Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89970 |
| ensemblid | ENSG00000159579.14 |
| hgncid | 29420 |
| symbol | RSPRY1 |
| name | ring finger and SPRY domain containing 1 |
| refseq_nuc | NM_133368.3 |
| refseq_prot | NP_588609.1 |
| ensembl_nuc | ENST00000394420.9 |
| ensembl_prot | ENSP00000377942.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 57186329 |
| end | 57240469 |
| strand | + |
| ver | v1.2 |
| region | chr16:57186329-57240469 |
| region5000 | chr16:57181329-57245469 |
| regionname0 | RSPRY1_chr16_57186329_57240469 |
| regionname5000 | RSPRY1_chr16_57181329_57245469 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 576 | 355 | 85 | 62 | 160 | 14 | 32 | 122 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | MIVFG others(571): Show |
chr16 | 57181329 | 57245469 |
| a0002 | 0/0 | 576 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | MIVFG others(571): Show |
chr16 | 57181329 | 57245469 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1728 | 352 | 82 | 62 | 160 | 14 | 32 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | ATGAT others(1723): Show |
chr16 | 57181329 | 57245469 | ||
| a0001c0003 | 0/0 | 1728 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | ATGAT others(1723): Show |
chr16 | 57181329 | 57245469 | ||
| a0001c0004 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | ATGAT others(1723): Show |
chr16 | 57181329 | 57245469 | ||
| a0002c0002 | 0/0 | 1728 | 3 | 3 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | ATGAT others(1723): Show |
chr16 | 57181329 | 57245469 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3503 | 186 | 59 | 45 | 64 | 8 | 9 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0002 | 0/0 | 3501 | 74 | 0 | 10 | 47 | 4 | 13 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3496): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0003 | 0/0 | 3494 | 40 | 0 | 1 | 31 | 0 | 8 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3489): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0004 | 0/0 | 3495 | 9 | 5 | 0 | 4 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3490): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0005 | 0/0 | 3503 | 7 | 4 | 2 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0006 | 0/1 | 3505 | 6 | 1 | 1 | 0 | 2 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3500): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0007 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0008 | 0/0 | 3505 | 4 | 1 | 1 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3500): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0009 | 0/0 | 3502 | 3 | 0 | 0 | 3 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0010 | 0/0 | 3502 | 3 | 2 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0011 | 0/0 | 3501 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3496): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0013 | 0/0 | 3495 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3490): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0014 | 0/0 | 3502 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0015 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0016 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3490): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0017 | 0/0 | 3505 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3500): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0019 | 0/0 | 3503 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0020 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0021 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0022 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0023 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3496): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0024 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0025 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3497): Show |
chr16 | 57181329 | 57245469 |
| a0001c0001t0026 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | GTGGC others(3476): Show |
chr16 | 57181329 | 57245469 |
| a0001c0003t0001 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0003t0007 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0001c0004t0001 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3498): Show |
chr16 | 57181329 | 57245469 |
| a0002c0002t0012 | 0/0 | 3504 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3499): Show |
chr16 | 57181329 | 57245469 |
| a0002c0002t0018 | 0/0 | 3504 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | CTCTG others(3499): Show |
chr16 | 57181329 | 57245469 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0010 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0011g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0013g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0014g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0017g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0019g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0020g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0021g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0022g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0023g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0024g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0025g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0001t0026g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0003t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0002c0002t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0002c0002t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| a0002c0002t0018g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0262 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0135 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0275 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00735 | hp1 | a0001 | c0001 | t0019 | g0119 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0164 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0333 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0260 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0148 | EUR | IBS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02280 | hp2 | a0001 | c0001 | t0025 | g0170 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02523 | hp1 | a0001 | c0001 | t0011 | g0218 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02647 | hp1 | a0001 | c0001 | t0021 | g0152 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0334 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0037 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02818 | hp1 | a0002 | c0002 | t0018 | g0284 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0137 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0163 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0032 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03195 | hp1 | a0001 | c0001 | t0022 | g0276 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03195 | hp2 | a0001 | c0001 | t0026 | g0237 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0168 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0326 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0336 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | STU | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0054 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18942 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18953 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18961 | hp1 | a0001 | c0001 | t0017 | g0288 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18963 | hp1 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18964 | hp2 | a0001 | c0001 | t0024 | g0012 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18973 | hp2 | a0001 | c0001 | t0023 | g0305 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0011 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19030 | hp1 | a0002 | c0002 | t0012 | g0285 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0172 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0251 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19083 | hp2 | a0001 | c0001 | t0014 | g0012 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19085 | hp2 | a0001 | c0001 | t0013 | g0306 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0183 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0263 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0324 | SAS | GIH | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | GIH | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0169 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG06807 | hp1 | a0002 | c0002 | t0012 | g0283 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0139 | REF | REF | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57204505 | A | G | 1 | a0001 | 1 | HG03195.hp1 | splice_region_variant | LOW | c.-154A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | chr16 | 57204505 | |||||||
| chr16:57227432 | A | G | 1 | a0002 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1252A>G | p.Ile418Val | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/15 | 1530/3503 | 1252/1731 | 418/576 | chr16 | 57227432 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57204847 | C | T | 1 | a0001c0004 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.189C>T | p.Ala63Ala | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | 467/3503 | 189/1731 | 63/576 | chr16 | 57204847 | |||
| chr16:57227371 | C | T | 1 | a0002c0002 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.1191C>T | p.Tyr397Tyr | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/15 | 1469/3503 | 1191/1731 | 397/576 | chr16 | 57227371 | |||
| chr16:57235142 | G | C | 1 | a0001c0003 | 2 | HG03139.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.1548G>C | p.Leu516Leu | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/15 | 1826/3503 | 1548/1731 | 516/576 | chr16 | 57235142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57186386 | C | T | 1 | a0001c0001t0025 | 1 | HG02280.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-221C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/15 | chr16 | 57186386 | |||||||
| chr16:57186428 | C | G | 5 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(2): Show |
46 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-179C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/15 | 18231 | chr16 | 57186428 | ||||||
| chr16:57204578 | C | A | 1 | a0001c0001t0015 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | 81 | chr16 | 57204578 | ||||||
| chr16:57239039 | GA | G | 3 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0024 |
43 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*74delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 74 | INFO_REALIGN_3_PRIME | chr16 | 57239039 | |||||
| chr16:57239049 | ACT | A | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(1): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*79_*80delCT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 79 | INFO_REALIGN_3_PRIME | chr16 | 57239049 | |||||
| chr16:57239079 | C | G | 1 | a0001c0001t0021 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 104 | chr16 | 57239079 | ||||||
| chr16:57239088 | A | C | 1 | a0001c0001t0020 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 113 | chr16 | 57239088 | ||||||
| chr16:57239163 | C | G | 1 | a0001c0001t0019 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 188 | chr16 | 57239163 | ||||||
| chr16:57239216 | T | G | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 241 | chr16 | 57239216 | ||||||
| chr16:57239613 | G | GT | 3 | a0001c0001t0009 a0002c0002t0012 a0002c0002t0018 |
6 | HG02818.hp1 HG06807.hp1 NA18950.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*650dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 651 | INFO_REALIGN_3_PRIME | chr16 | 57239613 | |||||
| chr16:57239973 | G | T | 1 | a0001c0001t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*998G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 998 | chr16 | 57239973 | ||||||
| chr16:57240004 | C | T | 1 | a0001c0001t0017 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1029 | chr16 | 57240004 | ||||||
| chr16:57240307 | AT | A | 3 | a0001c0001t0010 a0001c0001t0020 a0001c0001t0025 |
5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1339delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1339 | INFO_REALIGN_3_PRIME | chr16 | 57240307 | |||||
| chr16:57240339 | C | CCA | 2 | a0001c0001t0008 a0001c0001t0017 |
5 | HG01109.hp1 HG03130.hp1 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1383_*1384dupCA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1385 | INFO_REALIGN_3_PRIME | chr16 | 57240339 | |||||
| chr16:57240339 | CCACACAC others(1): Show |
C | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0013 others(1): Show |
52 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1377_*1384delCACA others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1377 | INFO_REALIGN_3_PRIME | chr16 | 57240339 | |||||
| chr16:57240358 | C | A | 6 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 others(3): Show |
13 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1383C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1383 | chr16 | 57240358 | ||||||
| chr16:57240360 | A | C | 3 | a0001c0001t0005 a0001c0001t0011 a0002c0002t0018 |
10 | HG00609.hp2 HG01361.hp2 HG01934.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1385A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1385 | chr16 | 57240360 | ||||||
| chr16:57240363 | A | AAT | 1 | a0001c0001t0006 | 5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1403dupTA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1404 | INFO_REALIGN_3_PRIME | chr16 | 57240363 | |||||
| chr16:57240363 | A | T | 1 | a0001c0001t0014 | 2 | NA18942.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1388A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1388 | chr16 | 57240363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57186463 | A | C | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(41): Show |
50 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.-156+12A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186463 | |||||||
| chr16:57186480 | C | T | 1 | a0001c0001t0003g0338 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-156+29C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186480 | |||||||
| chr16:57186614 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-156+163G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186614 | |||||||
| chr16:57186746 | G | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG02155.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-156+295G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186746 | |||||||
| chr16:57186762 | G | C | 40 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0013 others(37): Show |
42 | HG00621.hp1 HG01255.hp1 HG02165.hp1 others(39): Show |
intron_variant | MODIFIER | c.-156+311G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186762 | |||||||
| chr16:57186775 | A | G | 7 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(4): Show |
7 | HG02071.hp1 HG02155.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156+324A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186775 | |||||||
| chr16:57186833 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+382G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186833 | |||||||
| chr16:57186977 | G | A | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-156+526G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186977 | |||||||
| chr16:57187028 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00438.hp2 NA18991.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+577C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187028 | |||||||
| chr16:57187081 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156+630G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187081 | |||||||
| chr16:57187224 | A | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156+773A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187224 | |||||||
| chr16:57187520 | ACCT | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+1073_-156+107 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57187520 | ||||||
| chr16:57187522 | C | T | 3 | a0001c0001t0003g0310 a0001c0001t0003g0312 a0001c0001t0003g0313 |
3 | NA18977.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-156+1071C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187522 | |||||||
| chr16:57187525 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+1074C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187525 | |||||||
| chr16:57187649 | C | T | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(38): Show |
45 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.-156+1198C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187649 | |||||||
| chr16:57187953 | G | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+1502G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187953 | |||||||
| chr16:57188219 | G | A | 1 | a0001c0001t0005g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-156+1768G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188219 | |||||||
| chr16:57188303 | A | G | 1 | a0001c0001t0003g0336 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1852A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188303 | |||||||
| chr16:57188304 | C | G | 1 | a0001c0001t0003g0336 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1853C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188304 | |||||||
| chr16:57188317 | G | T | 1 | a0001c0001t0003g0336 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1866G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188317 | |||||||
| chr16:57188401 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+1950C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188401 | |||||||
| chr16:57188515 | T | TTTTG | 61 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(58): Show |
67 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-156+2076_-156+207 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188515 | ||||||
| chr16:57188527 | G | GTTTGT | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+2079_-156+208 others(9): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188527 | ||||||
| chr16:57188758 | C | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+2307C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188758 | |||||||
| chr16:57188776 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-156+2325A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188776 | |||||||
| chr16:57188990 | C | CT | 51 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(48): Show |
57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-156+2559dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188990 | ||||||
| chr16:57188990 | CT | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG00280.hp1 HG01169.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-156+2559delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188990 | ||||||
| chr16:57189090 | T | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-156+2639T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189090 | |||||||
| chr16:57189137 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG01074.hp1 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-156+2686G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189137 | |||||||
| chr16:57189155 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-156+2704T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189155 | |||||||
| chr16:57189175 | A | G | 1 | a0001c0003t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-156+2724A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189175 | |||||||
| chr16:57189194 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-156+2743C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189194 | |||||||
| chr16:57189509 | A | G | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+3058A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189509 | |||||||
| chr16:57189593 | C | CT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-156+3158dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189593 | ||||||
| chr16:57189593 | C | CTT | 48 | a0001c0001t0001g0122 a0001c0001t0001g0299 a0001c0001t0001g0300 others(45): Show |
54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+3157_-156+315 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189593 | ||||||
| chr16:57189674 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-156+3223C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189674 | |||||||
| chr16:57189823 | A | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+3372A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189823 | |||||||
| chr16:57189838 | AC | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+3389delC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189838 | ||||||
| chr16:57189893 | G | A | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-156+3442G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189893 | |||||||
| chr16:57190161 | A | AGAAC | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG03453.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-156+3711_-156+371 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57190161 | ||||||
| chr16:57190230 | G | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+3779G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190230 | |||||||
| chr16:57190357 | C | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+3906C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190357 | |||||||
| chr16:57190361 | T | C | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | NA18975.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-156+3910T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190361 | |||||||
| chr16:57190488 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-156+4037A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190488 | |||||||
| chr16:57190651 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-156+4200G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190651 | |||||||
| chr16:57190853 | T | C | 1 | a0001c0001t0007g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-156+4402T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190853 | |||||||
| chr16:57190928 | A | G | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-156+4477A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190928 | |||||||
| chr16:57191119 | A | G | 5 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(2): Show |
5 | HG00099.hp2 HG02735.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+4668A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191119 | |||||||
| chr16:57191193 | G | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+4742G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191193 | |||||||
| chr16:57191295 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-156+4844T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191295 | |||||||
| chr16:57191445 | G | A | 7 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156+4994G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191445 | |||||||
| chr16:57191538 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0125 others(3): Show |
6 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+5087G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191538 | |||||||
| chr16:57191561 | G | C | 1 | a0001c0001t0001g0033 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-156+5110G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191561 | |||||||
| chr16:57192292 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-156+5841T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192292 | |||||||
| chr16:57192393 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-156+5942C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192393 | |||||||
| chr16:57192564 | A | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-156+6113A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192564 | |||||||
| chr16:57192708 | C | CT | 12 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0297 others(9): Show |
12 | HG00735.hp1 HG01361.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156+6277dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | ||||||
| chr16:57192708 | C | CTT | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(33): Show |
42 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-156+6276_-156+627 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | ||||||
| chr16:57192708 | CT | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
11 | HG01167.hp1 HG01993.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-156+6277delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | ||||||
| chr16:57192708 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0010g0169 a0001c0001t0010g0171 a0001c0001t0010g0172 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+6267_-156+627 others(15): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | ||||||
| chr16:57192712 | T | TTC | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+6262_-156+626 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192712 | ||||||
| chr16:57192718 | T | C | 5 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156+6267T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192718 | |||||||
| chr16:57192769 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-156+6318G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192769 | |||||||
| chr16:57192798 | C | T | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-156+6347C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192798 | |||||||
| chr16:57192990 | A | G | 5 | a0001c0001t0010g0169 a0001c0001t0010g0171 a0001c0001t0010g0172 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+6539A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192990 | |||||||
| chr16:57193044 | C | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-156+6593C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193044 | |||||||
| chr16:57193101 | A | G | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-156+6650A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193101 | |||||||
| chr16:57193164 | T | C | 1 | a0001c0001t0005g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-156+6713T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193164 | |||||||
| chr16:57193295 | C | G | 1 | a0001c0001t0005g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-156+6844C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193295 | |||||||
| chr16:57193446 | A | G | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-156+6995A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193446 | |||||||
| chr16:57193491 | CT | C | 90 | a0001c0001t0001g0038 a0001c0001t0001g0158 a0001c0001t0001g0210 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-156+7054delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57193491 | ||||||
| chr16:57193491 | CTT | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(26): Show |
30 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-156+7053_-156+705 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57193491 | ||||||
| chr16:57193505 | T | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7054T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193505 | |||||||
| chr16:57193506 | C | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7055C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193506 | |||||||
| chr16:57193654 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-156+7203G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193654 | |||||||
| chr16:57193708 | T | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7257T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193708 | |||||||
| chr16:57193716 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-156+7265G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193716 | |||||||
| chr16:57193911 | C | G | 1 | a0001c0001t0006g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-156+7460C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193911 | |||||||
| chr16:57194096 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156+7645A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194096 | |||||||
| chr16:57194105 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-156+7654C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194105 | |||||||
| chr16:57194188 | A | G | 1 | a0001c0001t0002g0250 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-156+7737A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194188 | |||||||
| chr16:57194251 | C | G | 1 | a0001c0001t0003g0332 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-156+7800C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194251 | |||||||
| chr16:57194530 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-156+8079C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194530 | |||||||
| chr16:57194554 | G | T | 1 | a0001c0001t0003g0331 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-156+8103G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194554 | |||||||
| chr16:57194556 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+8105C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194556 | |||||||
| chr16:57195094 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-156+8643T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195094 | |||||||
| chr16:57195113 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-156+8662T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195113 | |||||||
| chr16:57195217 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-156+8766G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195217 | |||||||
| chr16:57195314 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+8863C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195314 | |||||||
| chr16:57195374 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-156+8923T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195374 | |||||||
| chr16:57195462 | A | G | 1 | a0001c0001t0002g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-156+9011A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195462 | |||||||
| chr16:57195664 | C | CT | 48 | a0001c0001t0002g0249 a0001c0001t0003g0003 a0001c0001t0003g0004 others(45): Show |
54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-155-8827dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57195664 | ||||||
| chr16:57195664 | CT | C | 9 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-8827delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57195664 | ||||||
| chr16:57195793 | T | C | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-155-8711T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195793 | |||||||
| chr16:57195904 | C | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0106 a0001c0001t0001g0107 others(5): Show |
8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-8600C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195904 | |||||||
| chr16:57195914 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0008g0163 a0001c0001t0008g0164 |
3 | HG01109.hp1 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-8590C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195914 | |||||||
| chr16:57195953 | T | C | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-155-8551T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195953 | |||||||
| chr16:57196020 | C | CA | 51 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(48): Show |
57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-155-8469dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196020 | ||||||
| chr16:57196020 | C | CAA | 8 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00738.hp1 HG01106.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-8470_-155-846 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196020 | ||||||
| chr16:57196030 | A | AAT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00642.hp2 HG01168.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-8473_-155-847 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196030 | ||||||
| chr16:57196032 | A | AAT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-155-8471_-155-847 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196032 | ||||||
| chr16:57196032 | A | ATAT | 4 | a0001c0001t0001g0197 a0001c0001t0001g0279 a0001c0001t0002g0016 others(1): Show |
4 | HG02055.hp1 HG02083.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-8472_-155-847 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196032 | |||||||
| chr16:57196032 | A | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00642.hp2 HG01168.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-8472A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196032 | |||||||
| chr16:57196034 | A | AAAT | 9 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG00140.hp2 HG02056.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-8469_-155-846 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196034 | ||||||
| chr16:57196034 | A | AAT | 53 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
54 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.-155-8452_-155-845 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196034 | ||||||
| chr16:57196034 | A | ATAT | 3 | a0001c0001t0001g0040 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01257.hp1 HG01258.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-155-8470_-155-846 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196034 | |||||||
| chr16:57196034 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-155-8470A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196034 | |||||||
| chr16:57196036 | T | A | 49 | a0001c0001t0001g0042 a0001c0001t0001g0140 a0001c0001t0001g0143 others(46): Show |
52 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.-155-8468T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196036 | |||||||
| chr16:57196038 | T | A | 7 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-8466T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196038 | |||||||
| chr16:57196040 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-155-8464T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196040 | |||||||
| chr16:57196334 | G | T | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-8170G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196334 | |||||||
| chr16:57196340 | T | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-8164T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196340 | |||||||
| chr16:57196532 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-155-7972T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196532 | |||||||
| chr16:57196675 | A | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-155-7829A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196675 | |||||||
| chr16:57197171 | T | C | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-7333T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197171 | |||||||
| chr16:57197185 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-7319C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197185 | |||||||
| chr16:57197317 | T | A | 1 | a0001c0001t0003g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-155-7187T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197317 | |||||||
| chr16:57197667 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-155-6837C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197667 | |||||||
| chr16:57197709 | TTTTTTG | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6772_-155-676 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57197709 | ||||||
| chr16:57197836 | A | C | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-6668A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197836 | |||||||
| chr16:57197863 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-6641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197863 | |||||||
| chr16:57197894 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-155-6610C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197894 | |||||||
| chr16:57197923 | GCTACATT others(37): Show |
G | 53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(50): Show |
59 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-155-6578_-155-653 others(48): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57197923 | ||||||
| chr16:57198046 | T | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6458T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198046 | |||||||
| chr16:57198110 | G | A | 9 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-6394G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198110 | |||||||
| chr16:57198167 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-155-6337C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198167 | |||||||
| chr16:57198294 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-155-6210G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198294 | |||||||
| chr16:57198316 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0279 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-155-6188G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198316 | |||||||
| chr16:57198371 | A | G | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-6133A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198371 | |||||||
| chr16:57198383 | C | CA | 123 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(120): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-155-6109dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57198383 | ||||||
| chr16:57198474 | A | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6030A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198474 | |||||||
| chr16:57198558 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-5946T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198558 | |||||||
| chr16:57198615 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-155-5889T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198615 | |||||||
| chr16:57198840 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-155-5664C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198840 | |||||||
| chr16:57199049 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-155-5455A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199049 | |||||||
| chr16:57199125 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-155-5379A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199125 | |||||||
| chr16:57199173 | A | G | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-155-5331A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199173 | |||||||
| chr16:57199179 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-155-5325A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199179 | |||||||
| chr16:57199220 | C | T | 1 | a0001c0001t0005g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-5284C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199220 | |||||||
| chr16:57199225 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-155-5279C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199225 | |||||||
| chr16:57199448 | T | C | 65 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(62): Show |
71 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-155-5056T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199448 | |||||||
| chr16:57199533 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-155-4971T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199533 | |||||||
| chr16:57199535 | T | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-4969T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199535 | |||||||
| chr16:57199696 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-155-4808T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199696 | |||||||
| chr16:57199838 | CT | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-155-4652delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199838 | ||||||
| chr16:57199838 | CTT | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0013 others(46): Show |
53 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-155-4653_-155-465 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199838 | ||||||
| chr16:57199895 | GT | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-155-4598delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199895 | ||||||
| chr16:57199896 | T | C | 9 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-4608T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199896 | |||||||
| chr16:57199913 | CT | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0154 others(16): Show |
19 | HG01169.hp2 HG01884.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-4576delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199913 | ||||||
| chr16:57200217 | TG | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0155 a0001c0001t0001g0156 others(10): Show |
14 | HG01099.hp2 HG01109.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-155-4282delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200217 | ||||||
| chr16:57200314 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-155-4190C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200314 | |||||||
| chr16:57200360 | C | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-4144C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200360 | |||||||
| chr16:57200417 | T | G | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-4087T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200417 | |||||||
| chr16:57200557 | G | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3947G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200557 | |||||||
| chr16:57200558 | G | T | 2 | a0001c0001t0004g0136 a0001c0001t0004g0138 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-3946G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200558 | |||||||
| chr16:57200560 | TGGGGCGG others(120): Show |
T | 1 | a0001c0001t0003g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-155-3866_-155-374 others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200560 | ||||||
| chr16:57200636 | G | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-3868G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200636 | |||||||
| chr16:57200638 | C | T | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3866C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200638 | |||||||
| chr16:57200651 | C | T | 1 | a0001c0001t0006g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-155-3853C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200651 | |||||||
| chr16:57200652 | G | GGGCTGGG others(41): Show |
1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3849_-155-384 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200652 | ||||||
| chr16:57200661 | G | A | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3843G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200661 | |||||||
| chr16:57200661 | G | GCTGACCC others(42): Show |
2 | a0001c0001t0001g0108 a0001c0001t0002g0249 |
2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-155-3832_-155-383 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | ||||||
| chr16:57200661 | G | GCTGACCC others(41): Show |
323 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(320): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-155-3833_-155-383 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | ||||||
| chr16:57200661 | G | GCTGACCC others(41): Show |
6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-3833_-155-383 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | ||||||
| chr16:57200661 | G | GGCTGACC others(42): Show |
1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-155-3843_-155-384 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200661 | |||||||
| chr16:57200663 | TGACCCCC others(121): Show |
T | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3839_-155-371 others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200663 | ||||||
| chr16:57200665 | A | ACCCCCCG others(42): Show |
1 | a0001c0001t0004g0014 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-155-3833_-155-383 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200665 | ||||||
| chr16:57200684 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-3820G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200684 | |||||||
| chr16:57200696 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-155-3808T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200696 | |||||||
| chr16:57200792 | GC | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(317): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-155-3704delC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200792 | ||||||
| chr16:57200793 | C | G | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3711C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200793 | |||||||
| chr16:57200816 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-155-3688G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200816 | |||||||
| chr16:57200829 | G | GGGCAGAG others(71): Show |
1 | a0001c0001t0002g0009 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-155-3651_-155-357 others(82): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200829 | ||||||
| chr16:57200842 | C | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(27): Show |
31 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-155-3662C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200842 | |||||||
| chr16:57200850 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-3654C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200850 | |||||||
| chr16:57200856 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-155-3648C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200856 | |||||||
| chr16:57200886 | T | C | 65 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(62): Show |
71 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-155-3618T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200886 | |||||||
| chr16:57200934 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-155-3570C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200934 | |||||||
| chr16:57200947 | C | CG | 36 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0049 others(33): Show |
36 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-3543dupG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | ||||||
| chr16:57200947 | C | CGG | 21 | a0001c0001t0001g0110 a0001c0001t0001g0155 a0001c0001t0001g0156 others(18): Show |
21 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-155-3544_-155-354 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | ||||||
| chr16:57200947 | CG | C | 72 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(69): Show |
73 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-155-3543delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | ||||||
| chr16:57200947 | CGG | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
75 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-155-3544_-155-354 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | ||||||
| chr16:57200947 | CGGGG | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(48): Show |
57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-155-3546_-155-354 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | ||||||
| chr16:57200952 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-155-3552G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200952 | |||||||
| chr16:57200953 | G | T | 1 | a0001c0001t0002g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-155-3551G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200953 | |||||||
| chr16:57200953 | GGGGGGGG others(43): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-155-3544_-155-349 others(54): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200953 | ||||||
| chr16:57200954 | G | T | 1 | a0001c0001t0005g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-3550G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200954 | |||||||
| chr16:57200954 | GGGGGGGG others(42): Show |
G | 1 | a0001c0001t0002g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-155-3543_-155-349 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200954 | ||||||
| chr16:57200955 | GGGGGGGC others(41): Show |
G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0249 a0001c0001t0023g0305 |
3 | HG02056.hp1 NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-155-3517_-155-347 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200955 | ||||||
| chr16:57200958 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0254 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-155-3546G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200958 | |||||||
| chr16:57200959 | G | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(46): Show |
55 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-155-3545G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200959 | |||||||
| chr16:57200995 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-155-3509T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200995 | |||||||
| chr16:57201035 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0002c0002t0018g0284 |
3 | HG02818.hp1 NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-155-3469T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201035 | |||||||
| chr16:57201056 | G | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-155-3448G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201056 | |||||||
| chr16:57201066 | C | G | 1 | a0001c0001t0009g0223 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-155-3438C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201066 | |||||||
| chr16:57201078 | A | G | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3426A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201078 | |||||||
| chr16:57201080 | A | C | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-3424A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201080 | |||||||
| chr16:57201082 | G | T | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3422G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201082 | |||||||
| chr16:57201086 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3418T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201086 | |||||||
| chr16:57201102 | A | G | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3402A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201102 | |||||||
| chr16:57201103 | C | CGCTCCTC others(33): Show |
1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-155-3388_-155-334 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201103 | ||||||
| chr16:57201103 | C | G | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3401C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201103 | |||||||
| chr16:57201109 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3395T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201109 | |||||||
| chr16:57201113 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3391T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201113 | |||||||
| chr16:57201117 | CAGGCGGA others(29): Show |
C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3386_-155-335 others(40): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201117 | |||||||
| chr16:57201124 | AGTGGCTG others(73): Show |
A | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-3300_-155-322 others(84): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201124 | ||||||
| chr16:57201137 | C | CGGAGGGG others(33): Show |
53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(50): Show |
59 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-155-3330_-155-329 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201137 | ||||||
| chr16:57201156 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3348T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201156 | |||||||
| chr16:57201160 | A | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3344A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201160 | |||||||
| chr16:57201162 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-155-3342G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201162 | |||||||
| chr16:57201164 | T | G | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3340T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201164 | |||||||
| chr16:57201174 | A | G | 2 | a0001c0001t0002g0270 a0002c0002t0018g0284 |
2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-155-3330A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201174 | |||||||
| chr16:57201177 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3327T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201177 | |||||||
| chr16:57201182 | G | A | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3322G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201182 | |||||||
| chr16:57201183 | G | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3321G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201183 | |||||||
| chr16:57201196 | T | C | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3308T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201196 | |||||||
| chr16:57201200 | A | G | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3304A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201200 | |||||||
| chr16:57201204 | T | A | 1 | a0002c0002t0018g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3300T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201204 | |||||||
| chr16:57201214 | G | A | 1 | a0001c0003t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-155-3290G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201214 | |||||||
| chr16:57201217 | C | T | 1 | a0001c0003t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-155-3287C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201217 | |||||||
| chr16:57201281 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-3223C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201281 | |||||||
| chr16:57201286 | C | T | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-3218C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201286 | |||||||
| chr16:57201287 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-155-3217G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201287 | |||||||
| chr16:57201304 | TCTCCTCA others(30): Show |
T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-3191_-155-315 others(41): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201304 | ||||||
| chr16:57201358 | C | T | 53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(50): Show |
59 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-155-3146C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201358 | |||||||
| chr16:57201407 | TGGCAGAG others(33): Show |
T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG01074.hp1 HG01175.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-3076_-155-303 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201407 | ||||||
| chr16:57201442 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-155-3062C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201442 | |||||||
| chr16:57201461 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-3043C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201461 | |||||||
| chr16:57201550 | C | CG | 8 | a0001c0001t0001g0065 a0001c0001t0001g0121 a0001c0001t0001g0180 others(5): Show |
8 | HG01243.hp2 HG01496.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-2950dupG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201550 | ||||||
| chr16:57201551 | G | C | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-2953G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201551 | |||||||
| chr16:57201686 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-155-2818C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201686 | |||||||
| chr16:57201690 | A | C | 53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(50): Show |
59 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-155-2814A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201690 | |||||||
| chr16:57201692 | T | A | 1 | a0002c0002t0012g0283 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-155-2812T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201692 | |||||||
| chr16:57201732 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-155-2772G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201732 | |||||||
| chr16:57201778 | G | A | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-2726G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201778 | |||||||
| chr16:57201794 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0128 |
2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-155-2710C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201794 | |||||||
| chr16:57201799 | A | G | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-155-2705A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201799 | |||||||
| chr16:57201824 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-2680C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201824 | |||||||
| chr16:57201851 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-155-2653C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201851 | |||||||
| chr16:57201864 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-2640C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201864 | |||||||
| chr16:57201958 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-155-2546A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201958 | |||||||
| chr16:57201960 | AGAGGGAG others(8): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-155-2525_-155-251 others(19): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201960 | ||||||
| chr16:57202053 | A | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0277 |
2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-155-2451A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202053 | |||||||
| chr16:57202056 | T | C | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-155-2448T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202056 | |||||||
| chr16:57202293 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-155-2211G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202293 | |||||||
| chr16:57202878 | T | TTA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0146 a0001c0001t0001g0147 others(10): Show |
13 | HG00735.hp2 HG01099.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-1598_-155-159 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATA | 6 | a0001c0001t0001g0281 a0001c0001t0002g0200 a0001c0001t0002g0221 others(3): Show |
6 | HG00140.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1600_-155-159 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATA | 3 | a0001c0001t0002g0002 a0001c0001t0002g0220 a0001c0001t0002g0240 |
3 | HG03492.hp1 NA19002.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-155-1602_-155-159 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(1): Show |
19 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(16): Show |
19 | HG00099.hp2 HG00408.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-1604_-155-159 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(3): Show |
23 | a0001c0001t0001g0232 a0001c0001t0002g0002 a0001c0001t0002g0008 others(20): Show |
26 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-155-1606_-155-159 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0273 a0001c0001t0002g0206 a0001c0001t0002g0247 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1608_-155-159 others(16): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0238 a0001c0001t0002g0002 a0001c0001t0002g0008 others(10): Show |
13 | HG00642.hp1 HG00738.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-1610_-155-159 others(18): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(9): Show |
15 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0165 others(12): Show |
15 | HG01257.hp2 HG02165.hp1 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.-155-1612_-155-159 others(20): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(11): Show |
11 | a0001c0001t0002g0211 a0001c0001t0002g0243 a0001c0001t0003g0004 others(8): Show |
11 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.-155-1614_-155-159 others(22): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(13): Show |
7 | a0001c0001t0002g0162 a0001c0001t0002g0231 a0001c0001t0002g0263 others(4): Show |
7 | HG02074.hp1 HG03017.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-1616_-155-159 others(24): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(15): Show |
8 | a0001c0001t0002g0282 a0001c0001t0003g0003 a0001c0001t0003g0308 others(5): Show |
8 | HG02145.hp2 HG02155.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-1618_-155-159 others(26): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(17): Show |
6 | a0001c0001t0002g0160 a0001c0001t0002g0176 a0001c0001t0002g0242 others(3): Show |
6 | HG02132.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1620_-155-159 others(28): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(19): Show |
1 | a0001c0001t0003g0312 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-155-1622_-155-159 others(30): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(21): Show |
3 | a0001c0001t0003g0330 a0001c0001t0003g0332 a0001c0001t0014g0012 |
3 | NA18939.hp2 NA19076.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-155-1624_-155-159 others(32): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTATATAT others(27): Show |
1 | a0001c0001t0013g0011 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-155-1597_-155-159 others(38): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTTTATAT others(11): Show |
1 | a0001c0001t0003g0335 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-155-1625_-155-162 others(22): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTTTATAT others(13): Show |
2 | a0001c0001t0003g0003 a0001c0001t0003g0315 |
2 | NA18951.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-155-1625_-155-162 others(24): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | T | TTTTATAT others(15): Show |
1 | a0001c0001t0003g0331 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-155-1625_-155-162 others(26): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | TTA | T | 17 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0197 others(14): Show |
17 | HG01891.hp2 HG01934.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-1598_-155-159 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | TTATA | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
12 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-1600_-155-159 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | TTATATA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(47): Show |
51 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-155-1602_-155-159 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | TTATATAT others(1): Show |
T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-155-1604_-155-159 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202878 | TTATATAT others(3): Show |
T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-1606_-155-159 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | ||||||
| chr16:57202888 | A | ATATATAT others(3): Show |
5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | NA18946.hp1 NA18959.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-1607_-155-160 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202888 | ||||||
| chr16:57202939 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-155-1565T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202939 | |||||||
| chr16:57202959 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-1545A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202959 | |||||||
| chr16:57203008 | TAAA | T | 5 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-1494_-155-149 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57203008 | ||||||
| chr16:57203113 | A | G | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-155-1391A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203113 | |||||||
| chr16:57203125 | C | T | 1 | a0001c0001t0016g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-155-1379C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203125 | |||||||
| chr16:57203349 | T | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-1155T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203349 | |||||||
| chr16:57203460 | A | G | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-1044A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203460 | |||||||
| chr16:57203496 | TTTTG | T | 3 | a0001c0001t0001g0079 a0001c0001t0002g0204 a0001c0001t0002g0206 |
3 | HG00140.hp1 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-155-992_-155-989d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57203496 | ||||||
| chr16:57203543 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-155-961A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203543 | |||||||
| chr16:57203746 | C | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-758C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203746 | |||||||
| chr16:57203960 | A | C | 1 | a0001c0001t0002g0173 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-155-544A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203960 | |||||||
| chr16:57204030 | G | A | 2 | a0001c0001t0003g0309 a0001c0003t0001g0123 |
2 | HG02698.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-155-474G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204030 | |||||||
| chr16:57204034 | G | A | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-470G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204034 | |||||||
| chr16:57204084 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0106 a0001c0001t0001g0107 others(5): Show |
8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-420G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204084 | |||||||
| chr16:57204190 | C | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-314C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204190 | |||||||
| chr16:57204397 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-155-107A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204397 | |||||||
| chr16:57205059 | C | T | 1 | a0001c0001t0006g0149 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.350+51C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205059 | |||||||
| chr16:57205060 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.350+52G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205060 | |||||||
| chr16:57205068 | G | A | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.350+60G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205068 | |||||||
| chr16:57205151 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.350+143G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205151 | |||||||
| chr16:57205155 | A | G | 6 | a0001c0001t0010g0169 a0001c0001t0010g0171 a0001c0001t0010g0172 others(3): Show |
6 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.350+147A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205155 | |||||||
| chr16:57205384 | A | G | 2 | a0001c0001t0006g0135 a0001c0001t0006g0149 |
2 | HG00280.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.350+376A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205384 | |||||||
| chr16:57205730 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350+722T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205730 | |||||||
| chr16:57205804 | T | C | 59 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(56): Show |
65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.350+796T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205804 | |||||||
| chr16:57205924 | G | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.350+916G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205924 | |||||||
| chr16:57206166 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350+1158G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206166 | |||||||
| chr16:57206313 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.350+1305G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206313 | |||||||
| chr16:57206429 | T | A | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.350+1421T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206429 | |||||||
| chr16:57206757 | G | GTC | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.351-1299_351-1298d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 57206757 | ||||||
| chr16:57206889 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.351-1169G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206889 | |||||||
| chr16:57207096 | C | T | 1 | a0001c0001t0003g0327 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.351-962C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207096 | |||||||
| chr16:57207258 | A | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(117): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.351-800A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207258 | |||||||
| chr16:57207461 | G | C | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.351-597G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207461 | |||||||
| chr16:57207462 | A | T | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.351-596A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207462 | |||||||
| chr16:57207617 | G | A | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.351-441G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207617 | |||||||
| chr16:57207833 | G | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.351-225G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207833 | |||||||
| chr16:57207862 | A | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18977.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.351-196A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207862 | |||||||
| chr16:57207890 | A | AC | 5 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.351-167dupC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 57207890 | ||||||
| chr16:57207893 | T | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0096 a0001c0001t0005g0083 |
3 | HG01934.hp1 HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.351-165T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207893 | |||||||
| chr16:57208174 | CT | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.403+68delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208174 | ||||||
| chr16:57208181 | TTTTTG | T | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.403+87_403+91delTT others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208181 | ||||||
| chr16:57208228 | T | G | 43 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(40): Show |
47 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.403+118T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208228 | |||||||
| chr16:57208231 | A | C | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+121A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208231 | |||||||
| chr16:57208297 | T | G | 1 | a0001c0001t0001g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.403+187T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208297 | |||||||
| chr16:57208302 | C | CT | 59 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0031 others(56): Show |
59 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.403+215dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208302 | ||||||
| chr16:57208302 | CT | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0044 others(3): Show |
6 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+215delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208302 | ||||||
| chr16:57208376 | TTA | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.403+290_403+291del others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208376 | ||||||
| chr16:57208376 | TTATATA | T | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.403+286_403+291del others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208376 | ||||||
| chr16:57208378 | A | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0071 a0001c0001t0001g0077 others(1): Show |
4 | HG02886.hp1 HG03540.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+268A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208378 | |||||||
| chr16:57208392 | A | T | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+282A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208392 | |||||||
| chr16:57208393 | TA | T | 4 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(1): Show |
4 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+284delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208393 | |||||||
| chr16:57208394 | A | T | 1 | a0001c0001t0021g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+284A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208394 | |||||||
| chr16:57208395 | TA | T | 7 | a0001c0001t0001g0186 a0001c0001t0001g0235 a0001c0001t0001g0238 others(4): Show |
9 | HG00642.hp1 HG02015.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+286delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208395 | |||||||
| chr16:57208395 | TATA | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0271 a0001c0001t0002g0208 others(2): Show |
5 | HG01167.hp2 HG01433.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+286_403+288del others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208395 | |||||||
| chr16:57208396 | A | T | 15 | a0001c0001t0001g0154 a0001c0001t0001g0187 a0001c0001t0002g0217 others(12): Show |
15 | HG00280.hp1 HG01070.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+286A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208396 | |||||||
| chr16:57208397 | TA | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0232 a0001c0001t0002g0272 |
3 | HG00438.hp1 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.403+288delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208397 | |||||||
| chr16:57208397 | TATA | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0076 others(12): Show |
15 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+288_403+290del others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208397 | |||||||
| chr16:57208398 | A | AT | 3 | a0001c0001t0001g0052 a0001c0001t0001g0297 a0001c0001t0003g0316 |
3 | HG03239.hp1 NA18997.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.403+289dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208398 | ||||||
| chr16:57208398 | A | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0045 others(125): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.403+288A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208398 | |||||||
| chr16:57208399 | TA | T | 8 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0071 others(5): Show |
8 | HG00738.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+290delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208399 | |||||||
| chr16:57208400 | A | AT | 35 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0106 others(32): Show |
39 | HG00558.hp1 HG01255.hp1 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.403+305dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208400 | ||||||
| chr16:57208400 | A | ATT | 12 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+304_403+305dup others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208400 | ||||||
| chr16:57208400 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.403+290A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208400 | |||||||
| chr16:57208403 | T | A | 1 | a0001c0001t0017g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403+293T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208403 | |||||||
| chr16:57208438 | C | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0001t0001g0143 others(130): Show |
138 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.403+328C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208438 | |||||||
| chr16:57208451 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.403+341G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208451 | |||||||
| chr16:57208460 | C | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(117): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.403+350C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208460 | |||||||
| chr16:57208864 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.404-211G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208864 | |||||||
| chr16:57208920 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.404-155G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208920 | |||||||
| chr16:57209015 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.404-60C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57209015 | |||||||
| chr16:57209057 | T | A | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.404-18T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57209057 | |||||||
| chr16:57209583 | T | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.516+396T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209583 | |||||||
| chr16:57209594 | C | G | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+407C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209594 | |||||||
| chr16:57209611 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.516+424G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209611 | |||||||
| chr16:57209713 | A | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0127 |
3 | HG01891.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.516+526A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209713 | |||||||
| chr16:57209764 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0002g0221 a0001c0001t0002g0241 |
3 | HG00642.hp1 HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.516+577C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209764 | |||||||
| chr16:57209847 | T | G | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.516+660T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209847 | |||||||
| chr16:57209849 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516+662T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209849 | |||||||
| chr16:57209880 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+693G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209880 | |||||||
| chr16:57209935 | C | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+748C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209935 | |||||||
| chr16:57209976 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.516+789A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209976 | |||||||
| chr16:57209988 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.516+801A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209988 | |||||||
| chr16:57210027 | T | TTCCC | 258 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.516+858_516+861dup others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210027 | ||||||
| chr16:57210041 | C | CCCTCCCT others(5): Show |
1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.516+861_516+862ins others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210041 | ||||||
| chr16:57210061 | C | CCCTT | 45 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(42): Show |
51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.516+884_516+887dup others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210061 | ||||||
| chr16:57210075 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.516+888T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210075 | |||||||
| chr16:57210089 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.516+902C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210089 | |||||||
| chr16:57210120 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.516+933C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210120 | |||||||
| chr16:57210329 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0034 |
2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.516+1142C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210329 | |||||||
| chr16:57210357 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.516+1170C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210357 | |||||||
| chr16:57210358 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.516+1171G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210358 | |||||||
| chr16:57210434 | G | A | 1 | a0001c0001t0017g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.516+1247G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210434 | |||||||
| chr16:57210532 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.516+1345G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210532 | |||||||
| chr16:57210577 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.516+1390G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210577 | |||||||
| chr16:57210664 | G | T | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.516+1477G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210664 | |||||||
| chr16:57210667 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.516+1480T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210667 | |||||||
| chr16:57210675 | T | G | 48 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(45): Show |
54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.516+1488T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210675 | |||||||
| chr16:57210699 | C | T | 10 | a0001c0001t0002g0009 a0001c0001t0002g0173 a0001c0001t0002g0201 others(7): Show |
11 | NA18953.hp2 NA18962.hp1 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+1512C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210699 | |||||||
| chr16:57210788 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.516+1601C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210788 | |||||||
| chr16:57211007 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516+1820G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211007 | |||||||
| chr16:57211022 | G | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+1835G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211022 | |||||||
| chr16:57211026 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.516+1839C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211026 | |||||||
| chr16:57211067 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.516+1880C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211067 | |||||||
| chr16:57211155 | G | A | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-1817G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211155 | |||||||
| chr16:57211244 | C | G | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-1728C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211244 | |||||||
| chr16:57211266 | T | TA | 116 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0041 others(113): Show |
121 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.517-1688dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57211266 | ||||||
| chr16:57211281 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.517-1691A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211281 | |||||||
| chr16:57211431 | C | T | 1 | a0001c0001t0003g0320 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.517-1541C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211431 | |||||||
| chr16:57211580 | C | A | 1 | a0001c0001t0002g0282 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.517-1392C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211580 | |||||||
| chr16:57211583 | A | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-1389A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211583 | |||||||
| chr16:57211720 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.517-1252T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211720 | |||||||
| chr16:57211956 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-1016G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211956 | |||||||
| chr16:57212054 | A | G | 7 | a0001c0001t0001g0074 a0001c0001t0001g0091 a0001c0001t0001g0100 others(4): Show |
7 | HG00438.hp2 HG00673.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-918A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212054 | |||||||
| chr16:57212187 | G | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.517-785G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212187 | |||||||
| chr16:57212426 | A | C | 1 | a0001c0001t0002g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.517-546A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212426 | |||||||
| chr16:57212550 | A | T | 47 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(44): Show |
53 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.517-422A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212550 | |||||||
| chr16:57212637 | C | T | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.517-335C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212637 | |||||||
| chr16:57212684 | G | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.517-288G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212684 | |||||||
| chr16:57212745 | G | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.517-227G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212745 | |||||||
| chr16:57212799 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.517-173G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212799 | |||||||
| chr16:57212835 | G | A | 4 | a0001c0001t0001g0047 a0002c0002t0012g0283 a0002c0002t0012g0285 others(1): Show |
4 | HG02818.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-137G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212835 | |||||||
| chr16:57212860 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-112G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212860 | |||||||
| chr16:57213150 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.643+52G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213150 | |||||||
| chr16:57213196 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.643+98G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213196 | |||||||
| chr16:57213347 | G | A | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0003t0001g0123 |
3 | HG02922.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.643+249G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213347 | |||||||
| chr16:57213458 | G | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.643+360G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213458 | |||||||
| chr16:57213664 | G | C | 120 | a0001c0001t0001g0007 a0001c0001t0001g0154 a0001c0001t0001g0155 others(117): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.644-224G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213664 | |||||||
| chr16:57213674 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.644-214T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213674 | |||||||
| chr16:57213742 | A | G | 65 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(62): Show |
71 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.644-146A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213742 | |||||||
| chr16:57213787 | A | C | 1 | a0001c0001t0003g0319 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.644-101A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213787 | |||||||
| chr16:57213791 | T | A | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.644-97T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213791 | |||||||
| chr16:57213962 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+16A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57213962 | |||||||
| chr16:57213965 | CTATT | C | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.702+24_702+27delTA others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57213965 | ||||||
| chr16:57214069 | T | G | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.702+123T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214069 | |||||||
| chr16:57214082 | T | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG03471.hp2 HG03486.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+136T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214082 | |||||||
| chr16:57214218 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+272G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214218 | |||||||
| chr16:57214465 | A | G | 1 | a0001c0001t0003g0325 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.702+519A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214465 | |||||||
| chr16:57214534 | TG | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.702+589delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214534 | |||||||
| chr16:57214567 | G | T | 47 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(44): Show |
53 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.702+621G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214567 | |||||||
| chr16:57214722 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+776A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214722 | |||||||
| chr16:57214750 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0001c0001t0001g0248 |
3 | HG02015.hp2 NA18994.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.702+804C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214750 | |||||||
| chr16:57214771 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.702+825A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214771 | |||||||
| chr16:57214860 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.702+914C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214860 | |||||||
| chr16:57214906 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.702+960G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214906 | |||||||
| chr16:57214921 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+975C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214921 | |||||||
| chr16:57215055 | G | A | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.703-1052G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215055 | |||||||
| chr16:57215107 | A | G | 1 | a0001c0001t0003g0318 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.703-1000A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215107 | |||||||
| chr16:57215196 | A | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0254 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.703-911A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215196 | |||||||
| chr16:57215355 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18964.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.703-752A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215355 | |||||||
| chr16:57215397 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.703-710G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215397 | |||||||
| chr16:57215466 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215466 | |||||||
| chr16:57215917 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.703-190A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215917 | |||||||
| chr16:57216069 | A | AT | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.703-20dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57216069 | ||||||
| chr16:57216069 | A | ATT | 7 | a0001c0001t0001g0021 a0001c0001t0001g0073 a0001c0001t0001g0090 others(4): Show |
7 | HG01109.hp1 HG01943.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-21_703-20dupTT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57216069 | ||||||
| chr16:57216475 | T | G | 1 | a0001c0001t0002g0263 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+302T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216475 | |||||||
| chr16:57216489 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0239 a0001c0001t0001g0281 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+316C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216489 | |||||||
| chr16:57216683 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.770-221G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216683 | |||||||
| chr16:57216684 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.770-220C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216684 | |||||||
| chr16:57216728 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-176A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216728 | |||||||
| chr16:57216735 | C | G | 58 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(55): Show |
64 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.770-169C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216735 | |||||||
| chr16:57217591 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0329 a0001c0001t0003g0330 |
4 | NA18939.hp2 NA18981.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+556A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217591 | |||||||
| chr16:57217659 | C | A | 1 | a0001c0001t0002g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.901+624C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217659 | |||||||
| chr16:57217707 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.901+672A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217707 | |||||||
| chr16:57217771 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.901+736G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217771 | |||||||
| chr16:57217791 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.901+756A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217791 | |||||||
| chr16:57218008 | T | C | 13 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+973T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218008 | |||||||
| chr16:57218158 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.901+1123A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218158 | |||||||
| chr16:57218352 | A | G | 6 | a0001c0001t0002g0233 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG00621.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.901+1317A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218352 | |||||||
| chr16:57218581 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1546C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218581 | |||||||
| chr16:57218590 | T | G | 45 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(42): Show |
51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.901+1555T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218590 | |||||||
| chr16:57218621 | C | T | 1 | a0001c0001t0006g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.901+1586C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218621 | |||||||
| chr16:57218669 | A | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0001t0001g0143 others(130): Show |
138 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.901+1634A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218669 | |||||||
| chr16:57218670 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1635T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218670 | |||||||
| chr16:57218709 | TGCCACAT others(316): Show |
T | 61 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(58): Show |
67 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.901+1689_902-1686d others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218709 | ||||||
| chr16:57218720 | CT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0064 others(11): Show |
14 | HG00735.hp2 HG01361.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+1718delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | ||||||
| chr16:57218720 | CTT | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(77): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.901+1717_901+1718d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | ||||||
| chr16:57218720 | CTTT | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0017 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.901+1716_901+1718d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | ||||||
| chr16:57218720 | CTTTT | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0116 others(3): Show |
6 | HG01169.hp2 HG01257.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+1715_901+1718d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | ||||||
| chr16:57218721 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1686T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218721 | |||||||
| chr16:57218738 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0067 others(4): Show |
8 | HG00408.hp1 HG00609.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.901+1703T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218738 | |||||||
| chr16:57218937 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.902-1795C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218937 | |||||||
| chr16:57219031 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.902-1701C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219031 | |||||||
| chr16:57219190 | C | T | 1 | a0001c0001t0003g0324 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.902-1542C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219190 | |||||||
| chr16:57219239 | G | C | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.902-1493G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219239 | |||||||
| chr16:57219361 | G | A | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.902-1371G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219361 | |||||||
| chr16:57219411 | A | G | 1 | a0001c0001t0005g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902-1321A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219411 | |||||||
| chr16:57219433 | A | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
12 | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.902-1299A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219433 | |||||||
| chr16:57219702 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.902-1030G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219702 | |||||||
| chr16:57219835 | G | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.902-897G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219835 | |||||||
| chr16:57220249 | G | A | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.902-483G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220249 | |||||||
| chr16:57220475 | T | C | 43 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(40): Show |
47 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.902-257T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220475 | |||||||
| chr16:57220723 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.902-9C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220723 | |||||||
| chr16:57220866 | G | A | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017+19G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 9/14 | chr16 | 57220866 | |||||||
| chr16:57221132 | C | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1018-140C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 9/14 | chr16 | 57221132 | |||||||
| chr16:57221451 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1161+36T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221451 | |||||||
| chr16:57221523 | T | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1161+108T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221523 | |||||||
| chr16:57221542 | A | T | 1 | a0001c0001t0001g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+127A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221542 | |||||||
| chr16:57221621 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1161+206C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221621 | |||||||
| chr16:57221622 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1161+207T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221622 | |||||||
| chr16:57221755 | C | A | 1 | a0001c0001t0001g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+340C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221755 | |||||||
| chr16:57221761 | A | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1161+346A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221761 | |||||||
| chr16:57221892 | T | C | 45 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(42): Show |
51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+477T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221892 | |||||||
| chr16:57222095 | T | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+680T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222095 | |||||||
| chr16:57222129 | C | A | 1 | a0001c0001t0001g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+714C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222129 | |||||||
| chr16:57222130 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+715C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222130 | |||||||
| chr16:57222134 | T | G | 1 | a0001c0001t0002g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1161+719T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222134 | |||||||
| chr16:57222137 | A | AT | 45 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(42): Show |
51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+724dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222137 | ||||||
| chr16:57222194 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+779G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222194 | |||||||
| chr16:57222212 | A | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+797A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222212 | |||||||
| chr16:57222217 | A | AT | 4 | a0001c0001t0001g0154 a0001c0001t0001g0187 a0001c0001t0002g0243 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+803dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222217 | ||||||
| chr16:57222343 | C | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+928C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222343 | |||||||
| chr16:57222372 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1161+957G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222372 | |||||||
| chr16:57222526 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1161+1111C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222526 | |||||||
| chr16:57222924 | C | G | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+1509C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222924 | |||||||
| chr16:57222940 | C | T | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+1525C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222940 | |||||||
| chr16:57222994 | G | GT | 45 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(42): Show |
51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+1586dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222994 | ||||||
| chr16:57222996 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+1581T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222996 | |||||||
| chr16:57223001 | T | TA | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+1587dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57223001 | ||||||
| chr16:57223003 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+1588T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223003 | |||||||
| chr16:57223037 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1161+1622T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223037 | |||||||
| chr16:57223049 | C | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1161+1634C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223049 | |||||||
| chr16:57223275 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+1860T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223275 | |||||||
| chr16:57223589 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0005g0037 |
3 | HG02735.hp1 NA18945.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1161+2174A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223589 | |||||||
| chr16:57223796 | C | A | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(38): Show |
45 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161+2381C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223796 | |||||||
| chr16:57224025 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161+2610G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224025 | |||||||
| chr16:57224036 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0277 |
2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1161+2621T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224036 | |||||||
| chr16:57224070 | A | C | 5 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+2655A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224070 | |||||||
| chr16:57224079 | C | T | 1 | a0001c0001t0003g0320 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1161+2664C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224079 | |||||||
| chr16:57224161 | C | T | 5 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+2746C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224161 | |||||||
| chr16:57224174 | A | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+2759A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224174 | |||||||
| chr16:57224196 | C | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2781C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224196 | |||||||
| chr16:57224512 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1162-2830A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224512 | |||||||
| chr16:57224630 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1162-2712G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224630 | |||||||
| chr16:57224720 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1162-2622G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224720 | |||||||
| chr16:57224920 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0019g0119 |
3 | HG00735.hp1 HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1162-2422G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224920 | |||||||
| chr16:57224925 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1162-2417G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224925 | |||||||
| chr16:57224960 | C | T | 1 | a0001c0003t0007g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162-2382C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224960 | |||||||
| chr16:57225023 | T | G | 58 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(55): Show |
64 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1162-2319T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225023 | |||||||
| chr16:57225083 | C | CAG | 58 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(55): Show |
64 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1162-2258_1162-225 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57225083 | ||||||
| chr16:57225151 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-2191C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225151 | |||||||
| chr16:57225257 | C | T | 58 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(55): Show |
64 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1162-2085C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225257 | |||||||
| chr16:57225341 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1162-2001G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225341 | |||||||
| chr16:57225562 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0121 |
3 | HG01261.hp1 HG01952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1162-1780C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225562 | |||||||
| chr16:57225571 | A | AAGTGAGG others(23): Show |
1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1771_1162-177 others(34): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225571 | |||||||
| chr16:57225574 | A | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1768A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225574 | |||||||
| chr16:57225576 | C | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1766C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225576 | |||||||
| chr16:57225578 | G | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1764G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225578 | |||||||
| chr16:57225583 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1759T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225583 | |||||||
| chr16:57225620 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1722T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225620 | |||||||
| chr16:57225625 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1717T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225625 | |||||||
| chr16:57225633 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1709T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225633 | |||||||
| chr16:57225636 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1706A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225636 | |||||||
| chr16:57225638 | C | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1704C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225638 | |||||||
| chr16:57225639 | T | C | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1703T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225639 | |||||||
| chr16:57225640 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1702T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225640 | |||||||
| chr16:57225644 | A | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1698A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225644 | |||||||
| chr16:57225648 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1694T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225648 | |||||||
| chr16:57225651 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1691T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225651 | |||||||
| chr16:57225654 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1688C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225654 | |||||||
| chr16:57225657 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1685A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225657 | |||||||
| chr16:57225660 | G | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1682G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225660 | |||||||
| chr16:57225670 | G | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1672G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225670 | |||||||
| chr16:57225688 | T | C | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1654T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225688 | |||||||
| chr16:57225692 | A | C | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1650A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225692 | |||||||
| chr16:57225694 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1648T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225694 | |||||||
| chr16:57225701 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225701 | |||||||
| chr16:57225703 | G | C | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1639G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225703 | |||||||
| chr16:57225704 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1638C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225704 | |||||||
| chr16:57225713 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1629T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225713 | |||||||
| chr16:57225716 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1626T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225716 | |||||||
| chr16:57225721 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1621T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225721 | |||||||
| chr16:57225723 | A | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1619A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225723 | |||||||
| chr16:57225726 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1616T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225726 | |||||||
| chr16:57225730 | A | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1612A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225730 | |||||||
| chr16:57225751 | G | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1591G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225751 | |||||||
| chr16:57225753 | T | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1589T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225753 | |||||||
| chr16:57225755 | T | C | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1587T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225755 | |||||||
| chr16:57225756 | G | T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1586G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225756 | |||||||
| chr16:57225758 | G | A | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1584G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225758 | |||||||
| chr16:57225759 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1583A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225759 | |||||||
| chr16:57225766 | TGAAAGGC others(9): Show |
T | 1 | a0001c0001t0003g0307 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1575_1162-156 others(20): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225766 | |||||||
| chr16:57225885 | C | G | 2 | a0001c0001t0005g0141 a0001c0001t0005g0142 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1162-1457C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225885 | |||||||
| chr16:57226082 | G | GA | 18 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0074 others(15): Show |
18 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1162-1251dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57226082 | ||||||
| chr16:57226314 | C | T | 4 | a0001c0001t0002g0265 a0002c0002t0012g0283 a0002c0002t0012g0285 others(1): Show |
4 | HG02738.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1028C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226314 | |||||||
| chr16:57226375 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1162-967A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226375 | |||||||
| chr16:57226410 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-932C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226410 | |||||||
| chr16:57226686 | G | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG01074.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-656G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226686 | |||||||
| chr16:57226739 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-603C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226739 | |||||||
| chr16:57226806 | T | G | 1 | a0001c0001t0017g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1162-536T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226806 | |||||||
| chr16:57226879 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0184 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-463C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226879 | |||||||
| chr16:57227124 | G | A | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1162-218G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227124 | |||||||
| chr16:57227146 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1162-196G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227146 | |||||||
| chr16:57227210 | A | C | 6 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0184 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-132A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227210 | |||||||
| chr16:57227234 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1162-108A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227234 | |||||||
| chr16:57227267 | C | T | 5 | a0001c0001t0010g0169 a0001c0001t0010g0171 a0001c0001t0010g0172 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-75C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227267 | |||||||
| chr16:57227559 | G | A | 1 | a0001c0001t0003g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1273+106G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227559 | |||||||
| chr16:57227765 | C | T | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+312C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227765 | |||||||
| chr16:57227887 | C | A | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+434C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227887 | |||||||
| chr16:57227940 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+487A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227940 | |||||||
| chr16:57228147 | C | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0063 a0001c0001t0001g0088 others(2): Show |
5 | HG01261.hp1 HG01433.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+694C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228147 | |||||||
| chr16:57228168 | G | T | 3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1273+715G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228168 | |||||||
| chr16:57228272 | C | CA | 8 | a0001c0001t0001g0297 a0001c0001t0006g0135 a0001c0001t0006g0148 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1273+840dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | ||||||
| chr16:57228272 | CA | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1273+840delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | ||||||
| chr16:57228272 | CAA | C | 6 | a0001c0001t0001g0279 a0001c0001t0004g0153 a0001c0001t0005g0134 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+839_1273+840d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | ||||||
| chr16:57228358 | G | GA | 58 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0003g0003 others(55): Show |
64 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1273+912dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228358 | ||||||
| chr16:57228421 | A | T | 1 | a0001c0001t0001g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1273+968A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228421 | |||||||
| chr16:57228659 | A | G | 1 | a0001c0001t0003g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1273+1206A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228659 | |||||||
| chr16:57229327 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1274-1384C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229327 | |||||||
| chr16:57229434 | A | T | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1274-1277A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229434 | |||||||
| chr16:57229652 | C | CTTAGAGT others(1): Show |
3 | a0001c0001t0004g0136 a0001c0001t0004g0138 a0001c0001t0016g0137 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1274-1055_1274-104 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229652 | ||||||
| chr16:57229690 | C | CT | 22 | a0001c0001t0001g0049 a0001c0001t0001g0295 a0001c0001t0001g0297 others(19): Show |
23 | HG00621.hp1 HG02165.hp1 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.1274-988dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | C | CTT | 11 | a0001c0001t0001g0068 a0001c0001t0003g0013 a0001c0001t0003g0309 others(8): Show |
12 | HG02698.hp1 HG03492.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.1274-989_1274-988d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | C | CTTT | 12 | a0001c0001t0003g0004 a0001c0001t0003g0316 a0001c0001t0003g0320 others(9): Show |
15 | HG00558.hp1 HG01255.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1274-990_1274-988d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | C | CTTTT | 5 | a0001c0001t0001g0069 a0001c0001t0003g0311 a0001c0001t0003g0318 others(2): Show |
6 | HG02280.hp1 NA18989.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-991_1274-988d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0004g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1274-997_1274-988d others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | CT | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0019 others(39): Show |
43 | HG00140.hp1 HG00438.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1274-988delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | CTT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(70): Show |
76 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1274-989_1274-988d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | CTTT | C | 89 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0030 others(86): Show |
90 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1274-990_1274-988d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | CTTTT | C | 65 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0050 others(62): Show |
69 | HG00099.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1274-991_1274-988d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229690 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1274-1001_1274-988 others(17): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | ||||||
| chr16:57229768 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0082 |
2 | NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1274-943C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229768 | |||||||
| chr16:57229892 | A | G | 1 | a0001c0001t0003g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1274-819A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229892 | |||||||
| chr16:57229908 | T | A | 1 | a0001c0001t0002g0159 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1274-803T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229908 | |||||||
| chr16:57229917 | T | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1274-794T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229917 | |||||||
| chr16:57229963 | C | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-748C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229963 | |||||||
| chr16:57230005 | C | CT | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1274-683dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57230005 | ||||||
| chr16:57230005 | C | CTT | 24 | a0001c0001t0001g0108 a0001c0001t0001g0143 a0001c0001t0001g0161 others(21): Show |
24 | HG01074.hp2 HG01981.hp1 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.1274-684_1274-683d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57230005 | ||||||
| chr16:57230555 | G | T | 1 | a0001c0001t0003g0321 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1274-156G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57230555 | |||||||
| chr16:57230668 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1274-43A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57230668 | |||||||
| chr16:57230904 | C | T | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1376+91C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230904 | |||||||
| chr16:57230907 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1376+94T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230907 | |||||||
| chr16:57230957 | G | T | 2 | a0001c0001t0003g0319 a0001c0001t0003g0332 |
2 | NA18959.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1376+144G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230957 | |||||||
| chr16:57231370 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1529+51A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231370 | |||||||
| chr16:57231428 | G | A | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1529+109G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231428 | |||||||
| chr16:57231632 | A | T | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1529+313A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231632 | |||||||
| chr16:57231769 | ACT | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0140 others(127): Show |
135 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1529+452_1529+453d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 57231769 | ||||||
| chr16:57231806 | A | G | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1529+487A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231806 | |||||||
| chr16:57231830 | C | G | 2 | a0001c0001t0011g0218 a0001c0001t0011g0275 |
2 | HG00609.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1529+511C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231830 | |||||||
| chr16:57232052 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1529+733A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232052 | |||||||
| chr16:57232063 | T | G | 1 | a0001c0001t0009g0251 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1529+744T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232063 | |||||||
| chr16:57232168 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1529+849G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232168 | |||||||
| chr16:57232294 | A | G | 2 | a0002c0002t0012g0283 a0002c0002t0012g0285 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1529+975A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232294 | |||||||
| chr16:57232542 | G | A | 50 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(47): Show |
56 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.1529+1223G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232542 | |||||||
| chr16:57232723 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1529+1404T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232723 | |||||||
| chr16:57233002 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1529+1683G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233002 | |||||||
| chr16:57233152 | T | C | 6 | a0001c0001t0006g0135 a0001c0001t0006g0148 a0001c0001t0006g0149 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1529+1833T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233152 | |||||||
| chr16:57233379 | T | A | 1 | a0001c0001t0016g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530-1745T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233379 | |||||||
| chr16:57233510 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1530-1614T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233510 | |||||||
| chr16:57233720 | G | A | 5 | a0001c0001t0010g0169 a0001c0001t0010g0171 a0001c0001t0010g0172 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530-1404G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233720 | |||||||
| chr16:57233751 | A | G | 3 | a0002c0002t0012g0283 a0002c0002t0012g0285 a0002c0002t0018g0284 |
3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1530-1373A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233751 | |||||||
| chr16:57233791 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1530-1333C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233791 | |||||||
| chr16:57234014 | T | C | 3 | a0001c0001t0010g0169 a0001c0001t0010g0172 a0001c0001t0020g0168 |
3 | HG01123.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1530-1110T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234014 | |||||||
| chr16:57234115 | C | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1530-1009C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234115 | |||||||
| chr16:57234198 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1530-926C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234198 | |||||||
| chr16:57234218 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0058 |
2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1530-906C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234218 | |||||||
| chr16:57234496 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG03471.hp2 HG03486.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530-628C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234496 | |||||||
| chr16:57234533 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0015 |
4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530-591G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234533 | |||||||
| chr16:57234625 | T | A | 1 | a0001c0001t0005g0260 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1530-499T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234625 | |||||||
| chr16:57234785 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1530-339T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234785 | |||||||
| chr16:57235019 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1530-105G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57235019 | |||||||
| chr16:57235041 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1530-83G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57235041 | |||||||
| chr16:57235419 | A | C | 1 | a0001c0001t0022g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1634+191A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57235419 | |||||||
| chr16:57236077 | C | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.1634+849C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236077 | |||||||
| chr16:57236270 | C | G | 1 | a0001c0003t0007g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1634+1042C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236270 | |||||||
| chr16:57236304 | A | G | 1 | a0001c0001t0010g0169 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1634+1076A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236304 | |||||||
| chr16:57236382 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1634+1154A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236382 | |||||||
| chr16:57236517 | GAGGA | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634+1290_1634+129 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236517 | |||||||
| chr16:57236522 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634+1294G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236522 | |||||||
| chr16:57236633 | T | G | 2 | a0001c0001t0003g0004 a0001c0001t0003g0337 |
4 | HG00558.hp1 NA18969.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+1405T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236633 | |||||||
| chr16:57236793 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1634+1565C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236793 | |||||||
| chr16:57236830 | C | G | 1 | a0001c0001t0016g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1634+1602C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236830 | |||||||
| chr16:57236842 | G | C | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1634+1614G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236842 | |||||||
| chr16:57236854 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1634+1626A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236854 | |||||||
| chr16:57236870 | AT | A | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1634+1644delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 57236870 | ||||||
| chr16:57236895 | G | A | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1634+1667G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236895 | |||||||
| chr16:57236900 | C | T | 1 | a0001c0001t0006g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1634+1672C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236900 | |||||||
| chr16:57236938 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0234 |
2 | NA18959.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1634+1710G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236938 | |||||||
| chr16:57236994 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1634+1766G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236994 | |||||||
| chr16:57237040 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1634+1812C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237040 | |||||||
| chr16:57237060 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0106 a0001c0001t0001g0107 others(5): Show |
8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-1819C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237060 | |||||||
| chr16:57237099 | G | A | 1 | a0001c0001t0003g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1635-1780G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237099 | |||||||
| chr16:57237155 | T | A | 1 | a0001c0001t0001g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1635-1724T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237155 | |||||||
| chr16:57237234 | C | T | 1 | a0001c0001t0009g0223 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1635-1645C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237234 | |||||||
| chr16:57237332 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG02257.hp1 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1635-1547C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237332 | |||||||
| chr16:57237333 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1635-1546G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237333 | |||||||
| chr16:57237387 | C | G | 1 | a0001c0001t0002g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1635-1492C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237387 | |||||||
| chr16:57237585 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1635-1294G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237585 | |||||||
| chr16:57237735 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0155 a0001c0001t0001g0156 others(10): Show |
14 | HG01099.hp2 HG01109.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1635-1144G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237735 | |||||||
| chr16:57237938 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.1635-941C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237938 | |||||||
| chr16:57238138 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635-741G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238138 | |||||||
| chr16:57238249 | T | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0252 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-630T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238249 | |||||||
| chr16:57238262 | A | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0154 others(117): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1635-617A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238262 | |||||||
| chr16:57238644 | T | C | 2 | a0001c0001t0008g0163 a0001c0001t0008g0164 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1635-235T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238644 | |||||||
| chr16:57238699 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635-180A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238699 | |||||||
| chr16:57238756 | C | A | 8 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0219 others(5): Show |
8 | HG00544.hp1 NA18946.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-123C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238756 | |||||||
| chr16:57238760 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1635-119T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238760 |