 | A | G | 1 | a0002c0002t0001g0091 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.974-693A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129302 | |||||||
chr2:135129363 | A | G | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.974-632A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129363 | |||||||
chr2:135129460 | A | T | 14 | a0001c0001t0002g0216 a0001c0001t0005g0007 a0001c0001t0005g0008 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-535A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129460 | |||||||
chr2:135129487 | T | C | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.974-508T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129487 | |||||||
chr2:135129496 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.974-499C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129496 | |||||||
chr2:135129497 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0054 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.974-498G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129497 | |||||||
chr2:135129635 | G | A | 2 | a0001c0001t0003g0276 a0002c0002t0002g0021 |
2 | HG00639.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.974-360G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129635 | |||||||
chr2:135129729 | A | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0193 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.974-266A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129729 | |||||||
chr2:135129813 | A | C | 2 | a0001c0004t0013g0257 a0001c0004t0026g0255 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.974-182A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129813 | |||||||
chr2:135129944 | AT | A | 22 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0241 others(19): Show |
22 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.974-38delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135129944 | ||||||
chr2:135130198 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066+111C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130198 | |||||||
chr2:135130323 | T | C | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1067-229T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130323 | |||||||
chr2:135130447 | G | C | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1067-105G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130447 | |||||||
chr2:135130508 | G | T | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1067-44G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130508 | |||||||
chr2:135130753 | A | G | 3 | a0001c0007t0002g0018 a0001c0007t0002g0019 a0001c0007t0002g0020 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1236+32A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135130753 | |||||||
chr2:135130978 | G | C | 1 | a0002c0002t0024g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1236+257G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135130978 | |||||||
chr2:135131064 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1236+343C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131064 | |||||||
chr2:135131257 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+536C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131257 | |||||||
chr2:135131479 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1236+758C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131479 | |||||||
chr2:135131859 | A | C | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1237-1036A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131859 | |||||||
chr2:135131873 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1237-1022A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131873 | |||||||
chr2:135132142 | G | T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1237-753G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132142 | |||||||
chr2:135132232 | A | G | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1237-663A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132232 | |||||||
chr2:135132311 | C | T | 3 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0072 |
3 | HG01243.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1237-584C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132311 | |||||||
chr2:135132416 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1237-479G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132416 | |||||||
chr2:135132467 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1237-428A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132467 | |||||||
chr2:135132540 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1237-355G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132540 | |||||||
chr2:135132651 | T | C | 4 | a0001c0001t0003g0245 a0001c0001t0003g0276 a0001c0001t0003g0277 others(1): Show |
4 | HG00639.hp1 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-244T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132651 | |||||||
chr2:135132810 | TTAAA | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-81_1237-78del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | 135132810 | ||||||
chr2:135133029 | G | A | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1326+45G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133029 | |||||||
chr2:135133038 | G | C | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1326+54G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133038 | |||||||
chr2:135133467 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1327-394G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133467 | |||||||
chr2:135133518 | T | C | 5 | a0001c0001t0003g0277 a0003c0006t0002g0248 a0003c0006t0009g0249 others(2): Show |
5 | HG02258.hp2 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-343T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133518 | |||||||
chr2:135133538 | G | A | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1327-323G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133538 | |||||||
chr2:135133711 | T | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1327-150T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133711 | |||||||
chr2:135133734 | T | A | 2 | a0001c0001t0004g0258 a0001c0001t0004g0261 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1327-127T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133734 | |||||||
chr2:135133790 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-71C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133790 | |||||||
chr2:135134739 | C | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | NA18990.hp1 NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1500-526C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135134739 | |||||||
chr2:135135115 | C | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-150C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135135115 | |||||||
chr2:135135190 | T | C | 1 | a0001c0001t0003g0275 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1500-75T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135135190 | |||||||
chr2:135135433 | T | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554+114T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 16/23 | chr2 | 135135433 | |||||||
chr2:135135490 | A | G | 1 | a0002c0002t0001g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1555-74A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 16/23 | chr2 | 135135490 | |||||||
chr2:135136001 | T | C | 4 | a0002c0002t0001g0092 a0002c0002t0001g0101 a0002c0002t0001g0217 others(1): Show |
4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+69T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136001 | |||||||
chr2:135136023 | T | G | 1 | a0001c0001t0002g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1923+91T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136023 | |||||||
chr2:135136105 | C | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1923+173C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136105 | |||||||
chr2:135136132 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1923+200T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136132 | |||||||
chr2:135136283 | A | G | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+351A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136283 | |||||||
chr2:135136311 | G | A | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1923+379G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136311 | |||||||
chr2:135136636 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1923+704T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136636 | |||||||
chr2:135136707 | C | G | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1923+775C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136707 | |||||||
chr2:135136848 | A | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1923+916A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136848 | |||||||
chr2:135136910 | A | G | 1 | a0002c0002t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1923+978A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136910 | |||||||
chr2:135136983 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1923+1051G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136983 | |||||||
chr2:135137096 | A | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1164A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137096 | |||||||
chr2:135137191 | T | G | 14 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1923+1259T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137191 | |||||||
chr2:135137267 | A | G | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1335A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137267 | |||||||
chr2:135137288 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1923+1356G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137288 | |||||||
chr2:135137309 | G | T | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1377G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137309 | |||||||
chr2:135137373 | A | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0200 |
2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1923+1441A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137373 | |||||||
chr2:135137515 | T | G | 4 | a0002c0002t0001g0088 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+1583T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137515 | |||||||
chr2:135137720 | T | C | 1 | a0001c0001t0021g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1923+1788T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137720 | |||||||
chr2:135137824 | T | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+1892T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137824 | |||||||
chr2:135137829 | T | G | 1 | a0002c0002t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1923+1897T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137829 | |||||||
chr2:135138003 | T | G | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1923+2071T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138003 | |||||||
chr2:135138239 | A | G | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.1923+2307A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138239 | |||||||
chr2:135138277 | C | G | 1 | a0002c0002t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1923+2345C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138277 | |||||||
chr2:135138281 | C | A | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1923+2349C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138281 | |||||||
chr2:135138281 | C | CA | 41 | a0001c0001t0001g0054 a0001c0001t0002g0160 a0001c0001t0002g0165 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923+2368dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135138281 | ||||||
chr2:135138281 | CA | C | 18 | a0001c0001t0002g0163 a0001c0001t0002g0247 a0001c0001t0005g0007 others(15): Show |
18 | HG00280.hp1 HG00423.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1923+2368delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135138281 | ||||||
chr2:135138300 | A | T | 2 | a0002c0002t0001g0047 a0002c0002t0001g0122 |
2 | HG00423.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1923+2368A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138300 | |||||||
chr2:135138309 | C | G | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+2377C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138309 | |||||||
chr2:135138318 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1923+2386C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138318 | |||||||
chr2:135138371 | G | C | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1923+2439G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138371 | |||||||
chr2:135138833 | T | A | 4 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | NA18942.hp1 NA18955.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+2901T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138833 | |||||||
chr2:135139072 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+3140C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139072 | |||||||
chr2:135139101 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1923+3169C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139101 | |||||||
chr2:135139415 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+3483G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139415 | |||||||
chr2:135139556 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0191 |
2 | HG03453.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1923+3624A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139556 | |||||||
chr2:135139562 | T | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0210 |
2 | NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1923+3630T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139562 | |||||||
chr2:135139709 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1923+3777T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139709 | |||||||
chr2:135139997 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+4065C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139997 | |||||||
chr2:135140065 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1923+4133G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140065 | |||||||
chr2:135140186 | A | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+4254A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140186 | |||||||
chr2:135140276 | CTA | C | 4 | a0002c0002t0001g0092 a0002c0002t0001g0101 a0002c0002t0001g0217 others(1): Show |
4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+4348_1923+434 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135140276 | ||||||
chr2:135140453 | C | T | 41 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(38): Show |
41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923+4521C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140453 | |||||||
chr2:135140504 | A | G | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1923+4572A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140504 | |||||||
chr2:135140817 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1923+4885G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140817 | |||||||
chr2:135141222 | T | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1923+5290T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141222 | |||||||
chr2:135141224 | A | ACTT | 35 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(32): Show |
35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1923+5296_1923+529 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141224 | ||||||
chr2:135141228 | C | CTTCT | 5 | a0001c0001t0002g0247 a0003c0006t0002g0248 a0003c0006t0009g0249 others(2): Show |
5 | HG01243.hp1 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1923+5298_1923+529 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141228 | ||||||
chr2:135141228 | C | CTTCTT | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1923+5298_1923+529 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141228 | ||||||
chr2:135141451 | C | G | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923+5519C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141451 | |||||||
chr2:135141499 | T | C | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+5567T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141499 | |||||||
chr2:135141772 | G | A | 1 | a0007c0014t0002g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1923+5840G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141772 | |||||||
chr2:135141849 | A | G | 2 | a0002c0002t0001g0094 a0002c0002t0001g0103 |
2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1923+5917A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141849 | |||||||
chr2:135141874 | CTATTTCT others(46): Show |
C | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1923+5945_1923+599 others(57): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141874 | ||||||
chr2:135142082 | T | C | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1923+6150T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142082 | |||||||
chr2:135142099 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1923+6167G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142099 | |||||||
chr2:135142153 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1923+6221T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142153 | |||||||
chr2:135142297 | T | C | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+6365T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142297 | |||||||
chr2:135142427 | ATTT | A | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1923+6496_1923+649 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142427 | |||||||
chr2:135142642 | C | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1923+6710C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142642 | |||||||
chr2:135142648 | A | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+6716A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142648 | |||||||
chr2:135142959 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1923+7027G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142959 | |||||||
chr2:135142969 | C | T | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923+7037C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142969 | |||||||
chr2:135143534 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1924-6835A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143534 | |||||||
chr2:135143550 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1924-6819A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143550 | |||||||
chr2:135143556 | C | CT | 44 | a0001c0001t0001g0042 a0001c0001t0003g0225 a0001c0001t0003g0227 others(41): Show |
44 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1924-6794dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135143556 | ||||||
chr2:135143556 | CT | C | 5 | a0001c0001t0002g0144 a0001c0001t0005g0014 a0001c0001t0012g0254 others(2): Show |
5 | HG01070.hp2 HG01993.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-6794delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135143556 | ||||||
chr2:135143580 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1924-6789C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143580 | |||||||
chr2:135143593 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-6776T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143593 | |||||||
chr2:135143800 | C | T | 14 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-6569C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143800 | |||||||
chr2:135144094 | C | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1924-6275C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144094 | |||||||
chr2:135144176 | C | G | 8 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(5): Show |
8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1924-6193C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144176 | |||||||
chr2:135144186 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1924-6183C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144186 | |||||||
chr2:135144222 | C | T | 10 | a0001c0001t0003g0234 a0001c0001t0003g0236 a0001c0001t0003g0237 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1924-6147C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144222 | |||||||
chr2:135144331 | TTTC | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-6036_1924-603 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135144331 | ||||||
chr2:135144457 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1924-5912G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144457 | |||||||
chr2:135144602 | C | A | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-5767C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144602 | |||||||
chr2:135144650 | C | T | 55 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-5719C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144650 | |||||||
chr2:135144671 | T | G | 1 | a0002c0002t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1924-5698T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144671 | |||||||
chr2:135144843 | G | A | 3 | a0003c0006t0009g0249 a0003c0006t0009g0250 a0003c0006t0009g0251 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1924-5526G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144843 | |||||||
chr2:135145301 | C | T | 1 | a0001c0001t0010g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1924-5068C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145301 | |||||||
chr2:135145360 | A | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-5009A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145360 | |||||||
chr2:135145399 | T | TAC | 5 | a0001c0001t0001g0110 a0001c0001t0003g0242 a0001c0001t0012g0252 others(2): Show |
5 | HG01175.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-4947_1924-494 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | ||||||
chr2:135145399 | TAC | T | 98 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(95): Show |
98 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.1924-4947_1924-494 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | ||||||
chr2:135145399 | TACAC | T | 16 | a0001c0001t0002g0178 a0001c0001t0002g0187 a0001c0001t0002g0191 others(13): Show |
16 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1924-4949_1924-494 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | ||||||
chr2:135145399 | TACACACA others(3): Show |
T | 2 | a0001c0001t0015g0272 a0001c0001t0015g0273 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1924-4955_1924-494 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | ||||||
chr2:135145469 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1924-4900C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145469 | |||||||
chr2:135146199 | C | CT | 91 | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0157 others(88): Show |
91 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1924-4147dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | ||||||
chr2:135146199 | C | CTT | 8 | a0001c0001t0001g0042 a0001c0001t0005g0015 a0001c0001t0012g0252 others(5): Show |
8 | HG02258.hp2 HG02293.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1924-4148_1924-414 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | ||||||
chr2:135146199 | CT | C | 5 | a0001c0001t0002g0146 a0001c0001t0002g0163 a0001c0001t0002g0247 others(2): Show |
5 | HG01243.hp1 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924-4147delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | ||||||
chr2:135146199 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1924-4158_1924-414 others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | ||||||
chr2:135146216 | T | C | 3 | a0001c0004t0013g0256 a0001c0004t0013g0257 a0001c0004t0026g0255 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1924-4153T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146216 | |||||||
chr2:135146302 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1924-4067G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146302 | |||||||
chr2:135146632 | C | T | 4 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
4 | NA18952.hp2 NA18966.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-3737C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146632 | |||||||
chr2:135146713 | A | G | 1 | a0002c0002t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1924-3656A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146713 | |||||||
chr2:135146810 | A | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0200 |
2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1924-3559A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146810 | |||||||
chr2:135146854 | A | AAC | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-3514_1924-351 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146854 | ||||||
chr2:135146939 | T | G | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1924-3430T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146939 | |||||||
chr2:135146971 | A | AAC | 93 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0046 others(90): Show |
93 | HG00438.hp1 HG00621.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.1924-3371_1924-337 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | ||||||
chr2:135146971 | A | AACAC | 13 | a0001c0001t0002g0196 a0001c0001t0002g0207 a0001c0004t0013g0246 others(10): Show |
13 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.1924-3373_1924-337 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | ||||||
chr2:135146971 | A | AACACAC | 4 | a0001c0001t0002g0159 a0001c0001t0012g0252 a0001c0001t0012g0253 others(1): Show |
4 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-3375_1924-337 others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | ||||||
chr2:135146971 | AAC | A | 40 | a0001c0001t0001g0080 a0001c0001t0002g0158 a0001c0001t0002g0247 others(37): Show |
40 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1924-3371_1924-337 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | ||||||
chr2:135147089 | T | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-3280T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147089 | |||||||
chr2:135147098 | C | T | 8 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1924-3271C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147098 | |||||||
chr2:135147301 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-3068G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147301 | |||||||
chr2:135147345 | C | CA | 6 | a0001c0001t0001g0052 a0001c0001t0002g0155 a0001c0001t0002g0186 others(3): Show |
6 | HG00621.hp2 HG01978.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1924-3008dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147345 | ||||||
chr2:135147426 | T | C | 2 | a0001c0001t0003g0277 a0001c0001t0003g0279 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1924-2943T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147426 | |||||||
chr2:135147615 | T | TC | 22 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0140 others(19): Show |
22 | HG01346.hp2 HG01981.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1924-2745dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | ||||||
chr2:135147615 | T | TCC | 37 | a0001c0001t0002g0141 a0001c0001t0002g0144 a0001c0001t0002g0145 others(34): Show |
37 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1924-2746_1924-274 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | ||||||
chr2:135147615 | T | TCCC | 16 | a0001c0001t0002g0139 a0001c0001t0002g0142 a0001c0001t0002g0149 others(13): Show |
16 | HG01192.hp1 HG01928.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1924-2747_1924-274 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | ||||||
chr2:135147623 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-2746C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147623 | |||||||
chr2:135147624 | C | CT | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-2735dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147624 | ||||||
chr2:135147625 | T | C | 3 | a0001c0001t0002g0148 a0001c0001t0002g0193 a0001c0001t0004g0262 |
3 | HG03225.hp1 NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1924-2744T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147625 | |||||||
chr2:135147786 | A | C | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1924-2583A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147786 | |||||||
chr2:135147993 | C | CCT | 269 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(266): Show |
270 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.1924-2372_1924-237 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147993 | ||||||
chr2:135148341 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0174 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1924-2028C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148341 | |||||||
chr2:135148379 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-1990C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148379 | |||||||
chr2:135148491 | CT | C | 144 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(141): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1924-1857delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148491 | ||||||
chr2:135148491 | CTT | C | 55 | a0001c0001t0001g0052 a0001c0001t0002g0181 a0001c0001t0002g0183 others(52): Show |
55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-1858_1924-185 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148491 | ||||||
chr2:135148668 | C | CT | 31 | a0001c0001t0003g0229 a0001c0001t0003g0234 a0001c0001t0003g0236 others(28): Show |
31 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1924-1679dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | ||||||
chr2:135148668 | CT | C | 11 | a0001c0001t0002g0162 a0001c0001t0002g0174 a0001c0001t0002g0181 others(8): Show |
11 | HG01070.hp1 HG01256.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1924-1679delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | ||||||
chr2:135148668 | CTT | C | 5 | a0001c0001t0002g0247 a0003c0006t0002g0248 a0004c0005t0011g0219 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-1680_1924-167 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | ||||||
chr2:135148668 | CTTT | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1924-1681_1924-167 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | ||||||
chr2:135148708 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1924-1661C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148708 | |||||||
chr2:135148731 | C | CG | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-1637dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148731 | ||||||
chr2:135148732 | G | A | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1924-1637G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148732 | |||||||
chr2:135149016 | A | G | 6 | a0001c0001t0002g0167 a0001c0001t0002g0169 a0001c0001t0002g0170 others(3): Show |
6 | HG00438.hp1 HG02040.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1924-1353A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149016 | |||||||
chr2:135149044 | A | G | 1 | a0001c0001t0017g0226 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1924-1325A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149044 | |||||||
chr2:135149122 | T | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-1247T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149122 | |||||||
chr2:135149509 | C | T | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1924-860C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149509 | |||||||
chr2:135149518 | A | G | 263 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(260): Show |
264 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.1924-851A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149518 | |||||||
chr2:135149635 | A | G | 1 | a0001c0001t0007g0151 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1924-734A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149635 | |||||||
chr2:135149661 | A | G | 3 | a0001c0001t0005g0008 a0001c0001t0005g0012 a0001c0001t0005g0013 |
3 | NA19002.hp1 NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1924-708A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149661 | |||||||
chr2:135149869 | G | A | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1924-500G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149869 | |||||||
chr2:135150003 | A | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1924-366A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150003 | |||||||
chr2:135150276 | T | C | 40 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(37): Show |
40 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.1924-93T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150276 | |||||||
chr2:135150308 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1924-61T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150308 | |||||||
chr2:135150654 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2061+148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135150654 | |||||||
chr2:135150775 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2061+269G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135150775 | |||||||
chr2:135151215 | A | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2061+709A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151215 | |||||||
chr2:135151581 | C | T | 3 | a0001c0001t0002g0204 a0001c0001t0002g0211 a0001c0001t0010g0208 |
3 | HG03017.hp2 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2061+1075C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151581 | |||||||
chr2:135151892 | G | A | 154 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(151): Show |
154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.2061+1386G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151892 | |||||||
chr2:135151938 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2061+1432T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151938 | |||||||
chr2:135152077 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061+1571T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152077 | |||||||
chr2:135152337 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-1312C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152337 | |||||||
chr2:135152350 | G | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2062-1299G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152350 | |||||||
chr2:135152748 | T | A | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2062-901T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152748 | |||||||
chr2:135152845 | G | A | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2062-804G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152845 | |||||||
chr2:135152975 | A | G | 1 | a0001c0007t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2062-674A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152975 | |||||||
chr2:135153177 | CTG | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2062-468_2062-467d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr2 | 135153177 | ||||||
chr2:135153192 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2062-457C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135153192 | |||||||
chr2:135154435 | C | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2289+559C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154435 | |||||||
chr2:135154456 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+580A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154456 | |||||||
chr2:135154465 | A | C | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2289+589A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154465 | |||||||
chr2:135154473 | T | TTACTAAG others(3): Show |
16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+600_2289+609d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135154473 | ||||||
chr2:135154549 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2289+673C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154549 | |||||||
chr2:135154685 | A | G | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289+809A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154685 | |||||||
chr2:135154707 | C | G | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+831C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154707 | |||||||
chr2:135155043 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0098 a0001c0001t0001g0106 |
3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2289+1167A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155043 | |||||||
chr2:135155075 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+1199T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155075 | |||||||
chr2:135155389 | T | C | 1 | a0001c0001t0004g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2289+1513T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155389 | |||||||
chr2:135155407 | G | T | 148 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(145): Show |
148 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.2289+1531G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155407 | |||||||
chr2:135155476 | T | A | 5 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0149 others(2): Show |
5 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289+1600T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155476 | |||||||
chr2:135156458 | T | C | 2 | a0001c0001t0010g0176 a0001c0001t0010g0177 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2289+2582T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156458 | |||||||
chr2:135156468 | C | T | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2289+2592C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156468 | |||||||
chr2:135156556 | T | C | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+2680T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156556 | |||||||
chr2:135156582 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2289+2706G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156582 | |||||||
chr2:135156652 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2289+2776A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156652 | |||||||
chr2:135156799 | C | G | 10 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(7): Show |
10 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.2289+2923C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156799 | |||||||
chr2:135157072 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3196C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157072 | |||||||
chr2:135157083 | C | T | 96 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(93): Show |
96 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.2289+3207C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157083 | |||||||
chr2:135157109 | G | A | 3 | a0001c0007t0002g0018 a0001c0007t0002g0019 a0001c0007t0002g0020 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2289+3233G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157109 | |||||||
chr2:135157344 | A | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289+3468A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157344 | |||||||
chr2:135157378 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2289+3502C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157378 | |||||||
chr2:135157431 | C | T | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3555C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157431 | |||||||
chr2:135157620 | T | C | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3744T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157620 | |||||||
chr2:135157788 | T | C | 217 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0098 others(214): Show |
218 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2289+3912T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157788 | |||||||
chr2:135157831 | C | CA | 8 | a0001c0001t0001g0042 a0001c0001t0018g0074 a0002c0002t0001g0075 others(5): Show |
8 | HG01192.hp2 HG02056.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.2289+3973dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | ||||||
chr2:135157831 | CA | C | 136 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(133): Show |
136 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2289+3973delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | ||||||
chr2:135157831 | CAA | C | 10 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(7): Show |
10 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2289+3972_2289+397 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | ||||||
chr2:135157839 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2289+3963A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157839 | |||||||
chr2:135157844 | A | C | 80 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(77): Show |
80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289+3968A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157844 | |||||||
chr2:135157846 | A | AC | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3970_2289+397 others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157846 | |||||||
chr2:135157850 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2289+3974C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157850 | |||||||
chr2:135158187 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289+4311A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158187 | |||||||
chr2:135158207 | C | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2289+4331C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158207 | |||||||
chr2:135158300 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2290-4255G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158300 | |||||||
chr2:135158426 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2290-4129T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158426 | |||||||
chr2:135158597 | A | G | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2290-3958A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158597 | |||||||
chr2:135158642 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2290-3913A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158642 | |||||||
chr2:135158920 | C | T | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2290-3635C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158920 | |||||||
chr2:135158938 | C | G | 1 | a0002c0002t0002g0021 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2290-3617C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158938 | |||||||
chr2:135159053 | C | G | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2290-3502C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159053 | |||||||
chr2:135159316 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2290-3239C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159316 | |||||||
chr2:135159381 | C | T | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2290-3174C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159381 | |||||||
chr2:135159656 | G | T | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2290-2899G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159656 | |||||||
chr2:135159677 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2290-2878G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159677 | |||||||
chr2:135159681 | A | G | 6 | a0001c0001t0002g0139 a0001c0001t0002g0155 a0001c0001t0002g0165 others(3): Show |
6 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2290-2874A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159681 | |||||||
chr2:135159889 | G | C | 9 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290-2666G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159889 | |||||||
chr2:135160327 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2290-2228A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160327 | |||||||
chr2:135160354 | T | C | 4 | a0001c0004t0013g0246 a0001c0004t0013g0256 a0001c0004t0013g0257 others(1): Show |
4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2290-2201T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160354 | |||||||
chr2:135160399 | C | T | 4 | a0004c0005t0011g0219 a0004c0005t0011g0221 a0004c0005t0011g0222 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2290-2156C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160399 | |||||||
chr2:135160530 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2290-2025G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160530 | |||||||
chr2:135160542 | C | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2290-2013C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160542 | |||||||
chr2:135160597 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2290-1958C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160597 | |||||||
chr2:135160674 | C | CA | 16 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0082 others(13): Show |
16 | HG00438.hp2 HG00639.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2290-1855dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | ||||||
chr2:135160674 | CA | C | 45 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0070 others(42): Show |
45 | HG00280.hp1 HG00741.hp2 HG01256.hp2 others(42): Show |
intron_variant | MODIFIER | c.2290-1855delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | ||||||
chr2:135160674 | CAA | C | 66 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(63): Show |
66 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(63): Show |
intron_variant | MODIFIER | c.2290-1856_2290-185 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | ||||||
chr2:135160674 | CAAA | C | 18 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0004g0258 others(15): Show |
18 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2290-1857_2290-185 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | ||||||
chr2:135160732 | A | G | 1 | a0002c0002t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2290-1823A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160732 | |||||||
chr2:135160798 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2290-1757C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160798 | |||||||
chr2:135161111 | A | G | 79 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(76): Show |
79 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.2290-1444A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161111 | |||||||
chr2:135161145 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2290-1410A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161145 | |||||||
chr2:135161320 | T | C | 5 | a0001c0001t0004g0261 a0004c0005t0011g0219 a0004c0005t0011g0221 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2290-1235T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161320 | |||||||
chr2:135161350 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2290-1205A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161350 | |||||||
chr2:135161391 | GA | G | 5 | a0001c0001t0003g0234 a0001c0001t0003g0240 a0001c0001t0003g0242 others(2): Show |
5 | HG01175.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290-1157delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135161391 | ||||||
chr2:135161802 | A | G | 3 | a0001c0001t0005g0010 a0001c0001t0005g0014 a0001c0001t0005g0015 |
3 | HG01358.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2290-753A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161802 | |||||||
chr2:135161891 | A | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0166 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2290-664A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161891 | |||||||
chr2:135161979 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2290-576A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161979 | |||||||
chr2:135162214 | G | A | 7 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0083 others(4): Show |
7 | HG00738.hp1 HG01943.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290-341G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162214 | |||||||
chr2:135162357 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2290-198A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162357 | |||||||
chr2:135162363 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2290-192A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162363 | |||||||
chr2:135162521 | C | T | 33 | a0001c0001t0002g0247 a0001c0001t0003g0225 a0001c0001t0003g0227 others(30): Show |
33 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2290-34C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162521 | |||||||
chr2:135162522 | G | A | 1 | a0001c0001t0010g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2290-33G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162522 | |||||||
chr2:135162538 | C | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2290-17C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162538 | |||||||
chr2:135162953 | C | T | 3 | a0001c0001t0012g0252 a0001c0001t0012g0253 a0001c0001t0012g0254 |
3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2491-33C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/23 | chr2 | 135162953 | |||||||
chr2:135163223 | A | G | 8 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(5): Show |
8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.2606+122A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135163223 | |||||||
chr2:135163704 | G | A | 4 | a0003c0006t0002g0248 a0003c0006t0009g0249 a0003c0006t0009g0250 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2606+603G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135163704 | |||||||
chr2:135164169 | G | A | 1 | a0006c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2607-425G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164169 | |||||||
chr2:135164269 | T | A | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2607-325T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164269 | |||||||
chr2:135164410 | T | A | 1 | a0001c0001t0007g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2607-184T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164410 | |||||||
chr2:135164720 | C | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+24C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135164720 | |||||||
chr2:135165334 | T | G | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2709+638T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165334 | |||||||
chr2:135165375 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+679G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165375 | |||||||
chr2:135165394 | C | T | 4 | a0002c0002t0001g0092 a0002c0002t0001g0101 a0002c0002t0001g0217 others(1): Show |
4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2709+698C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165394 | |||||||
chr2:135165501 | TAAC | T | 28 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2709+809_2709+811d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135165501 | ||||||
chr2:135165577 | T | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+881T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165577 | |||||||
chr2:135165908 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2709+1212G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165908 | |||||||
chr2:135166537 | C | T | 9 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(6): Show |
9 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2709+1841C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166537 | |||||||
chr2:135166555 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2709+1859C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166555 | |||||||
chr2:135166588 | A | G | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2709+1892A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166588 | |||||||
chr2:135166590 | T | G | 1 | a0008c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2709+1894T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166590 | |||||||
chr2:135166735 | A | C | 1 | a0001c0001t0021g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2710-1810A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166735 | |||||||
chr2:135166855 | C | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-1690C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166855 | |||||||
chr2:135166855 | C | T | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2710-1690C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166855 | |||||||
chr2:135166897 | A | G | 58 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(55): Show |
58 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(55): Show |
intron_variant | MODIFIER | c.2710-1648A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166897 | |||||||
chr2:135167217 | A | G | 16 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0260 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2710-1328A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167217 | |||||||
chr2:135167379 | C | CT | 5 | a0001c0001t0002g0212 a0001c0001t0007g0154 a0001c0003t0001g0059 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-1152dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | ||||||
chr2:135167379 | C | CTT | 27 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2710-1153_2710-115 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | ||||||
chr2:135167379 | CT | C | 9 | a0001c0001t0002g0168 a0001c0001t0004g0259 a0001c0001t0004g0260 others(6): Show |
9 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2710-1152delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | ||||||
chr2:135167432 | T | G | 151 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0139 others(148): Show |
151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2710-1113T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167432 | |||||||
chr2:135167841 | C | T | 2 | a0001c0003t0001g0045 a0001c0003t0001g0114 |
2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2710-704C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167841 | |||||||
chr2:135167924 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2710-621T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167924 | |||||||
chr2:135168021 | A | G | 5 | a0001c0001t0003g0225 a0001c0001t0003g0244 a0001c0001t0006g0232 others(2): Show |
5 | HG00558.hp1 HG00621.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-524A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168021 | |||||||
chr2:135168053 | G | A | 24 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0003g0229 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2710-492G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168053 | |||||||
chr2:135168262 | T | G | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2710-283T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168262 | |||||||
chr2:135168426 | C | A | 1 | a0001c0001t0002g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2710-119C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168426 |