Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5874 |
| ensemblid | ENSG00000041353.10 |
| hgncid | 9767 |
| symbol | RAB27B |
| name | RAB27B, member RAS oncogene family |
| refseq_nuc | NM_004163.4 |
| refseq_prot | NP_004154.2 |
| ensembl_nuc | ENST00000262094.10 |
| ensembl_prot | ENSP00000262094.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 54828477 |
| end | 54895516 |
| strand | + |
| ver | v1.2 |
| region | chr18:54828477-54895516 |
| region5000 | chr18:54823477-54900516 |
| regionname0 | RAB27B_chr18_54828477_54895516 |
| regionname5000 | RAB27B_chr18_54823477_54900516 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 218 | 331 | 81 | 74 | 126 | 8 | 40 | 102 | RAB27B_chr18_54823477_54900516 | RAB27B | MTDGD others(213): Show |
chr18 | 54823477 | 54900516 |
| a0002 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | MTDGD others(213): Show |
chr18 | 54823477 | 54900516 |
| a0003 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | MTDGD others(213): Show |
chr18 | 54823477 | 54900516 |
| a0004 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | MIDGD others(213): Show |
chr18 | 54823477 | 54900516 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 654 | 331 | 81 | 74 | 126 | 8 | 40 | RAB27B_chr18_54823477_54900516 | RAB27B | ATGAC others(649): Show |
chr18 | 54823477 | 54900516 | ||
| a0002c0003 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ATGAC others(649): Show |
chr18 | 54823477 | 54900516 | ||
| a0003c0002 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ATGAC others(649): Show |
chr18 | 54823477 | 54900516 | ||
| a0004c0004 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ATGAT others(649): Show |
chr18 | 54823477 | 54900516 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6999 | 140 | 23 | 31 | 67 | 1 | 17 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0002 | 0/0 | 6999 | 66 | 2 | 15 | 38 | 1 | 10 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0003 | 0/0 | 6999 | 16 | 0 | 10 | 0 | 2 | 4 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0004 | 1/0 | 7003 | 13 | 12 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6998): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0005 | 0/0 | 6999 | 11 | 0 | 8 | 0 | 2 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0006 | 0/0 | 6999 | 9 | 8 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0007 | 0/0 | 6999 | 7 | 5 | 1 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0008 | 0/0 | 6999 | 8 | 8 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0009 | 0/0 | 6999 | 7 | 1 | 4 | 1 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0010 | 0/0 | 6998 | 7 | 3 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6993): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0011 | 0/0 | 6999 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0012 | 0/0 | 6999 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0013 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0014 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0015 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0016 | 0/0 | 6999 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0017 | 0/0 | 6999 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0018 | 0/0 | 6840 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6835): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0019 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0020 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0021 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0022 | 0/0 | 6999 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0023 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0024 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6998): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0025 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6998): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0026 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6998): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0027 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0028 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0029 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0030 | 0/0 | 6998 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6993): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0032 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0033 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0034 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0035 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0036 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0037 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0038 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0039 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0040 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0041 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0042 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0043 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0044 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0045 | 0/0 | 6999 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0001c0001t0046 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6998): Show |
chr18 | 54823477 | 54900516 |
| a0002c0003t0031 | 0/0 | 6998 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6993): Show |
chr18 | 54823477 | 54900516 |
| a0003c0002t0001 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| a0004c0004t0007 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | ACTCG others(6994): Show |
chr18 | 54823477 | 54900516 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0305 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0015g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0015g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0017g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0017g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0021g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0022g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0023g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0024g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0025g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0026g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0027g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0028g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0030g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0032g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0033g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0034g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0035g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0036g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0037g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0038g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0039g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0040g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0041g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0042g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0043g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0044g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0045g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0046g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0002c0003t0031g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0003c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0004c0004t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0015 | g0058 | EUR | GBR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0095 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00738 | hp2 | a0001 | c0001 | t0030 | g0107 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0098 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0219 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0056 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0198 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0188 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0238 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0075 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01358 | hp2 | a0001 | c0001 | t0036 | g0209 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0059 | EUR | IBS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0151 | EUR | IBS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01891 | hp1 | a0001 | c0001 | t0019 | g0043 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01934 | hp1 | a0001 | c0001 | t0028 | g0041 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02004 | hp2 | a0001 | c0001 | t0032 | g0003 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02015 | hp1 | a0001 | c0001 | t0038 | g0190 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0312 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0093 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02074 | hp1 | a0001 | c0001 | t0009 | g0099 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02145 | hp1 | a0002 | c0003 | t0031 | g0114 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0147 | EAS | CDX | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0295 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0062 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02630 | hp1 | a0001 | c0001 | t0041 | g0302 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0118 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02723 | hp1 | a0001 | c0001 | t0034 | g0310 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02809 | hp1 | a0003 | c0002 | t0001 | g0306 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02965 | hp1 | a0001 | c0001 | t0018 | g0182 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02965 | hp2 | a0001 | c0001 | t0043 | g0115 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02970 | hp1 | a0001 | c0001 | t0046 | g0313 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0092 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0087 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0314 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0110 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03139 | hp1 | a0001 | c0001 | t0044 | g0316 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0211 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0191 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0046 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0102 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0101 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0205 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0239 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03834 | hp2 | a0001 | c0001 | t0015 | g0018 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0065 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04204 | hp1 | a0001 | c0001 | t0045 | g0042 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0055 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18941 | hp1 | a0001 | c0001 | t0012 | g0026 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0221 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0161 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18951 | hp1 | a0001 | c0001 | t0011 | g0194 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18972 | hp1 | a0001 | c0001 | t0037 | g0208 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18974 | hp1 | a0001 | c0001 | t0017 | g0150 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0142 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18986 | hp1 | a0001 | c0001 | t0017 | g0135 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18988 | hp1 | a0001 | c0001 | t0023 | g0181 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18992 | hp2 | a0001 | c0001 | t0035 | g0149 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19030 | hp1 | a0004 | c0004 | t0007 | g0074 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19030 | hp2 | a0001 | c0001 | t0040 | g0195 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19043 | hp1 | a0001 | c0001 | t0042 | g0111 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19075 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19078 | hp1 | a0001 | c0001 | t0027 | g0148 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19085 | hp1 | a0001 | c0001 | t0039 | g0108 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19087 | hp1 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19091 | hp1 | a0001 | c0001 | t0011 | g0249 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19240 | hp1 | a0001 | c0001 | t0024 | g0267 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | ASW | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20752 | hp1 | a0001 | c0001 | t0022 | g0097 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0117 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0261 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0222 | SAS | GIH | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0100 | SAS | GIH | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0096 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02486 | hp1 | a0001 | c0001 | t0033 | g0174 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0319 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0293 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03471 | hp2 | a0001 | c0001 | t0018 | g0116 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | USA | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0094 | AFR | USA | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0185 | REF | REF | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0305 | REF | REF | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54877590 | C | T | 1 | a0004 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.5C>T | p.Thr2Ile | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/6 | 248/7003 | 5/657 | 2/218 | chr18 | 54877590 | |||
| chr18:54888097 | G | T | 1 | a0002 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.446G>T | p.Arg149Leu | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/6 | 689/7003 | 446/657 | 149/218 | chr18 | 54888097 | |||
| chr18:54889335 | A | C | 1 | a0003 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.579A>C | p.Gln193His | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 822/7003 | 579/657 | 193/218 | chr18 | 54889335 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54828694 | C | A | 6 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0019 others(3): Show |
13 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-26C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/6 | 48892 | chr18 | 54828694 | ||||||
| chr18:54889677 | G | A | 1 | a0001c0001t0023 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 264 | chr18 | 54889677 | ||||||
| chr18:54889747 | C | T | 1 | a0001c0001t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 334 | chr18 | 54889747 | ||||||
| chr18:54889974 | G | T | 1 | a0001c0001t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 561 | chr18 | 54889974 | ||||||
| chr18:54890011 | C | T | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*598C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 598 | chr18 | 54890011 | ||||||
| chr18:54890017 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*604G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 604 | chr18 | 54890017 | ||||||
| chr18:54890033 | G | A | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 620 | chr18 | 54890033 | ||||||
| chr18:54890085 | T | C | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*672T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 672 | chr18 | 54890085 | ||||||
| chr18:54890118 | T | A | 1 | a0001c0001t0019 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 705 | chr18 | 54890118 | ||||||
| chr18:54890358 | C | A | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 945 | chr18 | 54890358 | ||||||
| chr18:54890366 | G | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*953G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 953 | chr18 | 54890366 | ||||||
| chr18:54890551 | C | T | 2 | a0001c0001t0008 a0001c0001t0044 |
9 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1138C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1138 | chr18 | 54890551 | ||||||
| chr18:54890606 | T | A | 1 | a0001c0001t0028 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1193 | chr18 | 54890606 | ||||||
| chr18:54890618 | A | C | 1 | a0001c0001t0028 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1205 | chr18 | 54890618 | ||||||
| chr18:54890718 | T | C | 3 | a0001c0001t0008 a0001c0001t0029 a0001c0001t0044 |
10 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1305T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1305 | chr18 | 54890718 | ||||||
| chr18:54890760 | TG | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*1348delG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1348 | chr18 | 54890760 | ||||||
| chr18:54890807 | G | A | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1394 | chr18 | 54890807 | ||||||
| chr18:54890987 | G | GT | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(37): Show |
307 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1583dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1584 | INFO_REALIGN_3_PRIME | chr18 | 54890987 | |||||
| chr18:54891012 | T | G | 3 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0032 |
19 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1599T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1599 | chr18 | 54891012 | ||||||
| chr18:54891198 | A | T | 1 | a0002c0003t0031 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1785 | chr18 | 54891198 | ||||||
| chr18:54891266 | TAATAATT others(152): Show |
T | 1 | a0001c0001t0018 | 2 | HG02965.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1857_*2015del | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1857 | INFO_REALIGN_3_PRIME | chr18 | 54891266 | |||||
| chr18:54891375 | G | T | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1962G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1962 | chr18 | 54891375 | ||||||
| chr18:54891435 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2022 | chr18 | 54891435 | ||||||
| chr18:54891532 | T | G | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2119 | chr18 | 54891532 | ||||||
| chr18:54891761 | A | T | 1 | a0001c0001t0030 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2348A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2348 | chr18 | 54891761 | ||||||
| chr18:54892035 | C | T | 4 | a0001c0001t0018 a0001c0001t0042 a0001c0001t0043 others(1): Show |
5 | HG02145.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2622C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2622 | chr18 | 54892035 | ||||||
| chr18:54892063 | G | A | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(2): Show |
22 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2650G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2650 | chr18 | 54892063 | ||||||
| chr18:54892151 | T | C | 1 | a0001c0001t0042 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2738T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2738 | chr18 | 54892151 | ||||||
| chr18:54892174 | C | T | 1 | a0001c0001t0012 | 4 | NA18941.hp1 NA19075.hp1 NA19081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2761 | chr18 | 54892174 | ||||||
| chr18:54892221 | A | G | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2808A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2808 | chr18 | 54892221 | ||||||
| chr18:54892229 | C | A | 1 | a0001c0001t0005 | 11 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2816 | chr18 | 54892229 | ||||||
| chr18:54892338 | G | A | 1 | a0001c0001t0034 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2925 | chr18 | 54892338 | ||||||
| chr18:54892404 | G | A | 1 | a0001c0001t0021 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2991G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2991 | chr18 | 54892404 | ||||||
| chr18:54892474 | T | A | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0015 others(10): Show |
88 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3061T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3061 | chr18 | 54892474 | ||||||
| chr18:54892702 | C | A | 1 | a0001c0001t0035 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3289C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3289 | chr18 | 54892702 | ||||||
| chr18:54892743 | C | T | 1 | a0001c0001t0032 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3330C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3330 | chr18 | 54892743 | ||||||
| chr18:54892747 | C | T | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3334 | chr18 | 54892747 | ||||||
| chr18:54892877 | C | T | 1 | a0001c0001t0011 | 4 | NA18948.hp1 NA18951.hp1 NA19087.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3464C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3464 | chr18 | 54892877 | ||||||
| chr18:54893262 | G | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*3849G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3849 | chr18 | 54893262 | ||||||
| chr18:54893473 | T | C | 1 | a0001c0001t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4060T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4060 | chr18 | 54893473 | ||||||
| chr18:54893519 | A | G | 1 | a0001c0001t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4106A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4106 | chr18 | 54893519 | ||||||
| chr18:54893555 | G | T | 1 | a0001c0001t0026 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4142G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4142 | chr18 | 54893555 | ||||||
| chr18:54893653 | C | T | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG02965.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4240C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4240 | chr18 | 54893653 | ||||||
| chr18:54893778 | C | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*4365C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4365 | chr18 | 54893778 | ||||||
| chr18:54893899 | A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4486A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4486 | chr18 | 54893899 | ||||||
| chr18:54893992 | C | T | 1 | a0001c0001t0006 | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4579C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4579 | chr18 | 54893992 | ||||||
| chr18:54894025 | A | G | 1 | a0001c0001t0036 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4612A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4612 | chr18 | 54894025 | ||||||
| chr18:54894085 | T | G | 1 | a0001c0001t0017 | 2 | NA18974.hp1 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4672T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4672 | chr18 | 54894085 | ||||||
| chr18:54894112 | G | A | 1 | a0001c0001t0006 | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4699G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4699 | chr18 | 54894112 | ||||||
| chr18:54894192 | G | T | 1 | a0001c0001t0016 | 2 | HG03130.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4779G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4779 | chr18 | 54894192 | ||||||
| chr18:54894215 | A | G | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*4802A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4802 | chr18 | 54894215 | ||||||
| chr18:54894281 | A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4868A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4868 | chr18 | 54894281 | ||||||
| chr18:54894615 | G | T | 1 | a0001c0001t0044 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5202G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5202 | chr18 | 54894615 | ||||||
| chr18:54895120 | TTTAG | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*5713_*5716delTAGT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5713 | INFO_REALIGN_3_PRIME | chr18 | 54895120 | |||||
| chr18:54895231 | G | A | 1 | a0001c0001t0037 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5818 | chr18 | 54895231 | ||||||
| chr18:54895257 | A | G | 1 | a0001c0001t0039 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5844A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5844 | chr18 | 54895257 | ||||||
| chr18:54895335 | A | G | 1 | a0001c0001t0038 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5922A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5922 | chr18 | 54895335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54828772 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-20+72C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828772 | |||||||
| chr18:54828792 | CTG | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
193 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.-20+107_-20+108del others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54828792 | ||||||
| chr18:54828811 | T | A | 1 | a0001c0001t0002g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-20+111T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828811 | |||||||
| chr18:54828821 | C | A | 1 | a0001c0001t0002g0193 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-20+121C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828821 | |||||||
| chr18:54828944 | A | G | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+244A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828944 | |||||||
| chr18:54829059 | T | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(30): Show |
34 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+359T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829059 | |||||||
| chr18:54829105 | T | C | 1 | a0001c0001t0011g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-20+405T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829105 | |||||||
| chr18:54829179 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+479T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829179 | |||||||
| chr18:54829254 | T | C | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+554T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829254 | |||||||
| chr18:54829690 | A | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+990A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829690 | |||||||
| chr18:54829973 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+1273A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829973 | |||||||
| chr18:54830305 | C | T | 1 | a0001c0001t0045g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-20+1605C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830305 | |||||||
| chr18:54830328 | T | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+1628T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830328 | |||||||
| chr18:54830379 | C | T | 1 | a0001c0001t0038g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-20+1679C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830379 | |||||||
| chr18:54830502 | G | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+1802G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830502 | |||||||
| chr18:54830610 | AT | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0039 others(9): Show |
12 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+1920delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54830610 | ||||||
| chr18:54830762 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-20+2062C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830762 | |||||||
| chr18:54830946 | T | A | 1 | a0001c0001t0040g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20+2246T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830946 | |||||||
| chr18:54830986 | T | C | 1 | a0001c0001t0039g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-20+2286T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830986 | |||||||
| chr18:54831059 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+2359C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831059 | |||||||
| chr18:54831069 | C | A | 47 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(44): Show |
47 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-20+2369C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831069 | |||||||
| chr18:54831129 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-20+2429A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831129 | |||||||
| chr18:54831318 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+2618C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831318 | |||||||
| chr18:54831389 | AATGGGGA others(9): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-20+2690_-20+2705d others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831389 | |||||||
| chr18:54831499 | C | T | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+2799C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831499 | |||||||
| chr18:54831545 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+2845C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831545 | |||||||
| chr18:54831546 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+2846G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831546 | |||||||
| chr18:54831570 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
92 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+2870G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831570 | |||||||
| chr18:54831781 | CT | C | 15 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
15 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+3090delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54831781 | ||||||
| chr18:54831838 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+3138C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831838 | |||||||
| chr18:54831868 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+3168C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831868 | |||||||
| chr18:54831929 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+3229C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831929 | |||||||
| chr18:54831982 | G | T | 7 | a0001c0001t0006g0084 a0001c0001t0006g0086 a0001c0001t0006g0088 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+3282G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831982 | |||||||
| chr18:54832053 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+3353T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832053 | |||||||
| chr18:54832054 | G | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+3354G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832054 | |||||||
| chr18:54832121 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-20+3421T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832121 | |||||||
| chr18:54832217 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+3517C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832217 | |||||||
| chr18:54832395 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+3695T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832395 | |||||||
| chr18:54832470 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-20+3770T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832470 | |||||||
| chr18:54832570 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+3870T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832570 | |||||||
| chr18:54832780 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
77 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.-20+4080G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832780 | |||||||
| chr18:54832829 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+4129C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832829 | |||||||
| chr18:54832854 | G | A | 12 | a0001c0001t0009g0092 a0001c0001t0009g0095 a0001c0001t0009g0096 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+4154G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832854 | |||||||
| chr18:54832892 | A | G | 15 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
15 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+4192A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832892 | |||||||
| chr18:54833000 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+4300A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833000 | |||||||
| chr18:54833020 | G | A | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-20+4320G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833020 | |||||||
| chr18:54833061 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+4361C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833061 | |||||||
| chr18:54833118 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-20+4418G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833118 | |||||||
| chr18:54833234 | C | CTTTT | 128 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0189 others(125): Show |
132 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.-20+4545_-20+4548d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | ||||||
| chr18:54833234 | C | CTTTTT | 68 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(65): Show |
69 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-20+4544_-20+4548d others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | ||||||
| chr18:54833234 | C | CTTTTTT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0039 others(11): Show |
14 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+4543_-20+4548d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | ||||||
| chr18:54833234 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-20+4534C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833234 | |||||||
| chr18:54833272 | G | C | 1 | a0001c0001t0006g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+4572G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833272 | |||||||
| chr18:54833274 | T | G | 1 | a0001c0001t0041g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+4574T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833274 | |||||||
| chr18:54833289 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0007g0295 |
2 | HG00735.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+4589C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833289 | |||||||
| chr18:54833370 | G | A | 1 | a0001c0001t0016g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+4670G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833370 | |||||||
| chr18:54833528 | T | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0039 others(9): Show |
12 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+4828T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833528 | |||||||
| chr18:54833588 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02602.hp2 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-20+4888A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833588 | |||||||
| chr18:54833662 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+4962C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833662 | |||||||
| chr18:54833781 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+5081A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833781 | |||||||
| chr18:54833784 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+5084G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833784 | |||||||
| chr18:54833785 | G | T | 1 | a0001c0001t0003g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+5085G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833785 | |||||||
| chr18:54833823 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+5123G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833823 | |||||||
| chr18:54833869 | CAG | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+5176_-20+5177d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833869 | ||||||
| chr18:54833939 | A | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+5239A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833939 | |||||||
| chr18:54833989 | T | C | 1 | a0001c0001t0004g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+5289T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833989 | |||||||
| chr18:54834331 | A | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
211 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.-20+5631A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834331 | |||||||
| chr18:54834573 | A | T | 1 | a0001c0001t0002g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+5873A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834573 | |||||||
| chr18:54834575 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+5875C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834575 | |||||||
| chr18:54834673 | G | GTA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
131 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-20+5981_-20+5982d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834673 | ||||||
| chr18:54834681 | A | ATATG | 123 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0120 others(120): Show |
128 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.-20+5982_-20+5983i others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | ||||||
| chr18:54834681 | A | ATATGTG | 4 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0004g0199 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+5982_-20+5983i others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | ||||||
| chr18:54834681 | A | ATG | 49 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(46): Show |
49 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.-20+5998_-20+5999d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | ||||||
| chr18:54834719 | GAAGAGAT others(2199): Show |
G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+6024_-20+8229d others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834719 | ||||||
| chr18:54834753 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-20+6053G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834753 | |||||||
| chr18:54834808 | T | C | 1 | a0001c0001t0007g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-20+6108T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834808 | |||||||
| chr18:54834949 | A | G | 7 | a0001c0001t0004g0303 a0001c0001t0004g0304 a0001c0001t0004g0315 others(4): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+6249A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834949 | |||||||
| chr18:54834959 | A | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0010g0147 others(2): Show |
5 | HG00609.hp2 HG02165.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+6259A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834959 | |||||||
| chr18:54835068 | A | G | 1 | a0001c0001t0037g0208 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-20+6368A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835068 | |||||||
| chr18:54835073 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-20+6373C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835073 | |||||||
| chr18:54835077 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0033 |
2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-20+6377T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835077 | |||||||
| chr18:54835333 | C | T | 1 | a0001c0001t0018g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+6633C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835333 | |||||||
| chr18:54835528 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+6828A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835528 | |||||||
| chr18:54835565 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
211 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.-20+6865C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835565 | |||||||
| chr18:54835566 | G | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+6866G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835566 | |||||||
| chr18:54835613 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0006g0014 a0001c0001t0008g0016 |
3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+6913C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835613 | |||||||
| chr18:54835629 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+6929A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835629 | |||||||
| chr18:54835652 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0002g0119 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-20+6952G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835652 | |||||||
| chr18:54835656 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+6956T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835656 | |||||||
| chr18:54835716 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-20+7016C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835716 | |||||||
| chr18:54835717 | C | T | 1 | a0001c0001t0033g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+7017C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835717 | |||||||
| chr18:54835747 | T | C | 1 | a0004c0004t0007g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20+7047T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835747 | |||||||
| chr18:54835821 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0002g0231 a0001c0001t0005g0198 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+7121C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835821 | |||||||
| chr18:54835869 | T | G | 79 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(76): Show |
80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-20+7169T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835869 | |||||||
| chr18:54835908 | C | T | 1 | a0001c0001t0039g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-20+7208C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835908 | |||||||
| chr18:54835969 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0131 others(9): Show |
15 | HG00609.hp1 HG01169.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+7269T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835969 | |||||||
| chr18:54835975 | C | A | 3 | a0001c0001t0004g0015 a0001c0001t0006g0014 a0001c0001t0008g0016 |
3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+7275C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835975 | |||||||
| chr18:54835979 | A | C | 1 | a0003c0002t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+7279A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835979 | |||||||
| chr18:54836082 | A | C | 95 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(92): Show |
96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-20+7382A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836082 | |||||||
| chr18:54836234 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+7534A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836234 | |||||||
| chr18:54836358 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+7658G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836358 | |||||||
| chr18:54836392 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-20+7692C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836392 | |||||||
| chr18:54836423 | T | G | 95 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(92): Show |
96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-20+7723T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836423 | |||||||
| chr18:54836796 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(294): Show |
308 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(305): Show |
intron_variant | MODIFIER | c.-20+8096A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836796 | |||||||
| chr18:54836811 | G | T | 1 | a0001c0001t0012g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-20+8111G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836811 | |||||||
| chr18:54837007 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-20+8307A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837007 | |||||||
| chr18:54837021 | CCTA | C | 116 | a0001c0001t0001g0011 a0001c0001t0001g0189 a0001c0001t0001g0201 others(113): Show |
120 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(117): Show |
intron_variant | MODIFIER | c.-20+8325_-20+8327d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54837021 | ||||||
| chr18:54837087 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-20+8387T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837087 | |||||||
| chr18:54837112 | TAGAG | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
211 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.-20+8415_-20+8418d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54837112 | ||||||
| chr18:54837124 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+8424T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837124 | |||||||
| chr18:54837267 | A | G | 67 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(64): Show |
68 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-20+8567A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837267 | |||||||
| chr18:54837482 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+8782G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837482 | |||||||
| chr18:54837538 | C | A | 3 | a0001c0001t0004g0015 a0001c0001t0006g0014 a0001c0001t0008g0016 |
3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+8838C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837538 | |||||||
| chr18:54837792 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-20+9092A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837792 | |||||||
| chr18:54837796 | A | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+9096A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837796 | |||||||
| chr18:54837880 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+9180G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837880 | |||||||
| chr18:54838095 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+9395A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838095 | |||||||
| chr18:54838484 | C | A | 2 | a0001c0001t0004g0106 a0001c0001t0030g0107 |
2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+9784C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838484 | |||||||
| chr18:54838636 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+9936A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838636 | |||||||
| chr18:54838651 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+9951A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838651 | |||||||
| chr18:54838722 | G | A | 2 | a0001c0001t0005g0117 a0001c0001t0018g0116 |
2 | HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-20+10022G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838722 | |||||||
| chr18:54838731 | G | A | 83 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(80): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-20+10031G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838731 | |||||||
| chr18:54838846 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+10146A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838846 | |||||||
| chr18:54838957 | A | G | 4 | a0001c0001t0009g0092 a0001c0001t0019g0043 a0001c0001t0020g0094 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+10257A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838957 | |||||||
| chr18:54838960 | G | A | 1 | a0001c0001t0041g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+10260G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838960 | |||||||
| chr18:54839004 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-20+10304G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839004 | |||||||
| chr18:54839181 | G | A | 4 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0042g0111 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+10481G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839181 | |||||||
| chr18:54839354 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+10654T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839354 | |||||||
| chr18:54839355 | A | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0002g0035 others(8): Show |
11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+10655A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839355 | |||||||
| chr18:54839698 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+10998C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839698 | |||||||
| chr18:54839736 | G | A | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+11036G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839736 | |||||||
| chr18:54839742 | G | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+11042G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839742 | |||||||
| chr18:54839847 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+11147T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839847 | |||||||
| chr18:54839859 | T | C | 67 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(64): Show |
68 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-20+11159T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839859 | |||||||
| chr18:54839940 | T | A | 1 | a0001c0001t0002g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-20+11240T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839940 | |||||||
| chr18:54840039 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+11339A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840039 | |||||||
| chr18:54840133 | G | A | 1 | a0001c0001t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-20+11433G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840133 | |||||||
| chr18:54840138 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-20+11438G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840138 | |||||||
| chr18:54840228 | C | G | 1 | a0001c0001t0002g0291 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-20+11528C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840228 | |||||||
| chr18:54840619 | A | AAAT | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+11922_-20+1192 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54840619 | ||||||
| chr18:54840646 | T | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+11946T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840646 | |||||||
| chr18:54840874 | G | C | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-20+12174G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840874 | |||||||
| chr18:54840944 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0010g0031 |
3 | HG00438.hp1 NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-20+12244C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840944 | |||||||
| chr18:54840976 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0015g0018 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-20+12276G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840976 | |||||||
| chr18:54841151 | T | TGGCG | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0060 others(10): Show |
13 | HG00099.hp1 HG01168.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+12454_-20+1245 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841151 | ||||||
| chr18:54841154 | C | CG | 23 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(20): Show |
24 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20+12458dupG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGG | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
120 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGGG | 38 | a0001c0001t0001g0007 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
39 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-20+12456_-20+1245 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGGGCG | 28 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0069 others(25): Show |
28 | HG01081.hp2 HG01106.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(9): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGGGCGG | 19 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(16): Show |
19 | HG00438.hp1 HG00558.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGGGCGGG | 7 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0048 others(4): Show |
7 | HG01123.hp1 HG01928.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(11): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841154 | C | CGGGG | 15 | a0001c0001t0001g0029 a0001c0001t0001g0283 a0001c0001t0001g0284 others(12): Show |
15 | HG02109.hp2 HG02922.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+12455_-20+1245 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | ||||||
| chr18:54841155 | G | GGGC | 12 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(9): Show |
12 | HG00639.hp2 HG00735.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841155 | ||||||
| chr18:54841159 | C | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(293): Show |
307 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(304): Show |
intron_variant | MODIFIER | c.-20+12459C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841159 | |||||||
| chr18:54841159 | C | T | 1 | a0001c0001t0012g0017 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-20+12459C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841159 | |||||||
| chr18:54841160 | G | GC | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0297 others(1): Show |
4 | NA18965.hp1 NA18969.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+12460_-20+1246 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841160 | |||||||
| chr18:54841162 | T | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(295): Show |
309 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(306): Show |
intron_variant | MODIFIER | c.-20+12462T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841162 | |||||||
| chr18:54841183 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+12483C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841183 | |||||||
| chr18:54841250 | A | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+12550A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841250 | |||||||
| chr18:54841405 | A | G | 2 | a0001c0001t0003g0002 a0001c0001t0015g0018 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-20+12705A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841405 | |||||||
| chr18:54841566 | G | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+12866G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841566 | |||||||
| chr18:54841732 | A | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+13032A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841732 | |||||||
| chr18:54841778 | T | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0136 others(10): Show |
13 | HG01074.hp1 HG01123.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+13078T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841778 | |||||||
| chr18:54841943 | C | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-20+13243C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841943 | |||||||
| chr18:54842079 | C | T | 1 | a0001c0001t0004g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+13379C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842079 | |||||||
| chr18:54842313 | T | TAGAG | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+13616_-20+1361 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54842313 | ||||||
| chr18:54842399 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+13699C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842399 | |||||||
| chr18:54842411 | A | G | 1 | a0001c0001t0004g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+13711A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842411 | |||||||
| chr18:54842521 | C | CA | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+13823dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54842521 | ||||||
| chr18:54842602 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
73 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-20+13902C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842602 | |||||||
| chr18:54842603 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-20+13903G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842603 | |||||||
| chr18:54842651 | C | T | 91 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): Show |
92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+13951C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842651 | |||||||
| chr18:54842768 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+14068G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842768 | |||||||
| chr18:54842778 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0029 others(2): Show |
5 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+14078C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842778 | |||||||
| chr18:54842863 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-20+14163C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842863 | |||||||
| chr18:54842974 | T | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+14274T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842974 | |||||||
| chr18:54842981 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-20+14281A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842981 | |||||||
| chr18:54843146 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-20+14446T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843146 | |||||||
| chr18:54843148 | A | G | 2 | a0001c0001t0004g0106 a0001c0001t0030g0107 |
2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+14448A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843148 | |||||||
| chr18:54843200 | G | C | 4 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0042g0111 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+14500G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843200 | |||||||
| chr18:54843357 | ACT | A | 3 | a0001c0001t0004g0015 a0001c0001t0006g0014 a0001c0001t0008g0016 |
3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+14660_-20+1466 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843357 | ||||||
| chr18:54843360 | CT | C | 203 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(200): Show |
208 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.-20+14671delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843360 | ||||||
| chr18:54843360 | CTT | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
91 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-20+14670_-20+1467 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843360 | ||||||
| chr18:54843758 | C | A | 2 | a0001c0001t0009g0092 a0001c0001t0021g0093 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-20+15058C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843758 | |||||||
| chr18:54843834 | C | G | 1 | a0001c0001t0029g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+15134C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843834 | |||||||
| chr18:54843871 | T | G | 1 | a0001c0001t0001g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-20+15171T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843871 | |||||||
| chr18:54844003 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+15303T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844003 | |||||||
| chr18:54844090 | A | C | 91 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): Show |
92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+15390A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844090 | |||||||
| chr18:54844143 | T | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0039 others(11): Show |
14 | HG01074.hp1 HG01123.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+15443T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844143 | |||||||
| chr18:54844345 | C | T | 1 | a0001c0001t0029g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+15645C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844345 | |||||||
| chr18:54844375 | C | CTTCT | 3 | a0001c0001t0001g0320 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG00642.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-20+15698_-20+1570 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | ||||||
| chr18:54844375 | CTTCT | C | 3 | a0001c0001t0001g0262 a0001c0001t0002g0263 a0001c0001t0009g0100 |
3 | HG00621.hp1 HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-20+15698_-20+1570 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | ||||||
| chr18:54844375 | CTTCTTTC others(1): Show |
C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0024 others(20): Show |
24 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-20+15694_-20+1570 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | ||||||
| chr18:54844408 | C | CTTT | 49 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0051 others(46): Show |
49 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.-20+15724_-20+1572 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | ||||||
| chr18:54844408 | CTT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0272 a0001c0001t0002g0119 others(9): Show |
13 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+15725_-20+1572 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | ||||||
| chr18:54844408 | CTTT | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(192): Show |
204 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(201): Show |
intron_variant | MODIFIER | c.-20+15724_-20+1572 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | ||||||
| chr18:54844412 | T | TC | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+15712_-20+1571 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844412 | |||||||
| chr18:54844418 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00673.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-20+15718T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844418 | |||||||
| chr18:54844481 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20+15781T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844481 | |||||||
| chr18:54844581 | A | G | 1 | a0001c0001t0004g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20+15881A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844581 | |||||||
| chr18:54844794 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-20+16094C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844794 | |||||||
| chr18:54844804 | C | T | 1 | a0001c0001t0003g0261 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-20+16104C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844804 | |||||||
| chr18:54845088 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-20+16388A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845088 | |||||||
| chr18:54845212 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+16512G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845212 | |||||||
| chr18:54845213 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+16513C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845213 | |||||||
| chr18:54845372 | A | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
26 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20+16672A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845372 | |||||||
| chr18:54845405 | C | CAAAA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
218 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(215): Show |
intron_variant | MODIFIER | c.-20+16716_-20+1671 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54845405 | ||||||
| chr18:54845405 | C | CAAAAA | 87 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(84): Show |
88 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-20+16715_-20+1671 others(9): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54845405 | ||||||
| chr18:54845415 | A | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0307 a0001c0001t0001g0308 others(15): Show |
19 | HG00642.hp1 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+16715A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845415 | |||||||
| chr18:54845420 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+16720T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845420 | |||||||
| chr18:54845421 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(295): Show |
309 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(306): Show |
intron_variant | MODIFIER | c.-20+16721A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845421 | |||||||
| chr18:54845426 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+16726A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845426 | |||||||
| chr18:54845545 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+16845G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845545 | |||||||
| chr18:54845549 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0131 others(1): Show |
7 | HG01169.hp2 HG01943.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16849C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845549 | |||||||
| chr18:54845616 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+16916G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845616 | |||||||
| chr18:54845836 | A | G | 2 | a0001c0001t0004g0318 a0001c0001t0026g0319 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-20+17136A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845836 | |||||||
| chr18:54845888 | C | A | 1 | a0001c0001t0029g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+17188C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845888 | |||||||
| chr18:54845992 | A | G | 4 | a0001c0001t0008g0061 a0001c0001t0008g0062 a0001c0001t0010g0046 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+17292A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845992 | |||||||
| chr18:54846111 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+17411C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846111 | |||||||
| chr18:54846132 | T | C | 2 | a0001c0001t0002g0214 a0001c0001t0002g0270 |
2 | HG02523.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-20+17432T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846132 | |||||||
| chr18:54846139 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+17439A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846139 | |||||||
| chr18:54846145 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+17445G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846145 | |||||||
| chr18:54846193 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+17493A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846193 | |||||||
| chr18:54846217 | C | T | 1 | a0001c0001t0014g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-20+17517C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846217 | |||||||
| chr18:54846219 | A | G | 2 | a0001c0001t0004g0015 a0001c0001t0008g0016 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+17519A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846219 | |||||||
| chr18:54846570 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+17870T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846570 | |||||||
| chr18:54846638 | T | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
26 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20+17938T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846638 | |||||||
| chr18:54846665 | G | A | 1 | a0001c0001t0041g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+17965G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846665 | |||||||
| chr18:54846728 | C | G | 1 | a0001c0001t0004g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+18028C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846728 | |||||||
| chr18:54846785 | A | T | 1 | a0001c0001t0012g0026 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-20+18085A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846785 | |||||||
| chr18:54846954 | G | T | 1 | a0001c0001t0033g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+18254G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846954 | |||||||
| chr18:54846995 | T | C | 92 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(89): Show |
93 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+18295T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846995 | |||||||
| chr18:54847122 | A | G | 1 | a0003c0002t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+18422A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847122 | |||||||
| chr18:54847177 | T | A | 91 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): Show |
92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+18477T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847177 | |||||||
| chr18:54847442 | T | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
311 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+18742T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847442 | |||||||
| chr18:54847522 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+18822A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847522 | |||||||
| chr18:54847612 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-20+18912T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847612 | |||||||
| chr18:54847836 | G | A | 4 | a0001c0001t0008g0061 a0001c0001t0008g0062 a0001c0001t0010g0046 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+19136G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847836 | |||||||
| chr18:54847855 | GA | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
217 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(214): Show |
intron_variant | MODIFIER | c.-20+19165delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54847855 | ||||||
| chr18:54847923 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-20+19223C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847923 | |||||||
| chr18:54848017 | A | G | 7 | a0001c0001t0006g0084 a0001c0001t0006g0086 a0001c0001t0006g0088 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+19317A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848017 | |||||||
| chr18:54848043 | G | A | 2 | a0001c0001t0005g0056 a0001c0001t0005g0064 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-20+19343G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848043 | |||||||
| chr18:54848043 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+19343G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848043 | |||||||
| chr18:54848256 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20+19556G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848256 | |||||||
| chr18:54848311 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-20+19611A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848311 | |||||||
| chr18:54848654 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
218 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(215): Show |
intron_variant | MODIFIER | c.-20+19954A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848654 | |||||||
| chr18:54848697 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+19997A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848697 | |||||||
| chr18:54848743 | C | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+20043C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848743 | |||||||
| chr18:54848810 | A | G | 1 | a0003c0002t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+20110A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848810 | |||||||
| chr18:54848844 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+20144T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848844 | |||||||
| chr18:54849061 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-20+20361C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849061 | |||||||
| chr18:54849115 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+20415G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849115 | |||||||
| chr18:54849483 | C | T | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-20+20783C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849483 | |||||||
| chr18:54849558 | A | G | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0004g0015 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+20858A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849558 | |||||||
| chr18:54849581 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0029g0055 |
2 | HG00673.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20+20881C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849581 | |||||||
| chr18:54849730 | A | G | 7 | a0001c0001t0004g0122 a0001c0001t0004g0303 a0001c0001t0004g0304 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+21030A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849730 | |||||||
| chr18:54849765 | G | T | 1 | a0003c0002t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+21065G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849765 | |||||||
| chr18:54849772 | T | G | 2 | a0001c0001t0004g0106 a0001c0001t0030g0107 |
2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+21072T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849772 | |||||||
| chr18:54849793 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0307 a0001c0001t0001g0308 others(14): Show |
18 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20+21093A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849793 | |||||||
| chr18:54849920 | T | C | 2 | a0001c0001t0010g0046 a0001c0001t0030g0107 |
2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-20+21220T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849920 | |||||||
| chr18:54849980 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+21280C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849980 | |||||||
| chr18:54850159 | A | C | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0296 |
3 | HG00735.hp2 HG01069.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-20+21459A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850159 | |||||||
| chr18:54850321 | GCAAA | G | 15 | a0001c0001t0001g0121 a0001c0001t0002g0119 a0001c0001t0004g0122 others(12): Show |
15 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+21628_-20+2163 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850321 | ||||||
| chr18:54850327 | A | AGGATATA others(9): Show |
2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21627_-20+2162 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850327 | |||||||
| chr18:54850329 | A | T | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21629A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850329 | |||||||
| chr18:54850330 | C | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21630C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850330 | |||||||
| chr18:54850331 | A | T | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21631A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850331 | |||||||
| chr18:54850332 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21632G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850332 | |||||||
| chr18:54850333 | G | GACATATA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(7): Show |
3 | a0001c0001t0001g0138 a0001c0001t0001g0189 a0001c0001t0001g0271 |
3 | HG00741.hp1 NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(9): Show |
3 | a0001c0001t0001g0265 a0001c0001t0001g0320 a0001c0001t0014g0065 |
3 | HG00558.hp2 HG00642.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(11): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0143 others(1): Show |
4 | HG01978.hp1 HG02523.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(13): Show |
2 | a0001c0001t0001g0127 a0001c0001t0010g0031 |
2 | NA18950.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(15): Show |
9 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0186 others(6): Show |
9 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(17): Show |
2 | a0001c0001t0001g0050 a0001c0001t0002g0171 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(28): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(19): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0124 a0001c0001t0001g0136 others(7): Show |
10 | HG01257.hp2 HG01975.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(21): Show |
8 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0177 others(5): Show |
8 | HG02004.hp2 HG02055.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(32): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(23): Show |
9 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0133 others(6): Show |
10 | HG01517.hp2 HG02683.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(34): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(25): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0128 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(36): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(27): Show |
7 | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0001g0178 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(29): Show |
4 | a0001c0001t0001g0129 a0001c0001t0002g0226 a0001c0001t0003g0036 others(1): Show |
4 | HG00438.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(40): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(31): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0003g0157 |
3 | HG01433.hp1 HG02004.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(42): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(33): Show |
1 | a0001c0001t0001g0160 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(44): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GACATATA others(35): Show |
1 | a0001c0001t0010g0161 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(46): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GAT | 10 | a0001c0001t0001g0311 a0001c0001t0003g0067 a0001c0001t0004g0106 others(7): Show |
10 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+21659_-20+2166 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATAT | 3 | a0001c0001t0002g0037 a0001c0001t0018g0116 a0001c0001t0028g0041 |
3 | HG01074.hp1 HG01934.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+21655_-20+2166 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(3): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0004g0315 others(1): Show |
4 | HG00099.hp1 HG01981.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+21651_-20+2166 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(5): Show |
11 | a0001c0001t0001g0024 a0001c0001t0001g0069 a0001c0001t0001g0105 others(8): Show |
11 | HG00558.hp1 HG01517.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+21649_-20+2166 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(7): Show |
8 | a0001c0001t0001g0030 a0001c0001t0001g0081 a0001c0001t0001g0282 others(5): Show |
8 | HG01081.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+21647_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(9): Show |
12 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0103 others(9): Show |
12 | HG01346.hp2 HG01934.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+21645_-20+2166 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(11): Show |
15 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0032 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+21643_-20+2166 others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(13): Show |
5 | a0001c0001t0001g0167 a0001c0001t0001g0183 a0001c0001t0001g0289 others(2): Show |
5 | HG02683.hp1 HG03239.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+21641_-20+2166 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(15): Show |
10 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0257 others(7): Show |
10 | HG01261.hp2 HG01346.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+21639_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(17): Show |
1 | a0001c0001t0006g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+21637_-20+2166 others(28): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(19): Show |
3 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0001g0213 |
3 | HG02602.hp2 NA18959.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-20+21635_-20+2166 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(23): Show |
2 | a0001c0001t0001g0168 a0001c0001t0013g0102 |
2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-20+21660_-20+2166 others(34): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | GATATATA others(27): Show |
1 | a0001c0001t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | G | T | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21633G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850333 | |||||||
| chr18:54850333 | GAT | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(97): Show |
108 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.-20+21659_-20+2166 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | GATATAT | G | 4 | a0001c0001t0008g0061 a0001c0001t0008g0062 a0001c0001t0030g0107 others(1): Show |
4 | HG00738.hp2 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+21655_-20+2166 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | GATATATA others(1): Show |
G | 13 | a0001c0001t0001g0121 a0001c0001t0002g0119 a0001c0001t0004g0122 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+21653_-20+2166 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850333 | GATATATA others(7): Show |
G | 2 | a0001c0001t0004g0015 a0001c0001t0008g0016 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+21647_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | ||||||
| chr18:54850335 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-20+21635T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850335 | |||||||
| chr18:54850337 | T | TATATATA others(147): Show |
1 | a0001c0001t0001g0292 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(158): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | ||||||
| chr18:54850337 | T | TATATATA others(147): Show |
1 | a0001c0001t0007g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(158): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | ||||||
| chr18:54850337 | T | TATATATA others(151): Show |
1 | a0001c0001t0004g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(162): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | ||||||
| chr18:54850338 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-20+21638A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850338 | |||||||
| chr18:54850339 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0268 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-20+21639T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850339 | |||||||
| chr18:54850341 | T | C | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-20+21641T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850341 | |||||||
| chr18:54850353 | T | C | 13 | a0001c0001t0001g0121 a0001c0001t0002g0119 a0001c0001t0004g0122 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+21653T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850353 | |||||||
| chr18:54850356 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(27): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | ||||||
| chr18:54850356 | A | ATATATAT others(15): Show |
1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | ||||||
| chr18:54850356 | A | ATATATAT others(9): Show |
1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | ||||||
| chr18:54850357 | T | C | 17 | a0001c0001t0001g0121 a0001c0001t0001g0176 a0001c0001t0002g0119 others(14): Show |
17 | HG01433.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-20+21657T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850357 | |||||||
| chr18:54850357 | T | TATATATA others(27): Show |
1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850357 | ||||||
| chr18:54850357 | T | TATATATA others(41): Show |
1 | a0001c0001t0033g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(52): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850357 | ||||||
| chr18:54850359 | T | TATATATA others(7): Show |
1 | a0001c0001t0004g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850359 | T | TATATATA others(151): Show |
1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(162): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850359 | T | TATATATA others(7): Show |
1 | a0001c0001t0016g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850359 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850359 | T | TATATATA others(13): Show |
1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-20+21660_-20+2166 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850359 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | ||||||
| chr18:54850361 | C | T | 11 | a0001c0001t0006g0014 a0001c0001t0006g0084 a0001c0001t0006g0086 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+21661C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850361 | |||||||
| chr18:54850435 | A | G | 5 | a0001c0001t0001g0060 a0001c0001t0004g0015 a0001c0001t0008g0004 others(2): Show |
6 | HG02257.hp1 HG02976.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21735A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850435 | |||||||
| chr18:54850559 | G | A | 1 | a0001c0001t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-20+21859G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850559 | |||||||
| chr18:54850593 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-20+21893C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850593 | |||||||
| chr18:54850646 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-20+21946G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850646 | |||||||
| chr18:54850675 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0020 others(105): Show |
111 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-20+21975A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850675 | |||||||
| chr18:54850675 | A | T | 1 | a0001c0001t0010g0142 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+21975A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850675 | |||||||
| chr18:54850736 | CT | C | 3 | a0001c0001t0018g0116 a0001c0001t0040g0195 a0002c0003t0031g0114 |
3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+22040delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850736 | ||||||
| chr18:54850765 | A | G | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+22065A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850765 | |||||||
| chr18:54850865 | T | C | 3 | a0001c0001t0001g0272 a0001c0001t0017g0135 a0001c0001t0017g0150 |
3 | NA18961.hp2 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-20+22165T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850865 | |||||||
| chr18:54850874 | G | T | 3 | a0001c0001t0018g0116 a0001c0001t0040g0195 a0002c0003t0031g0114 |
3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+22174G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850874 | |||||||
| chr18:54850886 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+22186A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850886 | |||||||
| chr18:54850925 | G | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+22225G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850925 | |||||||
| chr18:54851013 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-20+22313T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851013 | |||||||
| chr18:54851134 | A | G | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20+22434A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851134 | |||||||
| chr18:54851216 | A | G | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+22516A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851216 | |||||||
| chr18:54851275 | C | T | 2 | a0001c0001t0004g0015 a0001c0001t0008g0016 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+22575C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851275 | |||||||
| chr18:54851426 | T | G | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-20+22726T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851426 | |||||||
| chr18:54851652 | C | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-20+22952C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851652 | |||||||
| chr18:54851748 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0247 others(1): Show |
5 | NA18942.hp2 NA18990.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+23048C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851748 | |||||||
| chr18:54851831 | A | C | 3 | a0001c0001t0018g0116 a0001c0001t0040g0195 a0002c0003t0031g0114 |
3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+23131A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851831 | |||||||
| chr18:54852020 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0002g0119 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-20+23320C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852020 | |||||||
| chr18:54852152 | C | T | 1 | a0001c0001t0008g0004 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+23452C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852152 | |||||||
| chr18:54852380 | T | G | 1 | a0001c0001t0003g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-20+23680T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852380 | |||||||
| chr18:54852554 | C | A | 2 | a0001c0001t0004g0063 a0001c0001t0004g0106 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+23854C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852554 | |||||||
| chr18:54852620 | A | G | 1 | a0001c0001t0002g0279 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-20+23920A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852620 | |||||||
| chr18:54852743 | A | G | 1 | a0001c0001t0002g0276 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-20+24043A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852743 | |||||||
| chr18:54852854 | G | T | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+24154G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852854 | |||||||
| chr18:54852918 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
188 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(185): Show |
intron_variant | MODIFIER | c.-20+24218C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852918 | |||||||
| chr18:54852945 | T | G | 4 | a0001c0001t0004g0063 a0001c0001t0004g0106 a0001c0001t0018g0182 others(1): Show |
4 | HG00738.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+24245T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852945 | |||||||
| chr18:54853053 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0060 |
2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-20+24353A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853053 | |||||||
| chr18:54853153 | G | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-24414G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853153 | |||||||
| chr18:54853185 | G | A | 93 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(90): Show |
96 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19-24382G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853185 | |||||||
| chr18:54853449 | A | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-24118A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853449 | |||||||
| chr18:54853784 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
74 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-19-23783G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853784 | |||||||
| chr18:54853856 | C | T | 4 | a0001c0001t0002g0196 a0001c0001t0002g0245 a0001c0001t0002g0275 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-23711C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853856 | |||||||
| chr18:54854138 | T | G | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19-23429T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854138 | |||||||
| chr18:54854303 | G | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0003g0002 others(20): Show |
25 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19-23264G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854303 | |||||||
| chr18:54854492 | G | T | 1 | a0001c0001t0038g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-19-23075G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854492 | |||||||
| chr18:54854567 | A | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0244 |
2 | HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-19-23000A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854567 | |||||||
| chr18:54854577 | G | A | 1 | a0001c0001t0015g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-22990G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854577 | |||||||
| chr18:54854609 | A | G | 1 | a0001c0001t0008g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19-22958A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854609 | |||||||
| chr18:54854743 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-19-22824A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854743 | |||||||
| chr18:54854912 | G | C | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22655G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854912 | |||||||
| chr18:54854929 | C | T | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22638C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854929 | |||||||
| chr18:54854951 | A | G | 2 | a0001c0001t0008g0016 a0001c0001t0019g0043 |
2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-22616A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854951 | |||||||
| chr18:54855058 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(13): Show |
17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-22509C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855058 | |||||||
| chr18:54855094 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(13): Show |
17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-22473C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855094 | |||||||
| chr18:54855133 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(12): Show |
16 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-22434G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855133 | |||||||
| chr18:54855170 | G | T | 2 | a0001c0001t0008g0016 a0001c0001t0019g0043 |
2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-22397G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855170 | |||||||
| chr18:54855220 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.-19-22347T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855220 | |||||||
| chr18:54855221 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22346G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855221 | |||||||
| chr18:54855232 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-22335G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855232 | |||||||
| chr18:54855305 | C | T | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-22262C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855305 | |||||||
| chr18:54855332 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-19-22235C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855332 | |||||||
| chr18:54855429 | A | G | 1 | a0001c0001t0022g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-19-22138A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855429 | |||||||
| chr18:54855444 | T | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-22123T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855444 | |||||||
| chr18:54855495 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-19-22072A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855495 | |||||||
| chr18:54855502 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-19-22065A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855502 | |||||||
| chr18:54855512 | G | A | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-19-22055G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855512 | |||||||
| chr18:54855516 | T | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
80 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-19-22051T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855516 | |||||||
| chr18:54855587 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0289 |
2 | NA18966.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-19-21980G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855587 | |||||||
| chr18:54855610 | C | T | 81 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(78): Show |
84 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-21957C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855610 | |||||||
| chr18:54855802 | C | G | 1 | a0001c0001t0002g0243 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-19-21765C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855802 | |||||||
| chr18:54855850 | G | T | 2 | a0001c0001t0008g0016 a0001c0001t0019g0043 |
2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-21717G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855850 | |||||||
| chr18:54855899 | T | C | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-21668T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855899 | |||||||
| chr18:54855900 | C | T | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-21667C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855900 | |||||||
| chr18:54856147 | G | T | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-21420G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856147 | |||||||
| chr18:54856206 | T | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0020 others(98): Show |
103 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-19-21361T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856206 | |||||||
| chr18:54856230 | T | G | 8 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0079 others(5): Show |
8 | HG02602.hp2 HG02683.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-21337T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856230 | |||||||
| chr18:54856246 | G | A | 81 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(78): Show |
84 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-21321G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856246 | |||||||
| chr18:54856541 | G | A | 3 | a0001c0001t0018g0116 a0001c0001t0040g0195 a0002c0003t0031g0114 |
3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-19-21026G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856541 | |||||||
| chr18:54856759 | A | G | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-20808A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856759 | |||||||
| chr18:54857005 | C | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0073 a0001c0001t0003g0082 others(2): Show |
5 | HG00639.hp1 HG02602.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-20562C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857005 | |||||||
| chr18:54857077 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
81 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-20490A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857077 | |||||||
| chr18:54857253 | C | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0260 a0001c0001t0002g0276 |
4 | HG00673.hp1 HG02129.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-20314C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857253 | |||||||
| chr18:54857348 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-20219A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857348 | |||||||
| chr18:54857453 | C | T | 1 | a0002c0003t0031g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19-20114C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857453 | |||||||
| chr18:54857520 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-19-20047C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857520 | |||||||
| chr18:54857601 | A | G | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-19966A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857601 | |||||||
| chr18:54857623 | C | G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0106 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-19944C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857623 | |||||||
| chr18:54857683 | C | T | 1 | a0001c0001t0026g0319 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-19-19884C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857683 | |||||||
| chr18:54857729 | CA | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(13): Show |
17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-19836delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54857729 | ||||||
| chr18:54857787 | A | G | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-19780A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857787 | |||||||
| chr18:54857864 | C | A | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-19703C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857864 | |||||||
| chr18:54857967 | T | C | 1 | a0001c0001t0009g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-19-19600T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857967 | |||||||
| chr18:54858016 | T | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0027 others(77): Show |
82 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-19-19551T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858016 | |||||||
| chr18:54858126 | C | T | 3 | a0001c0001t0018g0116 a0001c0001t0040g0195 a0002c0003t0031g0114 |
3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-19-19441C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858126 | |||||||
| chr18:54858347 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-19220A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858347 | |||||||
| chr18:54858354 | G | T | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-19213G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858354 | |||||||
| chr18:54858357 | C | T | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-19210C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858357 | |||||||
| chr18:54858377 | GT | G | 110 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
113 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-19-19165delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | ||||||
| chr18:54858377 | GTT | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.-19-19166_-19-1916 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | ||||||
| chr18:54858377 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0106 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-19176_-19-1916 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | ||||||
| chr18:54858385 | T | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0002g0170 others(10): Show |
13 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-19182T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858385 | |||||||
| chr18:54858386 | T | G | 106 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(103): Show |
109 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-19-19181T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858386 | |||||||
| chr18:54858387 | T | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.-19-19180T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858387 | |||||||
| chr18:54858390 | T | G | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-19177T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858390 | |||||||
| chr18:54858477 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0009g0100 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-19-19090C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858477 | |||||||
| chr18:54858517 | GGGACTA | G | 4 | a0001c0001t0005g0056 a0001c0001t0005g0064 a0001c0001t0005g0066 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19049_-19-1904 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858517 | |||||||
| chr18:54858524 | C | T | 4 | a0001c0001t0005g0056 a0001c0001t0005g0064 a0001c0001t0005g0066 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19043C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858524 | |||||||
| chr18:54858527 | G | T | 4 | a0001c0001t0005g0056 a0001c0001t0005g0064 a0001c0001t0005g0066 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19040G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858527 | |||||||
| chr18:54858528 | T | C | 4 | a0001c0001t0005g0056 a0001c0001t0005g0064 a0001c0001t0005g0066 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19039T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858528 | |||||||
| chr18:54858544 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
81 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-19023C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858544 | |||||||
| chr18:54858581 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18986G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858581 | |||||||
| chr18:54858622 | G | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-18945G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858622 | |||||||
| chr18:54858817 | A | G | 3 | a0001c0001t0002g0218 a0001c0001t0002g0242 a0001c0001t0002g0291 |
3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-19-18750A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858817 | |||||||
| chr18:54858832 | A | G | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18735A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858832 | |||||||
| chr18:54858857 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-19-18710G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858857 | |||||||
| chr18:54858894 | A | G | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-18673A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858894 | |||||||
| chr18:54858940 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-19-18627T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858940 | |||||||
| chr18:54859098 | C | T | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18469C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859098 | |||||||
| chr18:54859203 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-18364A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859203 | |||||||
| chr18:54859207 | G | A | 1 | a0001c0001t0045g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19-18360G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859207 | |||||||
| chr18:54859406 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19-18161C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859406 | |||||||
| chr18:54859486 | C | CA | 18 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0081 others(15): Show |
18 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19-18066dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | ||||||
| chr18:54859486 | CA | C | 38 | a0001c0001t0001g0052 a0001c0001t0001g0103 a0001c0001t0001g0105 others(35): Show |
38 | HG00738.hp1 HG01070.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-18066delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | ||||||
| chr18:54859486 | CAA | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0027 others(62): Show |
67 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-19-18067_-19-1806 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | ||||||
| chr18:54859511 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-19-18056C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859511 | |||||||
| chr18:54859740 | A | T | 2 | a0001c0001t0008g0118 a0001c0001t0033g0174 |
2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-17827A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859740 | |||||||
| chr18:54859753 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19-17814G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859753 | |||||||
| chr18:54859839 | C | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.-19-17728C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859839 | |||||||
| chr18:54859990 | A | T | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-17577A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859990 | |||||||
| chr18:54860068 | T | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0020 others(99): Show |
104 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-17499T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860068 | |||||||
| chr18:54860075 | A | T | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-17492A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860075 | |||||||
| chr18:54860085 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19-17482T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860085 | |||||||
| chr18:54860234 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0027 others(79): Show |
84 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-17333T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860234 | |||||||
| chr18:54860655 | T | C | 1 | a0003c0002t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-16912T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860655 | |||||||
| chr18:54860760 | A | T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0281 |
2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-19-16807A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860760 | |||||||
| chr18:54860903 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0002g0009 a0001c0001t0002g0232 |
4 | HG01358.hp1 HG01978.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-16664T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860903 | |||||||
| chr18:54860906 | C | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-16661C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860906 | |||||||
| chr18:54861110 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19-16457T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861110 | |||||||
| chr18:54861142 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-19-16425T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861142 | |||||||
| chr18:54861304 | T | C | 1 | a0001c0001t0040g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-16263T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861304 | |||||||
| chr18:54861304 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-19-16263T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861304 | |||||||
| chr18:54861313 | A | T | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-16254A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861313 | |||||||
| chr18:54861457 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(75): Show |
81 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-19-16110G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861457 | |||||||
| chr18:54861494 | C | T | 2 | a0001c0001t0004g0063 a0001c0001t0004g0106 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-16073C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861494 | |||||||
| chr18:54861548 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-16019A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861548 | |||||||
| chr18:54861618 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(73): Show |
80 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-19-15949G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861618 | |||||||
| chr18:54861704 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19-15863C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861704 | |||||||
| chr18:54861731 | G | T | 1 | a0001c0001t0012g0026 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-19-15836G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861731 | |||||||
| chr18:54861739 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0268 |
3 | HG00099.hp2 HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-19-15828A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861739 | |||||||
| chr18:54861847 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(5): Show |
9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-15720A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861847 | |||||||
| chr18:54861897 | T | C | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-15670T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861897 | |||||||
| chr18:54861920 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-15647A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861920 | |||||||
| chr18:54862005 | T | C | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-15562T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862005 | |||||||
| chr18:54862059 | GA | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
285 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(282): Show |
intron_variant | MODIFIER | c.-19-15496delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54862059 | ||||||
| chr18:54862059 | GAA | G | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-15497_-19-1549 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54862059 | ||||||
| chr18:54862237 | T | C | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-15330T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862237 | |||||||
| chr18:54862398 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0002g0119 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19-15169A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862398 | |||||||
| chr18:54862401 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-15166G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862401 | |||||||
| chr18:54862491 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-19-15076G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862491 | |||||||
| chr18:54862787 | G | A | 90 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(87): Show |
93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-14780G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862787 | |||||||
| chr18:54862910 | T | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-14657T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862910 | |||||||
| chr18:54862915 | G | T | 1 | a0001c0001t0010g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-14652G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862915 | |||||||
| chr18:54862928 | T | G | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-19-14639T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862928 | |||||||
| chr18:54863154 | G | C | 93 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(90): Show |
96 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19-14413G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863154 | |||||||
| chr18:54863174 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(72): Show |
79 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-14393A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863174 | |||||||
| chr18:54863182 | T | C | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-14385T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863182 | |||||||
| chr18:54863183 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-19-14384G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863183 | |||||||
| chr18:54863208 | G | T | 1 | a0001c0001t0002g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-14359G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863208 | |||||||
| chr18:54863453 | A | G | 2 | a0001c0001t0002g0216 a0001c0001t0002g0237 |
2 | HG02083.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-19-14114A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863453 | |||||||
| chr18:54863570 | T | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0045 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-19-13997T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863570 | |||||||
| chr18:54863583 | C | A | 1 | a0001c0001t0003g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-13984C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863583 | |||||||
| chr18:54863647 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-19-13920G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863647 | |||||||
| chr18:54863766 | A | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-19-13801A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863766 | |||||||
| chr18:54863967 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(168): Show |
178 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.-19-13600T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863967 | |||||||
| chr18:54863977 | T | C | 6 | a0001c0001t0008g0004 a0001c0001t0008g0016 a0001c0001t0008g0061 others(3): Show |
7 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-13590T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863977 | |||||||
| chr18:54864136 | A | AGGAG | 13 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(10): Show |
14 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-13428_-19-1342 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54864136 | ||||||
| chr18:54864280 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19-13287C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864280 | |||||||
| chr18:54864496 | A | T | 1 | a0001c0001t0001g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-19-13071A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864496 | |||||||
| chr18:54864496 | AT | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(70): Show |
77 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-19-13062delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54864496 | ||||||
| chr18:54864931 | G | T | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12636G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864931 | |||||||
| chr18:54864943 | G | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(17): Show |
22 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-12624G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864943 | |||||||
| chr18:54864976 | G | C | 1 | a0001c0001t0003g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-19-12591G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864976 | |||||||
| chr18:54865031 | A | T | 2 | a0001c0001t0004g0063 a0001c0001t0004g0106 |
2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-12536A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865031 | |||||||
| chr18:54865089 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19-12478A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865089 | |||||||
| chr18:54865184 | C | T | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-12383C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865184 | |||||||
| chr18:54865200 | T | A | 1 | a0001c0001t0002g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-19-12367T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865200 | |||||||
| chr18:54865232 | G | T | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-12335G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865232 | |||||||
| chr18:54865237 | T | TTG | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(71): Show |
75 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-19-12294_-19-1229 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | T | TTGTG | 43 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(40): Show |
43 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-12296_-19-1229 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | T | TTGTGTG | 27 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0034 others(24): Show |
30 | HG00673.hp2 HG01081.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-12298_-19-1229 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | T | TTGTGTGT others(1): Show |
30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(27): Show |
31 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19-12300_-19-1229 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0103 a0001c0001t0001g0163 a0001c0001t0003g0068 others(4): Show |
7 | HG00099.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-12302_-19-1229 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0003g0073 a0001c0001t0003g0154 a0001c0001t0003g0157 others(1): Show |
4 | HG01433.hp1 HG01496.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-12304_-19-1229 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | TTG | T | 13 | a0001c0001t0001g0130 a0001c0001t0001g0153 a0001c0001t0001g0178 others(10): Show |
13 | HG00621.hp1 HG01109.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-12294_-19-1229 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | TTGTG | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0050 others(92): Show |
99 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-19-12296_-19-1229 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865237 | TTGTGTG | T | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0002g0192 others(2): Show |
5 | HG01069.hp1 HG01074.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-12298_-19-1229 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | ||||||
| chr18:54865355 | C | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-19-12212C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865355 | |||||||
| chr18:54865379 | TC | T | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12187delC | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865379 | |||||||
| chr18:54865403 | T | C | 97 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(94): Show |
100 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19-12164T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865403 | |||||||
| chr18:54865427 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-12140A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865427 | |||||||
| chr18:54865529 | T | C | 1 | a0001c0001t0008g0004 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-12038T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865529 | |||||||
| chr18:54865672 | C | T | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11895C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865672 | |||||||
| chr18:54865737 | A | G | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11830A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865737 | |||||||
| chr18:54865739 | T | A | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11828T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865739 | |||||||
| chr18:54865779 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(43): Show |
50 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-19-11788A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865779 | |||||||
| chr18:54865807 | C | T | 89 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(86): Show |
92 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19-11760C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865807 | |||||||
| chr18:54865845 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(303): Show |
318 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(315): Show |
intron_variant | MODIFIER | c.-19-11722T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865845 | |||||||
| chr18:54865860 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-19-11707A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865860 | |||||||
| chr18:54865946 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(34): Show |
40 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19-11621A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865946 | |||||||
| chr18:54865959 | G | T | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-11608G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865959 | |||||||
| chr18:54866095 | CA | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11462delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54866095 | ||||||
| chr18:54866105 | AC | A | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11461delC | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866105 | |||||||
| chr18:54866108 | G | C | 8 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11459G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866108 | |||||||
| chr18:54866149 | G | A | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-11418G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866149 | |||||||
| chr18:54866221 | T | A | 95 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(92): Show |
98 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.-19-11346T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866221 | |||||||
| chr18:54866263 | TCCTCCCC others(1): Show |
T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(72): Show |
79 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19-11285_-19-1127 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54866263 | ||||||
| chr18:54866299 | C | T | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-11268C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866299 | |||||||
| chr18:54866306 | T | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11261T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866306 | |||||||
| chr18:54866372 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0308 others(16): Show |
21 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-11195C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866372 | |||||||
| chr18:54866381 | C | T | 3 | a0001c0001t0007g0075 a0001c0001t0013g0101 a0001c0001t0013g0102 |
3 | HG01261.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-19-11186C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866381 | |||||||
| chr18:54866457 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11110G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866457 | |||||||
| chr18:54866532 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-19-11035A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866532 | |||||||
| chr18:54866645 | C | A | 1 | a0001c0001t0004g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-10922C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866645 | |||||||
| chr18:54866850 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-10717G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866850 | |||||||
| chr18:54866985 | C | A | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-10582C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866985 | |||||||
| chr18:54867018 | C | G | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-10549C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867018 | |||||||
| chr18:54867038 | G | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10529G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867038 | |||||||
| chr18:54867063 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-19-10504G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867063 | |||||||
| chr18:54867231 | G | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10336G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867231 | |||||||
| chr18:54867256 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19-10311C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867256 | |||||||
| chr18:54867438 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-10129T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867438 | |||||||
| chr18:54867442 | C | CT | 99 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0050 others(96): Show |
102 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19-10105dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | ||||||
| chr18:54867442 | C | CTT | 8 | a0001c0001t0001g0320 a0001c0001t0002g0236 a0001c0001t0002g0290 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-10106_-19-1010 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | ||||||
| chr18:54867442 | C | CTTTTCT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(66): Show |
73 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | ||||||
| chr18:54867442 | C | CTTTTCTT others(4): Show |
1 | a0001c0001t0003g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19-10121_-19-1012 others(15): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | ||||||
| chr18:54867445 | T | TTC | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(68): Show |
74 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867445 | ||||||
| chr18:54867446 | T | TC | 8 | a0001c0001t0001g0228 a0001c0001t0008g0004 a0001c0001t0008g0016 others(5): Show |
9 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867446 | |||||||
| chr18:54867446 | T | TCTTTTCT others(19): Show |
2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867446 | |||||||
| chr18:54867447 | T | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10120T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867447 | |||||||
| chr18:54867456 | T | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10111T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867456 | |||||||
| chr18:54867549 | C | T | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-10018C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867549 | |||||||
| chr18:54867718 | T | C | 1 | a0001c0001t0016g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19-9849T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867718 | |||||||
| chr18:54867725 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0002g0119 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19-9842G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867725 | |||||||
| chr18:54867740 | C | T | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-9827C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867740 | |||||||
| chr18:54867792 | G | T | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-9775G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867792 | |||||||
| chr18:54867834 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-19-9733A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867834 | |||||||
| chr18:54867966 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(69): Show |
76 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-19-9601G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867966 | |||||||
| chr18:54867973 | T | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-9594T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867973 | |||||||
| chr18:54868066 | T | C | 1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-9501T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868066 | |||||||
| chr18:54868138 | G | C | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-9429G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868138 | |||||||
| chr18:54868210 | A | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(17): Show |
22 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-9357A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868210 | |||||||
| chr18:54868257 | A | G | 1 | a0001c0001t0033g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-9310A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868257 | |||||||
| chr18:54868425 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-9142C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868425 | |||||||
| chr18:54868439 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-19-9128A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868439 | |||||||
| chr18:54868442 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19-9125T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868442 | |||||||
| chr18:54868522 | T | G | 1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-9045T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868522 | |||||||
| chr18:54868541 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-19-9026G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868541 | |||||||
| chr18:54868554 | T | C | 94 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(91): Show |
97 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.-19-9013T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868554 | |||||||
| chr18:54868603 | C | CGTT | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(89): Show |
96 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19-8945_-19-8943d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | ||||||
| chr18:54868603 | C | CGTTGTT | 125 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(122): Show |
128 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.-19-8948_-19-8943d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | ||||||
| chr18:54868603 | C | CGTTGTTG others(2): Show |
67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(64): Show |
71 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19-8951_-19-8943d others(11): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | ||||||
| chr18:54868603 | C | CGTTGTTG others(5): Show |
6 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0076 others(3): Show |
6 | HG02109.hp1 HG02602.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8954_-19-8943d others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | ||||||
| chr18:54868603 | C | CGTTGTTG others(8): Show |
1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-8957_-19-8943d others(17): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | ||||||
| chr18:54868641 | G | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-8926G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868641 | |||||||
| chr18:54868694 | A | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
intron_variant | MODIFIER | c.-19-8873A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868694 | |||||||
| chr18:54868751 | C | A | 3 | a0001c0001t0018g0182 a0001c0001t0042g0111 a0001c0001t0043g0115 |
3 | HG02965.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-8816C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868751 | |||||||
| chr18:54868776 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-8791G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868776 | |||||||
| chr18:54868961 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-19-8606G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868961 | |||||||
| chr18:54869054 | T | G | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-8513T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869054 | |||||||
| chr18:54869063 | G | A | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-8504G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869063 | |||||||
| chr18:54869097 | T | C | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-8470T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869097 | |||||||
| chr18:54869268 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-19-8299T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869268 | |||||||
| chr18:54869268 | T | G | 1 | a0001c0001t0006g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-8299T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869268 | |||||||
| chr18:54869378 | C | A | 2 | a0001c0001t0008g0118 a0001c0001t0033g0174 |
2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-8189C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869378 | |||||||
| chr18:54869471 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-8096G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869471 | |||||||
| chr18:54869493 | A | G | 90 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(87): Show |
93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-8074A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869493 | |||||||
| chr18:54869669 | A | C | 1 | a0001c0001t0004g0083 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-7898A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869669 | |||||||
| chr18:54869715 | A | G | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-7852A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869715 | |||||||
| chr18:54869773 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-19-7794G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869773 | |||||||
| chr18:54869944 | C | A | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-7623C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869944 | |||||||
| chr18:54869945 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-7622A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869945 | |||||||
| chr18:54869962 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-7605G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869962 | |||||||
| chr18:54869999 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0002g0009 a0001c0001t0002g0232 |
4 | HG01358.hp1 HG01978.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-7568A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869999 | |||||||
| chr18:54870032 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-7535A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870032 | |||||||
| chr18:54870093 | G | A | 87 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(84): Show |
90 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.-19-7474G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870093 | |||||||
| chr18:54870399 | C | A | 90 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(87): Show |
93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-7168C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870399 | |||||||
| chr18:54870518 | G | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-7049G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870518 | |||||||
| chr18:54870544 | A | T | 1 | a0001c0001t0004g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-7023A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870544 | |||||||
| chr18:54870578 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
intron_variant | MODIFIER | c.-19-6989G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870578 | |||||||
| chr18:54870840 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-6727C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870840 | |||||||
| chr18:54870847 | G | A | 4 | a0001c0001t0012g0017 a0001c0001t0012g0019 a0001c0001t0012g0026 others(1): Show |
4 | NA18941.hp1 NA19075.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-6720G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870847 | |||||||
| chr18:54870895 | A | T | 1 | a0001c0001t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-19-6672A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870895 | |||||||
| chr18:54871003 | A | G | 7 | a0001c0001t0005g0059 a0001c0001t0005g0117 a0001c0001t0005g0198 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-6564A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871003 | |||||||
| chr18:54871152 | A | T | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-6415A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871152 | |||||||
| chr18:54871233 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-6334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871233 | |||||||
| chr18:54871632 | C | T | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-5935C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871632 | |||||||
| chr18:54871682 | C | G | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-5885C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871682 | |||||||
| chr18:54871707 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-19-5860G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871707 | |||||||
| chr18:54871724 | C | G | 1 | a0001c0001t0014g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-19-5843C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871724 | |||||||
| chr18:54871849 | C | CA | 87 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0050 others(84): Show |
91 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.-19-5698dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | ||||||
| chr18:54871849 | C | CAA | 13 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0079 others(10): Show |
13 | HG00642.hp2 HG02258.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-5699_-19-5698d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | ||||||
| chr18:54871849 | CA | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(22): Show |
26 | HG00438.hp1 HG00735.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19-5698delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | ||||||
| chr18:54871849 | CAAA | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(8): Show |
12 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-5700_-19-5698d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | ||||||
| chr18:54871865 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-19-5702A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871865 | |||||||
| chr18:54871903 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(105): Show |
111 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-19-5664G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871903 | |||||||
| chr18:54872087 | A | T | 2 | a0001c0001t0002g0290 a0001c0001t0045g0042 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-19-5480A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872087 | |||||||
| chr18:54872100 | G | C | 1 | a0001c0001t0002g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19-5467G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872100 | |||||||
| chr18:54872114 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-5453A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872114 | |||||||
| chr18:54872374 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-5193C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872374 | |||||||
| chr18:54872397 | G | A | 2 | a0001c0001t0008g0118 a0001c0001t0033g0174 |
2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-5170G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872397 | |||||||
| chr18:54872438 | C | A | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-5129C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872438 | |||||||
| chr18:54872530 | CAGG | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(9): Show |
13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-5034_-19-5032d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872530 | ||||||
| chr18:54872565 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-19-5002C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872565 | |||||||
| chr18:54872625 | T | TA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(73): Show |
80 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-19-4927dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872625 | ||||||
| chr18:54872625 | TA | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
113 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-19-4927delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872625 | ||||||
| chr18:54873058 | A | C | 1 | a0001c0001t0002g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-4509A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873058 | |||||||
| chr18:54873069 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-4498C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873069 | |||||||
| chr18:54873094 | T | TCCTACTT others(309): Show |
2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-4461_-19-4460i others(318): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873094 | ||||||
| chr18:54873189 | G | A | 205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(202): Show |
211 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.-19-4378G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873189 | |||||||
| chr18:54873496 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-4071T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873496 | |||||||
| chr18:54873510 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(69): Show |
76 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-19-4057C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873510 | |||||||
| chr18:54873642 | C | CAAAAAAA others(308): Show |
3 | a0001c0001t0001g0320 a0001c0001t0018g0116 a0002c0003t0031g0114 |
3 | HG00642.hp1 HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-3911_-19-3910i others(317): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873642 | ||||||
| chr18:54873642 | C | CAAAAAAA others(309): Show |
1 | a0001c0001t0040g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-3911_-19-3910i others(318): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873642 | ||||||
| chr18:54873685 | C | CTG | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0027 others(56): Show |
63 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-19-3839_-19-3838d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | C | CTGTG | 28 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0134 others(25): Show |
28 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-3841_-19-3838d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | C | CTGTGTG | 17 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0156 others(14): Show |
17 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-3843_-19-3838d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0186 a0001c0001t0001g0272 others(3): Show |
6 | HG02129.hp1 HG04115.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-3845_-19-3838d others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0162 a0001c0001t0002g0192 a0001c0001t0033g0174 |
3 | HG00099.hp2 HG02486.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-19-3847_-19-3838d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTG | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0039 others(32): Show |
37 | HG01099.hp2 HG01243.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19-3839_-19-3838d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTG | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(27): Show |
30 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19-3841_-19-3838d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTG | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0079 others(12): Show |
15 | HG01175.hp2 HG02723.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-3843_-19-3838d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(1): Show |
C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(49): Show |
55 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-19-3845_-19-3838d others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(3): Show |
C | 14 | a0001c0001t0001g0070 a0001c0001t0003g0002 a0001c0001t0003g0067 others(11): Show |
15 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-3847_-19-3838d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(5): Show |
C | 1 | a0004c0004t0007g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-3849_-19-3838d others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0002g0226 a0001c0001t0008g0004 |
3 | HG01433.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-3851_-19-3838d others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0008g0061 a0001c0001t0008g0062 a0001c0001t0008g0087 |
3 | HG02622.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-19-3853_-19-3838d others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873685 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0002g0009 | 2 | HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-19-3857_-19-3838d others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | ||||||
| chr18:54873730 | A | T | 1 | a0001c0001t0004g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-3837A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873730 | |||||||
| chr18:54873752 | TAGAC | T | 4 | a0001c0001t0001g0172 a0001c0001t0004g0112 a0001c0001t0028g0041 others(1): Show |
4 | HG01934.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-3811_-19-3808d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873752 | ||||||
| chr18:54873836 | G | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.-19-3731G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873836 | |||||||
| chr18:54873872 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0163 others(4): Show |
7 | NA18941.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-3695G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873872 | |||||||
| chr18:54873880 | G | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.-19-3687G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873880 | |||||||
| chr18:54873899 | C | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0163 others(4): Show |
7 | NA18941.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-3668C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873899 | |||||||
| chr18:54874133 | G | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-3434G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874133 | |||||||
| chr18:54874174 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-3393A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874174 | |||||||
| chr18:54874268 | A | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.-19-3299A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874268 | |||||||
| chr18:54874519 | A | G | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-3048A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874519 | |||||||
| chr18:54874540 | G | A | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-3027G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874540 | |||||||
| chr18:54874547 | T | C | 1 | a0001c0001t0018g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-3020T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874547 | |||||||
| chr18:54874557 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
113 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-19-3010T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874557 | |||||||
| chr18:54874562 | T | TA | 11 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19-2988dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | ||||||
| chr18:54874562 | TA | T | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(198): Show |
206 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-19-2988delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | ||||||
| chr18:54874562 | TAA | T | 7 | a0001c0001t0001g0184 a0001c0001t0001g0256 a0001c0001t0001g0320 others(4): Show |
7 | HG00642.hp1 HG01070.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2989_-19-2988d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | ||||||
| chr18:54874656 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19-2911C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874656 | |||||||
| chr18:54874665 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(5): Show |
9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-2902A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874665 | |||||||
| chr18:54874708 | A | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0164 a0001c0001t0001g0179 |
3 | HG00609.hp1 HG02074.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-19-2859A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874708 | |||||||
| chr18:54874755 | G | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.-19-2812G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874755 | |||||||
| chr18:54874757 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.-19-2810A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874757 | |||||||
| chr18:54874776 | T | C | 7 | a0001c0001t0006g0014 a0001c0001t0006g0084 a0001c0001t0006g0086 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2791T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874776 | |||||||
| chr18:54874930 | T | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(6): Show |
10 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-2637T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874930 | |||||||
| chr18:54875081 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0286 |
2 | NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-19-2486C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875081 | |||||||
| chr18:54875194 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
113 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-19-2373C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875194 | |||||||
| chr18:54875341 | T | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-2226T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875341 | |||||||
| chr18:54875539 | AG | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(201): Show |
210 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.-19-2026delG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54875539 | ||||||
| chr18:54875540 | GGT | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(76): Show |
83 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-19-2026_-19-2025d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875540 | |||||||
| chr18:54875541 | GT | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-2012delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54875541 | ||||||
| chr18:54875542 | T | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(201): Show |
210 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.-19-2025T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875542 | |||||||
| chr18:54875543 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(76): Show |
83 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-19-2024T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875543 | |||||||
| chr18:54875583 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-19-1984A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875583 | |||||||
| chr18:54875727 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0016 a0001c0001t0008g0061 others(3): Show |
7 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1840G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875727 | |||||||
| chr18:54875917 | C | T | 1 | a0001c0001t0015g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-1650C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875917 | |||||||
| chr18:54875960 | T | G | 4 | a0001c0001t0001g0320 a0001c0001t0018g0116 a0001c0001t0040g0195 others(1): Show |
4 | HG00642.hp1 HG02145.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1607T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875960 | |||||||
| chr18:54876030 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-1537T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876030 | |||||||
| chr18:54876031 | A | C | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-1536A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876031 | |||||||
| chr18:54876053 | G | A | 1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-1514G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876053 | |||||||
| chr18:54876086 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-1481T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876086 | |||||||
| chr18:54876098 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-1469G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876098 | |||||||
| chr18:54876130 | G | A | 87 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(84): Show |
90 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.-19-1437G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876130 | |||||||
| chr18:54876387 | G | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-1180G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876387 | |||||||
| chr18:54876419 | GAGGTGGA others(22): Show |
G | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-1146_-19-1118d others(31): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54876419 | ||||||
| chr18:54876439 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(70): Show |
77 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-19-1128C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876439 | |||||||
| chr18:54876620 | C | T | 1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-947C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876620 | |||||||
| chr18:54876655 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-912T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876655 | |||||||
| chr18:54876904 | C | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-663C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876904 | |||||||
| chr18:54876941 | A | G | 2 | a0001c0001t0004g0112 a0001c0001t0029g0055 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-626A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876941 | |||||||
| chr18:54876985 | C | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0144 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-582C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876985 | |||||||
| chr18:54877023 | GT | G | 89 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(86): Show |
92 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19-541delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54877023 | ||||||
| chr18:54877211 | G | A | 1 | a0001c0001t0001g0005 | 2 | NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-19-356G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54877211 | |||||||
| chr18:54877776 | C | T | 5 | a0001c0001t0010g0046 a0001c0001t0018g0182 a0001c0001t0030g0107 others(2): Show |
5 | HG00738.hp2 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+38C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877776 | |||||||
| chr18:54877782 | A | G | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.153+44A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877782 | |||||||
| chr18:54877841 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.153+103G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877841 | |||||||
| chr18:54877983 | A | T | 1 | a0001c0001t0024g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.153+245A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877983 | |||||||
| chr18:54878017 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.153+279A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878017 | |||||||
| chr18:54878067 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153+329A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878067 | |||||||
| chr18:54878074 | T | C | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+336T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878074 | |||||||
| chr18:54878218 | C | T | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153+480C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878218 | |||||||
| chr18:54878580 | T | A | 1 | a0001c0001t0002g0187 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.154-789T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878580 | |||||||
| chr18:54878635 | A | G | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154-734A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878635 | |||||||
| chr18:54878658 | A | G | 95 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0051 others(92): Show |
98 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.154-711A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878658 | |||||||
| chr18:54878673 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0004g0122 a0001c0001t0004g0304 |
3 | HG02647.hp1 HG02809.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-696C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878673 | |||||||
| chr18:54878753 | A | AT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(83): Show |
90 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.154-609dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 54878753 | ||||||
| chr18:54878760 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.154-609T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878760 | |||||||
| chr18:54878760 | T | TA | 193 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(190): Show |
199 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.154-602dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 54878760 | ||||||
| chr18:54878781 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.154-588A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878781 | |||||||
| chr18:54879115 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
73 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.154-254T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54879115 | |||||||
| chr18:54879314 | T | A | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154-55T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54879314 | |||||||
| chr18:54879482 | T | C | 1 | a0001c0001t0041g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239+28T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879482 | |||||||
| chr18:54879507 | T | C | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.239+53T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879507 | |||||||
| chr18:54879639 | G | C | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+185G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879639 | |||||||
| chr18:54879698 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.239+244A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879698 | |||||||
| chr18:54879793 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.239+339G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879793 | |||||||
| chr18:54879826 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(188): Show |
198 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(195): Show |
intron_variant | MODIFIER | c.239+372G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879826 | |||||||
| chr18:54879911 | T | C | 24 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0072 others(21): Show |
24 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.239+457T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879911 | |||||||
| chr18:54879949 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.239+495C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879949 | |||||||
| chr18:54880059 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.239+605C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880059 | |||||||
| chr18:54880107 | CA | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
262 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(259): Show |
intron_variant | MODIFIER | c.239+654delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880107 | |||||||
| chr18:54880258 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0002g0119 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.239+804G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880258 | |||||||
| chr18:54880310 | A | G | 3 | a0001c0001t0010g0046 a0001c0001t0010g0314 a0001c0001t0040g0195 |
3 | HG03041.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.239+856A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880310 | |||||||
| chr18:54880510 | G | A | 7 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0038 others(4): Show |
7 | HG01123.hp1 HG01256.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1056G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880510 | |||||||
| chr18:54880525 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(74): Show |
81 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.239+1071G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880525 | |||||||
| chr18:54880844 | G | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
intron_variant | MODIFIER | c.239+1390G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880844 | |||||||
| chr18:54880878 | A | T | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+1424A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880878 | |||||||
| chr18:54880892 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(195): Show |
206 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(203): Show |
intron_variant | MODIFIER | c.239+1438G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880892 | |||||||
| chr18:54881014 | G | A | 75 | a0001c0001t0001g0039 a0001c0001t0001g0120 a0001c0001t0001g0241 others(72): Show |
78 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.239+1560G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881014 | |||||||
| chr18:54881130 | T | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(101): Show |
108 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.239+1676T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881130 | |||||||
| chr18:54881169 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(157): Show |
167 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.239+1715C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881169 | |||||||
| chr18:54881315 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.239+1861G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881315 | |||||||
| chr18:54881333 | A | G | 4 | a0001c0001t0001g0201 a0001c0001t0001g0246 a0001c0001t0001g0255 others(1): Show |
4 | HG01081.hp1 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1879A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881333 | |||||||
| chr18:54881339 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.239+1885G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881339 | |||||||
| chr18:54881374 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.239+1920T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881374 | |||||||
| chr18:54881395 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+1941C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881395 | |||||||
| chr18:54881445 | G | C | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.239+1991G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881445 | |||||||
| chr18:54881503 | C | T | 2 | a0001c0001t0009g0092 a0001c0001t0021g0093 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.239+2049C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881503 | |||||||
| chr18:54881702 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.239+2248T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881702 | |||||||
| chr18:54881720 | G | A | 3 | a0001c0001t0008g0016 a0001c0001t0014g0065 a0001c0001t0014g0205 |
3 | HG03471.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.239+2266G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881720 | |||||||
| chr18:54881764 | A | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.239+2310A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881764 | |||||||
| chr18:54881793 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.239+2339G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881793 | |||||||
| chr18:54882033 | G | T | 2 | a0001c0001t0009g0092 a0001c0001t0021g0093 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.240-2300G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882033 | |||||||
| chr18:54882165 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.240-2168G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882165 | |||||||
| chr18:54882368 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(70): Show |
77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.240-1965G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882368 | |||||||
| chr18:54882501 | G | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-1832G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882501 | |||||||
| chr18:54882518 | T | C | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240-1815T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882518 | |||||||
| chr18:54882541 | G | A | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240-1792G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882541 | |||||||
| chr18:54882597 | T | G | 1 | a0001c0001t0030g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.240-1736T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882597 | |||||||
| chr18:54882690 | G | C | 75 | a0001c0001t0001g0039 a0001c0001t0001g0120 a0001c0001t0001g0241 others(72): Show |
78 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.240-1643G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882690 | |||||||
| chr18:54882830 | C | T | 85 | a0001c0001t0001g0039 a0001c0001t0001g0120 a0001c0001t0001g0241 others(82): Show |
88 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.240-1503C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882830 | |||||||
| chr18:54882920 | A | T | 1 | a0001c0001t0004g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.240-1413A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882920 | |||||||
| chr18:54883055 | A | G | 1 | a0001c0001t0006g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.240-1278A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883055 | |||||||
| chr18:54883370 | T | A | 3 | a0001c0001t0010g0191 a0001c0001t0014g0065 a0001c0001t0014g0205 |
3 | HG03195.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-963T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883370 | |||||||
| chr18:54883387 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(159): Show |
169 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(166): Show |
intron_variant | MODIFIER | c.240-946A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883387 | |||||||
| chr18:54883390 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.240-943G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883390 | |||||||
| chr18:54883646 | G | A | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.240-687G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883646 | |||||||
| chr18:54883839 | A | G | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.240-494A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883839 | |||||||
| chr18:54884093 | CTG | C | 22 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0072 others(19): Show |
22 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.240-234_240-233del others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 54884093 | ||||||
| chr18:54884094 | T | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-239T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884094 | |||||||
| chr18:54884139 | T | TA | 14 | a0001c0001t0001g0069 a0001c0001t0001g0184 a0001c0001t0001g0262 others(11): Show |
14 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-183dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 54884139 | ||||||
| chr18:54884224 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0242 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.240-109T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884224 | |||||||
| chr18:54884310 | T | C | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-23T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884310 | |||||||
| chr18:54884466 | C | T | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343+30C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884466 | |||||||
| chr18:54884485 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(91): Show |
97 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.343+49C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884485 | |||||||
| chr18:54884575 | TGTGTCAC others(1): Show |
T | 3 | a0001c0001t0010g0191 a0001c0001t0014g0065 a0001c0001t0014g0205 |
3 | HG03195.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.343+140_343+147del others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884575 | |||||||
| chr18:54884596 | G | A | 2 | a0001c0001t0005g0217 a0001c0001t0005g0238 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.343+160G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884596 | |||||||
| chr18:54884610 | C | A | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343+174C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884610 | |||||||
| chr18:54884621 | G | C | 84 | a0001c0001t0001g0039 a0001c0001t0001g0120 a0001c0001t0001g0241 others(81): Show |
87 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.343+185G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884621 | |||||||
| chr18:54884678 | T | C | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.343+242T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884678 | |||||||
| chr18:54884800 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.343+364G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884800 | |||||||
| chr18:54884905 | G | A | 1 | a0001c0001t0007g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.343+469G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884905 | |||||||
| chr18:54884936 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.343+500T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884936 | |||||||
| chr18:54884953 | G | A | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.343+517G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884953 | |||||||
| chr18:54885623 | CATCACTC others(3): Show |
C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0001g0307 others(5): Show |
9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.343+1191_343+1200d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54885623 | ||||||
| chr18:54885630 | C | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(291): Show |
305 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(302): Show |
intron_variant | MODIFIER | c.343+1194C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885630 | |||||||
| chr18:54885641 | C | T | 1 | a0001c0001t0040g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343+1205C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885641 | |||||||
| chr18:54885648 | C | T | 5 | a0001c0001t0010g0046 a0001c0001t0010g0314 a0001c0001t0018g0116 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+1212C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885648 | |||||||
| chr18:54885655 | G | A | 9 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(6): Show |
10 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+1219G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885655 | |||||||
| chr18:54885671 | T | A | 1 | a0001c0001t0003g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.343+1235T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885671 | |||||||
| chr18:54885815 | G | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.343+1379G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885815 | |||||||
| chr18:54885864 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0023g0181 |
2 | NA18963.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.343+1428T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885864 | |||||||
| chr18:54885973 | A | G | 1 | a0001c0001t0004g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.343+1537A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885973 | |||||||
| chr18:54886121 | C | A | 9 | a0001c0001t0004g0112 a0001c0001t0008g0004 a0001c0001t0008g0016 others(6): Show |
10 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+1685C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886121 | |||||||
| chr18:54886121 | C | G | 1 | a0001c0001t0019g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.343+1685C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886121 | |||||||
| chr18:54886241 | T | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.344-1754T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886241 | |||||||
| chr18:54886313 | G | A | 83 | a0001c0001t0001g0039 a0001c0001t0001g0241 a0001c0001t0002g0008 others(80): Show |
86 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.344-1682G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886313 | |||||||
| chr18:54886397 | A | T | 39 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0060 others(36): Show |
40 | HG00735.hp1 HG00738.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.344-1598A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886397 | |||||||
| chr18:54886416 | A | G | 1 | a0001c0001t0020g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.344-1579A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886416 | |||||||
| chr18:54886423 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(290): Show |
304 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(301): Show |
intron_variant | MODIFIER | c.344-1572G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886423 | |||||||
| chr18:54886513 | A | C | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.344-1482A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886513 | |||||||
| chr18:54886640 | C | A | 1 | a0001c0001t0042g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.344-1355C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886640 | |||||||
| chr18:54886697 | T | C | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.344-1298T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886697 | |||||||
| chr18:54886798 | A | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0248 a0001c0001t0001g0272 others(1): Show |
4 | NA18961.hp2 NA19004.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-1197A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886798 | |||||||
| chr18:54886830 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
intron_variant | MODIFIER | c.344-1165A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886830 | |||||||
| chr18:54886929 | A | G | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.344-1066A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886929 | |||||||
| chr18:54887021 | T | TCCTC | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(70): Show |
77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.344-954_344-951dup others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | ||||||
| chr18:54887021 | T | TCCTCCCT others(1): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02602.hp2 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.344-958_344-951dup others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | ||||||
| chr18:54887021 | TCCTC | T | 10 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0004g0112 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.344-954_344-951del others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | ||||||
| chr18:54887094 | C | T | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344-901C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887094 | |||||||
| chr18:54887110 | G | C | 1 | a0001c0001t0043g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344-885G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887110 | |||||||
| chr18:54887327 | A | C | 1 | a0001c0001t0023g0181 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.344-668A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887327 | |||||||
| chr18:54887425 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.344-570G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887425 | |||||||
| chr18:54887429 | T | A | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.344-566T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887429 | |||||||
| chr18:54887463 | G | A | 1 | a0001c0001t0024g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344-532G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887463 | |||||||
| chr18:54887535 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344-460G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887535 | |||||||
| chr18:54887605 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.344-390G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887605 | |||||||
| chr18:54887661 | C | T | 1 | a0001c0001t0008g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344-334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887661 | |||||||
| chr18:54887704 | T | G | 1 | a0002c0003t0031g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.344-291T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887704 | |||||||
| chr18:54887866 | T | A | 1 | a0001c0001t0025g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344-129T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887866 | |||||||
| chr18:54888149 | C | A | 1 | a0002c0003t0031g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.467+31C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888149 | |||||||
| chr18:54888167 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.467+49G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888167 | |||||||
| chr18:54888261 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.467+143T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888261 | |||||||
| chr18:54888354 | T | G | 2 | a0001c0001t0002g0290 a0001c0001t0045g0042 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.467+236T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888354 | |||||||
| chr18:54888373 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.467+255G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888373 | |||||||
| chr18:54888431 | G | A | 4 | a0001c0001t0005g0056 a0001c0001t0005g0064 a0001c0001t0005g0066 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+313G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888431 | |||||||
| chr18:54888584 | G | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.467+466G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888584 | |||||||
| chr18:54888663 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.467+545C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888663 | |||||||
| chr18:54888751 | G | A | 1 | a0001c0001t0010g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.468-473G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888751 | |||||||
| chr18:54888972 | T | G | 2 | a0001c0001t0014g0065 a0001c0001t0014g0205 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.468-252T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888972 | |||||||
| chr18:54889017 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.468-207A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889017 | |||||||
| chr18:54889135 | G | A | 1 | a0001c0001t0033g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468-89G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889135 | |||||||
| chr18:54889174 | C | T | 1 | a0001c0001t0010g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.468-50C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889174 |