Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26003 |
| ensemblid | ENSG00000115806.13 |
| hgncid | 17500 |
| symbol | GORASP2 |
| name | golgi reassembly stacking protein 2 |
| refseq_nuc | NM_015530.5 |
| refseq_prot | NP_056345.3 |
| ensembl_nuc | ENST00000234160.5 |
| ensembl_prot | ENSP00000234160.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 170929253 |
| end | 170967130 |
| strand | + |
| ver | v1.2 |
| region | chr2:170929253-170967130 |
| region5000 | chr2:170924253-170972130 |
| regionname0 | GORASP2_chr2_170929253_170967130 |
| regionname5000 | GORASP2_chr2_170924253_170972130 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 301 | 85 | 55 | 107 | 16 | 36 | 76 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0002 | 0/0 | 452 | 68 | 0 | 9 | 53 | 0 | 6 | 39 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0003 | 0/0 | 452 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0004 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0005 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0006 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| a0007 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | MGSSQ others(447): Show |
chr2 | 170924253 | 170972130 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1356 | 253 | 45 | 51 | 107 | 15 | 34 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0001c0003 | 1/0 | 1356 | 46 | 38 | 4 | 0 | 1 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0001c0006 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0001c0009 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0002c0002 | 0/0 | 1356 | 68 | 0 | 9 | 53 | 0 | 6 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0003c0004 | 0/0 | 1356 | 8 | 6 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0004c0005 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0005c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0006c0007 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 | ||
| a0007c0008 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | ATGGG others(1351): Show |
chr2 | 170924253 | 170972130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2447 | 246 | 43 | 49 | 105 | 15 | 33 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0001t0003 | 0/0 | 2447 | 2 | 0 | 1 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0001t0004 | 0/0 | 2447 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0001t0005 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0001t0006 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0001t0007 | 0/0 | 2447 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0003t0001 | 1/0 | 2447 | 40 | 38 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0003t0002 | 0/0 | 2447 | 6 | 0 | 4 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0006t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0001c0009t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0002c0002t0001 | 0/0 | 2447 | 68 | 0 | 9 | 53 | 0 | 6 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0003c0004t0001 | 0/0 | 2447 | 8 | 6 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0004c0005t0001 | 0/0 | 2447 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0005c0010t0001 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0006c0007t0001 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| a0007c0008t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | AAGTG others(2442): Show |
chr2 | 170924253 | 170972130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 3 | 10 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 7 | 1 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0003 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0007 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0009t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0004c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0004c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0005c0010t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0006c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0007c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0073 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0232 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02015 | hp1 | a0005 | c0010 | t0001 | g0079 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0072 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0186 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0200 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0038 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0183 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03041 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0259 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0231 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0071 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | CHB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18972 | hp1 | a0006 | c0007 | t0001 | g0158 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19009 | hp2 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19068 | hp1 | a0004 | c0005 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ASW | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20129 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ASW | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | GIH | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA21309 | hp1 | a0007 | c0008 | t0001 | g0049 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0046 | REF | REF | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170956451 | G | T | 1 | a0005 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.715G>T | p.Val239Phe | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/10 | 803/2447 | 715/1359 | 239/452 | chr2 | 170956451 | |||
| chr2:170956461 | C | T | 1 | a0004 | 2 | NA19009.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.725C>T | p.Pro242Leu | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/10 | 813/2447 | 725/1359 | 242/452 | chr2 | 170956461 | |||
| chr2:170966015 | C | T | 1 | a0003 | 8 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(5): Show |
missense_variant | MODERATE | c.1244C>T | p.Thr415Met | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1332/2447 | 1244/1359 | 415/452 | chr2 | 170966015 | |||
| chr2:170966044 | G | A | 1 | a0006 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1273G>A | p.Val425Ile | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1361/2447 | 1273/1359 | 425/452 | chr2 | 170966044 | |||
| chr2:170966062 | G | A | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1291G>A | p.Asp431Asn | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1379/2447 | 1291/1359 | 431/452 | chr2 | 170966062 | |||
| chr2:170966066 | C | T | 1 | a0002 | 68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
missense_variant | MODERATE | c.1295C>T | p.Ser432Phe | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1383/2447 | 1295/1359 | 432/452 | chr2 | 170966066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170961679 | G | A | 1 | a0001c0006 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.840G>A | p.Pro280Pro | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/10 | 928/2447 | 840/1359 | 280/452 | chr2 | 170961679 | |||
| chr2:170965849 | C | T | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1078C>T | p.Leu360Leu | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1166/2447 | 1078/1359 | 360/452 | chr2 | 170965849 | |||
| chr2:170965956 | C | T | 9 | a0001c0001 a0001c0006 a0001c0009 others(6): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
synonymous_variant | LOW | c.1185C>T | p.Ser395Ser | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1273/2447 | 1185/1359 | 395/452 | chr2 | 170965956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170929265 | G | C | 1 | a0001c0001t0005 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/10 | 76 | chr2 | 170929265 | ||||||
| chr2:170966335 | C | T | 1 | a0001c0003t0002 | 6 | HG01069.hp1 HG01081.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 205 | chr2 | 170966335 | ||||||
| chr2:170966364 | T | C | 1 | a0001c0001t0006 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 234 | chr2 | 170966364 | ||||||
| chr2:170966420 | G | A | 1 | a0001c0001t0007 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 290 | chr2 | 170966420 | ||||||
| chr2:170966558 | C | G | 1 | a0001c0001t0004 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*428C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 428 | chr2 | 170966558 | ||||||
| chr2:170966638 | T | C | 1 | a0001c0001t0003 | 2 | HG00733.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*508T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 508 | chr2 | 170966638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170929509 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.63+106C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929509 | |||||||
| chr2:170929553 | G | A | 2 | a0001c0003t0001g0020 a0003c0004t0001g0038 |
3 | HG02970.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+150G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929553 | |||||||
| chr2:170929578 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(27): Show |
41 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.63+175C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929578 | |||||||
| chr2:170929659 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.63+256A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929659 | |||||||
| chr2:170929719 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
7 | HG00323.hp1 HG00738.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+316C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929719 | |||||||
| chr2:170929729 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+326C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929729 | |||||||
| chr2:170929737 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.63+334T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929737 | |||||||
| chr2:170929772 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(6): Show |
10 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+369G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929772 | |||||||
| chr2:170929784 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.63+381G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929784 | |||||||
| chr2:170929876 | C | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | NA18952.hp1 NA18962.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+473C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929876 | |||||||
| chr2:170929928 | C | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+525C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929928 | |||||||
| chr2:170929964 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
7 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+561G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929964 | |||||||
| chr2:170929969 | G | A | 4 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+566G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929969 | |||||||
| chr2:170930013 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+610C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930013 | |||||||
| chr2:170930053 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+650C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930053 | |||||||
| chr2:170930083 | TTA | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+683_63+684delTA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930083 | ||||||
| chr2:170930351 | A | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+948A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930351 | |||||||
| chr2:170930368 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01346.hp1 HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.63+965C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930368 | |||||||
| chr2:170930377 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+974G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930377 | |||||||
| chr2:170930651 | A | AT | 69 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0062 others(66): Show |
89 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.63+1258dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930651 | ||||||
| chr2:170930740 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(30): Show |
44 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+1337A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930740 | |||||||
| chr2:170930973 | CA | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(111): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.63+1587delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930973 | ||||||
| chr2:170930988 | A | AC | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.63+1585_63+1586ins others(1): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930988 | |||||||
| chr2:170930988 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(110): Show |
145 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.63+1585A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930988 | |||||||
| chr2:170931097 | G | GA | 8 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+1697dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170931097 | ||||||
| chr2:170931213 | C | T | 1 | a0001c0001t0006g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.63+1810C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931213 | |||||||
| chr2:170931514 | T | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+2111T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931514 | |||||||
| chr2:170931949 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.63+2546C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931949 | |||||||
| chr2:170932001 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.63+2598G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932001 | |||||||
| chr2:170932018 | G | A | 1 | a0005c0010t0001g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+2615G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932018 | |||||||
| chr2:170932136 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.63+2733A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932136 | |||||||
| chr2:170932203 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.63+2800G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932203 | |||||||
| chr2:170932296 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.63+2893A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932296 | |||||||
| chr2:170932403 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.63+3000T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932403 | |||||||
| chr2:170932693 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+3290C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932693 | |||||||
| chr2:170933192 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.63+3789T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933192 | |||||||
| chr2:170933214 | C | T | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+3811C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933214 | |||||||
| chr2:170933587 | A | C | 1 | a0002c0002t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+4184A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933587 | |||||||
| chr2:170933593 | C | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.63+4190C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933593 | |||||||
| chr2:170933657 | T | C | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.63+4254T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933657 | |||||||
| chr2:170933697 | G | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG02602.hp2 HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.63+4294G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933697 | |||||||
| chr2:170933707 | TAAAAG | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+4306_63+4310del others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170933707 | ||||||
| chr2:170933843 | A | G | 1 | a0001c0001t0003g0175 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.63+4440A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933843 | |||||||
| chr2:170933877 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.63+4474A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933877 | |||||||
| chr2:170933986 | T | TA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+4584dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170933986 | ||||||
| chr2:170933987 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.63+4584A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933987 | |||||||
| chr2:170934158 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0081 |
3 | NA18975.hp2 NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.63+4755T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934158 | |||||||
| chr2:170934197 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+4794C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934197 | |||||||
| chr2:170934244 | CCT | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+4842_63+4843del others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934244 | |||||||
| chr2:170934253 | T | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+4850T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934253 | |||||||
| chr2:170934256 | T | G | 20 | a0001c0001t0001g0082 a0001c0001t0001g0246 a0001c0001t0001g0247 others(17): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+4853T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934256 | |||||||
| chr2:170934258 | TG | T | 3 | a0001c0001t0001g0098 a0002c0002t0001g0199 a0003c0004t0001g0200 |
3 | HG02818.hp1 HG02965.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.63+4856delG | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934258 | |||||||
| chr2:170934259 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
260 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.63+4856G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934259 | |||||||
| chr2:170934262 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0002c0002t0001g0239 |
3 | HG02165.hp1 NA18947.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.63+4859G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934262 | |||||||
| chr2:170934305 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.63+4902C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934305 | |||||||
| chr2:170934556 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.63+5153C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934556 | |||||||
| chr2:170934801 | A | G | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+5398A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934801 | |||||||
| chr2:170934899 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.63+5496A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934899 | |||||||
| chr2:170935077 | T | C | 1 | a0002c0002t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+5674T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935077 | |||||||
| chr2:170935526 | A | G | 7 | a0002c0002t0001g0198 a0002c0002t0001g0233 a0002c0002t0001g0234 others(4): Show |
7 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+6123A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935526 | |||||||
| chr2:170935558 | C | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6155C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935558 | |||||||
| chr2:170935572 | C | CT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
9 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6187dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170935572 | ||||||
| chr2:170935585 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63+6182T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935585 | |||||||
| chr2:170935588 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.63+6185T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935588 | |||||||
| chr2:170935588 | T | TC | 4 | a0003c0004t0001g0011 a0003c0004t0001g0200 a0003c0004t0001g0231 others(1): Show |
7 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6185_63+6186ins others(1): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935588 | |||||||
| chr2:170935781 | G | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6378G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935781 | |||||||
| chr2:170935815 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+6412A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935815 | |||||||
| chr2:170935919 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.63+6516C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935919 | |||||||
| chr2:170935922 | C | T | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(17): Show |
22 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+6519C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935922 | |||||||
| chr2:170935953 | G | T | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+6550G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935953 | |||||||
| chr2:170936019 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.63+6616C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936019 | |||||||
| chr2:170936082 | C | G | 1 | a0001c0003t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.63+6679C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936082 | |||||||
| chr2:170936224 | C | CT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0027 others(33): Show |
51 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.63+6841dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | ||||||
| chr2:170936224 | C | CTT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.63+6840_63+6841dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | ||||||
| chr2:170936224 | C | CTTT | 8 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0170 others(5): Show |
9 | HG02486.hp1 HG02647.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6839_63+6841dup others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | ||||||
| chr2:170936406 | A | G | 12 | a0002c0002t0001g0009 a0002c0002t0001g0036 a0002c0002t0001g0188 others(9): Show |
17 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+7003A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936406 | |||||||
| chr2:170936420 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0080 |
3 | HG00280.hp1 HG03710.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.63+7017A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936420 | |||||||
| chr2:170936464 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.63+7061C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936464 | |||||||
| chr2:170936629 | A | G | 4 | a0001c0003t0002g0071 a0001c0003t0002g0072 a0001c0003t0002g0073 others(1): Show |
4 | HG01081.hp2 HG02735.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+7226A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936629 | |||||||
| chr2:170936758 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0093 others(2): Show |
5 | HG00140.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7355C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936758 | |||||||
| chr2:170936833 | G | A | 1 | a0001c0003t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+7430G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936833 | |||||||
| chr2:170936847 | C | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+7444C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936847 | |||||||
| chr2:170936876 | C | T | 4 | a0003c0004t0001g0011 a0003c0004t0001g0200 a0003c0004t0001g0231 others(1): Show |
7 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7473C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936876 | |||||||
| chr2:170936914 | A | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0063 others(12): Show |
20 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+7511A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936914 | |||||||
| chr2:170937058 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+7655A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937058 | |||||||
| chr2:170937077 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.63+7674G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937077 | |||||||
| chr2:170937187 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.63+7784G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937187 | |||||||
| chr2:170937786 | C | T | 1 | a0002c0002t0001g0223 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+8383C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937786 | |||||||
| chr2:170937797 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
9 | HG00140.hp1 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8394A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937797 | |||||||
| chr2:170937869 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.63+8466T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937869 | |||||||
| chr2:170937998 | C | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8595C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937998 | |||||||
| chr2:170938024 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+8621C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938024 | |||||||
| chr2:170938051 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0245 |
2 | HG01081.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.63+8648C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938051 | |||||||
| chr2:170938118 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.63+8715G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938118 | |||||||
| chr2:170938121 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+8718A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938121 | |||||||
| chr2:170938172 | A | C | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.63+8769A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938172 | |||||||
| chr2:170938509 | C | T | 2 | a0002c0002t0001g0221 a0002c0002t0001g0222 |
2 | NA18985.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.63+9106C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938509 | |||||||
| chr2:170938533 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.63+9130A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938533 | |||||||
| chr2:170938650 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+9247C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938650 | |||||||
| chr2:170938650 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+9247C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938650 | |||||||
| chr2:170939001 | G | GA | 4 | a0001c0001t0001g0096 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00099.hp1 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9342dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170939001 | ||||||
| chr2:170939110 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-9240A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939110 | |||||||
| chr2:170939158 | G | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9192G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939158 | |||||||
| chr2:170939202 | T | C | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-9148T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939202 | |||||||
| chr2:170939331 | G | A | 2 | a0001c0003t0001g0183 a0001c0003t0001g0184 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-9019G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939331 | |||||||
| chr2:170939429 | CA | C | 55 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(52): Show |
69 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-8920delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939429 | |||||||
| chr2:170939506 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | NA18942.hp1 NA18978.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.64-8844C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939506 | |||||||
| chr2:170939591 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-8759T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939591 | |||||||
| chr2:170939745 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.64-8605A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939745 | |||||||
| chr2:170939917 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-8433A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939917 | |||||||
| chr2:170940006 | TAGA | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-8340_64-8338del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170940006 | ||||||
| chr2:170940013 | G | A | 1 | a0001c0003t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-8337G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940013 | |||||||
| chr2:170940037 | A | G | 2 | a0001c0003t0001g0183 a0001c0003t0001g0184 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-8313A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940037 | |||||||
| chr2:170940087 | A | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8263A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940087 | |||||||
| chr2:170940221 | A | G | 2 | a0002c0002t0001g0189 a0002c0002t0001g0229 |
2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.64-8129A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940221 | |||||||
| chr2:170940259 | C | G | 1 | a0001c0003t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-8091C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940259 | |||||||
| chr2:170940369 | A | G | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-7981A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940369 | |||||||
| chr2:170940553 | TAAAAG | T | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-7786_64-7782del others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170940553 | ||||||
| chr2:170940609 | A | C | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-7741A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940609 | |||||||
| chr2:170940679 | G | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-7671G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940679 | |||||||
| chr2:170940724 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-7626A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940724 | |||||||
| chr2:170940881 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.64-7469T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940881 | |||||||
| chr2:170941339 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64-7011G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941339 | |||||||
| chr2:170941394 | A | G | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-6956A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941394 | |||||||
| chr2:170941574 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-6776A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941574 | |||||||
| chr2:170941619 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-6731T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941619 | |||||||
| chr2:170941868 | T | C | 1 | a0001c0003t0001g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-6482T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941868 | |||||||
| chr2:170941873 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
18 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-6477A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941873 | |||||||
| chr2:170942069 | G | A | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-6281G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942069 | |||||||
| chr2:170942084 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-6266T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942084 | |||||||
| chr2:170942267 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.64-6083A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942267 | |||||||
| chr2:170942304 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64-6046A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942304 | |||||||
| chr2:170942431 | A | G | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-5919A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942431 | |||||||
| chr2:170942447 | C | T | 1 | a0001c0003t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-5903C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942447 | |||||||
| chr2:170942450 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-5900A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942450 | |||||||
| chr2:170942456 | C | T | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-5894C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942456 | |||||||
| chr2:170942504 | T | G | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-5846T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942504 | |||||||
| chr2:170942547 | G | A | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-5803G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942547 | |||||||
| chr2:170942876 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-5474C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942876 | |||||||
| chr2:170942914 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-5436G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942914 | |||||||
| chr2:170943181 | GTTTTACC others(7): Show |
G | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-5163_64-5150del others(14): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170943181 | ||||||
| chr2:170943205 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-5145T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943205 | |||||||
| chr2:170943401 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18968.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.64-4949G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943401 | |||||||
| chr2:170943418 | T | G | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-4932T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943418 | |||||||
| chr2:170943632 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.64-4718A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943632 | |||||||
| chr2:170943655 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-4695A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943655 | |||||||
| chr2:170943771 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64-4579C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943771 | |||||||
| chr2:170943772 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-4578G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943772 | |||||||
| chr2:170943785 | G | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-4565G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943785 | |||||||
| chr2:170943792 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-4558C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943792 | |||||||
| chr2:170943873 | A | G | 3 | a0003c0004t0001g0011 a0003c0004t0001g0200 a0003c0004t0001g0232 |
6 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4477A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943873 | |||||||
| chr2:170943965 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64-4385C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943965 | |||||||
| chr2:170944043 | A | C | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-4307A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944043 | |||||||
| chr2:170944176 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.64-4174A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944176 | |||||||
| chr2:170944273 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-4077A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944273 | |||||||
| chr2:170944286 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64-4064T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944286 | |||||||
| chr2:170944311 | G | C | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-4039G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944311 | |||||||
| chr2:170944412 | A | C | 1 | a0001c0001t0001g0280 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64-3938A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944412 | |||||||
| chr2:170944437 | G | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-3913G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944437 | |||||||
| chr2:170944564 | A | C | 1 | a0001c0003t0001g0023 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.64-3786A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944564 | |||||||
| chr2:170944710 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
7 | HG02071.hp2 HG02135.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3640G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944710 | |||||||
| chr2:170944902 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.64-3448G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944902 | |||||||
| chr2:170945212 | G | A | 1 | a0002c0002t0001g0239 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-3138G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945212 | |||||||
| chr2:170945237 | G | A | 1 | a0003c0004t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-3113G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945237 | |||||||
| chr2:170945258 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.64-3092C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945258 | |||||||
| chr2:170945359 | C | CGT | 2 | a0001c0001t0001g0024 a0001c0001t0001g0058 |
3 | HG02886.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.64-2987_64-2986dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945359 | ||||||
| chr2:170945501 | C | CA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.64-2835dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945501 | ||||||
| chr2:170945501 | C | CAA | 16 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0001g0089 others(13): Show |
17 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-2836_64-2835dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945501 | ||||||
| chr2:170945515 | AGAAG | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2834_64-2831del others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945515 | |||||||
| chr2:170945516 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.64-2834G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945516 | |||||||
| chr2:170945649 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.64-2701G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945649 | |||||||
| chr2:170945688 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-2662T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945688 | |||||||
| chr2:170945726 | A | G | 6 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG03130.hp1 HG04199.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-2624A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945726 | |||||||
| chr2:170945823 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.64-2527T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945823 | |||||||
| chr2:170945964 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0279 |
2 | HG02559.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.64-2386A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945964 | |||||||
| chr2:170946010 | T | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0002c0002t0001g0224 |
3 | HG02523.hp2 HG02886.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.64-2340T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946010 | |||||||
| chr2:170946318 | C | T | 54 | a0002c0002t0001g0005 a0002c0002t0001g0009 a0002c0002t0001g0010 others(51): Show |
68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.64-2032C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946318 | |||||||
| chr2:170946424 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-1926A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946424 | |||||||
| chr2:170946620 | G | C | 1 | a0002c0002t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-1730G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946620 | |||||||
| chr2:170946768 | C | CA | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.64-1562dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170946768 | ||||||
| chr2:170946768 | C | CAA | 35 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0074 others(32): Show |
40 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1563_64-1562dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170946768 | ||||||
| chr2:170946881 | A | C | 1 | a0001c0003t0001g0148 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64-1469A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946881 | |||||||
| chr2:170947010 | G | A | 6 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG03130.hp1 HG04199.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-1340G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947010 | |||||||
| chr2:170947081 | T | C | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.64-1269T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947081 | |||||||
| chr2:170947129 | T | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(26): Show |
40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1221T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947129 | |||||||
| chr2:170947281 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64-1069A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947281 | |||||||
| chr2:170947368 | T | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
24 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-982T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947368 | |||||||
| chr2:170947382 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
18 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-968A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947382 | |||||||
| chr2:170947396 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.64-954C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947396 | |||||||
| chr2:170947413 | A | G | 2 | a0001c0003t0001g0047 a0007c0008t0001g0049 |
2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.64-937A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947413 | |||||||
| chr2:170947452 | T | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-898T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947452 | |||||||
| chr2:170947468 | C | T | 2 | a0001c0003t0001g0020 a0003c0004t0001g0038 |
3 | HG02970.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-882C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947468 | |||||||
| chr2:170947507 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-843C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947507 | |||||||
| chr2:170947592 | C | T | 6 | a0002c0002t0001g0198 a0002c0002t0001g0233 a0002c0002t0001g0234 others(3): Show |
6 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-758C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947592 | |||||||
| chr2:170947739 | C | T | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-611C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947739 | |||||||
| chr2:170947992 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0244 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.64-358G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947992 | |||||||
| chr2:170948143 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-207A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170948143 | |||||||
| chr2:170948153 | G | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0093 others(2): Show |
5 | HG00140.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-197G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170948153 | |||||||
| chr2:170948459 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.144+29A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948459 | |||||||
| chr2:170948557 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.144+127A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948557 | |||||||
| chr2:170948628 | A | C | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.144+198A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948628 | |||||||
| chr2:170948925 | G | A | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.144+495G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948925 | |||||||
| chr2:170949275 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.145-264A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949275 | |||||||
| chr2:170949360 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.145-179G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949360 | |||||||
| chr2:170949413 | T | A | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.145-126T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949413 | |||||||
| chr2:170949806 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.348+64A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170949806 | |||||||
| chr2:170949939 | T | C | 5 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+197T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170949939 | |||||||
| chr2:170950109 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0129 |
2 | HG00609.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.349-95A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950109 | |||||||
| chr2:170950113 | A | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-91A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950113 | |||||||
| chr2:170950134 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.349-70A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950134 | |||||||
| chr2:170950407 | C | G | 7 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+117C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950407 | |||||||
| chr2:170950494 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.435+204C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950494 | |||||||
| chr2:170950557 | A | G | 1 | a0001c0003t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.435+267A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950557 | |||||||
| chr2:170950843 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(8): Show |
19 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.436-485A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950843 | |||||||
| chr2:170950933 | A | T | 1 | a0001c0001t0001g0012 | 3 | HG02809.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.436-395A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950933 | |||||||
| chr2:170950974 | A | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.436-354A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950974 | |||||||
| chr2:170951127 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436-201A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170951127 | |||||||
| chr2:170951141 | G | A | 3 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 |
3 | NA18962.hp1 NA19055.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.436-187G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170951141 | |||||||
| chr2:170951502 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+44C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951502 | |||||||
| chr2:170951617 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.566+159T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951617 | |||||||
| chr2:170951710 | A | G | 4 | a0001c0001t0001g0096 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00099.hp1 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+252A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951710 | |||||||
| chr2:170951717 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.566+259C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951717 | |||||||
| chr2:170951890 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
2 | HG02602.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.566+432G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951890 | |||||||
| chr2:170951894 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.566+436C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951894 | |||||||
| chr2:170952115 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(31): Show |
45 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.566+657C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952115 | |||||||
| chr2:170952306 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.566+848C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952306 | |||||||
| chr2:170952608 | T | A | 3 | a0001c0003t0002g0071 a0001c0003t0002g0072 a0001c0003t0002g0073 |
3 | HG01081.hp2 HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.566+1150T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952608 | |||||||
| chr2:170952751 | C | T | 1 | a0001c0003t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566+1293C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952751 | |||||||
| chr2:170952893 | C | G | 2 | a0001c0003t0001g0007 a0001c0003t0001g0048 |
6 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+1435C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952893 | |||||||
| chr2:170952915 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566+1457A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952915 | |||||||
| chr2:170952975 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.566+1517C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952975 | |||||||
| chr2:170953179 | A | G | 2 | a0001c0003t0001g0007 a0001c0003t0001g0048 |
6 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-1471A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953179 | |||||||
| chr2:170953192 | CAAAAAAT others(3): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567-1453_567-1444d others(12): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953192 | ||||||
| chr2:170953233 | A | G | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.567-1417A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953233 | |||||||
| chr2:170953259 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.567-1391G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953259 | |||||||
| chr2:170953261 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.567-1389C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953261 | |||||||
| chr2:170953278 | C | T | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-1372C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953278 | |||||||
| chr2:170953333 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.567-1317G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953333 | |||||||
| chr2:170953355 | T | TAATA | 11 | a0001c0001t0001g0057 a0001c0003t0001g0020 a0001c0003t0001g0066 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-1268_567-1265d others(6): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | ||||||
| chr2:170953355 | T | TAATAAAT others(5): Show |
2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.567-1276_567-1265d others(14): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | ||||||
| chr2:170953355 | TAATA | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.567-1268_567-1265d others(6): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | ||||||
| chr2:170953513 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.567-1137G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953513 | |||||||
| chr2:170953532 | T | C | 1 | a0001c0003t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.567-1118T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953532 | |||||||
| chr2:170953597 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01106.hp1 HG01243.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.567-1053G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953597 | |||||||
| chr2:170953901 | A | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(33): Show |
57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.567-749A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953901 | |||||||
| chr2:170953946 | G | A | 30 | a0002c0002t0001g0005 a0002c0002t0001g0130 a0002c0002t0001g0191 others(27): Show |
35 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.567-704G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953946 | |||||||
| chr2:170953988 | C | T | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.567-662C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953988 | |||||||
| chr2:170954222 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.567-428G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954222 | |||||||
| chr2:170954333 | G | A | 1 | a0001c0003t0001g0020 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.567-317G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954333 | |||||||
| chr2:170954351 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.567-299A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954351 | |||||||
| chr2:170954530 | G | A | 5 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-120G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954530 | |||||||
| chr2:170954538 | T | C | 2 | a0002c0002t0001g0227 a0002c0002t0001g0228 |
2 | NA19001.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.567-112T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954538 | |||||||
| chr2:170954647 | T | A | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.567-3T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954647 | |||||||
| chr2:170954887 | G | A | 1 | a0002c0002t0001g0221 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.699+105G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170954887 | |||||||
| chr2:170955036 | T | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.699+254T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170955036 | |||||||
| chr2:170955558 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.699+776A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170955558 | |||||||
| chr2:170956151 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.700-285A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170956151 | |||||||
| chr2:170956742 | TAAA | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.823+193_823+195del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170956742 | ||||||
| chr2:170956806 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.823+247C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956806 | |||||||
| chr2:170956929 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.823+370T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956929 | |||||||
| chr2:170956932 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0058 |
3 | HG02886.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823+373T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956932 | |||||||
| chr2:170957148 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.823+589T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957148 | |||||||
| chr2:170957178 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.823+619C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957178 | |||||||
| chr2:170957199 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0204 |
3 | HG02257.hp2 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.823+640A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957199 | |||||||
| chr2:170957240 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0112 a0001c0001t0001g0129 others(3): Show |
6 | HG00323.hp2 HG00609.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+681C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957240 | |||||||
| chr2:170957371 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.823+812A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957371 | |||||||
| chr2:170957578 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG02602.hp2 HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.823+1019C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957578 | |||||||
| chr2:170957704 | A | T | 1 | a0002c0002t0001g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823+1145A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957704 | |||||||
| chr2:170957743 | A | C | 1 | a0002c0002t0001g0228 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.823+1184A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957743 | |||||||
| chr2:170957916 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.823+1357C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957916 | |||||||
| chr2:170957946 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+1387A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957946 | |||||||
| chr2:170957965 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823+1406A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957965 | |||||||
| chr2:170958128 | C | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1569C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958128 | |||||||
| chr2:170958181 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0244 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.823+1622C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958181 | |||||||
| chr2:170958240 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.823+1681C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958240 | |||||||
| chr2:170958380 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): Show |
39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.823+1821A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958380 | |||||||
| chr2:170958653 | CT | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
25 | HG01069.hp1 HG01081.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.823+2115delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958653 | ||||||
| chr2:170958653 | CTT | C | 6 | a0001c0001t0001g0040 a0001c0003t0001g0133 a0001c0003t0001g0148 others(3): Show |
6 | HG02630.hp2 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2114_823+2115d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958653 | ||||||
| chr2:170958674 | T | A | 2 | a0001c0003t0001g0050 a0007c0008t0001g0049 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.823+2115T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958674 | |||||||
| chr2:170958674 | TA | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0098 a0001c0001t0001g0110 others(12): Show |
15 | HG00408.hp2 HG00621.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.823+2129delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | ||||||
| chr2:170958674 | TAA | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.823+2128_823+2129d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | ||||||
| chr2:170958674 | TAAA | T | 21 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0081 others(18): Show |
23 | HG00323.hp2 HG01081.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+2127_823+2129d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | ||||||
| chr2:170958675 | A | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(18): Show |
32 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.823+2116A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958675 | |||||||
| chr2:170958676 | A | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(29): Show |
43 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.823+2117A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958676 | |||||||
| chr2:170958677 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.823+2118A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958677 | |||||||
| chr2:170958678 | A | T | 8 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0002c0002t0001g0188 others(5): Show |
11 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+2119A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958678 | |||||||
| chr2:170958684 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.823+2125A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958684 | |||||||
| chr2:170958810 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.823+2251C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958810 | |||||||
| chr2:170958851 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.823+2292G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958851 | |||||||
| chr2:170958913 | G | A | 7 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+2354G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958913 | |||||||
| chr2:170958966 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
2 | HG02602.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.823+2407G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958966 | |||||||
| chr2:170959023 | C | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2464C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959023 | |||||||
| chr2:170959058 | T | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2499T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959058 | |||||||
| chr2:170959063 | C | T | 6 | a0001c0001t0001g0272 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG00408.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2504C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959063 | |||||||
| chr2:170959085 | C | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2526C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959085 | |||||||
| chr2:170959093 | T | G | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2534T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959093 | |||||||
| chr2:170959094 | G | T | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2535G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959094 | |||||||
| chr2:170959095 | G | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2536G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959095 | |||||||
| chr2:170959219 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2444C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959219 | |||||||
| chr2:170959260 | C | G | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2403C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959260 | |||||||
| chr2:170959306 | A | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2357A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959306 | |||||||
| chr2:170959316 | T | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2347T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959316 | |||||||
| chr2:170959522 | G | C | 10 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(7): Show |
11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-2141G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959522 | |||||||
| chr2:170959594 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-2069A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959594 | |||||||
| chr2:170959610 | A | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(17): Show |
26 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-2053A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959610 | |||||||
| chr2:170959722 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.824-1941G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959722 | |||||||
| chr2:170959787 | C | G | 1 | a0001c0003t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.824-1876C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959787 | |||||||
| chr2:170959821 | C | CT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.824-1824dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170959821 | ||||||
| chr2:170959860 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.824-1803C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959860 | |||||||
| chr2:170960021 | A | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.824-1642A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960021 | |||||||
| chr2:170960057 | G | A | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01346.hp1 HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.824-1606G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960057 | |||||||
| chr2:170960077 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1586T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960077 | |||||||
| chr2:170960086 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.824-1577G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960086 | |||||||
| chr2:170960091 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0140 |
2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.824-1572G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960091 | |||||||
| chr2:170960141 | A | G | 2 | a0002c0002t0001g0036 a0002c0002t0001g0193 |
3 | HG02155.hp2 NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.824-1522A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960141 | |||||||
| chr2:170960214 | C | A | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.824-1449C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960214 | |||||||
| chr2:170960247 | A | G | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.824-1416A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960247 | |||||||
| chr2:170960258 | T | G | 5 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-1405T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960258 | |||||||
| chr2:170960361 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.824-1302T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960361 | |||||||
| chr2:170960442 | T | C | 1 | a0001c0003t0002g0021 | 2 | HG01069.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.824-1221T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960442 | |||||||
| chr2:170960564 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0276 a0001c0001t0001g0284 |
5 | NA18940.hp2 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1099C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960564 | |||||||
| chr2:170960788 | G | C | 3 | a0001c0003t0001g0133 a0001c0003t0001g0148 a0001c0003t0001g0190 |
3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.824-875G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960788 | |||||||
| chr2:170960989 | G | A | 3 | a0001c0003t0001g0133 a0001c0003t0001g0148 a0001c0003t0001g0190 |
3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.824-674G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960989 | |||||||
| chr2:170961162 | C | T | 24 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0040 others(21): Show |
27 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.824-501C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961162 | |||||||
| chr2:170961284 | C | T | 1 | a0003c0004t0001g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.824-379C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961284 | |||||||
| chr2:170961302 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.824-361G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961302 | |||||||
| chr2:170961403 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.824-260C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961403 | |||||||
| chr2:170961415 | CTGG | C | 10 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(7): Show |
11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-247_824-245del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961415 | |||||||
| chr2:170961418 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.824-245G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961418 | |||||||
| chr2:170961419 | G | C | 10 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(7): Show |
11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-244G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961419 | |||||||
| chr2:170961619 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0244 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.824-44C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961619 | |||||||
| chr2:170961776 | G | T | 1 | a0001c0003t0001g0020 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.910+27G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961776 | |||||||
| chr2:170961779 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.910+30G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961779 | |||||||
| chr2:170961998 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
5 | HG01074.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+249A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961998 | |||||||
| chr2:170962020 | C | G | 3 | a0001c0003t0001g0133 a0001c0003t0001g0148 a0001c0003t0001g0190 |
3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.910+271C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962020 | |||||||
| chr2:170962079 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.910+330A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962079 | |||||||
| chr2:170962087 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.910+338T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962087 | |||||||
| chr2:170962091 | C | T | 1 | a0002c0002t0001g0035 | 2 | NA18612.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.910+342C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962091 | |||||||
| chr2:170962236 | A | C | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.910+487A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962236 | |||||||
| chr2:170962490 | A | G | 2 | a0001c0001t0003g0125 a0001c0001t0003g0175 |
2 | HG00733.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.911-349A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962490 | |||||||
| chr2:170962979 | C | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018+33C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170962979 | |||||||
| chr2:170963355 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(19): Show |
33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1018+409A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963355 | |||||||
| chr2:170963374 | C | CA | 29 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(26): Show |
31 | HG00438.hp2 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1018+445dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963374 | ||||||
| chr2:170963426 | GCTGCTA | G | 10 | a0001c0001t0001g0017 a0001c0003t0001g0020 a0001c0003t0001g0066 others(7): Show |
13 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018+486_1018+491d others(8): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963426 | ||||||
| chr2:170963431 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
6 | HG02615.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018+485T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963431 | |||||||
| chr2:170963432 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
14 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1018+486A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963432 | |||||||
| chr2:170963447 | G | C | 2 | a0001c0003t0001g0183 a0001c0003t0001g0184 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1018+501G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963447 | |||||||
| chr2:170963450 | G | C | 11 | a0001c0003t0001g0020 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018+504G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963450 | |||||||
| chr2:170963450 | G | GCTC | 48 | a0002c0002t0001g0005 a0002c0002t0001g0009 a0002c0002t0001g0010 others(45): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1018+524_1018+526d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963450 | ||||||
| chr2:170963453 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1018+507C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963453 | |||||||
| chr2:170963462 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1018+516C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963462 | |||||||
| chr2:170963469 | CT | C | 6 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018+524delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963469 | |||||||
| chr2:170963470 | T | C | 5 | a0001c0003t0001g0020 a0001c0003t0001g0078 a0001c0003t0001g0183 others(2): Show |
6 | HG02630.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+524T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963470 | |||||||
| chr2:170963470 | T | TC | 14 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG00621.hp2 HG01192.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1018+529dupC | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963470 | ||||||
| chr2:170963473 | C | CCCTCCT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0275 a0001c0001t0001g0278 others(4): Show |
8 | HG00140.hp2 HG00642.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+536_1018+541d others(8): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963473 | ||||||
| chr2:170963473 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1018+527C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963473 | |||||||
| chr2:170963476 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1018+530T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963476 | |||||||
| chr2:170963488 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1018+542C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963488 | |||||||
| chr2:170963523 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1018+577A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963523 | |||||||
| chr2:170963775 | T | A | 1 | a0001c0003t0001g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1018+829T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963775 | |||||||
| chr2:170963960 | T | TA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(27): Show |
41 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1018+1024dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963960 | ||||||
| chr2:170963980 | A | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(33): Show |
57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1018+1034A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963980 | |||||||
| chr2:170964017 | C | T | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1018+1071C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964017 | |||||||
| chr2:170964426 | G | GT | 3 | a0001c0003t0001g0133 a0001c0003t0001g0148 a0001c0003t0001g0190 |
3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1019-1363dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964426 | ||||||
| chr2:170964574 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1019-1216A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964574 | |||||||
| chr2:170964607 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1019-1183C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964607 | |||||||
| chr2:170964608 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(26): Show |
40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1019-1182G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964608 | |||||||
| chr2:170964623 | A | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-1167A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964623 | |||||||
| chr2:170964635 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1019-1155A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964635 | |||||||
| chr2:170964716 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1019-1074G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964716 | |||||||
| chr2:170964883 | T | G | 4 | a0002c0002t0001g0211 a0002c0002t0001g0221 a0002c0002t0001g0222 others(1): Show |
4 | NA18980.hp2 NA18985.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019-907T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964883 | |||||||
| chr2:170964892 | A | AT | 27 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0065 others(24): Show |
28 | HG00140.hp2 HG01081.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.1019-871dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | ||||||
| chr2:170964892 | A | ATT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0024 others(23): Show |
37 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1019-872_1019-871d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | ||||||
| chr2:170964892 | A | ATTT | 9 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0058 others(6): Show |
9 | HG01175.hp1 HG01433.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1019-873_1019-871d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | ||||||
| chr2:170964892 | AT | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(85): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1019-871delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | ||||||
| chr2:170964892 | ATT | A | 51 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0061 others(48): Show |
65 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1019-872_1019-871d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | ||||||
| chr2:170965067 | C | T | 2 | a0002c0002t0001g0036 a0002c0002t0001g0193 |
3 | HG02155.hp2 NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1019-723C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965067 | |||||||
| chr2:170965082 | TGTACTTT others(26): Show |
T | 1 | a0002c0002t0001g0130 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1019-707_1019-675d others(35): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965082 | |||||||
| chr2:170965323 | C | T | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1019-467C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965323 | |||||||
| chr2:170965425 | G | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
11 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1019-365G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965425 | |||||||
| chr2:170965428 | TG | T | 54 | a0002c0002t0001g0005 a0002c0002t0001g0009 a0002c0002t0001g0010 others(51): Show |
68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1019-359delG | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170965428 | ||||||
| chr2:170965609 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
11 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1019-181G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965609 | |||||||
| chr2:170965755 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-35G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965755 |