Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5899 |
| ensemblid | ENSG00000144118.14 |
| hgncid | 9840 |
| symbol | RALB |
| name | RAS like proto-oncogene B |
| refseq_nuc | NM_002881.3 |
| refseq_prot | NP_002872.1 |
| ensembl_nuc | ENST00000272519.10 |
| ensembl_prot | ENSP00000272519.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 120252852 |
| end | 120294710 |
| strand | + |
| ver | v1.2 |
| region | chr2:120252852-120294710 |
| region5000 | chr2:120247852-120299710 |
| regionname0 | RALB_chr2_120252852_120294710 |
| regionname5000 | RALB_chr2_120247852_120299710 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 618 | 342 | 86 | 60 | 147 | 11 | 36 | RALB_chr2_120247852_120299710 | RALB | ATGGC others(613): Show |
chr2 | 120247852 | 120299710 | ||
| a0001c0002 | 0/0 | 618 | 15 | 0 | 6 | 0 | 5 | 4 | RALB_chr2_120247852_120299710 | RALB | ATGGC others(613): Show |
chr2 | 120247852 | 120299710 | ||
| a0001c0003 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | ATGGC others(613): Show |
chr2 | 120247852 | 120299710 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2247 | 157 | 39 | 28 | 58 | 8 | 24 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0002 | 1/1 | 2247 | 131 | 20 | 27 | 71 | 2 | 9 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0003 | 0/0 | 2247 | 14 | 0 | 1 | 13 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0004 | 0/0 | 2247 | 11 | 10 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0005 | 0/0 | 2247 | 10 | 10 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0006 | 0/0 | 2247 | 6 | 4 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0007 | 0/0 | 2247 | 4 | 0 | 0 | 2 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0008 | 0/0 | 2247 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0009 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0010 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0011 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0012 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0001t0014 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0002t0001 | 0/0 | 2247 | 15 | 0 | 6 | 0 | 5 | 4 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| a0001c0003t0003 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | GAAAG others(2242): Show |
chr2 | 120247852 | 120299710 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0001 | 1/0 | 27 | 6 | 10 | 8 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0036 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0005g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0008g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0001t0014g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 0 | 4 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| a0001c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | GBR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0152 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0150 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0008 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18954 | hp1 | a0001 | c0001 | t0013 | g0035 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18978 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0135 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19084 | hp2 | a0001 | c0001 | t0010 | g0196 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0154 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0085 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0036 | REF | REF | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:120278757 | G | A | 1 | a0001c0002 | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
synonymous_variant | LOW | c.93G>A | p.Thr31Thr | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/5 | 269/2247 | 93/621 | 31/206 | chr2 | 120278757 | |||
| chr2:120286029 | T | A | 1 | a0001c0003 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.270T>A | p.Leu90Leu | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/5 | 446/2247 | 270/621 | 90/206 | chr2 | 120286029 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:120252867 | A | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-161A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | chr2 | 120252867 | |||||||
| chr2:120252942 | G | A | 1 | a0001c0001t0005 | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | 25723 | chr2 | 120252942 | ||||||
| chr2:120252943 | C | A | 1 | a0001c0001t0011 | 1 | NA19000.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | 25722 | chr2 | 120252943 | ||||||
| chr2:120293413 | T | A | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*153T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 153 | chr2 | 120293413 | ||||||
| chr2:120293564 | A | G | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*304A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 304 | chr2 | 120293564 | ||||||
| chr2:120293605 | C | T | 1 | a0001c0001t0014 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*345C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 345 | chr2 | 120293605 | ||||||
| chr2:120293619 | G | A | 1 | a0001c0001t0009 | 2 | HG03209.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 359 | chr2 | 120293619 | ||||||
| chr2:120293818 | G | A | 1 | a0001c0001t0004 | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*558G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 558 | chr2 | 120293818 | ||||||
| chr2:120294196 | C | T | 1 | a0001c0001t0013 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 936 | chr2 | 120294196 | ||||||
| chr2:120294224 | T | A | 1 | a0001c0001t0012 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 964 | chr2 | 120294224 | ||||||
| chr2:120294538 | C | T | 1 | a0001c0001t0010 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1278 | chr2 | 120294538 | ||||||
| chr2:120294558 | C | A | 2 | a0001c0001t0003 a0001c0003t0003 |
15 | HG00609.hp1 HG01928.hp2 HG02165.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1298C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1298 | chr2 | 120294558 | ||||||
| chr2:120294678 | C | T | 1 | a0001c0001t0008 | 2 | HG01243.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1418C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1418 | chr2 | 120294678 | ||||||
| chr2:120294692 | A | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1432 | chr2 | 120294692 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:120253200 | CTGGGGCT others(3): Show |
C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+221_-48+230del others(10): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253200 | |||||||
| chr2:120253333 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48+353C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253333 | |||||||
| chr2:120253387 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48+407C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253387 | |||||||
| chr2:120253563 | C | T | 1 | a0001c0001t0002g0044 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-48+583C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253563 | |||||||
| chr2:120253586 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+606T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253586 | |||||||
| chr2:120253630 | T | G | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+650T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253630 | |||||||
| chr2:120254084 | C | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1104C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254084 | |||||||
| chr2:120254194 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1214A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254194 | |||||||
| chr2:120254353 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-48+1373A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254353 | |||||||
| chr2:120254404 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-48+1424A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254404 | |||||||
| chr2:120254453 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1473A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254453 | |||||||
| chr2:120254457 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1477A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254457 | |||||||
| chr2:120254655 | A | G | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+1675A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254655 | |||||||
| chr2:120254681 | TTTTG | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+1709_-48+1712d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120254681 | ||||||
| chr2:120254695 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-48+1715G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254695 | |||||||
| chr2:120254779 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-48+1799G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254779 | |||||||
| chr2:120254783 | G | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1803G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254783 | |||||||
| chr2:120254852 | T | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+1872T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254852 | |||||||
| chr2:120254895 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+1915C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254895 | |||||||
| chr2:120254948 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-48+1968A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254948 | |||||||
| chr2:120254965 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1985C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254965 | |||||||
| chr2:120254966 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1986C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254966 | |||||||
| chr2:120254967 | C | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1987C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254967 | |||||||
| chr2:120255082 | TA | T | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG01192.hp2 HG01257.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2103delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255082 | |||||||
| chr2:120255090 | T | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2110T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255090 | |||||||
| chr2:120255255 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-48+2275G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255255 | |||||||
| chr2:120255258 | TG | T | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+2280delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120255258 | ||||||
| chr2:120255259 | G | GT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0134 others(6): Show |
11 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48+2279_-48+2280i others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255259 | |||||||
| chr2:120255260 | G | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+2280G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255260 | |||||||
| chr2:120255293 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2313T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255293 | |||||||
| chr2:120255326 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2346C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255326 | |||||||
| chr2:120255335 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2355A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255335 | |||||||
| chr2:120255480 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2500T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255480 | |||||||
| chr2:120255593 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+2613G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255593 | |||||||
| chr2:120255716 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+2736A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255716 | |||||||
| chr2:120255765 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48+2785C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255765 | |||||||
| chr2:120255781 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-48+2801T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255781 | |||||||
| chr2:120255930 | C | CTATGTGA others(10): Show |
158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2953_-48+2954i others(19): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120255930 | ||||||
| chr2:120255936 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-48+2956G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255936 | |||||||
| chr2:120256040 | C | A | 1 | a0001c0001t0002g0172 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-48+3060C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256040 | |||||||
| chr2:120256096 | T | TTC | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3117_-48+3118i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120256096 | ||||||
| chr2:120256099 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3119A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256099 | |||||||
| chr2:120256135 | A | G | 1 | a0001c0001t0004g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+3155A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256135 | |||||||
| chr2:120256205 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3225G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256205 | |||||||
| chr2:120256256 | G | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3276G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256256 | |||||||
| chr2:120256286 | C | G | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+3306C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256286 | |||||||
| chr2:120256306 | C | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+3326C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256306 | |||||||
| chr2:120256338 | GATA | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+3361_-48+3363d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120256338 | ||||||
| chr2:120256470 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+3490T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256470 | |||||||
| chr2:120256531 | G | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0031 others(22): Show |
32 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-48+3551G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256531 | |||||||
| chr2:120256546 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+3566G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256546 | |||||||
| chr2:120256558 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48+3578C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256558 | |||||||
| chr2:120256568 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3588A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256568 | |||||||
| chr2:120256647 | C | T | 4 | a0001c0002t0001g0012 a0001c0002t0001g0085 a0001c0002t0001g0086 others(1): Show |
7 | HG00099.hp2 HG00280.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+3667C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256647 | |||||||
| chr2:120256696 | C | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0218 a0001c0001t0002g0219 |
5 | NA18939.hp1 NA18973.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+3716C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256696 | |||||||
| chr2:120256734 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-48+3754C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256734 | |||||||
| chr2:120256794 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3814C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256794 | |||||||
| chr2:120257013 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+4033C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257013 | |||||||
| chr2:120257014 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-48+4034G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257014 | |||||||
| chr2:120257107 | T | TG | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+4128dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120257107 | ||||||
| chr2:120257115 | T | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4135T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257115 | |||||||
| chr2:120257128 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-48+4148A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257128 | |||||||
| chr2:120257225 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-48+4245C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257225 | |||||||
| chr2:120257254 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4274G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257254 | |||||||
| chr2:120257277 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0221 |
2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-48+4297C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257277 | |||||||
| chr2:120257319 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+4339G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257319 | |||||||
| chr2:120257422 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-48+4442A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257422 | |||||||
| chr2:120257511 | AT | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+4541delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120257511 | ||||||
| chr2:120257526 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+4546C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257526 | |||||||
| chr2:120257769 | C | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4789C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257769 | |||||||
| chr2:120257773 | C | T | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+4793C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257773 | |||||||
| chr2:120257938 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48+4958A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257938 | |||||||
| chr2:120258071 | G | T | 10 | a0001c0001t0001g0076 a0001c0001t0004g0018 a0001c0001t0004g0048 others(7): Show |
12 | HG00735.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+5091G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258071 | |||||||
| chr2:120258171 | G | A | 29 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(26): Show |
40 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-48+5191G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258171 | |||||||
| chr2:120258231 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0165 |
5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+5251C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258231 | |||||||
| chr2:120258254 | T | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+5274T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258254 | |||||||
| chr2:120258471 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48+5491A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258471 | |||||||
| chr2:120258488 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+5508G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258488 | |||||||
| chr2:120258613 | G | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+5633G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258613 | |||||||
| chr2:120258794 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-48+5814G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258794 | |||||||
| chr2:120258834 | G | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+5854G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258834 | |||||||
| chr2:120258858 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-48+5878C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258858 | |||||||
| chr2:120258860 | C | G | 1 | a0001c0001t0002g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+5880C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258860 | |||||||
| chr2:120258898 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+5918A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258898 | |||||||
| chr2:120258931 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-48+5951G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258931 | |||||||
| chr2:120259002 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48+6022G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259002 | |||||||
| chr2:120259155 | G | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
8 | NA18944.hp1 NA18964.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6175G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259155 | |||||||
| chr2:120259175 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6195T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259175 | |||||||
| chr2:120259197 | C | T | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48+6217C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259197 | |||||||
| chr2:120259198 | G | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+6218G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259198 | |||||||
| chr2:120259294 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-48+6314C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259294 | |||||||
| chr2:120259295 | G | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0220 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-48+6315G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259295 | |||||||
| chr2:120259316 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-48+6336C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259316 | |||||||
| chr2:120259443 | G | A | 1 | a0001c0001t0002g0037 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-48+6463G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259443 | |||||||
| chr2:120259535 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-48+6555G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259535 | |||||||
| chr2:120259650 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-48+6670C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259650 | |||||||
| chr2:120259705 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+6725C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259705 | |||||||
| chr2:120259712 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0050 others(22): Show |
36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48+6732G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259712 | |||||||
| chr2:120259742 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6762A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259742 | |||||||
| chr2:120259781 | C | T | 6 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(3): Show |
8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6801C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259781 | |||||||
| chr2:120259787 | G | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+6807G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259787 | |||||||
| chr2:120259797 | A | AG | 8 | a0001c0001t0001g0062 a0001c0001t0001g0121 a0001c0001t0001g0164 others(5): Show |
8 | HG00735.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6822dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120259797 | ||||||
| chr2:120259813 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0165 |
5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+6833C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259813 | |||||||
| chr2:120259823 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-48+6843C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259823 | |||||||
| chr2:120259829 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+6849G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259829 | |||||||
| chr2:120259869 | T | C | 1 | a0001c0002t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-48+6889T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259869 | |||||||
| chr2:120259883 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-48+6903C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259883 | |||||||
| chr2:120259884 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6904A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259884 | |||||||
| chr2:120259888 | C | G | 2 | a0001c0001t0004g0018 a0001c0001t0004g0093 |
4 | HG02451.hp1 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6908C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259888 | |||||||
| chr2:120259936 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6956T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259936 | |||||||
| chr2:120260006 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+7026T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260006 | |||||||
| chr2:120260014 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG01943.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+7034C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260014 | |||||||
| chr2:120260041 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+7061C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260041 | |||||||
| chr2:120260074 | C | T | 4 | a0001c0001t0002g0171 a0001c0001t0002g0221 a0001c0001t0004g0018 others(1): Show |
6 | HG01175.hp1 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+7094C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260074 | |||||||
| chr2:120260112 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-48+7132C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260112 | |||||||
| chr2:120260198 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-48+7218C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260198 | |||||||
| chr2:120260278 | C | T | 4 | a0001c0002t0001g0012 a0001c0002t0001g0085 a0001c0002t0001g0086 others(1): Show |
7 | HG00099.hp2 HG00280.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+7298C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260278 | |||||||
| chr2:120260279 | G | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+7299G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260279 | |||||||
| chr2:120260437 | G | A | 2 | a0001c0002t0001g0078 a0001c0002t0001g0079 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+7457G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260437 | |||||||
| chr2:120260577 | C | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-48+7597C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260577 | |||||||
| chr2:120260621 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+7641A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260621 | |||||||
| chr2:120260641 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+7661G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260641 | |||||||
| chr2:120260893 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+7913A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260893 | |||||||
| chr2:120260896 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+7916G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260896 | |||||||
| chr2:120260961 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-48+7981A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260961 | |||||||
| chr2:120261032 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-48+8052C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261032 | |||||||
| chr2:120261056 | C | T | 1 | a0001c0001t0005g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+8076C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261056 | |||||||
| chr2:120261063 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-48+8083A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261063 | |||||||
| chr2:120261070 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-48+8090T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261070 | |||||||
| chr2:120261111 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+8131C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261111 | |||||||
| chr2:120261171 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+8191A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261171 | |||||||
| chr2:120261177 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-48+8197G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261177 | |||||||
| chr2:120261184 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+8204T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261184 | |||||||
| chr2:120261185 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+8205G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261185 | |||||||
| chr2:120261575 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0098 |
4 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+8595C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261575 | |||||||
| chr2:120261668 | G | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+8688G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261668 | |||||||
| chr2:120261840 | T | G | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+8860T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261840 | |||||||
| chr2:120261846 | T | G | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+8866T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261846 | |||||||
| chr2:120262023 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+9043G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262023 | |||||||
| chr2:120262207 | G | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+9227G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262207 | |||||||
| chr2:120262224 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-48+9244G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262224 | |||||||
| chr2:120262378 | A | G | 6 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(3): Show |
8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+9398A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262378 | |||||||
| chr2:120262858 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+9878G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262858 | |||||||
| chr2:120262895 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+9915C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262895 | |||||||
| chr2:120263065 | A | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+10085A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263065 | |||||||
| chr2:120263207 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0220 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-48+10227C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263207 | |||||||
| chr2:120263226 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+10246C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263226 | |||||||
| chr2:120263402 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-48+10422G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263402 | |||||||
| chr2:120263579 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-48+10599A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263579 | |||||||
| chr2:120263772 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-48+10792C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263772 | |||||||
| chr2:120263773 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+10793G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263773 | |||||||
| chr2:120263827 | G | T | 1 | a0001c0001t0001g0023 | 3 | HG02155.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-48+10847G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263827 | |||||||
| chr2:120263886 | C | T | 1 | a0001c0001t0004g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+10906C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263886 | |||||||
| chr2:120263992 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+11012A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263992 | |||||||
| chr2:120264049 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(24): Show |
38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.-48+11069A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264049 | |||||||
| chr2:120264205 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+11225T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264205 | |||||||
| chr2:120264219 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-48+11239C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264219 | |||||||
| chr2:120264260 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+11280C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264260 | |||||||
| chr2:120264336 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG03453.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-48+11356G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264336 | |||||||
| chr2:120264554 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11574A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264554 | |||||||
| chr2:120264555 | C | A | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11575C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264555 | |||||||
| chr2:120264555 | CA | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+11577delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120264555 | ||||||
| chr2:120264556 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11576A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264556 | |||||||
| chr2:120264583 | T | A | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-48+11603T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264583 | |||||||
| chr2:120264610 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+11630A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264610 | |||||||
| chr2:120264678 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-48+11698T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264678 | |||||||
| chr2:120264680 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(24): Show |
39 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-48+11700C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264680 | |||||||
| chr2:120264778 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-48+11798C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264778 | |||||||
| chr2:120264786 | C | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+11806C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264786 | |||||||
| chr2:120264820 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-48+11840A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264820 | |||||||
| chr2:120264864 | T | G | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+11884T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264864 | |||||||
| chr2:120264946 | A | AATAC | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+11967_-48+1196 others(8): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120264946 | ||||||
| chr2:120265157 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-48+12177A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265157 | |||||||
| chr2:120265164 | G | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(156): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-48+12184G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265164 | |||||||
| chr2:120265588 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+12608A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265588 | |||||||
| chr2:120265772 | ATAGAAG | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+12808_-48+1281 others(10): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120265772 | ||||||
| chr2:120265920 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47-12698C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265920 | |||||||
| chr2:120266175 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-12443G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266175 | |||||||
| chr2:120266305 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-12313C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266305 | |||||||
| chr2:120266321 | T | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-47-12297T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266321 | |||||||
| chr2:120266352 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-12266A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266352 | |||||||
| chr2:120266384 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-47-12234A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266384 | |||||||
| chr2:120266401 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(56): Show |
94 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-47-12217C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266401 | |||||||
| chr2:120266414 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47-12204T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266414 | |||||||
| chr2:120266571 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-47-12047C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266571 | |||||||
| chr2:120266685 | T | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-11933T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266685 | |||||||
| chr2:120266777 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-11841A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266777 | |||||||
| chr2:120266843 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-11775A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266843 | |||||||
| chr2:120266856 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-11762A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266856 | |||||||
| chr2:120266868 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-11750T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266868 | |||||||
| chr2:120267138 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47-11480G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267138 | |||||||
| chr2:120267220 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-11398G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267220 | |||||||
| chr2:120267222 | G | A | 10 | a0001c0002t0001g0012 a0001c0002t0001g0029 a0001c0002t0001g0078 others(7): Show |
14 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-11396G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267222 | |||||||
| chr2:120267396 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-47-11222A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267396 | |||||||
| chr2:120267403 | GT | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-11213delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120267403 | ||||||
| chr2:120267411 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-11207A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267411 | |||||||
| chr2:120267449 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-47-11169G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267449 | |||||||
| chr2:120267503 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47-11115G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267503 | |||||||
| chr2:120267536 | G | GCTCC | 2 | a0001c0001t0002g0014 a0001c0001t0002g0185 |
5 | HG02040.hp1 HG02155.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-11082_-47-1108 others(8): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267536 | |||||||
| chr2:120267609 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47-11009A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267609 | |||||||
| chr2:120267665 | G | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-10953G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267665 | |||||||
| chr2:120267672 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-47-10946C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267672 | |||||||
| chr2:120267679 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0050 others(22): Show |
36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-10939C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267679 | |||||||
| chr2:120267686 | A | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0178 a0001c0001t0002g0207 |
7 | NA18952.hp2 NA18955.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-10932A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267686 | |||||||
| chr2:120267753 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-47-10865G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267753 | |||||||
| chr2:120267801 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0013g0035 |
2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47-10817A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267801 | |||||||
| chr2:120268025 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-10593C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268025 | |||||||
| chr2:120268110 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-10508C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268110 | |||||||
| chr2:120268192 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-47-10426G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268192 | |||||||
| chr2:120268269 | T | A | 1 | a0001c0001t0002g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-47-10349T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268269 | |||||||
| chr2:120268319 | C | CA | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-10298dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120268319 | ||||||
| chr2:120268443 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-47-10175T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268443 | |||||||
| chr2:120268566 | C | T | 2 | a0001c0002t0001g0080 a0001c0002t0001g0081 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-47-10052C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268566 | |||||||
| chr2:120268578 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0129 |
4 | NA18961.hp2 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-10040T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268578 | |||||||
| chr2:120268579 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-10039G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268579 | |||||||
| chr2:120268669 | A | G | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-9949A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268669 | |||||||
| chr2:120268696 | T | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0050 others(22): Show |
36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-9922T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268696 | |||||||
| chr2:120268750 | A | G | 1 | a0001c0001t0014g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47-9868A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268750 | |||||||
| chr2:120268794 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-47-9824C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268794 | |||||||
| chr2:120268937 | A | AT | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9674dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120268937 | ||||||
| chr2:120269006 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-9612A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269006 | |||||||
| chr2:120269076 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9542T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269076 | |||||||
| chr2:120269085 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-47-9533T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269085 | |||||||
| chr2:120269117 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0221 |
2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47-9501G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269117 | |||||||
| chr2:120269195 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-47-9423T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269195 | |||||||
| chr2:120269213 | TGGAGTTT others(17): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-47-9392_-47-9369d others(26): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120269213 | ||||||
| chr2:120269302 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-9316G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269302 | |||||||
| chr2:120269315 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9303T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269315 | |||||||
| chr2:120269397 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(68): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-9221C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269397 | |||||||
| chr2:120269398 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0186 |
2 | HG00642.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-47-9220G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269398 | |||||||
| chr2:120269417 | G | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG01192.hp2 HG01257.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-9201G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269417 | |||||||
| chr2:120269417 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-47-9201G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269417 | |||||||
| chr2:120269425 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-47-9193C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269425 | |||||||
| chr2:120269475 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-47-9143T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269475 | |||||||
| chr2:120269498 | AG | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(68): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-9119delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269498 | |||||||
| chr2:120269508 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0050 others(22): Show |
36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-9110T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269508 | |||||||
| chr2:120269592 | C | T | 6 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(3): Show |
8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-9026C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269592 | |||||||
| chr2:120269785 | T | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-8833T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269785 | |||||||
| chr2:120269995 | A | G | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-8623A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269995 | |||||||
| chr2:120270178 | GTTC | G | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-8434_-47-8432d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270178 | ||||||
| chr2:120270600 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-47-8018A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270600 | |||||||
| chr2:120270615 | C | CG | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-8001dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270615 | ||||||
| chr2:120270761 | T | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7857T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270761 | |||||||
| chr2:120270873 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-47-7745G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270873 | |||||||
| chr2:120270884 | ATAT | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(33): Show |
48 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-7730_-47-7728d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270884 | ||||||
| chr2:120270933 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-7685G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270933 | |||||||
| chr2:120270968 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-7650G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270968 | |||||||
| chr2:120270999 | G | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-7619G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270999 | |||||||
| chr2:120271161 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-47-7457A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271161 | |||||||
| chr2:120271191 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-47-7427C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271191 | |||||||
| chr2:120271192 | G | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7426G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271192 | |||||||
| chr2:120271257 | T | TA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-7360dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120271257 | ||||||
| chr2:120271267 | T | C | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7351T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271267 | |||||||
| chr2:120271276 | G | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7342G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271276 | |||||||
| chr2:120271357 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-7261G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271357 | |||||||
| chr2:120271437 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-47-7181T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271437 | |||||||
| chr2:120271489 | A | G | 1 | a0001c0001t0002g0014 | 4 | HG02040.hp1 HG02155.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-7129A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271489 | |||||||
| chr2:120271782 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-47-6836C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271782 | |||||||
| chr2:120271941 | C | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-6677C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271941 | |||||||
| chr2:120272010 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-6608G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272010 | |||||||
| chr2:120272096 | C | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0221 |
2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47-6522C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272096 | |||||||
| chr2:120272262 | A | G | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-6356A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272262 | |||||||
| chr2:120272264 | G | A | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-6354G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272264 | |||||||
| chr2:120272367 | G | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-47-6251G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272367 | |||||||
| chr2:120272673 | GCTTCCTA others(21): Show |
G | 1 | a0001c0001t0002g0205 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-47-5938_-47-5911d others(30): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120272673 | ||||||
| chr2:120272771 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0007g0150 a0001c0001t0007g0152 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-5847C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272771 | |||||||
| chr2:120272783 | C | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-5835C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272783 | |||||||
| chr2:120272879 | C | A | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-5739C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272879 | |||||||
| chr2:120273042 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47-5576C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273042 | |||||||
| chr2:120273172 | C | T | 14 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-5446C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273172 | |||||||
| chr2:120273173 | T | TA | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-47-5442dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120273173 | ||||||
| chr2:120273182 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-47-5436A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273182 | |||||||
| chr2:120273356 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-47-5262G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273356 | |||||||
| chr2:120273377 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-47-5241A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273377 | |||||||
| chr2:120273438 | C | T | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-5180C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273438 | |||||||
| chr2:120273490 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-5128G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273490 | |||||||
| chr2:120273613 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-47-5005A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273613 | |||||||
| chr2:120273684 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-4934G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273684 | |||||||
| chr2:120273686 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-47-4932C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273686 | |||||||
| chr2:120273743 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01515.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-47-4875G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273743 | |||||||
| chr2:120273830 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-4788A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273830 | |||||||
| chr2:120273857 | G | A | 3 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 |
3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-4761G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273857 | |||||||
| chr2:120274050 | G | C | 1 | a0001c0001t0006g0051 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-47-4568G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274050 | |||||||
| chr2:120274119 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-4499G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274119 | |||||||
| chr2:120274157 | G | A | 3 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 |
3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-4461G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274157 | |||||||
| chr2:120274232 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-4386C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274232 | |||||||
| chr2:120274247 | C | G | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-4371C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274247 | |||||||
| chr2:120274283 | T | C | 6 | a0001c0001t0002g0038 a0001c0001t0002g0173 a0001c0001t0002g0187 others(3): Show |
7 | HG01192.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-4335T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274283 | |||||||
| chr2:120274342 | T | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-4276T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274342 | |||||||
| chr2:120274386 | C | T | 1 | a0001c0001t0004g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-4232C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274386 | |||||||
| chr2:120274414 | A | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-4204A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274414 | |||||||
| chr2:120274467 | A | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-4151A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274467 | |||||||
| chr2:120274507 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-4111T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274507 | |||||||
| chr2:120275156 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-3462G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275156 | |||||||
| chr2:120275164 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-3454G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275164 | |||||||
| chr2:120275283 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
6 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-3335C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275283 | |||||||
| chr2:120275373 | C | G | 1 | a0001c0001t0009g0034 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-3245C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275373 | |||||||
| chr2:120275495 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-47-3123C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275495 | |||||||
| chr2:120275690 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-47-2928C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275690 | |||||||
| chr2:120275842 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-2776C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275842 | |||||||
| chr2:120275914 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-2704T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275914 | |||||||
| chr2:120275935 | T | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-2683T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275935 | |||||||
| chr2:120276049 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-2569C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276049 | |||||||
| chr2:120276131 | TG | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-2482delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120276131 | ||||||
| chr2:120276195 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01175.hp2 HG02293.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2423C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276195 | |||||||
| chr2:120276419 | A | G | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-2199A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276419 | |||||||
| chr2:120276557 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(24): Show |
38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.-47-2061C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276557 | |||||||
| chr2:120276722 | A | T | 1 | a0001c0001t0002g0043 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-47-1896A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276722 | |||||||
| chr2:120276954 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1664A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276954 | |||||||
| chr2:120277075 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0165 |
5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1543G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277075 | |||||||
| chr2:120277243 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0031 others(11): Show |
21 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-1375G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277243 | |||||||
| chr2:120277290 | C | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-1328C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277290 | |||||||
| chr2:120277290 | C | T | 2 | a0001c0001t0005g0101 a0001c0001t0005g0102 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-47-1328C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277290 | |||||||
| chr2:120277293 | G | A | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-1325G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277293 | |||||||
| chr2:120277326 | TTG | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1285_-47-1284d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277326 | ||||||
| chr2:120277330 | G | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1288G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277330 | |||||||
| chr2:120277350 | C | CATGT | 36 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(33): Show |
49 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47-1267_-47-1264d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277350 | ||||||
| chr2:120277353 | G | GTA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-47-1264_-47-1263i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277353 | ||||||
| chr2:120277360 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-47-1258A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277360 | |||||||
| chr2:120277365 | ATG | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1246_-47-1245d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277365 | ||||||
| chr2:120277411 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47-1207G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277411 | |||||||
| chr2:120277418 | CAT | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1199_-47-1198d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277418 | |||||||
| chr2:120277429 | C | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(60): Show |
87 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-47-1189C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277429 | |||||||
| chr2:120277431 | C | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1187C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277431 | |||||||
| chr2:120277458 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-47-1160G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277458 | |||||||
| chr2:120277463 | T | TGTGA | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-47-1153_-47-1152i others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277463 | ||||||
| chr2:120277511 | C | CAT | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1107_-47-1106i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277511 | |||||||
| chr2:120277519 | CGTAT | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-1096_-47-1093d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277519 | ||||||
| chr2:120277520 | G | A | 1 | a0001c0001t0004g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-47-1098G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277520 | |||||||
| chr2:120277523 | TGTGA | T | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1091_-47-1088d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277523 | ||||||
| chr2:120277536 | T | TTG | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-1069_-47-1068d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277536 | ||||||
| chr2:120277537 | TGTG | T | 15 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0130 others(12): Show |
19 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47-1080_-47-1078d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277537 | |||||||
| chr2:120277594 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-1024A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277594 | |||||||
| chr2:120277641 | C | G | 1 | a0001c0001t0002g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-47-977C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277641 | |||||||
| chr2:120277654 | GTGT | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(64): Show |
88 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.-47-960_-47-958del others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277654 | ||||||
| chr2:120277681 | ATGAG | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-47-933_-47-930del others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277681 | ||||||
| chr2:120277684 | AGT | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(69): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-932_-47-931del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277684 | ||||||
| chr2:120277687 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(69): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-931G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277687 | |||||||
| chr2:120277689 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(69): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-929A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277689 | |||||||
| chr2:120277690 | A | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(69): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-928A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277690 | |||||||
| chr2:120277697 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-921A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277697 | |||||||
| chr2:120277699 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-919G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277699 | |||||||
| chr2:120277702 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-916G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277702 | |||||||
| chr2:120277704 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-914T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277704 | |||||||
| chr2:120277759 | GTA | G | 1 | a0001c0001t0001g0023 | 3 | HG02155.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-47-857_-47-856del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277759 | ||||||
| chr2:120277768 | CGT | C | 3 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0204 |
3 | HG02280.hp2 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-47-846_-47-845del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277768 | ||||||
| chr2:120277781 | G | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-837G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277781 | |||||||
| chr2:120277828 | AAT | A | 14 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-787_-47-786del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277828 | ||||||
| chr2:120277831 | ATG | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-47-781_-47-780del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277831 | ||||||
| chr2:120277843 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-775A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277843 | |||||||
| chr2:120277867 | ATG | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-748_-47-747del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277867 | ||||||
| chr2:120277877 | A | ATG | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-47-740_-47-739dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277877 | ||||||
| chr2:120277877 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47-741A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277877 | |||||||
| chr2:120277900 | CGT | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0191 a0001c0001t0007g0015 |
5 | NA18990.hp1 NA18994.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-710_-47-709del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277900 | ||||||
| chr2:120277920 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-698A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277920 | |||||||
| chr2:120277928 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-47-690C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277928 | |||||||
| chr2:120277947 | A | ATG | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-47-666_-47-665dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277947 | ||||||
| chr2:120277976 | T | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47-642T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277976 | |||||||
| chr2:120277984 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47-634T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277984 | |||||||
| chr2:120278000 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-47-618C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278000 | |||||||
| chr2:120278036 | C | CGT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-47-580_-47-579dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120278036 | ||||||
| chr2:120278038 | TGA | T | 6 | a0001c0001t0001g0138 a0001c0001t0005g0005 a0001c0001t0005g0099 others(3): Show |
11 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-578_-47-577del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120278038 | ||||||
| chr2:120278347 | AC | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 |
4 | HG02071.hp2 HG02074.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-270delC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278347 | |||||||
| chr2:120278348 | CT | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-47-269delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278348 | |||||||
| chr2:120278449 | G | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-169G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278449 | |||||||
| chr2:120278476 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-47-142A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278476 | |||||||
| chr2:120278482 | G | A | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-136G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278482 | |||||||
| chr2:120278483 | C | T | 1 | a0001c0001t0002g0042 | 2 | NA18946.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-47-135C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278483 | |||||||
| chr2:120278587 | G | A | 1 | a0001c0001t0002g0038 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-47-31G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278587 | |||||||
| chr2:120278591 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-47-27C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278591 | |||||||
| chr2:120278800 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.114+22C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278800 | |||||||
| chr2:120278809 | T | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+31T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278809 | |||||||
| chr2:120278810 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+32T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278810 | |||||||
| chr2:120278983 | C | T | 18 | a0001c0001t0002g0003 a0001c0001t0002g0025 a0001c0001t0002g0041 others(15): Show |
32 | HG00673.hp1 HG00673.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.114+205C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278983 | |||||||
| chr2:120278996 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.114+218G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278996 | |||||||
| chr2:120279001 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0031 others(22): Show |
32 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.114+223C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279001 | |||||||
| chr2:120279022 | T | C | 1 | a0001c0001t0002g0043 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114+244T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279022 | |||||||
| chr2:120279085 | T | G | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+307T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279085 | |||||||
| chr2:120279325 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+547C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279325 | |||||||
| chr2:120279353 | G | C | 1 | a0001c0001t0002g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.114+575G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279353 | |||||||
| chr2:120279353 | G | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0073 |
2 | HG02165.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.114+575G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279353 | |||||||
| chr2:120279442 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.114+664A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279442 | |||||||
| chr2:120279486 | C | G | 1 | a0001c0001t0002g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.114+708C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279486 | |||||||
| chr2:120279622 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+844T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279622 | |||||||
| chr2:120279657 | A | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+879A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279657 | |||||||
| chr2:120279703 | CA | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+926delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279703 | |||||||
| chr2:120279707 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.114+929G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279707 | |||||||
| chr2:120279799 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+1021A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279799 | |||||||
| chr2:120279954 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1176T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279954 | |||||||
| chr2:120280075 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1297T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280075 | |||||||
| chr2:120280080 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1302C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280080 | |||||||
| chr2:120280221 | C | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1443C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280221 | |||||||
| chr2:120280506 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.114+1728C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280506 | |||||||
| chr2:120280508 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1730C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280508 | |||||||
| chr2:120280543 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.114+1765C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280543 | |||||||
| chr2:120280668 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.114+1890A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280668 | |||||||
| chr2:120280714 | GA | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.114+1949delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280714 | ||||||
| chr2:120280774 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114+1996C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280774 | |||||||
| chr2:120280774 | CAA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(24): Show |
38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.114+1999_114+2000d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280774 | ||||||
| chr2:120280982 | G | GT | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+2212dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280982 | ||||||
| chr2:120281035 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.114+2257C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281035 | |||||||
| chr2:120281093 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.114+2315C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281093 | |||||||
| chr2:120281198 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0002g0192 a0001c0001t0002g0212 others(1): Show |
8 | NA18944.hp1 NA18955.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+2420T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281198 | |||||||
| chr2:120281241 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.114+2463C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281241 | |||||||
| chr2:120281261 | G | C | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+2483G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281261 | |||||||
| chr2:120281302 | C | T | 1 | a0001c0002t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+2524C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281302 | |||||||
| chr2:120281324 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+2546C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281324 | |||||||
| chr2:120281687 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+2909G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281687 | |||||||
| chr2:120281732 | T | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+2954T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281732 | |||||||
| chr2:120281816 | G | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.114+3038G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281816 | |||||||
| chr2:120281818 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+3040G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281818 | |||||||
| chr2:120281890 | G | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+3112G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281890 | |||||||
| chr2:120281997 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0068 others(1): Show |
7 | NA18948.hp1 NA18982.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+3219C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281997 | |||||||
| chr2:120282137 | G | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0056 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+3359G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282137 | |||||||
| chr2:120282176 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.114+3398C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282176 | |||||||
| chr2:120282342 | G | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-3532G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282342 | |||||||
| chr2:120282392 | C | T | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-3482C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282392 | |||||||
| chr2:120282432 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.115-3442C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282432 | |||||||
| chr2:120282478 | CA | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(69): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.115-3385delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120282478 | ||||||
| chr2:120282518 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.115-3356C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282518 | |||||||
| chr2:120282564 | A | AG | 9 | a0001c0001t0001g0132 a0001c0001t0001g0145 a0001c0001t0002g0040 others(6): Show |
10 | HG01261.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-3304dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120282564 | ||||||
| chr2:120282609 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.115-3265G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282609 | |||||||
| chr2:120282816 | A | C | 17 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0005g0005 others(14): Show |
26 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-3058A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282816 | |||||||
| chr2:120282822 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.115-3052G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282822 | |||||||
| chr2:120283104 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.115-2770G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283104 | |||||||
| chr2:120283142 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.115-2732C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283142 | |||||||
| chr2:120283143 | T | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-2731T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283143 | |||||||
| chr2:120283427 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115-2447C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283427 | |||||||
| chr2:120283458 | G | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-2416G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283458 | |||||||
| chr2:120283575 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.115-2299G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283575 | |||||||
| chr2:120283586 | C | A | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
30 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.115-2288C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283586 | |||||||
| chr2:120283738 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.115-2136A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283738 | |||||||
| chr2:120283771 | A | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.115-2103A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283771 | |||||||
| chr2:120283898 | A | T | 1 | a0001c0002t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.115-1976A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283898 | |||||||
| chr2:120284220 | T | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-1654T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284220 | |||||||
| chr2:120284274 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-1600C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284274 | |||||||
| chr2:120284403 | AT | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.115-1459delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120284403 | ||||||
| chr2:120284416 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.115-1458G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284416 | |||||||
| chr2:120284578 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0125 |
4 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1296T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284578 | |||||||
| chr2:120284634 | A | T | 9 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(6): Show |
11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-1240A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284634 | |||||||
| chr2:120284684 | T | G | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1190T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284684 | |||||||
| chr2:120284755 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1119C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284755 | |||||||
| chr2:120284757 | A | C | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1117A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284757 | |||||||
| chr2:120284758 | AC | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.115-1114delC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120284758 | ||||||
| chr2:120284759 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1115C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284759 | |||||||
| chr2:120284782 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.115-1092C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284782 | |||||||
| chr2:120284965 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-909C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284965 | |||||||
| chr2:120284969 | C | T | 4 | a0001c0002t0001g0029 a0001c0002t0001g0078 a0001c0002t0001g0079 others(1): Show |
5 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-905C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284969 | |||||||
| chr2:120285270 | G | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(8): Show |
15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.115-604G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285270 | |||||||
| chr2:120285270 | G | GC | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-599dupC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285270 | ||||||
| chr2:120285359 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.115-515G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285359 | |||||||
| chr2:120285570 | T | TAAAA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.115-301_115-298dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285570 | ||||||
| chr2:120285570 | T | TAAAAA | 16 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0005g0005 others(13): Show |
25 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.115-302_115-298dup others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285570 | ||||||
| chr2:120285614 | A | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.115-260A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285614 | |||||||
| chr2:120285827 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.115-47G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285827 | |||||||
| chr2:120285853 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0032 others(25): Show |
40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-21C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285853 | |||||||
| chr2:120286138 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0107 |
2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.323+56A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286138 | |||||||
| chr2:120286337 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.323+255G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286337 | |||||||
| chr2:120286570 | C | T | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+488C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286570 | |||||||
| chr2:120286573 | G | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0032 others(25): Show |
40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.323+491G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286573 | |||||||
| chr2:120286719 | G | A | 2 | a0001c0001t0006g0052 a0001c0001t0006g0053 |
2 | HG00639.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.323+637G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286719 | |||||||
| chr2:120286818 | A | G | 1 | a0001c0001t0005g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.323+736A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286818 | |||||||
| chr2:120286831 | G | A | 5 | a0001c0001t0006g0026 a0001c0001t0006g0051 a0001c0001t0006g0052 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+749G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286831 | |||||||
| chr2:120286878 | T | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.323+796T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286878 | |||||||
| chr2:120286917 | A | C | 10 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(7): Show |
13 | HG00735.hp1 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.323+835A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286917 | |||||||
| chr2:120286917 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+835A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286917 | |||||||
| chr2:120286945 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.323+863T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286945 | |||||||
| chr2:120286980 | C | CA | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.323+898_323+899ins others(1): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286980 | |||||||
| chr2:120287008 | A | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0023 others(19): Show |
32 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.323+926A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287008 | |||||||
| chr2:120287228 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.323+1146C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287228 | |||||||
| chr2:120287230 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.323+1148C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287230 | |||||||
| chr2:120287257 | C | A | 1 | a0001c0001t0004g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1175C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287257 | |||||||
| chr2:120287271 | T | C | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(8): Show |
15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1189T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287271 | |||||||
| chr2:120287346 | G | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(8): Show |
15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1264G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287346 | |||||||
| chr2:120287397 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.323+1315T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287397 | |||||||
| chr2:120287478 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.323+1396G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287478 | |||||||
| chr2:120287537 | C | T | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0001g0012 others(8): Show |
15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1455C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287537 | |||||||
| chr2:120287553 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0179 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.323+1471C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287553 | |||||||
| chr2:120287599 | G | A | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.323+1517G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287599 | |||||||
| chr2:120288083 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.324-1497C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288083 | |||||||
| chr2:120288197 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.324-1383C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288197 | |||||||
| chr2:120288308 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-1272G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288308 | |||||||
| chr2:120288342 | G | GTT | 27 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0057 others(24): Show |
39 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.324-1228_324-1227d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | ||||||
| chr2:120288342 | G | GTTT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0032 others(37): Show |
53 | HG00609.hp1 HG00741.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.324-1229_324-1227d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | ||||||
| chr2:120288342 | G | GTTTT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
97 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.324-1230_324-1227d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | ||||||
| chr2:120288342 | G | GTTTTT | 26 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0103 others(23): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.324-1231_324-1227d others(7): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | ||||||
| chr2:120288354 | G | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.324-1226G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288354 | |||||||
| chr2:120288431 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0032 others(25): Show |
40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.324-1149C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288431 | |||||||
| chr2:120288477 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.324-1103G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288477 | |||||||
| chr2:120288540 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-1040C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288540 | |||||||
| chr2:120288701 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0089 a0001c0001t0004g0090 others(3): Show |
8 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-879C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288701 | |||||||
| chr2:120288857 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-723C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288857 | |||||||
| chr2:120288977 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.324-603C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288977 | |||||||
| chr2:120288997 | T | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-583T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288997 | |||||||
| chr2:120289048 | G | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0010g0196 |
3 | NA18994.hp2 NA19077.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.324-532G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289048 | |||||||
| chr2:120289109 | A | G | 3 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 |
3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-471A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289109 | |||||||
| chr2:120289238 | C | CT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0060 others(2): Show |
5 | HG02486.hp1 HG03486.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-337dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289238 | ||||||
| chr2:120289238 | C | CTT | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-338_324-337dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289238 | ||||||
| chr2:120289243 | TG | T | 18 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0004g0018 others(15): Show |
24 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.324-336delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289243 | |||||||
| chr2:120289244 | G | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(49): Show |
71 | HG00609.hp1 HG00639.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.324-336G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289244 | |||||||
| chr2:120289244 | GT | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.324-325delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289244 | ||||||
| chr2:120289254 | T | G | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0004g0088 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.324-326T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289254 | |||||||
| chr2:120289313 | C | CACTT | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-266_324-263dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289313 | ||||||
| chr2:120289534 | G | A | 1 | a0001c0001t0008g0028 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.324-46G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289534 | |||||||
| chr2:120289941 | C | T | 2 | a0001c0001t0004g0018 a0001c0001t0004g0093 |
4 | HG02451.hp1 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+184C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120289941 | |||||||
| chr2:120289999 | TG | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.501+243delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120289999 | |||||||
| chr2:120290099 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.501+342A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290099 | |||||||
| chr2:120290163 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.501+406G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290163 | |||||||
| chr2:120290273 | G | A | 1 | a0001c0002t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.501+516G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290273 | |||||||
| chr2:120290287 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
14 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+530C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290287 | |||||||
| chr2:120290353 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.501+596G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290353 | |||||||
| chr2:120290433 | G | C | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.501+676G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290433 | |||||||
| chr2:120290434 | C | G | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.501+677C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290434 | |||||||
| chr2:120290435 | G | A | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.501+678G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290435 | |||||||
| chr2:120290626 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.501+869G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290626 | |||||||
| chr2:120290632 | C | CT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0142 a0001c0001t0002g0191 others(4): Show |
8 | HG00639.hp2 HG01074.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+887dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | ||||||
| chr2:120290632 | C | CTT | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.501+886_501+887dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | ||||||
| chr2:120290632 | C | CTTT | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0098 others(9): Show |
16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+885_501+887dup others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | ||||||
| chr2:120290632 | C | CTTTT | 10 | a0001c0001t0004g0018 a0001c0001t0004g0048 a0001c0001t0004g0088 others(7): Show |
13 | HG00735.hp1 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+884_501+887dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | ||||||
| chr2:120290830 | G | T | 1 | a0001c0001t0003g0066 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.501+1073G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290830 | |||||||
| chr2:120291136 | T | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.501+1379T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291136 | |||||||
| chr2:120291276 | A | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.501+1519A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291276 | |||||||
| chr2:120291302 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0030 others(70): Show |
99 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.501+1545C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291302 | |||||||
| chr2:120291500 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.502-1641G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291500 | |||||||
| chr2:120291502 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502-1639G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291502 | |||||||
| chr2:120291590 | G | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.502-1551G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291590 | |||||||
| chr2:120291635 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.502-1506G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291635 | |||||||
| chr2:120291878 | C | T | 1 | a0001c0001t0006g0051 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502-1263C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291878 | |||||||
| chr2:120292029 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502-1112C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292029 | |||||||
| chr2:120292037 | G | T | 32 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 others(29): Show |
45 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.502-1104G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292037 | |||||||
| chr2:120292515 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.502-626C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292515 | |||||||
| chr2:120292560 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502-581T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292560 | |||||||
| chr2:120292598 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.502-543C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292598 | |||||||
| chr2:120292790 | T | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0021 others(24): Show |
43 | HG00609.hp2 HG01123.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.502-351T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292790 | |||||||
| chr2:120292803 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.502-338A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292803 | |||||||
| chr2:120292830 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0013g0035 |
2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.502-311C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292830 | |||||||
| chr2:120292839 | T | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0099 a0001c0001t0005g0100 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-302T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292839 | |||||||
| chr2:120292848 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 |
4 | HG02071.hp2 HG02074.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-293C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292848 | |||||||
| chr2:120292851 | G | C | 4 | a0001c0001t0001g0134 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG00609.hp2 HG02040.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-290G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292851 | |||||||
| chr2:120292861 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.502-280G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292861 | |||||||
| chr2:120292888 | T | G | 1 | a0001c0001t0004g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502-253T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292888 | |||||||
| chr2:120292984 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.502-157A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292984 | |||||||
| chr2:120293013 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0155 |
2 | HG01496.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.502-128C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120293013 | |||||||
| chr2:120293022 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.502-119T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120293022 |