Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27342 |
| ensemblid | ENSG00000154710.18 |
| hgncid | 17676 |
| symbol | RABGEF1 |
| name | RAB guanine nucleotide exchange factor 1 |
| refseq_nuc | NM_014504.3 |
| refseq_prot | NP_055319.1 |
| ensembl_nuc | ENST00000284957.9 |
| ensembl_prot | ENSP00000284957.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 66740733 |
| end | 66811464 |
| strand | + |
| ver | v1.2 |
| region | chr7:66740733-66811464 |
| region5000 | chr7:66735733-66816464 |
| regionname0 | RABGEF1_chr7_66740733_66811464 |
| regionname5000 | RABGEF1_chr7_66735733_66816464 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 491 | 398 | 90 | 72 | 184 | 12 | 38 | 140 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | MSLKS others(486): Show |
chr7 | 66735733 | 66816464 |
| a0002 | 0/0 | 491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | MSLKS others(486): Show |
chr7 | 66735733 | 66816464 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1473 | 396 | 90 | 72 | 183 | 12 | 37 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | ATGAG others(1468): Show |
chr7 | 66735733 | 66816464 | ||
| a0001c0003 | 0/0 | 1473 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | ATGAG others(1468): Show |
chr7 | 66735733 | 66816464 | ||
| a0001c0004 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | ATGAG others(1468): Show |
chr7 | 66735733 | 66816464 | ||
| a0002c0002 | 0/0 | 1473 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | ATGAG others(1468): Show |
chr7 | 66735733 | 66816464 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3733 | 186 | 47 | 38 | 72 | 8 | 20 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0002 | 0/0 | 3734 | 56 | 5 | 11 | 35 | 2 | 3 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3729): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0003 | 0/0 | 3733 | 52 | 18 | 6 | 18 | 0 | 10 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0004 | 0/0 | 3733 | 28 | 1 | 5 | 20 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0005 | 0/0 | 3733 | 25 | 0 | 2 | 23 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0006 | 0/0 | 3733 | 21 | 0 | 7 | 13 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0007 | 0/0 | 3733 | 15 | 15 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0008 | 0/1 | 3735 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3730): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0009 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3729): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0010 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3729): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0011 | 0/0 | 3743 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3738): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0012 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0013 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0014 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0015 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0016 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0017 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0018 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0019 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0001t0020 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0003t0001 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0001c0004t0001 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| a0002c0002t0001 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | AGACC others(3728): Show |
chr7 | 66735733 | 66816464 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0008g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0010g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0013g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0015g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0016g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0017g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0018g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0019g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0002c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | GBR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00558 | hp2 | a0001 | c0001 | t0011 | g0074 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0341 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0353 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0185 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0346 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0344 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0371 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0372 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0314 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0318 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0178 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02004 | hp1 | a0001 | c0001 | t0015 | g0113 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02027 | hp2 | a0001 | c0001 | t0019 | g0032 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0260 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02148 | hp2 | a0001 | c0001 | t0014 | g0175 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0345 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0356 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0246 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0373 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0358 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0085 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0303 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0249 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0333 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0374 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0076 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0250 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0245 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0332 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0151 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0124 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0184 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04199 | hp2 | a0001 | c0001 | t0017 | g0295 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0200 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0360 | EAS | CHB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0203 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0251 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0361 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0202 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0297 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0078 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0336 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0098 | REF | REF | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0220 | REF | REF | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66805218 | A | G | 1 | a0002 | 2 | HG02970.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.899A>G | p.Asn300Ser | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/9 | 976/3733 | 899/1476 | 300/491 | chr7 | 66805218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66771941 | A | G | 1 | a0001c0004 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.42A>G | p.Gln14Gln | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/9 | 119/3733 | 42/1476 | 14/491 | chr7 | 66771941 | |||
| chr7:66797390 | C | T | 1 | a0001c0003 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.612C>T | p.Val204Val | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/9 | 689/3733 | 612/1476 | 204/491 | chr7 | 66797390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66809603 | G | A | 1 | a0001c0001t0009 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 319 | chr7 | 66809603 | ||||||
| chr7:66809885 | C | G | 1 | a0001c0001t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*601C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 601 | chr7 | 66809885 | ||||||
| chr7:66809968 | G | A | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(2): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 684 | chr7 | 66809968 | ||||||
| chr7:66810064 | C | T | 1 | a0001c0001t0019 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*780C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 780 | chr7 | 66810064 | ||||||
| chr7:66810279 | A | G | 1 | a0001c0001t0005 | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*995A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 995 | chr7 | 66810279 | ||||||
| chr7:66810628 | C | G | 1 | a0001c0001t0018 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1344 | chr7 | 66810628 | ||||||
| chr7:66810693 | G | C | 1 | a0001c0001t0012 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1409G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1409 | chr7 | 66810693 | ||||||
| chr7:66810748 | A | G | 1 | a0001c0001t0017 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1464A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1464 | chr7 | 66810748 | ||||||
| chr7:66810918 | C | T | 1 | a0001c0001t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1634 | chr7 | 66810918 | ||||||
| chr7:66810999 | A | C | 1 | a0001c0001t0007 | 15 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1715A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1715 | chr7 | 66810999 | ||||||
| chr7:66811077 | A | T | 1 | a0001c0001t0016 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1793A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1793 | chr7 | 66811077 | ||||||
| chr7:66811135 | T | C | 1 | a0001c0001t0013 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1851 | chr7 | 66811135 | ||||||
| chr7:66811155 | C | CT | 3 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 |
58 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1872dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1873 | INFO_REALIGN_3_PRIME | chr7 | 66811155 | |||||
| chr7:66811155 | C | CTTTACAC others(3): Show |
1 | a0001c0001t0011 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1872_*1873insTTAC others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1873 | INFO_REALIGN_3_PRIME | chr7 | 66811155 | |||||
| chr7:66811166 | A | G | 1 | a0001c0001t0004 | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1882A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1882 | chr7 | 66811166 | ||||||
| chr7:66811230 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(10): Show |
190 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1946T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1946 | chr7 | 66811230 | ||||||
| chr7:66811325 | G | C | 3 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2041 | chr7 | 66811325 | ||||||
| chr7:66811334 | C | T | 1 | a0001c0001t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2050C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2050 | chr7 | 66811334 | ||||||
| chr7:66811337 | C | T | 1 | a0001c0001t0015 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2053 | chr7 | 66811337 | ||||||
| chr7:66811341 | C | T | 2 | a0001c0001t0006 a0001c0001t0014 |
22 | HG00408.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2057C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2057 | chr7 | 66811341 | ||||||
| chr7:66811445 | A | G | 1 | a0001c0001t0014 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2161A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2161 | chr7 | 66811445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66740807 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+15G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740807 | |||||||
| chr7:66740835 | A | G | 2 | a0001c0001t0007g0373 a0001c0001t0007g0374 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+43A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740835 | |||||||
| chr7:66740901 | C | G | 2 | a0001c0001t0004g0371 a0001c0001t0004g0372 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+109C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740901 | |||||||
| chr7:66740941 | C | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+149C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740941 | |||||||
| chr7:66740949 | C | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+157C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740949 | |||||||
| chr7:66741005 | T | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0022 |
3 | HG01255.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-18+213T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741005 | |||||||
| chr7:66741077 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+285C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741077 | |||||||
| chr7:66741126 | C | G | 1 | a0001c0001t0001g0337 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18+334C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741126 | |||||||
| chr7:66741130 | C | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+338C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741130 | |||||||
| chr7:66741388 | G | T | 1 | a0001c0001t0001g0335 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+596G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741388 | |||||||
| chr7:66741534 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-18+742C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741534 | |||||||
| chr7:66741543 | C | T | 2 | a0002c0002t0001g0332 a0002c0002t0001g0333 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-18+751C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741543 | |||||||
| chr7:66741672 | C | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+880C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741672 | |||||||
| chr7:66741769 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+977T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741769 | |||||||
| chr7:66741886 | C | T | 1 | a0001c0001t0003g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+1094C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741886 | |||||||
| chr7:66741941 | C | T | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+1149C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741941 | |||||||
| chr7:66741978 | T | TA | 234 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(231): Show |
250 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-18+1198dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66741978 | ||||||
| chr7:66741978 | T | TAA | 15 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
16 | HG00609.hp2 HG00621.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+1197_-18+1198d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66741978 | ||||||
| chr7:66741993 | A | G | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1201A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741993 | |||||||
| chr7:66741997 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1205G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741997 | |||||||
| chr7:66742099 | C | T | 2 | a0001c0001t0005g0329 a0001c0001t0005g0330 |
2 | NA18939.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-18+1307C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742099 | |||||||
| chr7:66742150 | C | CA | 151 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(148): Show |
160 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-18+1368dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66742150 | ||||||
| chr7:66742150 | C | CAA | 47 | a0001c0001t0001g0075 a0001c0001t0002g0001 a0001c0001t0002g0007 others(44): Show |
54 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+1367_-18+1368d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66742150 | ||||||
| chr7:66742161 | C | A | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+1369C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742161 | |||||||
| chr7:66742259 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+1467G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742259 | |||||||
| chr7:66742380 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-18+1588A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742380 | |||||||
| chr7:66742493 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+1701A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742493 | |||||||
| chr7:66742527 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-18+1735C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742527 | |||||||
| chr7:66742705 | G | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+1913G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742705 | |||||||
| chr7:66742714 | C | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-18+1922C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742714 | |||||||
| chr7:66742768 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02155.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-18+1976A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742768 | |||||||
| chr7:66742852 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+2060C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742852 | |||||||
| chr7:66742897 | G | C | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+2105G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742897 | |||||||
| chr7:66743019 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18+2227G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743019 | |||||||
| chr7:66743080 | C | T | 1 | a0001c0001t0007g0303 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+2288C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743080 | |||||||
| chr7:66743169 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-18+2377G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743169 | |||||||
| chr7:66743189 | G | A | 2 | a0002c0002t0001g0332 a0002c0002t0001g0333 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-18+2397G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743189 | |||||||
| chr7:66743197 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-18+2405C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743197 | |||||||
| chr7:66743198 | T | A | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+2406T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743198 | |||||||
| chr7:66743325 | AT | A | 6 | a0001c0001t0001g0193 a0001c0001t0003g0194 a0001c0001t0003g0195 others(3): Show |
6 | HG01517.hp2 HG03195.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2536delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66743325 | ||||||
| chr7:66743327 | T | TA | 11 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(8): Show |
12 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+2535_-18+2536i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743327 | |||||||
| chr7:66743327 | T | TAA | 44 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(41): Show |
51 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-18+2535_-18+2536i others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743327 | |||||||
| chr7:66743328 | T | A | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+2536T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743328 | |||||||
| chr7:66743359 | C | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+2567C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743359 | |||||||
| chr7:66743540 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(47): Show |
57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-18+2748C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743540 | |||||||
| chr7:66743647 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-18+2855G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743647 | |||||||
| chr7:66743798 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+3006G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743798 | |||||||
| chr7:66743918 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0338 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-18+3126A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743918 | |||||||
| chr7:66743968 | G | T | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+3176G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743968 | |||||||
| chr7:66744021 | TTTTTC | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
55 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-18+3249_-18+3253d others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744021 | ||||||
| chr7:66744070 | A | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+3278A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744070 | |||||||
| chr7:66744082 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+3290G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744082 | |||||||
| chr7:66744092 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18+3300A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744092 | |||||||
| chr7:66744110 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-18+3318A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744110 | |||||||
| chr7:66744147 | T | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+3355T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744147 | |||||||
| chr7:66744190 | C | T | 26 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(23): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18+3398C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744190 | |||||||
| chr7:66744193 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0201 a0001c0001t0001g0206 |
4 | HG01109.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3401G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744193 | |||||||
| chr7:66744200 | C | T | 3 | a0001c0001t0004g0359 a0001c0001t0004g0360 a0001c0001t0004g0361 |
3 | NA18612.hp2 NA18959.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-18+3408C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744200 | |||||||
| chr7:66744266 | C | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(141): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-18+3474C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744266 | |||||||
| chr7:66744283 | C | T | 4 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(1): Show |
4 | NA18960.hp2 NA18980.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3491C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744283 | |||||||
| chr7:66744324 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3532G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744324 | |||||||
| chr7:66744444 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3652G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744444 | |||||||
| chr7:66744536 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-18+3744C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744536 | |||||||
| chr7:66744590 | C | G | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+3798C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744590 | |||||||
| chr7:66744667 | C | CA | 63 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(60): Show |
67 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.-18+3895dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | ||||||
| chr7:66744667 | C | CAA | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0004g0339 others(3): Show |
6 | HG00642.hp2 HG02080.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3894_-18+3895d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | ||||||
| chr7:66744667 | CA | C | 72 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0298 others(69): Show |
79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-18+3895delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | ||||||
| chr7:66744667 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+3886_-18+3895d others(12): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | ||||||
| chr7:66744697 | C | T | 15 | a0001c0001t0001g0212 a0001c0001t0007g0202 a0001c0001t0007g0245 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+3905C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744697 | |||||||
| chr7:66744749 | T | C | 2 | a0001c0001t0003g0080 a0001c0001t0012g0085 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-18+3957T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744749 | |||||||
| chr7:66744807 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+4015A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744807 | |||||||
| chr7:66744912 | G | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+4120G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744912 | |||||||
| chr7:66744915 | G | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+4123G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744915 | |||||||
| chr7:66745020 | A | G | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+4228A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745020 | |||||||
| chr7:66745076 | C | T | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+4284C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745076 | |||||||
| chr7:66745109 | G | A | 1 | a0001c0001t0007g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-18+4317G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745109 | |||||||
| chr7:66745191 | C | CA | 28 | a0001c0001t0001g0213 a0001c0001t0001g0284 a0001c0001t0004g0018 others(25): Show |
29 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18+4413dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745191 | ||||||
| chr7:66745208 | A | T | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+4416A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745208 | |||||||
| chr7:66745261 | C | T | 5 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(2): Show |
5 | NA18941.hp1 NA18948.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+4469C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745261 | |||||||
| chr7:66745376 | A | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(49): Show |
59 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-18+4584A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745376 | |||||||
| chr7:66745460 | C | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01261.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-18+4668C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745460 | |||||||
| chr7:66745630 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+4838A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745630 | |||||||
| chr7:66745663 | G | C | 46 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(43): Show |
53 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-18+4871G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745663 | |||||||
| chr7:66745741 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-18+4949C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745741 | |||||||
| chr7:66745768 | C | CA | 80 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
83 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-18+4994dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | ||||||
| chr7:66745768 | C | CAAA | 24 | a0001c0001t0004g0018 a0001c0001t0004g0340 a0001c0001t0004g0341 others(21): Show |
25 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+4992_-18+4994d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | ||||||
| chr7:66745768 | CA | C | 57 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0003g0014 others(54): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18+4994delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | ||||||
| chr7:66745843 | C | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+5051C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745843 | |||||||
| chr7:66745905 | A | T | 90 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+5113A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745905 | |||||||
| chr7:66746023 | T | A | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+5231T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746023 | |||||||
| chr7:66746106 | T | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+5314T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746106 | |||||||
| chr7:66746207 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-18+5415T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746207 | |||||||
| chr7:66746224 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0197 others(1): Show |
4 | HG02155.hp2 NA18612.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5432G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746224 | |||||||
| chr7:66746289 | A | AT | 16 | a0001c0001t0001g0128 a0001c0001t0001g0212 a0001c0001t0007g0202 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+5509dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746289 | ||||||
| chr7:66746410 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
11 | HG00609.hp2 HG00621.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+5618C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746410 | |||||||
| chr7:66746559 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+5767G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746559 | |||||||
| chr7:66746618 | C | CT | 15 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(12): Show |
15 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+5848dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | ||||||
| chr7:66746618 | CT | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(177): Show |
189 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-18+5848delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | ||||||
| chr7:66746618 | CTT | C | 8 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG01168.hp1 HG03942.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5847_-18+5848d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | ||||||
| chr7:66746781 | G | A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG00438.hp1 NA18954.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+5989G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746781 | |||||||
| chr7:66746784 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18+5992C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746784 | |||||||
| chr7:66746790 | A | AT | 147 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(144): Show |
156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-18+6009dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746790 | ||||||
| chr7:66746941 | G | GC | 90 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+6150dupC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746941 | ||||||
| chr7:66747138 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+6346G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747138 | |||||||
| chr7:66747202 | C | G | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+6410C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747202 | |||||||
| chr7:66747226 | C | T | 1 | a0001c0001t0007g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18+6434C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747226 | |||||||
| chr7:66747272 | A | G | 1 | a0001c0001t0006g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-18+6480A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747272 | |||||||
| chr7:66747328 | C | A | 4 | a0001c0001t0003g0129 a0001c0001t0003g0145 a0001c0001t0003g0146 others(1): Show |
4 | HG03669.hp1 HG03710.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6536C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747328 | |||||||
| chr7:66747333 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6541G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747333 | |||||||
| chr7:66747437 | T | A | 1 | a0001c0001t0003g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+6645T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747437 | |||||||
| chr7:66747523 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18+6731A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747523 | |||||||
| chr7:66747541 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+6749G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747541 | |||||||
| chr7:66747610 | G | A | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-18+6818G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747610 | |||||||
| chr7:66747774 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18+6982C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747774 | |||||||
| chr7:66747819 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+7027C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747819 | |||||||
| chr7:66747885 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18+7093A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747885 | |||||||
| chr7:66747900 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+7108T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747900 | |||||||
| chr7:66747917 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-18+7125A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747917 | |||||||
| chr7:66748015 | G | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+7223G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748015 | |||||||
| chr7:66748121 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
61 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18+7329C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748121 | |||||||
| chr7:66748142 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-18+7350G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748142 | |||||||
| chr7:66748213 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+7421C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748213 | |||||||
| chr7:66748504 | G | A | 172 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(169): Show |
182 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.-18+7712G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748504 | |||||||
| chr7:66748541 | A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+7749A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748541 | |||||||
| chr7:66749023 | G | A | 249 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(246): Show |
266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-18+8231G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749023 | |||||||
| chr7:66749262 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+8470C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749262 | |||||||
| chr7:66749358 | A | C | 2 | a0001c0001t0007g0245 a0001c0001t0007g0254 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-18+8566A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749358 | |||||||
| chr7:66749367 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+8575T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749367 | |||||||
| chr7:66749390 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+8598G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749390 | |||||||
| chr7:66749580 | C | T | 174 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(171): Show |
184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-18+8788C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749580 | |||||||
| chr7:66749657 | A | C | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+8865A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749657 | |||||||
| chr7:66749659 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-18+8867G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749659 | |||||||
| chr7:66749710 | A | G | 1 | a0001c0001t0005g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-18+8918A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749710 | |||||||
| chr7:66749746 | C | A | 1 | a0001c0001t0001g0026 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18+8954C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749746 | |||||||
| chr7:66749788 | A | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+8996A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749788 | |||||||
| chr7:66749798 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+9006C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749798 | |||||||
| chr7:66749819 | A | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+9027A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749819 | |||||||
| chr7:66749861 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-18+9069C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749861 | |||||||
| chr7:66749946 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+9154C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749946 | |||||||
| chr7:66750043 | C | T | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18+9251C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750043 | |||||||
| chr7:66750260 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-18+9468A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750260 | |||||||
| chr7:66750313 | A | G | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18+9521A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750313 | |||||||
| chr7:66750459 | A | G | 1 | a0001c0001t0017g0295 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18+9667A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750459 | |||||||
| chr7:66750659 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+9867T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750659 | |||||||
| chr7:66750727 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+9935G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750727 | |||||||
| chr7:66750963 | T | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+10171T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750963 | |||||||
| chr7:66751032 | C | CT | 88 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0023 others(85): Show |
93 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-18+10254dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66751032 | ||||||
| chr7:66751179 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-18+10387C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751179 | |||||||
| chr7:66751185 | C | T | 22 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+10393C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751185 | |||||||
| chr7:66751206 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+10414T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751206 | |||||||
| chr7:66751612 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18+10820C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751612 | |||||||
| chr7:66751613 | G | C | 1 | a0001c0001t0003g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+10821G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751613 | |||||||
| chr7:66751640 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18+10848C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751640 | |||||||
| chr7:66751700 | C | G | 1 | a0001c0001t0004g0355 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-18+10908C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751700 | |||||||
| chr7:66751742 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+10950A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751742 | |||||||
| chr7:66751929 | G | T | 5 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+11137G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751929 | |||||||
| chr7:66751966 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18+11174G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751966 | |||||||
| chr7:66751968 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+11176G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751968 | |||||||
| chr7:66751993 | T | TC | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+11202dupC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66751993 | ||||||
| chr7:66752108 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+11316A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752108 | |||||||
| chr7:66752125 | A | G | 249 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(246): Show |
266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-18+11333A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752125 | |||||||
| chr7:66752195 | TA | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+11414delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752195 | ||||||
| chr7:66752196 | A | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+11404A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752196 | |||||||
| chr7:66752269 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+11477G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752269 | |||||||
| chr7:66752314 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-18+11522G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752314 | |||||||
| chr7:66752349 | G | A | 2 | a0001c0001t0001g0363 a0001c0001t0001g0364 |
2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-18+11557G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752349 | |||||||
| chr7:66752474 | A | G | 9 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+11682A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752474 | |||||||
| chr7:66752493 | T | TA | 29 | a0001c0001t0001g0079 a0001c0001t0001g0275 a0001c0001t0002g0042 others(26): Show |
30 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+11716dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752493 | ||||||
| chr7:66752493 | TA | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0091 others(7): Show |
10 | HG00438.hp1 HG01256.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+11716delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752493 | ||||||
| chr7:66752521 | G | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+11729G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752521 | |||||||
| chr7:66752632 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18+11840A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752632 | |||||||
| chr7:66752676 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+11884A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752676 | |||||||
| chr7:66752787 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
10 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+11995A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752787 | |||||||
| chr7:66752982 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-18+12190C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752982 | |||||||
| chr7:66752983 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-18+12191T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752983 | |||||||
| chr7:66753061 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18+12269G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753061 | |||||||
| chr7:66753146 | A | C | 1 | a0001c0001t0007g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+12354A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753146 | |||||||
| chr7:66753209 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-18+12417G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753209 | |||||||
| chr7:66753234 | T | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+12442T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753234 | |||||||
| chr7:66753365 | A | T | 1 | a0001c0001t0007g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+12573A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753365 | |||||||
| chr7:66753623 | C | G | 2 | a0001c0001t0002g0077 a0001c0001t0020g0078 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+12831C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753623 | |||||||
| chr7:66753692 | T | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
78 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-18+12900T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753692 | |||||||
| chr7:66753694 | T | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
78 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-18+12902T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753694 | |||||||
| chr7:66753700 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0004g0353 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+12908_-18+1290 others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753700 | |||||||
| chr7:66753701 | G | GT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0204 others(38): Show |
46 | HG00621.hp2 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18+12932dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTT | 51 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
54 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+12931_-18+1293 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTT | 57 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0034 others(54): Show |
59 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+12930_-18+1293 others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTT | 25 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0087 others(22): Show |
26 | HG00597.hp1 HG00738.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18+12929_-18+1293 others(8): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTT | 9 | a0001c0001t0003g0177 a0001c0001t0003g0180 a0001c0001t0003g0186 others(6): Show |
9 | HG00735.hp2 HG01106.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+12928_-18+1293 others(9): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTT | 9 | a0001c0001t0005g0307 a0001c0001t0005g0309 a0001c0001t0005g0314 others(6): Show |
9 | HG01928.hp1 HG02523.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+12927_-18+1293 others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT | 11 | a0001c0001t0005g0310 a0001c0001t0005g0318 a0001c0001t0005g0319 others(8): Show |
11 | HG00438.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+12926_-18+1293 others(11): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0360 a0001c0001t0004g0371 |
2 | HG01515.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18+12923_-18+1293 others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(4): Show |
5 | a0001c0001t0004g0341 a0001c0001t0004g0344 a0001c0001t0004g0355 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+12922_-18+1293 others(15): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(5): Show |
4 | a0001c0001t0004g0342 a0001c0001t0004g0345 a0001c0001t0004g0346 others(1): Show |
4 | HG01257.hp2 HG02155.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+12921_-18+1293 others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(6): Show |
7 | a0001c0001t0004g0339 a0001c0001t0004g0340 a0001c0001t0004g0343 others(4): Show |
7 | NA18939.hp1 NA18963.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12920_-18+1293 others(17): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(7): Show |
4 | a0001c0001t0004g0018 a0001c0001t0004g0351 a0001c0001t0004g0352 others(1): Show |
5 | NA18950.hp1 NA18953.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+12919_-18+1293 others(18): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0004g0354 a0001c0001t0004g0356 a0001c0001t0004g0358 |
3 | HG02165.hp1 HG02300.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-18+12918_-18+1293 others(19): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753701 | G | T | 1 | a0001c0001t0004g0353 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+12909G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753701 | |||||||
| chr7:66753701 | GT | G | 43 | a0001c0001t0001g0259 a0001c0001t0001g0288 a0001c0001t0002g0001 others(40): Show |
50 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.-18+12932delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | ||||||
| chr7:66753832 | G | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+13040G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753832 | |||||||
| chr7:66753860 | T | C | 266 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(263): Show |
283 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.-18+13068T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753860 | |||||||
| chr7:66753895 | TGGGGTTT others(290): Show |
T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+13111_-18+1340 others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753895 | ||||||
| chr7:66754005 | A | AT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0216 others(6): Show |
9 | HG01074.hp1 HG02056.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+13228dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66754005 | ||||||
| chr7:66754006 | T | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+13214T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754006 | |||||||
| chr7:66754012 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+13220T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754012 | |||||||
| chr7:66754192 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(15): Show |
19 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+13400C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754192 | |||||||
| chr7:66754371 | C | CT | 27 | a0001c0001t0003g0181 a0001c0001t0004g0336 a0001c0001t0005g0307 others(24): Show |
27 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+13594dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66754371 | ||||||
| chr7:66754387 | A | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+13595A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754387 | |||||||
| chr7:66754399 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-18+13607C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754399 | |||||||
| chr7:66754507 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+13715G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754507 | |||||||
| chr7:66754554 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+13762G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754554 | |||||||
| chr7:66754947 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+14155G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754947 | |||||||
| chr7:66754973 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+14181G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754973 | |||||||
| chr7:66755293 | CA | C | 368 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(365): Show |
394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.-18+14511delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66755293 | ||||||
| chr7:66755354 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-18+14562A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755354 | |||||||
| chr7:66755515 | G | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(50): Show |
57 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+14723G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755515 | |||||||
| chr7:66755821 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0039 a0001c0001t0002g0056 |
4 | NA18956.hp1 NA18971.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15029C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755821 | |||||||
| chr7:66755910 | T | C | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+15118T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755910 | |||||||
| chr7:66756005 | G | A | 3 | a0001c0001t0005g0313 a0001c0001t0005g0314 a0001c0001t0005g0318 |
3 | HG01928.hp1 HG01934.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-18+15213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756005 | |||||||
| chr7:66756162 | T | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+15370T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756162 | |||||||
| chr7:66756210 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+15418C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756210 | |||||||
| chr7:66756268 | T | G | 3 | a0001c0001t0003g0129 a0001c0001t0003g0145 a0001c0001t0003g0183 |
3 | HG03669.hp1 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+15476T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756268 | |||||||
| chr7:66756273 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+15481G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756273 | |||||||
| chr7:66756425 | C | G | 4 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15458C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756425 | |||||||
| chr7:66756502 | A | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(47): Show |
57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-15381A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756502 | |||||||
| chr7:66756505 | T | C | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(47): Show |
57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-15378T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756505 | |||||||
| chr7:66756596 | T | A | 1 | a0001c0001t0003g0181 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-17-15287T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756596 | |||||||
| chr7:66756746 | T | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-15137T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756746 | |||||||
| chr7:66756956 | G | A | 73 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
76 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-17-14927G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756956 | |||||||
| chr7:66757120 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-14763G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757120 | |||||||
| chr7:66757180 | TTTTATGT others(3): Show |
T | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-17-14700_-17-1469 others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757180 | ||||||
| chr7:66757201 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-17-14682T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757201 | |||||||
| chr7:66757280 | ATTGT | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-14600_-17-1459 others(8): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757280 | ||||||
| chr7:66757442 | CAT | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0286 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-17-14438_-17-1443 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757442 | ||||||
| chr7:66757547 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-14336A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757547 | |||||||
| chr7:66757813 | G | A | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-14070G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757813 | |||||||
| chr7:66757877 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-17-14005_-17-1400 others(46): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757877 | ||||||
| chr7:66757878 | TGGGATTA others(35): Show |
T | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-17-14004_-17-1396 others(46): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757878 | |||||||
| chr7:66757891 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-13992G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757891 | |||||||
| chr7:66757911 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-13972G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757911 | |||||||
| chr7:66757920 | A | AT | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-13954dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757920 | ||||||
| chr7:66758084 | C | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-13799C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758084 | |||||||
| chr7:66758085 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-13798C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758085 | |||||||
| chr7:66758430 | A | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-13453A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758430 | |||||||
| chr7:66758432 | T | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-13451T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758432 | |||||||
| chr7:66758474 | T | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-13409T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758474 | |||||||
| chr7:66758522 | C | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-13361C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758522 | |||||||
| chr7:66758597 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-17-13286G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758597 | |||||||
| chr7:66758688 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0223 |
2 | HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-17-13195C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758688 | |||||||
| chr7:66758701 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-17-13182T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758701 | |||||||
| chr7:66758703 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-17-13180C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758703 | |||||||
| chr7:66758705 | G | GT | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-13177dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66758705 | ||||||
| chr7:66758961 | T | C | 2 | a0001c0001t0003g0148 a0001c0001t0003g0181 |
2 | HG00423.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-17-12922T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758961 | |||||||
| chr7:66758985 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0188 |
2 | NA19058.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-17-12898G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758985 | |||||||
| chr7:66758990 | A | G | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-12893A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758990 | |||||||
| chr7:66759075 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-12808C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759075 | |||||||
| chr7:66759213 | G | A | 1 | a0001c0001t0001g0365 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-12670G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759213 | |||||||
| chr7:66759397 | C | G | 1 | a0001c0001t0002g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-17-12486C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759397 | |||||||
| chr7:66759492 | T | C | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-12391T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759492 | |||||||
| chr7:66759494 | G | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-12389G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759494 | |||||||
| chr7:66759510 | T | C | 174 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(171): Show |
184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-17-12373T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759510 | |||||||
| chr7:66759519 | A | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(85): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-17-12364A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759519 | |||||||
| chr7:66759566 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17-12317C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759566 | |||||||
| chr7:66759704 | A | G | 9 | a0001c0001t0001g0216 a0001c0001t0001g0229 a0001c0001t0001g0232 others(6): Show |
9 | HG02257.hp2 HG02723.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-12179A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759704 | |||||||
| chr7:66759705 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-12178T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759705 | |||||||
| chr7:66759724 | A | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-12159A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759724 | |||||||
| chr7:66759725 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-12158T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759725 | |||||||
| chr7:66759771 | T | G | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-12112T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759771 | |||||||
| chr7:66759822 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-12061G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759822 | |||||||
| chr7:66760109 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-11774C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760109 | |||||||
| chr7:66760122 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-11761G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760122 | |||||||
| chr7:66760237 | A | G | 1 | a0001c0001t0005g0317 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-17-11646A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760237 | |||||||
| chr7:66760325 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-11558C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760325 | |||||||
| chr7:66760442 | A | AT | 57 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0125 others(54): Show |
64 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-17-11423dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66760442 | ||||||
| chr7:66760442 | A | ATTTTTT | 22 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(19): Show |
23 | HG00735.hp1 HG01257.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-11428_-17-1142 others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66760442 | ||||||
| chr7:66760475 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-11408G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760475 | |||||||
| chr7:66760480 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-17-11403A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760480 | |||||||
| chr7:66760604 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-17-11279C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760604 | |||||||
| chr7:66760771 | T | TC | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-11112_-17-1111 others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760771 | |||||||
| chr7:66760823 | C | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-11060C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760823 | |||||||
| chr7:66760852 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-11031C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760852 | |||||||
| chr7:66760909 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17-10974G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760909 | |||||||
| chr7:66761304 | A | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-10579A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761304 | |||||||
| chr7:66761389 | G | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-10494G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761389 | |||||||
| chr7:66761452 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-10431G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761452 | |||||||
| chr7:66761620 | G | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(5): Show |
10 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-10263G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761620 | |||||||
| chr7:66761633 | C | T | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-10250C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761633 | |||||||
| chr7:66761676 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-10207A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761676 | |||||||
| chr7:66761737 | C | T | 1 | a0001c0001t0005g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-17-10146C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761737 | |||||||
| chr7:66761838 | G | A | 46 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(43): Show |
53 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-17-10045G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761838 | |||||||
| chr7:66761848 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-17-10035C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761848 | |||||||
| chr7:66761890 | A | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-9993A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761890 | |||||||
| chr7:66761930 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0197 others(1): Show |
4 | HG02155.hp2 NA18612.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9953A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761930 | |||||||
| chr7:66761975 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-17-9908C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761975 | |||||||
| chr7:66761982 | T | C | 1 | a0001c0001t0005g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-17-9901T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761982 | |||||||
| chr7:66762063 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9820C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762063 | |||||||
| chr7:66762064 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9819A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762064 | |||||||
| chr7:66762083 | CAT | C | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-9798_-17-9797d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66762083 | ||||||
| chr7:66762160 | A | G | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9723A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762160 | |||||||
| chr7:66762220 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-9663T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762220 | |||||||
| chr7:66762495 | C | T | 145 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-17-9388C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762495 | |||||||
| chr7:66762718 | A | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9165A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762718 | |||||||
| chr7:66762723 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9160C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762723 | |||||||
| chr7:66762801 | C | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-9082C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762801 | |||||||
| chr7:66762834 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9049A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762834 | |||||||
| chr7:66763260 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-17-8623C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763260 | |||||||
| chr7:66763267 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-8616C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763267 | |||||||
| chr7:66763303 | C | G | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-8580C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763303 | |||||||
| chr7:66763518 | A | G | 9 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-8365A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763518 | |||||||
| chr7:66763688 | G | A | 1 | a0001c0001t0005g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-17-8195G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763688 | |||||||
| chr7:66763745 | G | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-8138G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763745 | |||||||
| chr7:66763746 | T | G | 2 | a0002c0002t0001g0332 a0002c0002t0001g0333 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17-8137T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763746 | |||||||
| chr7:66763811 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0034 |
2 | HG00609.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-17-8072A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763811 | |||||||
| chr7:66763816 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-8067A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763816 | |||||||
| chr7:66763897 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-7986G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763897 | |||||||
| chr7:66764117 | A | G | 2 | a0001c0001t0004g0356 a0001c0001t0020g0078 |
2 | HG02109.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-17-7766A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764117 | |||||||
| chr7:66764245 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-17-7638A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764245 | |||||||
| chr7:66764249 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-7634T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764249 | |||||||
| chr7:66764252 | C | G | 1 | a0001c0001t0006g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-17-7631C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764252 | |||||||
| chr7:66764275 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-7608A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764275 | |||||||
| chr7:66764322 | T | TTTA | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-7558_-17-7556d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66764322 | ||||||
| chr7:66764391 | TG | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(85): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-17-7491delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764391 | |||||||
| chr7:66764476 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-17-7407A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764476 | |||||||
| chr7:66764566 | TCTGAGAG others(11): Show |
T | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-7316_-17-7299d others(20): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764566 | |||||||
| chr7:66764613 | C | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-7270C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764613 | |||||||
| chr7:66764648 | T | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-7235T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764648 | |||||||
| chr7:66764650 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0112 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-7233T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764650 | |||||||
| chr7:66764885 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-6998T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764885 | |||||||
| chr7:66764932 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-17-6951A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764932 | |||||||
| chr7:66764948 | A | C | 1 | a0001c0001t0001g0008 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-17-6935A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764948 | |||||||
| chr7:66764951 | T | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-6932T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764951 | |||||||
| chr7:66765008 | C | A | 1 | a0001c0001t0013g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-17-6875C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765008 | |||||||
| chr7:66765066 | A | G | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-6817A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765066 | |||||||
| chr7:66765159 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-17-6724T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765159 | |||||||
| chr7:66765184 | T | G | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-6699T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765184 | |||||||
| chr7:66765195 | G | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-6688G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765195 | |||||||
| chr7:66765315 | C | G | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-6568C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765315 | |||||||
| chr7:66765485 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(60): Show |
68 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-17-6398G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765485 | |||||||
| chr7:66765537 | G | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(85): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-17-6346G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765537 | |||||||
| chr7:66765542 | C | T | 147 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(144): Show |
156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-17-6341C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765542 | |||||||
| chr7:66765626 | G | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-6257G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765626 | |||||||
| chr7:66765743 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-6140C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765743 | |||||||
| chr7:66765873 | T | C | 174 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(171): Show |
184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-17-6010T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765873 | |||||||
| chr7:66765947 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5936T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765947 | |||||||
| chr7:66765959 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-5924T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765959 | |||||||
| chr7:66765983 | T | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5900T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765983 | |||||||
| chr7:66765984 | T | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0221 a0001c0001t0001g0222 others(27): Show |
33 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-5899T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765984 | |||||||
| chr7:66765985 | A | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0221 a0001c0001t0001g0222 |
5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5898A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765985 | |||||||
| chr7:66766108 | G | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-5775G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766108 | |||||||
| chr7:66766245 | G | C | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0012g0085 |
3 | HG02615.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-5638G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766245 | |||||||
| chr7:66766304 | C | CA | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0127 others(5): Show |
8 | HG00738.hp2 HG01358.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-5564dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766304 | ||||||
| chr7:66766304 | CA | C | 30 | a0001c0001t0001g0238 a0001c0001t0001g0300 a0001c0001t0004g0018 others(27): Show |
31 | HG00642.hp2 HG00735.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-5564delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766304 | ||||||
| chr7:66766420 | G | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-5463G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766420 | |||||||
| chr7:66766683 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5200G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766683 | |||||||
| chr7:66766710 | C | CTTAT | 65 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0030 others(62): Show |
66 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-17-5146_-17-5143d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | ||||||
| chr7:66766710 | C | CTTATTTA others(1): Show |
68 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0023 others(65): Show |
74 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-5150_-17-5143d others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | ||||||
| chr7:66766710 | C | CTTATTTA others(5): Show |
19 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0031 others(16): Show |
19 | HG00609.hp2 HG00735.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-5154_-17-5143d others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | ||||||
| chr7:66766710 | CTTAT | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
6 | HG01081.hp1 HG01106.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-5146_-17-5143d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | ||||||
| chr7:66766808 | T | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-5075T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766808 | |||||||
| chr7:66766887 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-17-4996G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766887 | |||||||
| chr7:66767000 | C | CT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0209 others(8): Show |
13 | HG00544.hp1 HG02015.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-4863dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | ||||||
| chr7:66767000 | CT | C | 195 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0023 others(192): Show |
207 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-17-4863delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | ||||||
| chr7:66767000 | CTT | C | 35 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0003g0002 others(32): Show |
39 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-17-4864_-17-4863d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | ||||||
| chr7:66767005 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0094 others(3): Show |
7 | HG00280.hp2 HG01346.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-4878T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767005 | |||||||
| chr7:66767015 | T | A | 1 | a0001c0001t0006g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-4868T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767015 | |||||||
| chr7:66767059 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-17-4824A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767059 | |||||||
| chr7:66767234 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-4649C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767234 | |||||||
| chr7:66767257 | C | G | 1 | a0001c0001t0001g0301 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-17-4626C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767257 | |||||||
| chr7:66767391 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-17-4492G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767391 | |||||||
| chr7:66767599 | C | A | 2 | a0001c0001t0003g0130 a0001c0001t0003g0152 |
2 | NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-17-4284C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767599 | |||||||
| chr7:66767968 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-3915G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767968 | |||||||
| chr7:66767978 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-3905G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767978 | |||||||
| chr7:66767991 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-3892A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767991 | |||||||
| chr7:66768073 | G | A | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-3810G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768073 | |||||||
| chr7:66768150 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-3733G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768150 | |||||||
| chr7:66768166 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-17-3717G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768166 | |||||||
| chr7:66768235 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-3648C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768235 | |||||||
| chr7:66768292 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-3591G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768292 | |||||||
| chr7:66768302 | C | G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(47): Show |
57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-3581C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768302 | |||||||
| chr7:66768456 | T | G | 1 | a0001c0001t0001g0365 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-3427T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768456 | |||||||
| chr7:66768515 | G | T | 1 | a0001c0001t0003g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-3368G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768515 | |||||||
| chr7:66768636 | A | G | 147 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(144): Show |
156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-17-3247A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768636 | |||||||
| chr7:66768647 | TCTGAGAC | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0223 |
3 | HG01071.hp1 HG01123.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-17-3232_-17-3226d others(9): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66768647 | ||||||
| chr7:66768726 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-17-3157T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768726 | |||||||
| chr7:66769160 | A | G | 1 | a0001c0001t0004g0356 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-17-2723A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769160 | |||||||
| chr7:66769165 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-17-2718T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769165 | |||||||
| chr7:66769254 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-2629G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769254 | |||||||
| chr7:66769381 | C | T | 2 | a0001c0001t0003g0156 a0001c0001t0003g0171 |
2 | NA18952.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-17-2502C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769381 | |||||||
| chr7:66769424 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-2459C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769424 | |||||||
| chr7:66769598 | A | G | 21 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-2285A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769598 | |||||||
| chr7:66769651 | A | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-2232A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769651 | |||||||
| chr7:66770140 | T | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-1743T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770140 | |||||||
| chr7:66770484 | T | C | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01261.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1399T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770484 | |||||||
| chr7:66770571 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-17-1312A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770571 | |||||||
| chr7:66770844 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0255 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-17-1039T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770844 | |||||||
| chr7:66770969 | T | G | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-914T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770969 | |||||||
| chr7:66771048 | T | C | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-835T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771048 | |||||||
| chr7:66771141 | A | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-742A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771141 | |||||||
| chr7:66771207 | T | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-676T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771207 | |||||||
| chr7:66771284 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-17-599G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771284 | |||||||
| chr7:66771392 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-491G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771392 | |||||||
| chr7:66771517 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-366A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771517 | |||||||
| chr7:66771556 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-17-327C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771556 | |||||||
| chr7:66771620 | G | T | 250 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(247): Show |
267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.-17-263G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771620 | |||||||
| chr7:66771632 | AATTTTTT | A | 9 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-231_-17-225del others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66771632 | ||||||
| chr7:66771781 | A | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-102A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771781 | |||||||
| chr7:66772114 | C | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.179+36C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772114 | |||||||
| chr7:66772261 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.179+183C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772261 | |||||||
| chr7:66772358 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179+280A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772358 | |||||||
| chr7:66772422 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.179+344G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772422 | |||||||
| chr7:66772454 | A | AT | 16 | a0001c0001t0001g0212 a0001c0001t0007g0202 a0001c0001t0007g0227 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.179+378dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66772454 | ||||||
| chr7:66772595 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.179+517G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772595 | |||||||
| chr7:66772672 | G | T | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179+594G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772672 | |||||||
| chr7:66772738 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0052 |
2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.179+660C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772738 | |||||||
| chr7:66772769 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0286 a0001c0001t0004g0336 |
4 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+691G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772769 | |||||||
| chr7:66772913 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.179+835A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772913 | |||||||
| chr7:66772921 | T | A | 212 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(209): Show |
225 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.179+843T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772921 | |||||||
| chr7:66772924 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0121 |
4 | HG00597.hp2 HG02040.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+846A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772924 | |||||||
| chr7:66772925 | T | A | 71 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
75 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.179+847T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772925 | |||||||
| chr7:66772929 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.179+851T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772929 | |||||||
| chr7:66772971 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.179+893A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772971 | |||||||
| chr7:66773028 | G | C | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179+950G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773028 | |||||||
| chr7:66773078 | TG | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0094 a0001c0001t0001g0104 others(1): Show |
5 | HG00280.hp2 HG01346.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+1001delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773078 | |||||||
| chr7:66773081 | TTG | T | 30 | a0001c0001t0002g0057 a0001c0001t0002g0063 a0001c0001t0004g0018 others(27): Show |
31 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.179+1005_179+1006d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66773081 | ||||||
| chr7:66773082 | TG | T | 183 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0023 others(180): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.179+1005delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773082 | |||||||
| chr7:66773083 | G | T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0094 a0001c0001t0001g0104 others(33): Show |
37 | HG00280.hp2 HG00438.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.179+1005G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773083 | |||||||
| chr7:66773096 | C | T | 145 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.179+1018C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773096 | |||||||
| chr7:66773115 | TGTTGA | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.179+1040_179+1044d others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66773115 | ||||||
| chr7:66773209 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179+1131A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773209 | |||||||
| chr7:66773370 | A | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0193 others(2): Show |
5 | HG00408.hp1 HG02083.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+1292A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773370 | |||||||
| chr7:66773395 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179+1317G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773395 | |||||||
| chr7:66773553 | G | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.179+1475G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773553 | |||||||
| chr7:66773561 | A | G | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.179+1483A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773561 | |||||||
| chr7:66773566 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0001g0335 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+1488A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773566 | |||||||
| chr7:66773615 | G | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179+1537G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773615 | |||||||
| chr7:66773734 | C | A | 1 | a0001c0001t0003g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.180-1493C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773734 | |||||||
| chr7:66773746 | A | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.180-1481A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773746 | |||||||
| chr7:66773839 | T | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.180-1388T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773839 | |||||||
| chr7:66773912 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.180-1315C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773912 | |||||||
| chr7:66774142 | C | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.180-1085C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774142 | |||||||
| chr7:66774357 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.180-870C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774357 | |||||||
| chr7:66774392 | C | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-835C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774392 | |||||||
| chr7:66774399 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.180-828G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774399 | |||||||
| chr7:66774601 | T | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(145): Show |
157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.180-626T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774601 | |||||||
| chr7:66774816 | C | T | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.180-411C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774816 | |||||||
| chr7:66774844 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-383G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774844 | |||||||
| chr7:66774877 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0001g0335 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-350G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774877 | |||||||
| chr7:66774975 | A | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.180-252A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774975 | |||||||
| chr7:66775021 | A | G | 175 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(172): Show |
185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.180-206A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775021 | |||||||
| chr7:66775197 | A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180-30A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775197 | |||||||
| chr7:66775208 | A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180-19A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775208 | |||||||
| chr7:66775402 | C | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0052 |
2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.346+9C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775402 | |||||||
| chr7:66775535 | G | C | 8 | a0001c0001t0003g0014 a0001c0001t0003g0164 a0001c0001t0003g0165 others(5): Show |
9 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+142G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775535 | |||||||
| chr7:66775536 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0286 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.346+143G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775536 | |||||||
| chr7:66775565 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.346+172C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775565 | |||||||
| chr7:66775652 | C | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.346+259C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775652 | |||||||
| chr7:66775851 | G | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.346+458G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775851 | |||||||
| chr7:66776005 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.346+612T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776005 | |||||||
| chr7:66776073 | C | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.346+680C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776073 | |||||||
| chr7:66776131 | G | C | 1 | a0001c0001t0002g0050 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.346+738G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776131 | |||||||
| chr7:66776263 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0121 |
4 | HG00597.hp2 HG02040.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+870G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776263 | |||||||
| chr7:66776389 | T | G | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+996T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776389 | |||||||
| chr7:66776461 | G | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1068G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776461 | |||||||
| chr7:66776905 | T | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346+1512T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776905 | |||||||
| chr7:66776986 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.346+1593A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776986 | |||||||
| chr7:66777189 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.346+1796G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777189 | |||||||
| chr7:66777429 | G | A | 73 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
76 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.346+2036G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777429 | |||||||
| chr7:66777606 | A | G | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.346+2213A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777606 | |||||||
| chr7:66777644 | C | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2251C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777644 | |||||||
| chr7:66777660 | C | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+2267C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777660 | |||||||
| chr7:66777669 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+2276T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777669 | |||||||
| chr7:66777675 | C | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+2282C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777675 | |||||||
| chr7:66777729 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+2336G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777729 | |||||||
| chr7:66777742 | C | G | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.346+2349C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777742 | |||||||
| chr7:66777843 | A | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0049 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.346+2450A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777843 | |||||||
| chr7:66777845 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.346+2452A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777845 | |||||||
| chr7:66777848 | T | A | 49 | a0001c0001t0003g0014 a0001c0001t0003g0130 a0001c0001t0003g0131 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.346+2455T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777848 | |||||||
| chr7:66777883 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2490C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777883 | |||||||
| chr7:66777968 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2575G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777968 | |||||||
| chr7:66778052 | C | G | 26 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(23): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.346+2659C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778052 | |||||||
| chr7:66778276 | G | GACAAATA others(8): Show |
25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2883_346+2884i others(17): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778276 | |||||||
| chr7:66778280 | G | C | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2887G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778280 | |||||||
| chr7:66778281 | G | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2888G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778281 | |||||||
| chr7:66778282 | T | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2889T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778282 | |||||||
| chr7:66778386 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0338 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346+2993G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778386 | |||||||
| chr7:66778401 | A | C | 4 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+3008A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778401 | |||||||
| chr7:66778461 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.346+3068A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778461 | |||||||
| chr7:66778684 | G | T | 8 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(5): Show |
11 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+3291G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778684 | |||||||
| chr7:66778775 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+3382G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778775 | |||||||
| chr7:66779234 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.346+3841G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779234 | |||||||
| chr7:66779302 | G | GAGACCAG others(7): Show |
5 | a0001c0001t0001g0229 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+3911_346+3924d others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779302 | ||||||
| chr7:66779322 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+3929G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779322 | |||||||
| chr7:66779350 | A | G | 2 | a0002c0002t0001g0332 a0002c0002t0001g0333 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.346+3957A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779350 | |||||||
| chr7:66779376 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.346+3983T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779376 | |||||||
| chr7:66779408 | G | T | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+4015G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779408 | |||||||
| chr7:66779434 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0116 others(2): Show |
5 | HG00741.hp2 HG01192.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+4041G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779434 | |||||||
| chr7:66779436 | G | A | 1 | a0001c0001t0004g0341 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.346+4043G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779436 | |||||||
| chr7:66779670 | T | TA | 50 | a0001c0001t0001g0091 a0001c0001t0001g0229 a0001c0001t0001g0235 others(47): Show |
57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.347-3988dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779670 | ||||||
| chr7:66779670 | T | TAA | 6 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-3989_347-3988d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779670 | ||||||
| chr7:66779683 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.347-3992A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779683 | |||||||
| chr7:66779690 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0297 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.347-3985C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779690 | |||||||
| chr7:66779720 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.347-3955G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779720 | |||||||
| chr7:66779768 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.347-3907G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779768 | |||||||
| chr7:66779779 | T | C | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-3896T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779779 | |||||||
| chr7:66779815 | C | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0255 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.347-3860C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779815 | |||||||
| chr7:66779827 | G | A | 4 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3848G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779827 | |||||||
| chr7:66779829 | A | C | 53 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(50): Show |
60 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.347-3846A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779829 | |||||||
| chr7:66779994 | A | G | 76 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.347-3681A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779994 | |||||||
| chr7:66780255 | A | AC | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-3420_347-3419i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780255 | |||||||
| chr7:66780299 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.347-3376G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780299 | |||||||
| chr7:66780314 | T | C | 9 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3361T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780314 | |||||||
| chr7:66780414 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347-3261T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780414 | |||||||
| chr7:66780462 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.347-3213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780462 | |||||||
| chr7:66780615 | C | G | 1 | a0001c0001t0006g0179 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.347-3060C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780615 | |||||||
| chr7:66780913 | A | G | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-2762A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780913 | |||||||
| chr7:66781193 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.347-2482G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66781193 | |||||||
| chr7:66781487 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.347-2188T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66781487 | |||||||
| chr7:66782128 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.347-1547C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782128 | |||||||
| chr7:66782189 | T | C | 1 | a0001c0001t0003g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.347-1486T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782189 | |||||||
| chr7:66782274 | T | G | 1 | a0001c0001t0002g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.347-1401T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782274 | |||||||
| chr7:66782290 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.347-1385T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782290 | |||||||
| chr7:66782346 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.347-1329A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782346 | |||||||
| chr7:66782465 | CT | C | 101 | a0001c0001t0001g0261 a0001c0001t0002g0001 a0001c0001t0002g0007 others(98): Show |
109 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.347-1195delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782465 | ||||||
| chr7:66782493 | G | A | 2 | a0001c0001t0007g0247 a0001c0001t0007g0250 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.347-1182G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782493 | |||||||
| chr7:66782520 | G | A | 25 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(22): Show |
26 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.347-1155G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782520 | |||||||
| chr7:66782602 | G | A | 24 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(21): Show |
24 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.347-1073G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782602 | |||||||
| chr7:66782622 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1053C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782622 | |||||||
| chr7:66782700 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02055.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.347-975C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782700 | |||||||
| chr7:66782708 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.347-967C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782708 | |||||||
| chr7:66782785 | C | CA | 29 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(26): Show |
30 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.347-880dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782785 | ||||||
| chr7:66782791 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.347-884A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782791 | |||||||
| chr7:66782840 | T | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-835T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782840 | |||||||
| chr7:66782926 | T | TGGTAGTT others(2760): Show |
1 | a0001c0001t0001g0223 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.347-732_347-731ins others(2767): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782926 | ||||||
| chr7:66783024 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-651G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783024 | |||||||
| chr7:66783025 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-650A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783025 | |||||||
| chr7:66783067 | C | T | 1 | a0001c0001t0007g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.347-608C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783067 | |||||||
| chr7:66783113 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.347-562G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783113 | |||||||
| chr7:66783320 | T | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-355T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783320 | |||||||
| chr7:66783395 | T | C | 343 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.347-280T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783395 | |||||||
| chr7:66783419 | T | C | 1 | a0001c0001t0012g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-256T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783419 | |||||||
| chr7:66783463 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.347-212A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783463 | |||||||
| chr7:66783643 | A | T | 9 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-32A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783643 | |||||||
| chr7:66783870 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+29T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66783870 | |||||||
| chr7:66783921 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.513+80C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66783921 | |||||||
| chr7:66784185 | G | C | 2 | a0001c0001t0007g0202 a0001c0001t0007g0227 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.513+344G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784185 | |||||||
| chr7:66784310 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+469A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784310 | |||||||
| chr7:66784623 | G | T | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513+782G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784623 | |||||||
| chr7:66784652 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+811G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784652 | |||||||
| chr7:66784693 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784693 | |||||||
| chr7:66784694 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+853A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784694 | |||||||
| chr7:66785248 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+1407C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785248 | |||||||
| chr7:66785258 | C | G | 1 | a0001c0001t0007g0303 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513+1417C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785258 | |||||||
| chr7:66785308 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+1467C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785308 | |||||||
| chr7:66785460 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.513+1619C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785460 | |||||||
| chr7:66785543 | G | A | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0012g0085 |
3 | HG02615.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.513+1702G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785543 | |||||||
| chr7:66785624 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+1783C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785624 | |||||||
| chr7:66785641 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.513+1800G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785641 | |||||||
| chr7:66785734 | C | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+1893C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785734 | |||||||
| chr7:66785743 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.513+1902A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785743 | |||||||
| chr7:66785746 | C | T | 2 | a0001c0001t0005g0317 a0001c0001t0006g0176 |
2 | NA18963.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.513+1905C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785746 | |||||||
| chr7:66785857 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+2016G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785857 | |||||||
| chr7:66785872 | TG | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
76 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.513+2038delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66785872 | ||||||
| chr7:66785878 | G | GA | 3 | a0001c0001t0002g0054 a0001c0001t0003g0093 a0001c0001t0009g0076 |
3 | HG02055.hp1 HG03098.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.513+2037_513+2038i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785878 | |||||||
| chr7:66785879 | G | A | 151 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0002g0001 others(148): Show |
164 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.513+2038G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785879 | |||||||
| chr7:66785879 | GA | G | 19 | a0001c0001t0001g0206 a0001c0001t0001g0212 a0001c0001t0001g0224 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+2049delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66785879 | ||||||
| chr7:66785882 | A | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+2041A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785882 | |||||||
| chr7:66785956 | A | T | 1 | a0001c0001t0013g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+2115A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785956 | |||||||
| chr7:66786107 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+2266G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786107 | |||||||
| chr7:66786154 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+2313C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786154 | |||||||
| chr7:66786164 | A | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0269 |
2 | HG02080.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.513+2323A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786164 | |||||||
| chr7:66786170 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+2329C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786170 | |||||||
| chr7:66786306 | A | C | 1 | a0001c0001t0004g0358 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.513+2465A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786306 | |||||||
| chr7:66786382 | T | C | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.513+2541T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786382 | |||||||
| chr7:66786440 | A | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+2599A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786440 | |||||||
| chr7:66786440 | A | G | 1 | a0001c0001t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.513+2599A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786440 | |||||||
| chr7:66786521 | A | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+2680A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786521 | |||||||
| chr7:66786693 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.513+2852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786693 | |||||||
| chr7:66786786 | C | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(102): Show |
113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.513+2945C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786786 | |||||||
| chr7:66786817 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+2976G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786817 | |||||||
| chr7:66786821 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+2980T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786821 | |||||||
| chr7:66787186 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.513+3345C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787186 | |||||||
| chr7:66787194 | T | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02055.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.513+3353T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787194 | |||||||
| chr7:66787206 | T | C | 1 | a0001c0001t0002g0334 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.513+3365T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787206 | |||||||
| chr7:66787336 | A | AT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0089 others(39): Show |
44 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.513+3520dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66787336 | ||||||
| chr7:66787336 | AT | A | 82 | a0001c0001t0001g0110 a0001c0001t0001g0192 a0001c0001t0001g0228 others(79): Show |
90 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.513+3520delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66787336 | ||||||
| chr7:66787396 | T | C | 1 | a0001c0001t0003g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.513+3555T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787396 | |||||||
| chr7:66787794 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.513+3953G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787794 | |||||||
| chr7:66787810 | A | G | 1 | a0001c0001t0004g0355 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+3969A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787810 | |||||||
| chr7:66788211 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+4370C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788211 | |||||||
| chr7:66788273 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.513+4432T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788273 | |||||||
| chr7:66788290 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.513+4449C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788290 | |||||||
| chr7:66788453 | C | CA | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+4618dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66788453 | ||||||
| chr7:66788666 | T | C | 1 | a0001c0001t0006g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.513+4825T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788666 | |||||||
| chr7:66788736 | T | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+4895T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788736 | |||||||
| chr7:66788780 | C | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.513+4939C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788780 | |||||||
| chr7:66788783 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+4942G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788783 | |||||||
| chr7:66788816 | G | A | 1 | a0001c0001t0004g0358 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.513+4975G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788816 | |||||||
| chr7:66788824 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513+4983G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788824 | |||||||
| chr7:66788965 | A | T | 29 | a0001c0001t0001g0079 a0001c0001t0004g0018 a0001c0001t0004g0336 others(26): Show |
30 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+5124A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788965 | |||||||
| chr7:66788968 | T | A | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513+5127T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788968 | |||||||
| chr7:66789021 | T | C | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+5180T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789021 | |||||||
| chr7:66789134 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+5293T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789134 | |||||||
| chr7:66789303 | G | A | 161 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(158): Show |
172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.513+5462G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789303 | |||||||
| chr7:66789614 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.513+5773C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789614 | |||||||
| chr7:66789659 | A | G | 265 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(262): Show |
282 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.513+5818A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789659 | |||||||
| chr7:66789665 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.513+5824G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789665 | |||||||
| chr7:66789682 | C | CA | 62 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(59): Show |
67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.514-5803dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | ||||||
| chr7:66789682 | C | CAA | 6 | a0001c0001t0001g0259 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG00609.hp1 HG00621.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5804_514-5803d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | ||||||
| chr7:66789682 | CA | C | 119 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
123 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.514-5803delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | ||||||
| chr7:66789682 | CAA | C | 76 | a0001c0001t0001g0128 a0001c0001t0003g0014 a0001c0001t0003g0129 others(73): Show |
80 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.514-5804_514-5803d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | ||||||
| chr7:66789682 | CAAA | C | 6 | a0001c0001t0003g0155 a0001c0001t0004g0342 a0001c0001t0004g0349 others(3): Show |
6 | HG00558.hp1 HG01515.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5805_514-5803d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | ||||||
| chr7:66789780 | C | T | 55 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(52): Show |
58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.514-5731C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789780 | |||||||
| chr7:66790251 | G | A | 161 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(158): Show |
172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.514-5260G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790251 | |||||||
| chr7:66790265 | G | C | 4 | a0001c0001t0003g0013 a0001c0001t0003g0134 a0001c0001t0003g0137 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-5246G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790265 | |||||||
| chr7:66790324 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0052 |
2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.514-5187C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790324 | |||||||
| chr7:66790341 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.514-5170T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790341 | |||||||
| chr7:66790343 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-5168G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790343 | |||||||
| chr7:66790464 | T | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(49): Show |
59 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.514-5047T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790464 | |||||||
| chr7:66790659 | G | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(248): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.514-4852G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790659 | |||||||
| chr7:66790872 | T | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-4639T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790872 | |||||||
| chr7:66790930 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0261 others(3): Show |
7 | HG02083.hp2 HG02129.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-4581A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790930 | |||||||
| chr7:66791159 | G | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-4352G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791159 | |||||||
| chr7:66791433 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.514-4078C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791433 | |||||||
| chr7:66791964 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-3547T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791964 | |||||||
| chr7:66792068 | C | G | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3443C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792068 | |||||||
| chr7:66792069 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3442G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792069 | |||||||
| chr7:66792070 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3441C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792070 | |||||||
| chr7:66792072 | A | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3439A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792072 | |||||||
| chr7:66792110 | CA | C | 55 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0120 others(52): Show |
62 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.514-3385delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66792110 | ||||||
| chr7:66792110 | CAA | C | 26 | a0001c0001t0002g0057 a0001c0001t0005g0307 a0001c0001t0005g0308 others(23): Show |
26 | HG00438.hp2 HG01515.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.514-3386_514-3385d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66792110 | ||||||
| chr7:66792185 | C | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.514-3326C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792185 | |||||||
| chr7:66792194 | C | T | 1 | a0001c0001t0007g0303 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.514-3317C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792194 | |||||||
| chr7:66792537 | G | A | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.514-2974G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792537 | |||||||
| chr7:66792599 | G | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01261.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2912G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792599 | |||||||
| chr7:66792706 | A | G | 1 | a0001c0001t0006g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.514-2805A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792706 | |||||||
| chr7:66792706 | A | T | 1 | a0002c0002t0001g0333 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514-2805A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792706 | |||||||
| chr7:66792744 | G | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-2767G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792744 | |||||||
| chr7:66792760 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.514-2751C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792760 | |||||||
| chr7:66792942 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-2569G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792942 | |||||||
| chr7:66792974 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.514-2537G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792974 | |||||||
| chr7:66792997 | CTG | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.514-2513_514-2512d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792997 | |||||||
| chr7:66793006 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.514-2505A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793006 | |||||||
| chr7:66793024 | C | T | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.514-2487C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793024 | |||||||
| chr7:66793093 | G | A | 248 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(245): Show |
265 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.514-2418G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793093 | |||||||
| chr7:66793109 | G | A | 1 | a0001c0001t0001g0008 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.514-2402G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793109 | |||||||
| chr7:66793123 | A | C | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.514-2388A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793123 | |||||||
| chr7:66793132 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.514-2379A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793132 | |||||||
| chr7:66793355 | T | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-2156T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793355 | |||||||
| chr7:66793478 | A | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.514-2033A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793478 | |||||||
| chr7:66793538 | A | G | 1 | a0001c0001t0013g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514-1973A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793538 | |||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4579): Show |
1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4588): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4586): Show |
1 | a0001c0001t0005g0328 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4586): Show |
2 | a0001c0001t0005g0309 a0001c0001t0005g0331 |
2 | NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4587): Show |
4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4586): Show |
15 | a0001c0001t0005g0307 a0001c0001t0005g0310 a0001c0001t0005g0312 others(12): Show |
15 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0002g0050 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4587): Show |
45 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(42): Show |
52 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4587): Show |
1 | a0001c0001t0005g0308 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4586): Show |
5 | a0001c0001t0005g0311 a0001c0001t0005g0320 a0001c0001t0005g0322 others(2): Show |
5 | NA18947.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4585): Show |
1 | a0001c0001t0005g0323 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4594): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4589): Show |
1 | a0001c0001t0004g0354 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4598): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
21 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0341 others(18): Show |
22 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0343 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4587): Show |
1 | a0001c0001t0004g0355 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0350 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793679 | G | GTACCTGC others(4587): Show |
1 | a0001c0001t0004g0340 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | ||||||
| chr7:66793681 | G | A | 1 | a0001c0001t0006g0173 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.514-1830G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793681 | |||||||
| chr7:66793684 | T | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-1827T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793684 | |||||||
| chr7:66793734 | AC | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0093 others(5): Show |
11 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-1776delC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793734 | |||||||
| chr7:66793800 | G | C | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1711G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793800 | |||||||
| chr7:66793801 | T | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1710T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793801 | |||||||
| chr7:66793802 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1709C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793802 | |||||||
| chr7:66793803 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1708C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793803 | |||||||
| chr7:66793805 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1706G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793805 | |||||||
| chr7:66793806 | C | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1705C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793806 | |||||||
| chr7:66793817 | G | C | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1694G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793817 | |||||||
| chr7:66793874 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0001g0335 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-1637C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793874 | |||||||
| chr7:66793903 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0221 a0001c0001t0001g0222 |
5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-1608A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793903 | |||||||
| chr7:66794015 | C | T | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.514-1496C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794015 | |||||||
| chr7:66794039 | A | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1472A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794039 | |||||||
| chr7:66794060 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514-1451A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794060 | |||||||
| chr7:66794207 | A | AT | 16 | a0001c0001t0001g0210 a0001c0001t0001g0219 a0001c0001t0001g0228 others(13): Show |
16 | HG01952.hp1 HG01978.hp2 HG02897.hp1 others(13): Show |
intron_variant | MODIFIER | c.514-1279dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | ||||||
| chr7:66794207 | AT | A | 100 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.514-1279delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | ||||||
| chr7:66794207 | ATT | A | 71 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0123 others(68): Show |
79 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.514-1280_514-1279d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | ||||||
| chr7:66794234 | C | T | 2 | a0001c0001t0007g0202 a0001c0001t0007g0227 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.514-1277C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794234 | |||||||
| chr7:66794252 | A | T | 6 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1259A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794252 | |||||||
| chr7:66794258 | T | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1253T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794258 | |||||||
| chr7:66794259 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.514-1252A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794259 | |||||||
| chr7:66794409 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.514-1102A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794409 | |||||||
| chr7:66794733 | T | C | 1 | a0001c0001t0006g0157 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.514-778T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794733 | |||||||
| chr7:66794746 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-765C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794746 | |||||||
| chr7:66794967 | C | T | 104 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(101): Show |
112 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.514-544C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794967 | |||||||
| chr7:66795055 | C | T | 1 | a0001c0001t0001g0008 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.514-456C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795055 | |||||||
| chr7:66795109 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.514-402C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795109 | |||||||
| chr7:66795189 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.514-322C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795189 | |||||||
| chr7:66795216 | C | G | 2 | a0001c0001t0003g0156 a0001c0001t0003g0171 |
2 | NA18952.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.514-295C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795216 | |||||||
| chr7:66795302 | A | G | 288 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(285): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.514-209A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795302 | |||||||
| chr7:66795318 | A | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-193A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795318 | |||||||
| chr7:66795320 | T | G | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-191T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795320 | |||||||
| chr7:66795835 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.595+243G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795835 | |||||||
| chr7:66795937 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+345G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795937 | |||||||
| chr7:66795974 | A | G | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.595+382A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795974 | |||||||
| chr7:66796069 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0037 others(1): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+477G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796069 | |||||||
| chr7:66796128 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.595+536C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796128 | |||||||
| chr7:66796175 | G | C | 56 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.595+583G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796175 | |||||||
| chr7:66796224 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.595+632T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796224 | |||||||
| chr7:66796228 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595+636A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796228 | |||||||
| chr7:66796238 | T | TAA | 78 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(75): Show |
85 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.595+655_595+656dup others(2): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66796238 | ||||||
| chr7:66796248 | AG | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.595+657delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796248 | |||||||
| chr7:66796351 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.595+759A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796351 | |||||||
| chr7:66796382 | A | G | 21 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0208 others(18): Show |
21 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.595+790A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796382 | |||||||
| chr7:66796444 | C | T | 5 | a0001c0001t0004g0341 a0001c0001t0004g0344 a0001c0001t0004g0353 others(2): Show |
5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796444 | |||||||
| chr7:66796531 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.596-843G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796531 | |||||||
| chr7:66796582 | TTTTG | T | 6 | a0001c0001t0004g0342 a0001c0001t0004g0343 a0001c0001t0004g0349 others(3): Show |
6 | NA18612.hp2 NA18959.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-772_596-769del others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66796582 | ||||||
| chr7:66796738 | G | A | 1 | a0001c0001t0001g0367 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.596-636G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796738 | |||||||
| chr7:66796828 | C | T | 1 | a0001c0001t0004g0358 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.596-546C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796828 | |||||||
| chr7:66796881 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.596-493C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796881 | |||||||
| chr7:66796907 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0338 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.596-467T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796907 | |||||||
| chr7:66796992 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.596-382A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796992 | |||||||
| chr7:66797229 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.596-145A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797229 | |||||||
| chr7:66797297 | CTT | C | 161 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(158): Show |
172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.596-75_596-74delTT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797297 | ||||||
| chr7:66797306 | C | CA | 10 | a0001c0001t0001g0081 a0001c0001t0001g0278 a0001c0001t0002g0019 others(7): Show |
10 | HG02074.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.596-53dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797306 | ||||||
| chr7:66797306 | C | CAA | 44 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(41): Show |
51 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.596-54_596-53dupAA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797306 | ||||||
| chr7:66797321 | AG | A | 33 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0106 others(30): Show |
34 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.596-52delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797321 | |||||||
| chr7:66797322 | G | A | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.596-52G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797322 | |||||||
| chr7:66797324 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0272 a0001c0001t0001g0282 |
5 | HG00741.hp1 HG01346.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-50G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797324 | |||||||
| chr7:66797528 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.728+22C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797528 | |||||||
| chr7:66797781 | G | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.728+275G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797781 | |||||||
| chr7:66797839 | G | A | 3 | a0001c0001t0004g0346 a0001c0001t0004g0352 a0001c0001t0004g0354 |
3 | HG01257.hp2 NA18994.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.728+333G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797839 | |||||||
| chr7:66797986 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.728+480G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797986 | |||||||
| chr7:66798082 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.728+576A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798082 | |||||||
| chr7:66798313 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.728+807C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798313 | |||||||
| chr7:66798357 | AG | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.728+855delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 66798357 | ||||||
| chr7:66798414 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0223 |
2 | HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.728+908C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798414 | |||||||
| chr7:66798482 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.729-841G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798482 | |||||||
| chr7:66798563 | T | A | 172 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(169): Show |
186 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.729-760T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798563 | |||||||
| chr7:66798576 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.729-747G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798576 | |||||||
| chr7:66798797 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.729-526C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798797 | |||||||
| chr7:66798861 | C | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0001g0335 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-462C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798861 | |||||||
| chr7:66799007 | C | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(102): Show |
113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.729-316C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799007 | |||||||
| chr7:66799077 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.729-246C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799077 | |||||||
| chr7:66799123 | A | G | 1 | a0001c0001t0006g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.729-200A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799123 | |||||||
| chr7:66799279 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0255 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.729-44C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799279 | |||||||
| chr7:66799492 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0240 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.820+78A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66799492 | |||||||
| chr7:66799681 | C | CT | 8 | a0001c0001t0001g0258 a0001c0001t0005g0307 a0001c0001t0005g0309 others(5): Show |
8 | NA18939.hp2 NA18953.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+275dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66799681 | ||||||
| chr7:66800041 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+627C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800041 | |||||||
| chr7:66800263 | A | G | 1 | a0001c0001t0005g0327 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.820+849A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800263 | |||||||
| chr7:66800458 | A | G | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(102): Show |
113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.820+1044A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800458 | |||||||
| chr7:66800560 | G | A | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.820+1146G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800560 | |||||||
| chr7:66800574 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.820+1160C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800574 | |||||||
| chr7:66800582 | C | G | 2 | a0001c0001t0001g0368 a0001c0001t0001g0370 |
2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.820+1168C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800582 | |||||||
| chr7:66800622 | G | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0221 a0001c0001t0001g0222 |
5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1208G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800622 | |||||||
| chr7:66800649 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0030 others(1): Show |
4 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+1235G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800649 | |||||||
| chr7:66800745 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.820+1331C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800745 | |||||||
| chr7:66801203 | T | C | 1 | a0001c0001t0001g0368 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.820+1789T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801203 | |||||||
| chr7:66801247 | TTTTTAAT others(9): Show |
T | 1 | a0001c0001t0003g0143 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.820+1835_820+1850d others(18): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66801247 | ||||||
| chr7:66801316 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+1902G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801316 | |||||||
| chr7:66801678 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.820+2264C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801678 | |||||||
| chr7:66801795 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.820+2381T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801795 | |||||||
| chr7:66801886 | G | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+2472G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801886 | |||||||
| chr7:66801903 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.820+2489G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801903 | |||||||
| chr7:66801911 | G | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(102): Show |
113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.820+2497G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801911 | |||||||
| chr7:66801919 | G | T | 165 | a0001c0001t0001g0192 a0001c0001t0001g0338 a0001c0001t0002g0001 others(162): Show |
176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.820+2505G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801919 | |||||||
| chr7:66802056 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.820+2642C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802056 | |||||||
| chr7:66802152 | C | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0201 a0001c0001t0001g0206 others(3): Show |
7 | HG01071.hp1 HG01109.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+2738C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802152 | |||||||
| chr7:66802197 | A | C | 1 | a0001c0001t0003g0181 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.820+2783A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802197 | |||||||
| chr7:66802307 | A | G | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2833A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802307 | |||||||
| chr7:66802606 | C | G | 1 | a0001c0001t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.821-2534C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802606 | |||||||
| chr7:66802616 | G | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-2524G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802616 | |||||||
| chr7:66802707 | A | G | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2433A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802707 | |||||||
| chr7:66802726 | A | C | 2 | a0001c0001t0007g0202 a0001c0001t0007g0227 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.821-2414A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802726 | |||||||
| chr7:66802772 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821-2368T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802772 | |||||||
| chr7:66802874 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.821-2266A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802874 | |||||||
| chr7:66803061 | T | C | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2079T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803061 | |||||||
| chr7:66803075 | G | A | 1 | a0001c0001t0003g0143 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.821-2065G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803075 | |||||||
| chr7:66803143 | A | G | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-1997A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803143 | |||||||
| chr7:66803254 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1886G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803254 | |||||||
| chr7:66803315 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1825C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803315 | |||||||
| chr7:66803347 | A | G | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-1793A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803347 | |||||||
| chr7:66803431 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0034 |
2 | HG00609.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.821-1709T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803431 | |||||||
| chr7:66803580 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0118 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.821-1560A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803580 | |||||||
| chr7:66803686 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.821-1454C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803686 | |||||||
| chr7:66803786 | G | A | 1 | a0001c0001t0004g0356 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.821-1354G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803786 | |||||||
| chr7:66803900 | A | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1240A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803900 | |||||||
| chr7:66803917 | T | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-1223T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803917 | |||||||
| chr7:66803962 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.821-1178C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803962 | |||||||
| chr7:66803985 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.821-1155A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803985 | |||||||
| chr7:66804064 | T | C | 55 | a0001c0001t0003g0014 a0001c0001t0003g0129 a0001c0001t0003g0130 others(52): Show |
58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.821-1076T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804064 | |||||||
| chr7:66804086 | A | AT | 9 | a0001c0001t0001g0107 a0001c0001t0001g0206 a0001c0001t0001g0225 others(6): Show |
9 | HG02486.hp1 HG03704.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-1037dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804086 | ||||||
| chr7:66804086 | AT | A | 9 | a0001c0001t0001g0192 a0001c0001t0001g0290 a0001c0001t0002g0042 others(6): Show |
11 | HG02055.hp1 HG02572.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-1037delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804086 | ||||||
| chr7:66804208 | C | T | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-932C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804208 | |||||||
| chr7:66804219 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.821-921G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804219 | |||||||
| chr7:66804293 | A | G | 2 | a0001c0001t0005g0329 a0001c0001t0005g0330 |
2 | NA18939.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.821-847A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804293 | |||||||
| chr7:66804333 | G | A | 1 | a0001c0001t0001g0367 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.821-807G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804333 | |||||||
| chr7:66804402 | T | C | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-738T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804402 | |||||||
| chr7:66804604 | G | C | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.821-536G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804604 | |||||||
| chr7:66804738 | G | GA | 11 | a0001c0001t0001g0087 a0001c0001t0001g0213 a0001c0001t0001g0287 others(8): Show |
12 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-384dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804738 | ||||||
| chr7:66804738 | GA | G | 84 | a0001c0001t0001g0133 a0001c0001t0001g0219 a0001c0001t0001g0229 others(81): Show |
92 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.821-384delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804738 | ||||||
| chr7:66804739 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.821-401A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804739 | |||||||
| chr7:66804756 | AG | A | 24 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(21): Show |
24 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.821-383delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804756 | |||||||
| chr7:66804891 | G | A | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-249G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804891 | |||||||
| chr7:66804902 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-238G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804902 | |||||||
| chr7:66805399 | G | A | 1 | a0001c0001t0006g0184 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.1077+3G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805399 | |||||||
| chr7:66805417 | T | C | 1 | a0001c0001t0020g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1077+21T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805417 | |||||||
| chr7:66805609 | G | A | 8 | a0001c0001t0003g0014 a0001c0001t0003g0164 a0001c0001t0003g0165 others(5): Show |
9 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805609 | |||||||
| chr7:66805708 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1077+312G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805708 | |||||||
| chr7:66805711 | T | C | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077+315T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805711 | |||||||
| chr7:66805739 | C | CTCAT | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+351_1077+354d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66805739 | ||||||
| chr7:66805745 | C | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0240 |
3 | HG02965.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1077+349C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805745 | |||||||
| chr7:66805781 | A | G | 25 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0005g0309 others(22): Show |
25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077+385A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805781 | |||||||
| chr7:66805911 | A | AT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0221 others(9): Show |
14 | HG01081.hp1 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1077+530dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66805911 | ||||||
| chr7:66805937 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0236 a0001c0001t0001g0239 |
3 | HG02257.hp2 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1077+541G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805937 | |||||||
| chr7:66806248 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1077+852G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806248 | |||||||
| chr7:66806386 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0036 |
4 | NA18955.hp1 NA19002.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+990G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806386 | |||||||
| chr7:66806419 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0001g0299 |
3 | HG01074.hp1 HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1077+1023C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806419 | |||||||
| chr7:66806640 | C | CT | 92 | a0001c0001t0001g0025 a0001c0001t0001g0118 a0001c0001t0001g0217 others(89): Show |
102 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077+1265dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | ||||||
| chr7:66806640 | C | CTT | 5 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0004g0018 others(2): Show |
6 | NA18953.hp1 NA18968.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+1264_1077+126 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | ||||||
| chr7:66806640 | CT | C | 28 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0123 others(25): Show |
28 | HG01123.hp1 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+1265delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | ||||||
| chr7:66806827 | A | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+1431A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806827 | |||||||
| chr7:66806897 | G | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0009 others(101): Show |
112 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1077+1501G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806897 | |||||||
| chr7:66806922 | G | T | 1 | a0001c0001t0001g0008 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1077+1526G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806922 | |||||||
| chr7:66806983 | G | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0039 a0001c0001t0002g0045 others(1): Show |
5 | NA18940.hp2 NA18956.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+1587G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806983 | |||||||
| chr7:66807034 | C | G | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1077+1638C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807034 | |||||||
| chr7:66807297 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-1589C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807297 | |||||||
| chr7:66807441 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1078-1445G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807441 | |||||||
| chr7:66807517 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078-1369C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807517 | |||||||
| chr7:66808134 | A | T | 1 | a0001c0001t0004g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1078-752A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808134 | |||||||
| chr7:66808145 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078-741C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808145 | |||||||
| chr7:66808234 | C | T | 27 | a0001c0001t0004g0018 a0001c0001t0004g0336 a0001c0001t0004g0339 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1078-652C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808234 | |||||||
| chr7:66808332 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-554C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808332 | |||||||
| chr7:66808372 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02155.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1078-514C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808372 | |||||||
| chr7:66808422 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-464G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808422 | |||||||
| chr7:66808504 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-382G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808504 | |||||||
| chr7:66808763 | A | G | 1 | a0001c0001t0003g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1078-123A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808763 | |||||||
| chr7:66808802 | G | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0339 a0001c0001t0004g0340 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-84G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808802 | |||||||
| chr7:66808863 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1078-23G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808863 |