Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 131544 |
|---|---|
| ensemblid | ENSG00000080200.10 |
| hgncid | 34427 |
| symbol | CRYBG3 |
| name | crystallin beta-gamma domain containing 3 |
| refseq_nuc | NM_153605.4 |
| refseq_prot | NP_705833.3 |
| ensembl_nuc | ENST00000389622.7 |
| ensembl_prot | ENSP00000374273.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 97822011 |
| end | 97944984 |
| strand | + |
| ver | v1.2 |
| region | chr3:97822011-97944984 |
| region5000 | chr3:97817011-97949984 |
| regionname0 | CRYBG3_chr3_97822011_97944984 |
| regionname5000 | CRYBG3_chr3_97817011_97949984 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2970 | 95 | 17 | 20 | 45 | 5 | 8 | 36 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002 | 1/0 | 2970 | 88 | 33 | 15 | 27 | 3 | 9 | 18 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0003 | 0/0 | 2970 | 59 | 5 | 18 | 22 | 5 | 9 | 13 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0004 | 0/0 | 2970 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0005 | 0/0 | 2970 | 7 | 0 | 1 | 5 | 0 | 1 | 5 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0006 | 0/0 | 2970 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0007 | 0/0 | 2970 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008 | 0/0 | 2970 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0009 | 0/0 | 2970 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0010 | 0/0 | 2970 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0011 | 0/0 | 2970 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0012 | 0/0 | 2970 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0013 | 0/0 | 2970 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0014 | 0/0 | 2970 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0015 | 0/0 | 2970 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0016 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0017 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0018 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0019 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0020 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0021 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0022 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0023 | 0/1 | 2970 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0024 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0025 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0026 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0027 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0028 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0029 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0030 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0031 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0032 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0033 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0034 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0035 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0036 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0037 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0038 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0039 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0040 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0041 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0042 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 8913 | 74 | 27 | 15 | 19 | 3 | 9 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0002 | 0/0 | 8913 | 59 | 5 | 18 | 22 | 5 | 9 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0003 | 0/0 | 8913 | 55 | 11 | 12 | 22 | 3 | 7 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0004 | 0/0 | 8913 | 37 | 6 | 8 | 20 | 2 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0005 | 0/0 | 8913 | 7 | 6 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0006 | 0/0 | 8913 | 7 | 0 | 1 | 5 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0007 | 0/0 | 8913 | 6 | 3 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0008 | 0/0 | 8913 | 5 | 5 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0009 | 0/0 | 8913 | 4 | 4 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0010 | 0/0 | 8913 | 3 | 0 | 2 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0011 | 0/0 | 8913 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0012 | 0/0 | 8913 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0013 | 0/0 | 8913 | 3 | 3 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0014 | 0/0 | 8913 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0015 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0016 | 0/0 | 8913 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0017 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0018 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0019 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0020 | 0/0 | 8913 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0021 | 0/0 | 8913 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0022 | 0/0 | 8913 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0023 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0024 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0025 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0026 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0027 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0028 | 0/1 | 8913 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0029 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0030 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0031 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0032 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0033 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0034 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0035 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0036 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0037 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0038 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0039 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0040 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0041 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0042 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0043 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0044 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0045 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0046 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0047 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0048 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0049 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0050 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0051 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0052 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| c0053 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1867 | 172 | 55 | 36 | 53 | 8 | 19 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0002 | 0/1 | 1870 | 114 | 18 | 27 | 49 | 8 | 11 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0003 | 0/0 | 1870 | 7 | 3 | 1 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0004 | 0/0 | 1870 | 7 | 0 | 1 | 5 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0005 | 0/0 | 1867 | 4 | 4 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0006 | 0/0 | 1866 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0007 | 0/0 | 1867 | 3 | 3 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0008 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0009 | 0/0 | 1870 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0010 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| t0011 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0002 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0026 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 8913 | 55 | 11 | 12 | 22 | 3 | 7 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0004 | 0/0 | 8913 | 37 | 6 | 8 | 20 | 2 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0022 | 0/0 | 8913 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0032 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0001 | 1/0 | 8913 | 74 | 27 | 15 | 19 | 3 | 9 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0007 | 0/0 | 8913 | 6 | 3 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0011 | 0/0 | 8913 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0018 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0026 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0036 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0052 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0003c0002 | 0/0 | 8913 | 59 | 5 | 18 | 22 | 5 | 9 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0004c0005 | 0/0 | 8913 | 7 | 6 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0005c0006 | 0/0 | 8913 | 7 | 0 | 1 | 5 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0006c0008 | 0/0 | 8913 | 5 | 5 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0007c0009 | 0/0 | 8913 | 4 | 4 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0015 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0039 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0042 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0009c0014 | 0/0 | 8913 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0010c0013 | 0/0 | 8913 | 3 | 3 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0011c0010 | 0/0 | 8913 | 3 | 0 | 2 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0012c0012 | 0/0 | 8913 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0013c0021 | 0/0 | 8913 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0014c0016 | 0/0 | 8913 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0015c0020 | 0/0 | 8913 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0016c0019 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0017c0017 | 0/0 | 8913 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0018c0051 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0019c0049 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0020c0050 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0021c0045 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0022c0044 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0023c0028 | 0/1 | 8913 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0024c0034 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0025c0035 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0026c0033 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0027c0029 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0028c0027 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0029c0053 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0030c0041 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0031c0031 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0032c0038 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0033c0037 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0034c0043 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0035c0040 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0036c0030 | 0/0 | 8913 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0037c0046 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0038c0047 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0039c0048 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0040c0025 | 0/0 | 8913 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0041c0024 | 0/0 | 8913 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0042c0023 | 0/0 | 8913 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002 | 0/0 | 10782 | 55 | 11 | 12 | 22 | 3 | 7 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0004t0002 | 0/0 | 10782 | 37 | 6 | 8 | 20 | 2 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0022t0002 | 0/0 | 10782 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0001c0032t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0001t0001 | 1/0 | 10779 | 71 | 25 | 15 | 19 | 3 | 8 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0001t0007 | 0/0 | 10779 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0001t0010 | 0/0 | 10779 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0007t0001 | 0/0 | 10779 | 6 | 3 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0011t0001 | 0/0 | 10779 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0018t0001 | 0/0 | 10779 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0026t0007 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0036t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0002c0052t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0003c0002t0001 | 0/0 | 10779 | 59 | 5 | 18 | 22 | 5 | 9 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0004c0005t0001 | 0/0 | 10779 | 7 | 6 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0005c0006t0004 | 0/0 | 10782 | 7 | 0 | 1 | 5 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0006c0008t0001 | 0/0 | 10779 | 5 | 5 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0007c0009t0005 | 0/0 | 10779 | 4 | 4 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0015t0003 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0039t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0008c0042t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0009c0014t0003 | 0/0 | 10782 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0010c0013t0001 | 0/0 | 10779 | 3 | 3 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0011c0010t0002 | 0/0 | 10782 | 3 | 0 | 2 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0012c0012t0006 | 0/0 | 10778 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0013c0021t0002 | 0/0 | 10782 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0014c0016t0002 | 0/0 | 10782 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0015c0020t0009 | 0/0 | 10782 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0016c0019t0001 | 0/0 | 10779 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0017c0017t0008 | 0/0 | 10779 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0018c0051t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0019c0049t0001 | 0/0 | 10779 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0020c0050t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0021c0045t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0022c0044t0001 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0023c0028t0002 | 0/1 | 10782 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0024c0034t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0025c0035t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0026c0033t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0027c0029t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0028c0027t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0029c0053t0011 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0030c0041t0001 | 0/0 | 10779 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0031c0031t0001 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0032c0038t0003 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0033c0037t0001 | 0/0 | 10779 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0034c0043t0001 | 0/0 | 10779 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0035c0040t0001 | 0/0 | 10779 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0036c0030t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0037c0046t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0038c0047t0001 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0039c0048t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0040c0025t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0041c0024t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| a0042c0023t0001 | 0/0 | 10779 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | copy fasta | chr3 | 97817011 | 97949984 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0022t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0022t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0001c0032t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0026 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0011t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0011t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0011t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0018t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0018t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0026t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0036t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0002c0052t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0004c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0005c0006t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0006c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0006c0008t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0006c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0006c0008t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0006c0008t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0007c0009t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0007c0009t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0007c0009t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0008c0015t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0008c0015t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0008c0039t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0008c0042t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0009c0014t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0009c0014t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0010c0013t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0010c0013t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0010c0013t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0011c0010t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0011c0010t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0011c0010t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0012c0012t0006g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0013c0021t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0013c0021t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0014c0016t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0015c0020t0009g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0016c0019t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0016c0019t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0017c0017t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0018c0051t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0019c0049t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0020c0050t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0021c0045t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0022c0044t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0023c0028t0002g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0024c0034t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0025c0035t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0026c0033t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0027c0029t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0028c0027t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0029c0053t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0030c0041t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0031c0031t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0032c0038t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0033c0037t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0034c0043t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0035c0040t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0036c0030t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0037c0046t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0038c0047t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0039c0048t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0040c0025t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0041c0024t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| a0042c0023t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0211 | EUR | GBR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00099 | hp2 | a0003 | c0002 | t0001 | g0017 | EUR | GBR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00140 | hp1 | a0001 | c0004 | t0002 | g0196 | EUR | GBR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0002 | EUR | GBR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0016 | EUR | FIN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00280 | hp2 | a0011 | c0010 | t0002 | g0200 | EUR | FIN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0085 | EUR | FIN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00323 | hp2 | a0003 | c0002 | t0001 | g0016 | EUR | FIN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00408 | hp2 | a0003 | c0002 | t0001 | g0051 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00423 | hp1 | a0001 | c0022 | t0002 | g0187 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00423 | hp2 | a0002 | c0011 | t0001 | g0112 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0220 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00597 | hp2 | a0003 | c0002 | t0001 | g0052 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00621 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00621 | hp2 | a0013 | c0021 | t0002 | g0167 | EAS | CHS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00642 | hp1 | a0004 | c0005 | t0001 | g0161 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0210 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00733 | hp2 | a0034 | c0043 | t0001 | g0102 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0240 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0229 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0020 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0083 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG00741 | hp2 | a0003 | c0002 | t0001 | g0072 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0203 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01070 | hp2 | a0003 | c0002 | t0001 | g0046 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01071 | hp1 | a0003 | c0002 | t0001 | g0045 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0020 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01074 | hp1 | a0026 | c0033 | t0002 | g0170 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01074 | hp2 | a0003 | c0002 | t0001 | g0060 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01106 | hp1 | a0012 | c0012 | t0006 | g0008 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0076 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01109 | hp1 | a0003 | c0002 | t0001 | g0015 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0145 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0245 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0030 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0030 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01169 | hp2 | a0003 | c0002 | t0001 | g0018 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0127 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01175 | hp2 | a0028 | c0027 | t0002 | g0236 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01243 | hp1 | a0003 | c0002 | t0001 | g0058 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01243 | hp2 | a0011 | c0010 | t0002 | g0216 | AMR | PUR | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01255 | hp1 | a0003 | c0002 | t0001 | g0070 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01255 | hp2 | a0001 | c0004 | t0002 | g0184 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0232 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01256 | hp2 | a0033 | c0037 | t0001 | g0137 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0231 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01257 | hp2 | a0003 | c0002 | t0001 | g0015 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01261 | hp1 | a0039 | c0048 | t0002 | g0246 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01261 | hp2 | a0003 | c0002 | t0001 | g0063 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01358 | hp1 | a0003 | c0002 | t0001 | g0061 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01358 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01361 | hp1 | a0001 | c0004 | t0002 | g0186 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01433 | hp2 | a0027 | c0029 | t0002 | g0177 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01496 | hp1 | a0003 | c0002 | t0001 | g0064 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01496 | hp2 | a0011 | c0010 | t0002 | g0217 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0002 | EUR | IBS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01516 | hp2 | a0014 | c0016 | t0002 | g0034 | EUR | IBS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01517 | hp1 | a0003 | c0002 | t0001 | g0038 | EUR | IBS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01517 | hp2 | a0014 | c0016 | t0002 | g0034 | EUR | IBS | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01884 | hp1 | a0002 | c0018 | t0001 | g0159 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0025 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01891 | hp1 | a0006 | c0008 | t0001 | g0151 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01891 | hp2 | a0010 | c0013 | t0001 | g0142 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01934 | hp1 | a0003 | c0002 | t0001 | g0048 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0091 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01943 | hp2 | a0005 | c0006 | t0004 | g0224 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01975 | hp1 | a0001 | c0004 | t0002 | g0195 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01975 | hp2 | a0032 | c0038 | t0003 | g0138 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01978 | hp1 | a0041 | c0024 | t0002 | g0192 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01978 | hp2 | a0003 | c0002 | t0001 | g0050 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0026 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01981 | hp2 | a0001 | c0003 | t0002 | g0256 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01993 | hp1 | a0003 | c0002 | t0001 | g0012 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0148 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0247 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02004 | hp2 | a0003 | c0002 | t0001 | g0071 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0207 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02027 | hp2 | a0002 | c0036 | t0001 | g0088 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02055 | hp1 | a0010 | c0013 | t0001 | g0140 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02055 | hp2 | a0042 | c0023 | t0001 | g0075 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02056 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02080 | hp1 | a0001 | c0004 | t0002 | g0179 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02080 | hp2 | a0003 | c0002 | t0001 | g0049 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02129 | hp1 | a0003 | c0002 | t0001 | g0043 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02129 | hp2 | a0001 | c0022 | t0002 | g0178 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02135 | hp2 | a0003 | c0002 | t0001 | g0074 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02145 | hp1 | a0007 | c0009 | t0005 | g0254 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0205 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0191 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02148 | hp2 | a0001 | c0004 | t0002 | g0185 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0214 | EAS | CDX | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02155 | hp2 | a0003 | c0002 | t0001 | g0003 | EAS | CDX | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CDX | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02165 | hp2 | a0002 | c0007 | t0001 | g0100 | EAS | CDX | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02257 | hp1 | a0007 | c0009 | t0005 | g0035 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02257 | hp2 | a0003 | c0002 | t0001 | g0014 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0031 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02258 | hp2 | a0017 | c0017 | t0008 | g0011 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02273 | hp1 | a0003 | c0002 | t0001 | g0047 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | PEL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02280 | hp1 | a0006 | c0008 | t0001 | g0152 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0118 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0128 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02451 | hp2 | a0004 | c0005 | t0001 | g0163 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02523 | hp1 | a0001 | c0003 | t0002 | g0242 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02523 | hp2 | a0003 | c0002 | t0001 | g0003 | EAS | KHV | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0108 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02572 | hp2 | a0038 | c0047 | t0001 | g0119 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0227 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0081 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02615 | hp1 | a0008 | c0039 | t0003 | g0124 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02615 | hp2 | a0002 | c0026 | t0007 | g0114 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0109 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0143 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02630 | hp2 | a0003 | c0002 | t0001 | g0068 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0130 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02698 | hp1 | a0021 | c0045 | t0002 | g0001 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0080 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0132 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02717 | hp2 | a0002 | c0007 | t0001 | g0105 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0129 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0248 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02735 | hp2 | a0003 | c0002 | t0001 | g0073 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02809 | hp1 | a0002 | c0001 | t0007 | g0123 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0031 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0116 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0252 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02886 | hp1 | a0006 | c0008 | t0001 | g0153 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02886 | hp2 | a0008 | c0015 | t0003 | g0115 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0136 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02896 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02897 | hp1 | a0001 | c0004 | t0002 | g0028 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02897 | hp2 | a0002 | c0001 | t0007 | g0113 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02922 | hp1 | a0001 | c0004 | t0002 | g0249 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0027 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02965 | hp1 | a0003 | c0002 | t0001 | g0057 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0122 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02970 | hp1 | a0004 | c0005 | t0001 | g0164 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02970 | hp2 | a0003 | c0002 | t0001 | g0014 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02976 | hp1 | a0012 | c0012 | t0006 | g0008 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0024 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03041 | hp1 | a0022 | c0044 | t0001 | g0149 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03041 | hp2 | a0002 | c0007 | t0001 | g0111 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0135 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03130 | hp2 | a0004 | c0005 | t0001 | g0162 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0032 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03139 | hp2 | a0017 | c0017 | t0008 | g0011 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0134 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03195 | hp2 | a0029 | c0053 | t0011 | g0258 | AFR | ESN | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03209 | hp1 | a0031 | c0031 | t0001 | g0160 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0025 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0121 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03225 | hp2 | a0002 | c0018 | t0001 | g0158 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03239 | hp1 | a0003 | c0002 | t0001 | g0017 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03239 | hp2 | a0002 | c0001 | t0010 | g0096 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0032 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0024 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03486 | hp1 | a0006 | c0008 | t0001 | g0154 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03486 | hp2 | a0002 | c0007 | t0001 | g0103 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03490 | hp1 | a0019 | c0049 | t0001 | g0059 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0022 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03491 | hp1 | a0015 | c0020 | t0009 | g0029 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03491 | hp2 | a0003 | c0002 | t0001 | g0037 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03492 | hp1 | a0015 | c0020 | t0009 | g0029 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0022 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0126 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03540 | hp2 | a0016 | c0019 | t0001 | g0156 | AFR | GWD | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03579 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0120 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0069 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03669 | hp2 | a0003 | c0002 | t0001 | g0053 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0097 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0197 | SAS | PJL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0209 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03834 | hp2 | a0035 | c0040 | t0001 | g0098 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03927 | hp1 | a0003 | c0002 | t0001 | g0039 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03927 | hp2 | a0003 | c0002 | t0001 | g0147 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03942 | hp1 | a0001 | c0003 | t0002 | g0174 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03942 | hp2 | a0001 | c0004 | t0002 | g0173 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04115 | hp1 | a0024 | c0034 | t0002 | g0223 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04115 | hp2 | a0005 | c0006 | t0004 | g0241 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0171 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0077 | SAS | BEB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0251 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04204 | hp2 | a0003 | c0002 | t0001 | g0018 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04228 | hp1 | a0003 | c0002 | t0001 | g0054 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0019 | SAS | STU | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0234 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18522 | hp2 | a0003 | c0002 | t0001 | g0066 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18747 | hp1 | a0002 | c0007 | t0001 | g0104 | EAS | CHB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | CHB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18906 | hp1 | a0007 | c0009 | t0005 | g0035 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18939 | hp1 | a0013 | c0021 | t0002 | g0169 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18939 | hp2 | a0001 | c0004 | t0002 | g0033 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18941 | hp1 | a0002 | c0052 | t0001 | g0021 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0233 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18942 | hp1 | a0020 | c0050 | t0001 | g0044 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18943 | hp2 | a0001 | c0004 | t0002 | g0189 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18944 | hp1 | a0003 | c0002 | t0001 | g0007 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18944 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18945 | hp1 | a0001 | c0004 | t0002 | g0033 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18945 | hp2 | a0003 | c0002 | t0001 | g0004 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18950 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18950 | hp2 | a0003 | c0002 | t0001 | g0062 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18954 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18954 | hp2 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18957 | hp2 | a0001 | c0004 | t0002 | g0238 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18970 | hp1 | a0009 | c0014 | t0003 | g0013 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18970 | hp2 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18971 | hp1 | a0005 | c0006 | t0004 | g0230 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18971 | hp2 | a0002 | c0011 | t0001 | g0106 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0239 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18979 | hp1 | a0003 | c0002 | t0001 | g0007 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18979 | hp2 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18980 | hp1 | a0018 | c0051 | t0001 | g0056 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18981 | hp1 | a0001 | c0004 | t0002 | g0199 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18981 | hp2 | a0001 | c0004 | t0002 | g0168 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18984 | hp2 | a0003 | c0002 | t0001 | g0041 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18986 | hp2 | a0003 | c0002 | t0001 | g0004 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18989 | hp1 | a0001 | c0004 | t0002 | g0188 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18989 | hp2 | a0009 | c0014 | t0003 | g0013 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18990 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18990 | hp2 | a0003 | c0002 | t0001 | g0004 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18991 | hp1 | a0001 | c0032 | t0002 | g0206 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18991 | hp2 | a0002 | c0007 | t0001 | g0110 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18993 | hp1 | a0005 | c0006 | t0004 | g0253 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18993 | hp2 | a0003 | c0002 | t0001 | g0004 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18994 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19002 | hp2 | a0005 | c0006 | t0004 | g0225 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19004 | hp1 | a0003 | c0002 | t0001 | g0012 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19009 | hp2 | a0001 | c0004 | t0002 | g0190 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19011 | hp1 | a0036 | c0030 | t0002 | g0010 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0007 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0125 | AFR | LWK | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19030 | hp2 | a0037 | c0046 | t0002 | g0172 | AFR | LWK | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19058 | hp2 | a0001 | c0004 | t0002 | g0250 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19065 | hp2 | a0030 | c0041 | t0001 | g0089 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19066 | hp1 | a0001 | c0004 | t0002 | g0183 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19066 | hp2 | a0002 | c0011 | t0001 | g0107 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19075 | hp1 | a0025 | c0035 | t0002 | g0221 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19075 | hp2 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0212 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19079 | hp1 | a0003 | c0002 | t0001 | g0040 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19079 | hp2 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19082 | hp1 | a0005 | c0006 | t0004 | g0226 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19082 | hp2 | a0008 | c0042 | t0001 | g0101 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19086 | hp1 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19086 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19087 | hp1 | a0009 | c0014 | t0003 | g0055 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19087 | hp2 | a0005 | c0006 | t0004 | g0201 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19240 | hp1 | a0001 | c0004 | t0002 | g0237 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA19240 | hp2 | a0002 | c0001 | t0001 | g0133 | AFR | YRI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20129 | hp1 | a0001 | c0004 | t0002 | g0194 | AFR | ASW | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20129 | hp2 | a0008 | c0015 | t0003 | g0139 | AFR | ASW | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0204 | EUR | TSI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20752 | hp2 | a0003 | c0002 | t0001 | g0065 | EUR | TSI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0006 | EUR | TSI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0202 | EUR | TSI | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0093 | SAS | GIH | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20905 | hp2 | a0040 | c0025 | t0002 | g0218 | SAS | GIH | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01123 | hp1 | a0003 | c0002 | t0001 | g0042 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0144 | AMR | CLM | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0131 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02109 | hp2 | a0001 | c0004 | t0002 | g0193 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02486 | hp1 | a0004 | c0005 | t0001 | g0165 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02486 | hp2 | a0016 | c0019 | t0001 | g0155 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02559 | hp1 | a0012 | c0012 | t0006 | g0008 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG02559 | hp2 | a0007 | c0009 | t0005 | g0255 | AFR | ACB | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0117 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0150 | AFR | MSL | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20300 | hp1 | a0006 | c0008 | t0001 | g0157 | AFR | USA | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| NA20300 | hp2 | a0010 | c0013 | t0001 | g0141 | AFR | USA | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| homoSapiens_chm13v2 | hp1 | a0023 | c0028 | t0002 | g0176 | REF | REF | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0026 | REF | REF | CRYBG3_chr3_97817011_97949984 | CRYBG3 | chr3 | 97817011 | 97949984 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:97822260
|
C | A | 1 | a0006 | 5 | HG01891.hp1 HG02280.hp1 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.54C>A | p.Phe18Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/22 | 250/10779 | 54/8913 | 18/2970 | chr3 | 97822260 | ||
| chr3:97872000
|
T | C | 1 | a0042 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.806T>C | p.Ile269Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1002/10779 | 806/8913 | 269/2970 | chr3 | 97872000 | ||
| chr3:97872143
|
T | G | 1 | a0041 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.949T>G | p.Leu317Val | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1145/10779 | 949/8913 | 317/2970 | chr3 | 97872143 | ||
| chr3:97872309
|
C | T | 5 | a0003a0009a0018others(2): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
missense_variant | MODERATE | c.1115C>T | p.Ser372Phe | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1311/10779 | 1115/8913 | 372/2970 | chr3 | 97872309 | ||
| chr3:97872414
|
C | T | 1 | a0018 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.1220C>T | p.Thr407Met | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1416/10779 | 1220/8913 | 407/2970 | chr3 | 97872414 | ||
| chr3:97872495
|
T | C | 1 | a0040 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1301T>C | p.Ile434Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1497/10779 | 1301/8913 | 434/2970 | chr3 | 97872495 | ||
| chr3:97872684
|
A | G | 1 | a0039 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.1490A>G | p.Gln497Arg | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1686/10779 | 1490/8913 | 497/2970 | chr3 | 97872684 | ||
| chr3:97872921
|
A | G | 1 | a0038 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1727A>G | p.Asp576Gly | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1923/10779 | 1727/8913 | 576/2970 | chr3 | 97872921 | ||
| chr3:97873640
|
G | T | 1 | a0037 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2446G>T | p.Ala816Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 2642/10779 | 2446/8913 | 816/2970 | chr3 | 97873640 | ||
| chr3:97873709
|
T | C | 1 | a0019 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.2515T>C | p.Ser839Pro | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 2711/10779 | 2515/8913 | 839/2970 | chr3 | 97873709 | ||
| chr3:97873734
|
A | C | 1 | a0021 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2540A>C | p.Glu847Ala | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 2736/10779 | 2540/8913 | 847/2970 | chr3 | 97873734 | ||
| chr3:97874480
|
G | T | 2 | a0010a0022 | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.3286G>T | p.Gly1096Cys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3482/10779 | 3286/8913 | 1096/2970 | chr3 | 97874480 | ||
| chr3:97874492
|
A | T | 2 | a0010a0022 | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.3298A>T | p.Thr1100Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3494/10779 | 3298/8913 | 1100/2970 | chr3 | 97874492 | ||
| chr3:97874720
|
G | A | 1 | a0036 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.3526G>A | p.Ala1176Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3722/10779 | 3526/8913 | 1176/2970 | chr3 | 97874720 | ||
| chr3:97875341
|
C | G | 1 | a0005 | 7 | HG01943.hp2 HG04115.hp2 NA18971.hp1 others(4): Show |
missense_variant | MODERATE | c.4147C>G | p.Leu1383Val | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4343/10779 | 4147/8913 | 1383/2970 | chr3 | 97875341 | ||
| chr3:97875417
|
G | A | 19 | a0001a0005a0007others(16): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
missense_variant | MODERATE | c.4223G>A | p.Gly1408Glu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4419/10779 | 4223/8913 | 1408/2970 | chr3 | 97875417 | ||
| chr3:97875489
|
C | T | 1 | a0004 | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
missense_variant | MODERATE | c.4295C>T | p.Ser1432Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4491/10779 | 4295/8913 | 1432/2970 | chr3 | 97875489 | ||
| chr3:97875498
|
G | A | 1 | a0007 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
missense_variant | MODERATE | c.4304G>A | p.Arg1435Gln | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4500/10779 | 4304/8913 | 1435/2970 | chr3 | 97875498 | ||
| chr3:97875501
|
T | C | 1 | a0028 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.4307T>C | p.Leu1436Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4503/10779 | 4307/8913 | 1436/2970 | chr3 | 97875501 | ||
| chr3:97875912
|
T | C | 1 | a0015 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.4718T>C | p.Ile1573Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4914/10779 | 4718/8913 | 1573/2970 | chr3 | 97875912 | ||
| chr3:97875942
|
C | T | 2 | a0006a0016 | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
missense_variant | MODERATE | c.4748C>T | p.Thr1583Met | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4944/10779 | 4748/8913 | 1583/2970 | chr3 | 97875942 | ||
| chr3:97876161
|
T | G | 1 | a0029 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.4967T>G | p.Val1656Gly | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5163/10779 | 4967/8913 | 1656/2970 | chr3 | 97876161 | ||
| chr3:97876178
|
C | A | 2 | a0004a0017 | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.4984C>A | p.Pro1662Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5180/10779 | 4984/8913 | 1662/2970 | chr3 | 97876178 | ||
| chr3:97876398
|
G | C | 1 | a0020 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.5204G>C | p.Arg1735Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5400/10779 | 5204/8913 | 1735/2970 | chr3 | 97876398 | ||
| chr3:97876535
|
G | A | 20 | a0001a0005a0007others(17): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
missense_variant | MODERATE | c.5341G>A | p.Val1781Met | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5537/10779 | 5341/8913 | 1781/2970 | chr3 | 97876535 | ||
| chr3:97876722
|
T | C | 1 | a0011 | 3 | HG00280.hp2 HG01243.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.5528T>C | p.Ile1843Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5724/10779 | 5528/8913 | 1843/2970 | chr3 | 97876722 | ||
| chr3:97877375
|
A | T | 1 | a0030 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.6181A>T | p.Thr2061Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6377/10779 | 6181/8913 | 2061/2970 | chr3 | 97877375 | ||
| chr3:97877417
|
G | A | 2 | a0010a0022 | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.6223G>A | p.Ala2075Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6419/10779 | 6223/8913 | 2075/2970 | chr3 | 97877417 | ||
| chr3:97877466
|
A | T | 1 | a0035 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.6272A>T | p.Asp2091Val | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6468/10779 | 6272/8913 | 2091/2970 | chr3 | 97877466 | ||
| chr3:97877514
|
A | G | 1 | a0017 | 2 | HG02258.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.6320A>G | p.His2107Arg | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6516/10779 | 6320/8913 | 2107/2970 | chr3 | 97877514 | ||
| chr3:97877529
|
A | C | 1 | a0034 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.6335A>C | p.Lys2112Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6531/10779 | 6335/8913 | 2112/2970 | chr3 | 97877529 | ||
| chr3:97877670
|
A | G | 1 | a0027 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.6476A>G | p.His2159Arg | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6672/10779 | 6476/8913 | 2159/2970 | chr3 | 97877670 | ||
| chr3:97877793
|
C | T | 1 | a0012 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.6599C>T | p.Pro2200Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6795/10779 | 6599/8913 | 2200/2970 | chr3 | 97877793 | ||
| chr3:97877991
|
A | G | 2 | a0010a0022 | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.6797A>G | p.Tyr2266Cys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6993/10779 | 6797/8913 | 2266/2970 | chr3 | 97877991 | ||
| chr3:97878035
|
G | A | 1 | a0026 | 1 | HG01074.hp1 | missense_variant&splice_region_variant | MODERATE | c.6841G>A | p.Glu2281Lys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 7037/10779 | 6841/8913 | 2281/2970 | chr3 | 97878035 | ||
| chr3:97881209
|
G | A | 1 | a0022 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.7142G>A | p.Arg2381His | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/22 | 7338/10779 | 7142/8913 | 2381/2970 | chr3 | 97881209 | ||
| chr3:97881209
|
G | T | 1 | a0012 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.7142G>T | p.Arg2381Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/22 | 7338/10779 | 7142/8913 | 2381/2970 | chr3 | 97881209 | ||
| chr3:97892899
|
A | G | 1 | a0013 | 2 | HG00621.hp2 NA18939.hp1 |
missense_variant | MODERATE | c.7480A>G | p.Lys2494Glu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/22 | 7676/10779 | 7480/8913 | 2494/2970 | chr3 | 97892899 | ||
| chr3:97892961
|
C | G | 1 | a0025 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.7542C>G | p.His2514Gln | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/22 | 7738/10779 | 7542/8913 | 2514/2970 | chr3 | 97892961 | ||
| chr3:97898977
|
A | G | 1 | a0014 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.7796A>G | p.Glu2599Gly | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 13/22 | 7992/10779 | 7796/8913 | 2599/2970 | chr3 | 97898977 | ||
| chr3:97899235
|
T | C | 2 | a0032a0033 | 2 | HG01256.hp2 HG01975.hp2 |
missense_variant | MODERATE | c.7943T>C | p.Ile2648Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/22 | 8139/10779 | 7943/8913 | 2648/2970 | chr3 | 97899235 | ||
| chr3:97915621
|
A | G | 1 | a0023 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.8126A>G | p.Tyr2709Cys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/22 | 8322/10779 | 8126/8913 | 2709/2970 | chr3 | 97915621 | ||
| chr3:97941166
|
A | G | 1 | a0031 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.8524A>G | p.Ile2842Val | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/22 | 8720/10779 | 8524/8913 | 2842/2970 | chr3 | 97941166 | ||
| chr3:97941262
|
A | C | 21 | a0001a0005a0008others(18): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
missense_variant | MODERATE | c.8620A>C | p.Asn2874His | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/22 | 8816/10779 | 8620/8913 | 2874/2970 | chr3 | 97941262 | ||
| chr3:97942309
|
T | G | 1 | a0031 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.8690T>G | p.Ile2897Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 21/22 | 8886/10779 | 8690/8913 | 2897/2970 | chr3 | 97942309 | ||
| chr3:97943228
|
G | C | 1 | a0024 | 1 | HG04115.hp1 | missense_variant&splice_region_variant | MODERATE | c.8827G>C | p.Gly2943Arg | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 9023/10779 | 8827/8913 | 2943/2970 | chr3 | 97943228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:97822254
|
C | T | 1 | a0029c0053 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.48C>T | p.Ser16Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/22 | 244/10779 | 48/8913 | 16/2970 | chr3 | 97822254 | ||
| chr3:97864411
|
A | G | 1 | a0002c0052 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.411A>G | p.Leu137Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/22 | 607/10779 | 411/8913 | 137/2970 | chr3 | 97864411 | ||
| chr3:97864495
|
C | T | 1 | a0001c0022 | 2 | HG00423.hp1 HG02129.hp2 |
synonymous_variant | LOW | c.495C>T | p.Asp165Asp | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/22 | 691/10779 | 495/8913 | 165/2970 | chr3 | 97864495 | ||
| chr3:97872685
|
G | A | 2 | a0002c0026a0008c0015 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1491G>A | p.Gln497Gln | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 1687/10779 | 1491/8913 | 497/2970 | chr3 | 97872685 | ||
| chr3:97874536
|
G | A | 9 | a0001c0004a0001c0022a0014c0016others(6): Show | 47 | HG00140.hp1 HG00423.hp1 HG00738.hp1 others(44): Show |
synonymous_variant | LOW | c.3342G>A | p.Thr1114Thr | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3538/10779 | 3342/8913 | 1114/2970 | chr3 | 97874536 | ||
| chr3:97874596
|
G | A | 1 | a0017c0017 | 2 | HG02258.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.3402G>A | p.Gly1134Gly | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3598/10779 | 3402/8913 | 1134/2970 | chr3 | 97874596 | ||
| chr3:97874641
|
C | T | 9 | a0002c0007a0003c0002a0008c0042others(6): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
synonymous_variant | LOW | c.3447C>T | p.Leu1149Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3643/10779 | 3447/8913 | 1149/2970 | chr3 | 97874641 | ||
| chr3:97874830
|
G | A | 4 | a0002c0018a0006c0008a0016c0019others(1): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.3636G>A | p.Arg1212Arg | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 3832/10779 | 3636/8913 | 1212/2970 | chr3 | 97874830 | ||
| chr3:97875409
|
A | C | 1 | a0029c0053 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.4215A>C | p.Leu1405Leu | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 4411/10779 | 4215/8913 | 1405/2970 | chr3 | 97875409 | ||
| chr3:97876057
|
T | A | 1 | a0002c0036 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.4863T>A | p.Ala1621Ala | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 5059/10779 | 4863/8913 | 1621/2970 | chr3 | 97876057 | ||
| chr3:97877230
|
G | A | 1 | a0001c0032 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.6036G>A | p.Lys2012Lys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/22 | 6232/10779 | 6036/8913 | 2012/2970 | chr3 | 97877230 | ||
| chr3:97886711
|
C | T | 1 | a0029c0053 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.7233C>T | p.Pro2411Pro | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/22 | 7429/10779 | 7233/8913 | 2411/2970 | chr3 | 97886711 | ||
| chr3:97888446
|
G | A | 9 | a0002c0007a0003c0002a0008c0042others(6): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
synonymous_variant | LOW | c.7395G>A | p.Pro2465Pro | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/22 | 7591/10779 | 7395/8913 | 2465/2970 | chr3 | 97888446 | ||
| chr3:97899245
|
G | A | 1 | a0002c0011 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
synonymous_variant | LOW | c.7953G>A | p.Ser2651Ser | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/22 | 8149/10779 | 7953/8913 | 2651/2970 | chr3 | 97899245 | ||
| chr3:97941240
|
C | T | 7 | a0002c0007a0003c0002a0018c0051others(4): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
synonymous_variant | LOW | c.8598C>T | p.Cys2866Cys | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/22 | 8794/10779 | 8598/8913 | 2866/2970 | chr3 | 97941240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:97822026
|
C | A | 1 | a0012c0012t0006 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-181C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/22 | 181 | chr3 | 97822026 | |||||
| chr3:97822124
|
C | T | 1 | a0007c0009t0005 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-83C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/22 | 83 | chr3 | 97822124 | |||||
| chr3:97822174
|
C | T | 21 | a0001c0003t0002a0001c0004t0002a0001c0022t0002others(18): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/22 | 33 | chr3 | 97822174 | |||||
| chr3:97943349
|
A | G | 2 | a0007c0009t0005a0029c0053t0011 | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*35A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 35 | chr3 | 97943349 | |||||
| chr3:97943362
|
A | G | 1 | a0002c0001t0010 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 48 | chr3 | 97943362 | |||||
| chr3:97943363
|
C | T | 1 | a0015c0020t0009 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*49C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 49 | chr3 | 97943363 | |||||
| chr3:97943475
|
T | C | 2 | a0002c0001t0007a0002c0026t0007 | 3 | HG02615.hp2 HG02809.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 161 | chr3 | 97943475 | |||||
| chr3:97943762
|
A | AGAT | 25 | a0001c0003t0002a0001c0004t0002a0001c0022t0002others(22): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*451_*453dupTGA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 454 | INFO_REALIGN_3_PRIME | chr3 | 97943762 | ||||
| chr3:97944074
|
T | A | 1 | a0007c0009t0005 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*760T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 760 | chr3 | 97944074 | |||||
| chr3:97944175
|
C | A | 2 | a0007c0009t0005a0029c0053t0011 | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*861C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 861 | chr3 | 97944175 | |||||
| chr3:97944223
|
TA | T | 1 | a0012c0012t0006 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 912 | INFO_REALIGN_3_PRIME | chr3 | 97944223 | ||||
| chr3:97944360
|
T | G | 1 | a0017c0017t0008 | 2 | HG02258.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1046T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 1046 | chr3 | 97944360 | |||||
| chr3:97944834
|
A | C | 1 | a0029c0053t0011 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 1520 | chr3 | 97944834 | |||||
| chr3:97944842
|
A | C | 1 | a0005c0006t0004 | 7 | HG01943.hp2 HG04115.hp2 NA18971.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1528A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 22/22 | 1528 | chr3 | 97944842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:97822651
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149+296A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97822651 | ||||||
| chr3:97823011
|
C | T | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.149+656C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97823011 | ||||||
| chr3:97823021
|
T | C | 1 | a0001c0003t0002g0166 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.149+666T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97823021 | ||||||
| chr3:97823053
|
G | T | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+698G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97823053 | ||||||
| chr3:97823395
|
T | C | 3 | a0001c0004t0002g0168a0013c0021t0002g0167a0013c0021t0002g0169 | 3 | HG00621.hp2 NA18939.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.149+1040T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97823395 | ||||||
| chr3:97823801
|
A | G | 1 | a0001c0003t0002g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.149+1446A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97823801 | ||||||
| chr3:97824046
|
C | T | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+1691C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824046 | ||||||
| chr3:97824338
|
A | G | 1 | a0002c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.149+1983A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824338 | ||||||
| chr3:97824373
|
T | C | 1 | a0003c0002t0001g0037 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.149+2018T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824373 | ||||||
| chr3:97824445
|
A | G | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.149+2090A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824445 | ||||||
| chr3:97824644
|
C | A | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.149+2289C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824644 | ||||||
| chr3:97824684
|
A | C | 1 | a0002c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.149+2329A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824684 | ||||||
| chr3:97824771
|
A | G | 1 | a0001c0003t0002g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.149+2416A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824771 | ||||||
| chr3:97824879
|
A | G | 2 | a0007c0009t0005g0254a0007c0009t0005g0255 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.149+2524A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97824879 | ||||||
| chr3:97825106
|
A | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.149+2751A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825106 | ||||||
| chr3:97825332
|
T | A | 1 | a0026c0033t0002g0170 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.149+2977T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825332 | ||||||
| chr3:97825400
|
C | G | 5 | a0004c0005t0001g0027a0004c0005t0001g0162a0004c0005t0001g0163others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+3045C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825400 | ||||||
| chr3:97825481
|
C | G | 1 | a0003c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.149+3126C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825481 | ||||||
| chr3:97825484
|
T | C | 254 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(251): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.149+3129T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825484 | ||||||
| chr3:97825560
|
A | G | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+3205A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825560 | ||||||
| chr3:97825651
|
G | A | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.149+3296G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97825651 | ||||||
| chr3:97826055
|
C | T | 223 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(220): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.149+3700C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97826055 | ||||||
| chr3:97826401
|
T | G | 14 | a0002c0001t0001g0108a0002c0001t0001g0109a0002c0007t0001g0100others(11): Show | 16 | HG00423.hp2 HG00733.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.149+4046T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97826401 | ||||||
| chr3:97826490
|
C | T | 1 | a0008c0015t0003g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.149+4135C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97826490 | ||||||
| chr3:97826700
|
A | G | 1 | a0005c0006t0004g0253 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.149+4345A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97826700 | ||||||
| chr3:97827129
|
C | T | 2 | a0001c0003t0002g0036a0001c0003t0002g0252 | 3 | HG02723.hp2 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.149+4774C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827129 | ||||||
| chr3:97827232
|
G | C | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.149+4877G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827232 | ||||||
| chr3:97827366
|
A | C | 1 | a0002c0001t0001g0099 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.149+5011A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827366 | ||||||
| chr3:97827536
|
A | G | 1 | a0002c0001t0001g0146 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.149+5181A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827536 | ||||||
| chr3:97827671
|
G | A | 1 | a0001c0003t0002g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.149+5316G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827671 | ||||||
| chr3:97827724
|
G | A | 1 | a0001c0004t0002g0009 | 3 | NA18954.hp2 NA18970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.149+5369G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827724 | ||||||
| chr3:97827773
|
A | G | 3 | a0002c0001t0001g0097a0002c0001t0010g0096a0035c0040t0001g0098 | 3 | HG03239.hp2 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.149+5418A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827773 | ||||||
| chr3:97827783
|
CAA | C | 103 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(100): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.149+5431_149+5432d others(4): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97827783 | |||||
| chr3:97827849
|
A | T | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+5494A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827849 | ||||||
| chr3:97827874
|
T | C | 1 | a0002c0001t0007g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.149+5519T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827874 | ||||||
| chr3:97827875
|
T | A | 1 | a0003c0002t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.149+5520T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97827875 | ||||||
| chr3:97828119
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149+5764C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828119 | ||||||
| chr3:97828140
|
A | T | 1 | a0003c0002t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.149+5785A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828140 | ||||||
| chr3:97828141
|
C | A | 1 | a0003c0002t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.149+5786C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828141 | ||||||
| chr3:97828236
|
A | C | 1 | a0002c0011t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.149+5881A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828236 | ||||||
| chr3:97828252
|
A | G | 1 | a0002c0001t0001g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.149+5897A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828252 | ||||||
| chr3:97828366
|
G | A | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.149+6011G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828366 | ||||||
| chr3:97828457
|
A | G | 1 | a0002c0011t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.149+6102A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828457 | ||||||
| chr3:97828528
|
T | TA | 22 | a0001c0003t0002g0174a0001c0003t0002g0175a0001c0004t0002g0173others(19): Show | 22 | HG00423.hp2 HG00733.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.149+6190dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97828528 | |||||
| chr3:97828659
|
T | A | 3 | a0002c0026t0007g0114a0008c0015t0003g0115a0008c0015t0003g0139 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.149+6304T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828659 | ||||||
| chr3:97828718
|
T | C | 1 | a0023c0028t0002g0176 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.149+6363T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828718 | ||||||
| chr3:97828724
|
A | T | 1 | a0003c0002t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.149+6369A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97828724 | ||||||
| chr3:97828828
|
C | CA | 48 | a0001c0004t0002g0179a0001c0004t0002g0180a0001c0022t0002g0178others(45): Show | 64 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.149+6490dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97828828 | |||||
| chr3:97828828
|
CA | C | 83 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(80): Show | 96 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.149+6490delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97828828 | |||||
| chr3:97828867
|
CAAAA | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.149+6518_149+6521d others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97828867 | |||||
| chr3:97829188
|
G | C | 1 | a0001c0003t0002g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.149+6833G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97829188 | ||||||
| chr3:97829479
|
T | A | 2 | a0006c0008t0001g0151a0006c0008t0001g0152 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.149+7124T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97829479 | ||||||
| chr3:97829779
|
A | G | 1 | a0035c0040t0001g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.149+7424A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97829779 | ||||||
| chr3:97829817
|
A | G | 1 | a0002c0018t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.149+7462A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97829817 | ||||||
| chr3:97830064
|
A | G | 1 | a0001c0003t0002g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.149+7709A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830064 | ||||||
| chr3:97830167
|
C | T | 1 | a0003c0002t0001g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149+7812C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830167 | ||||||
| chr3:97830205
|
G | T | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.149+7850G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830205 | ||||||
| chr3:97830252
|
G | T | 1 | a0002c0007t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.149+7897G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830252 | ||||||
| chr3:97830431
|
T | C | 1 | a0002c0007t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.149+8076T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830431 | ||||||
| chr3:97830464
|
C | G | 1 | a0001c0004t0002g0009 | 3 | NA18954.hp2 NA18970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.149+8109C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830464 | ||||||
| chr3:97830466
|
T | C | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+8111T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830466 | ||||||
| chr3:97830470
|
TCTTGGTT others(8): Show |
T | 2 | a0032c0038t0003g0138a0033c0037t0001g0137 | 2 | HG01256.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.149+8119_149+8133d others(17): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97830470 | |||||
| chr3:97830571
|
T | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.149+8216T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830571 | ||||||
| chr3:97830639
|
T | G | 1 | a0003c0002t0001g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.149+8284T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97830639 | ||||||
| chr3:97831016
|
A | G | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.149+8661A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831016 | ||||||
| chr3:97831174
|
A | T | 1 | a0003c0002t0001g0068 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+8819A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831174 | ||||||
| chr3:97831254
|
C | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149+8899C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831254 | ||||||
| chr3:97831258
|
G | A | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.149+8903G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831258 | ||||||
| chr3:97831519
|
A | G | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.149+9164A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831519 | ||||||
| chr3:97831699
|
G | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+9344G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831699 | ||||||
| chr3:97831883
|
C | G | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+9528C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97831883 | ||||||
| chr3:97832005
|
T | G | 163 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(160): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.149+9650T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832005 | ||||||
| chr3:97832169
|
C | G | 1 | a0003c0002t0001g0067 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.149+9814C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832169 | ||||||
| chr3:97832227
|
C | CA | 19 | a0001c0004t0002g0028a0001c0004t0002g0168a0001c0004t0002g0181others(16): Show | 21 | HG00621.hp2 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.149+9889dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97832227 | |||||
| chr3:97832348
|
A | G | 1 | a0002c0007t0001g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.149+9993A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832348 | ||||||
| chr3:97832471
|
G | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.149+10116G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832471 | ||||||
| chr3:97832492
|
G | A | 4 | a0003c0002t0001g0004a0003c0002t0001g0007a0003c0002t0001g0040others(1): Show | 9 | NA18944.hp1 NA18945.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+10137G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832492 | ||||||
| chr3:97832510
|
A | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+10155A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832510 | ||||||
| chr3:97832727
|
A | G | 1 | a0002c0018t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.149+10372A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832727 | ||||||
| chr3:97832964
|
A | G | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-10231A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97832964 | ||||||
| chr3:97833039
|
T | C | 169 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.150-10156T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833039 | ||||||
| chr3:97833052
|
A | T | 1 | a0001c0004t0002g0250 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.150-10143A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833052 | ||||||
| chr3:97833316
|
A | G | 1 | a0003c0002t0001g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.150-9879A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833316 | ||||||
| chr3:97833338
|
A | G | 1 | a0001c0003t0002g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.150-9857A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833338 | ||||||
| chr3:97833346
|
A | T | 1 | a0001c0004t0002g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.150-9849A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833346 | ||||||
| chr3:97833410
|
C | T | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150-9785C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833410 | ||||||
| chr3:97833564
|
G | A | 1 | a0004c0005t0001g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.150-9631G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833564 | ||||||
| chr3:97833619
|
A | G | 3 | a0002c0007t0001g0103a0002c0007t0001g0105a0002c0007t0001g0111 | 3 | HG02717.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.150-9576A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833619 | ||||||
| chr3:97833673
|
A | G | 1 | a0035c0040t0001g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.150-9522A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833673 | ||||||
| chr3:97833878
|
G | A | 1 | a0002c0001t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-9317G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97833878 | ||||||
| chr3:97834084
|
C | G | 1 | a0002c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.150-9111C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834084 | ||||||
| chr3:97834152
|
C | G | 2 | a0001c0003t0002g0247a0001c0003t0002g0248 | 2 | HG02004.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.150-9043C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834152 | ||||||
| chr3:97834417
|
G | T | 192 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(189): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.150-8778G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834417 | ||||||
| chr3:97834784
|
C | T | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.150-8411C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834784 | ||||||
| chr3:97834823
|
C | T | 2 | a0001c0004t0002g0245a0039c0048t0002g0246 | 2 | HG01168.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.150-8372C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834823 | ||||||
| chr3:97834879
|
A | T | 1 | a0002c0018t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.150-8316A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834879 | ||||||
| chr3:97834916
|
A | G | 3 | a0002c0026t0007g0114a0008c0015t0003g0115a0008c0015t0003g0139 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.150-8279A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97834916 | ||||||
| chr3:97835121
|
G | A | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-8074G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835121 | ||||||
| chr3:97835314
|
A | G | 3 | a0003c0002t0001g0004a0003c0002t0001g0007a0003c0002t0001g0041 | 8 | NA18944.hp1 NA18945.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-7881A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835314 | ||||||
| chr3:97835479
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150-7716G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835479 | ||||||
| chr3:97835509
|
G | C | 2 | a0002c0001t0001g0078a0002c0001t0001g0079 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.150-7686G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835509 | ||||||
| chr3:97835668
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150-7527T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835668 | ||||||
| chr3:97835869
|
A | T | 1 | a0001c0003t0002g0244 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.150-7326A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835869 | ||||||
| chr3:97835918
|
A | G | 1 | a0006c0008t0001g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-7277A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97835918 | ||||||
| chr3:97836018
|
G | T | 1 | a0001c0004t0002g0243 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150-7177G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836018 | ||||||
| chr3:97836081
|
G | A | 1 | a0005c0006t0004g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.150-7114G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836081 | ||||||
| chr3:97836287
|
A | G | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-6908A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836287 | ||||||
| chr3:97836514
|
C | T | 3 | a0002c0007t0001g0103a0002c0007t0001g0105a0002c0007t0001g0111 | 3 | HG02717.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.150-6681C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836514 | ||||||
| chr3:97836599
|
A | G | 1 | a0003c0002t0001g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.150-6596A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836599 | ||||||
| chr3:97836651
|
A | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150-6544A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836651 | ||||||
| chr3:97836667
|
A | G | 1 | a0001c0003t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150-6528A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836667 | ||||||
| chr3:97836954
|
T | A | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.150-6241T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97836954 | ||||||
| chr3:97837148
|
G | A | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-6047G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97837148 | ||||||
| chr3:97837194
|
T | C | 1 | a0001c0004t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.150-6001T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97837194 | ||||||
| chr3:97837228
|
G | A | 13 | a0002c0001t0001g0108a0002c0001t0001g0109a0002c0007t0001g0100others(10): Show | 13 | HG00423.hp2 HG00733.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-5967G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97837228 | ||||||
| chr3:97837816
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150-5379A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97837816 | ||||||
| chr3:97837875
|
C | T | 169 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.150-5320C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97837875 | ||||||
| chr3:97838211
|
G | A | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-4984G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838211 | ||||||
| chr3:97838231
|
A | C | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.150-4964A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838231 | ||||||
| chr3:97838339
|
C | T | 1 | a0001c0003t0002g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.150-4856C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838339 | ||||||
| chr3:97838376
|
T | C | 1 | a0002c0001t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.150-4819T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838376 | ||||||
| chr3:97838542
|
G | A | 1 | a0003c0002t0001g0042 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.150-4653G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838542 | ||||||
| chr3:97838616
|
A | G | 15 | a0002c0001t0001g0108a0002c0001t0001g0109a0002c0007t0001g0100others(12): Show | 18 | HG00423.hp2 HG00733.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.150-4579A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838616 | ||||||
| chr3:97838624
|
C | T | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150-4571C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838624 | ||||||
| chr3:97838657
|
T | C | 40 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(37): Show | 47 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.150-4538T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838657 | ||||||
| chr3:97838927
|
C | T | 1 | a0001c0003t0002g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.150-4268C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97838927 | ||||||
| chr3:97839067
|
T | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-4128T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839067 | ||||||
| chr3:97839092
|
C | G | 1 | a0002c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-4103C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839092 | ||||||
| chr3:97839332
|
A | G | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150-3863A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839332 | ||||||
| chr3:97839451
|
T | G | 1 | a0001c0003t0002g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.150-3744T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839451 | ||||||
| chr3:97839707
|
C | T | 1 | a0003c0002t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.150-3488C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839707 | ||||||
| chr3:97839708
|
G | A | 10 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(7): Show | 13 | HG00642.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-3487G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839708 | ||||||
| chr3:97839755
|
CT | C | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150-3428delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97839755 | |||||
| chr3:97839756
|
T | C | 2 | a0001c0003t0002g0256a0029c0053t0011g0258 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.150-3439T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839756 | ||||||
| chr3:97839884
|
T | C | 1 | a0001c0003t0002g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.150-3311T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839884 | ||||||
| chr3:97839931
|
C | T | 7 | a0002c0001t0001g0025a0002c0001t0001g0130a0002c0001t0001g0131others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-3264C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97839931 | ||||||
| chr3:97840158
|
A | G | 1 | a0005c0006t0004g0241 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.150-3037A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97840158 | ||||||
| chr3:97840441
|
T | G | 1 | a0007c0009t0005g0035 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.150-2754T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97840441 | ||||||
| chr3:97840498
|
T | C | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.150-2697T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97840498 | ||||||
| chr3:97840755
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150-2440C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97840755 | ||||||
| chr3:97841092
|
A | G | 3 | a0002c0001t0001g0133a0002c0001t0001g0134a0002c0001t0001g0135 | 3 | HG03130.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.150-2103A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841092 | ||||||
| chr3:97841192
|
G | GTGTATAT others(1): Show |
6 | a0001c0003t0002g0030a0001c0003t0002g0202a0001c0003t0002g0203others(3): Show | 7 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-1979_150-1972d others(10): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97841192 | |||||
| chr3:97841192
|
GTGTATAT others(1): Show |
G | 6 | a0001c0003t0002g0240a0001c0004t0002g0185a0007c0009t0005g0035others(3): Show | 7 | HG00733.hp2 HG00735.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-1979_150-1972d others(10): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97841192 | |||||
| chr3:97841218
|
G | GTATATGT others(19): Show |
9 | a0002c0018t0001g0159a0006c0008t0001g0151a0006c0008t0001g0152others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-1959_150-1934d others(28): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97841218 | |||||
| chr3:97841241
|
T | C | 1 | a0001c0003t0002g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.150-1954T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841241 | ||||||
| chr3:97841241
|
TACATATA others(17): Show |
T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-1942_150-1919d others(26): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97841241 | |||||
| chr3:97841296
|
A | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.150-1899A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841296 | ||||||
| chr3:97841319
|
C | T | 1 | a0002c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.150-1876C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841319 | ||||||
| chr3:97841342
|
A | G | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.150-1853A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841342 | ||||||
| chr3:97841492
|
TTTG | T | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-1700_150-1698d others(5): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 97841492 | |||||
| chr3:97841621
|
A | G | 169 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.150-1574A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841621 | ||||||
| chr3:97841754
|
C | T | 2 | a0003c0002t0001g0042a0003c0002t0001g0064 | 2 | HG01123.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.150-1441C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841754 | ||||||
| chr3:97841913
|
T | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.150-1282T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841913 | ||||||
| chr3:97841983
|
G | A | 1 | a0001c0032t0002g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.150-1212G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97841983 | ||||||
| chr3:97842233
|
T | A | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-962T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842233 | ||||||
| chr3:97842272
|
A | G | 1 | a0006c0008t0001g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.150-923A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842272 | ||||||
| chr3:97842373
|
G | T | 1 | a0042c0023t0001g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.150-822G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842373 | ||||||
| chr3:97842477
|
C | T | 1 | a0002c0001t0001g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150-718C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842477 | ||||||
| chr3:97842497
|
A | G | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.150-698A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842497 | ||||||
| chr3:97842542
|
A | C | 1 | a0002c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.150-653A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842542 | ||||||
| chr3:97842677
|
T | C | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-518T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97842677 | ||||||
| chr3:97843065
|
G | A | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.150-130G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 1/21 | chr3 | 97843065 | ||||||
| chr3:97843367
|
A | G | 5 | a0001c0003t0002g0242a0002c0001t0001g0025a0002c0001t0001g0130others(2): Show | 6 | HG01884.hp2 HG02109.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+106A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97843367 | ||||||
| chr3:97843921
|
A | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+660A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97843921 | ||||||
| chr3:97843996
|
G | A | 1 | a0024c0034t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.216+735G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97843996 | ||||||
| chr3:97844388
|
C | T | 1 | a0003c0002t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.216+1127C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844388 | ||||||
| chr3:97844527
|
A | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+1266A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844527 | ||||||
| chr3:97844541
|
C | T | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.216+1280C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844541 | ||||||
| chr3:97844601
|
C | T | 1 | a0002c0001t0001g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.216+1340C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844601 | ||||||
| chr3:97844736
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+1475C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844736 | ||||||
| chr3:97844953
|
C | T | 1 | a0002c0001t0001g0078 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.216+1692C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844953 | ||||||
| chr3:97844967
|
T | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.216+1706T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97844967 | ||||||
| chr3:97845060
|
C | T | 1 | a0002c0001t0001g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.216+1799C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845060 | ||||||
| chr3:97845221
|
A | G | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216+1960A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845221 | ||||||
| chr3:97845263
|
C | A | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+2002C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845263 | ||||||
| chr3:97845458
|
A | G | 1 | a0002c0011t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.216+2197A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845458 | ||||||
| chr3:97845522
|
T | C | 1 | a0001c0003t0002g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.216+2261T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845522 | ||||||
| chr3:97845633
|
C | T | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.216+2372C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845633 | ||||||
| chr3:97845674
|
C | A | 1 | a0002c0001t0001g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.216+2413C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845674 | ||||||
| chr3:97845730
|
C | T | 1 | a0001c0004t0002g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.216+2469C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845730 | ||||||
| chr3:97845815
|
A | T | 1 | a0003c0002t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.216+2554A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845815 | ||||||
| chr3:97845899
|
CT | C | 3 | a0006c0008t0001g0153a0006c0008t0001g0154a0006c0008t0001g0157 | 3 | HG02886.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.216+2642delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97845899 | |||||
| chr3:97845966
|
G | A | 1 | a0003c0002t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.216+2705G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97845966 | ||||||
| chr3:97846320
|
T | C | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.216+3059T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97846320 | ||||||
| chr3:97846582
|
A | G | 10 | a0002c0001t0001g0121a0002c0001t0001g0122a0002c0001t0001g0125others(7): Show | 10 | HG01175.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+3321A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97846582 | ||||||
| chr3:97846744
|
A | G | 1 | a0002c0001t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.216+3483A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97846744 | ||||||
| chr3:97846921
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+3660G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97846921 | ||||||
| chr3:97847064
|
G | A | 49 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(46): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.216+3803G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847064 | ||||||
| chr3:97847421
|
A | G | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+4160A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847421 | ||||||
| chr3:97847448
|
T | A | 1 | a0003c0002t0001g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.216+4187T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847448 | ||||||
| chr3:97847480
|
C | T | 2 | a0002c0001t0001g0025a0002c0001t0001g0132 | 3 | HG01884.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.216+4219C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847480 | ||||||
| chr3:97847507
|
C | T | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+4246C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847507 | ||||||
| chr3:97847508
|
G | A | 1 | a0002c0001t0001g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.216+4247G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847508 | ||||||
| chr3:97847583
|
G | A | 162 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(159): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.216+4322G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847583 | ||||||
| chr3:97847729
|
G | A | 254 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(251): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.216+4468G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847729 | ||||||
| chr3:97847738
|
C | T | 3 | a0001c0004t0002g0033a0001c0004t0002g0239a0001c0004t0002g0250 | 4 | NA18939.hp2 NA18945.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+4477C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847738 | ||||||
| chr3:97847944
|
A | G | 2 | a0002c0001t0001g0024a0002c0001t0001g0120 | 3 | HG02976.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.216+4683A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97847944 | ||||||
| chr3:97848063
|
G | A | 1 | a0010c0013t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+4802G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848063 | ||||||
| chr3:97848168
|
C | T | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216+4907C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848168 | ||||||
| chr3:97848203
|
A | C | 1 | a0002c0001t0001g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.216+4942A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848203 | ||||||
| chr3:97848254
|
T | A | 1 | a0020c0050t0001g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.216+4993T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848254 | ||||||
| chr3:97848363
|
G | A | 2 | a0003c0002t0001g0045a0003c0002t0001g0046 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.216+5102G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848363 | ||||||
| chr3:97848522
|
C | T | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+5261C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848522 | ||||||
| chr3:97848542
|
C | T | 1 | a0002c0001t0001g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.216+5281C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848542 | ||||||
| chr3:97848544
|
G | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.216+5283G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848544 | ||||||
| chr3:97848559
|
C | A | 2 | a0002c0001t0001g0024a0002c0001t0001g0120 | 3 | HG02976.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.216+5298C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848559 | ||||||
| chr3:97848605
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5344T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848605 | ||||||
| chr3:97848607
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5346T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848607 | ||||||
| chr3:97848608
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5347T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848608 | ||||||
| chr3:97848609
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5348T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848609 | ||||||
| chr3:97848610
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5349T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848610 | ||||||
| chr3:97848612
|
T | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5351T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848612 | ||||||
| chr3:97848723
|
C | T | 13 | a0002c0001t0001g0108a0002c0001t0001g0109a0002c0007t0001g0100others(10): Show | 13 | HG00423.hp2 HG00733.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.216+5462C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848723 | ||||||
| chr3:97848730
|
T | C | 169 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.216+5469T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848730 | ||||||
| chr3:97848778
|
G | A | 26 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0116others(23): Show | 28 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.216+5517G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97848778 | ||||||
| chr3:97849174
|
A | G | 1 | a0003c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.216+5913A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97849174 | ||||||
| chr3:97849438
|
T | TA | 7 | a0006c0008t0001g0151a0006c0008t0001g0152a0006c0008t0001g0153others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+6188dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97849438 | |||||
| chr3:97849719
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+6458T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97849719 | ||||||
| chr3:97849751
|
T | G | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+6490T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97849751 | ||||||
| chr3:97850035
|
A | G | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.216+6774A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97850035 | ||||||
| chr3:97850215
|
G | A | 2 | a0002c0001t0001g0130a0002c0001t0001g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.216+6954G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97850215 | ||||||
| chr3:97850225
|
C | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.216+6964C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97850225 | ||||||
| chr3:97850697
|
C | T | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.216+7436C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97850697 | ||||||
| chr3:97851082
|
G | A | 1 | a0002c0001t0001g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.216+7821G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851082 | ||||||
| chr3:97851131
|
C | CA | 96 | a0001c0003t0002g0031a0001c0004t0002g0186a0001c0022t0002g0187others(93): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.216+7889dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97851131 | |||||
| chr3:97851131
|
C | CAA | 6 | a0002c0001t0001g0077a0002c0001t0001g0082a0002c0007t0001g0100others(3): Show | 6 | HG02165.hp2 HG04184.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+7888_216+7889d others(4): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97851131 | |||||
| chr3:97851172
|
A | G | 7 | a0006c0008t0001g0151a0006c0008t0001g0152a0006c0008t0001g0153others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+7911A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851172 | ||||||
| chr3:97851291
|
A | C | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.216+8030A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851291 | ||||||
| chr3:97851428
|
A | G | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.216+8167A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851428 | ||||||
| chr3:97851602
|
G | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.216+8341G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851602 | ||||||
| chr3:97851691
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+8430G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851691 | ||||||
| chr3:97851920
|
C | G | 1 | a0005c0006t0004g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.216+8659C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97851920 | ||||||
| chr3:97852025
|
C | T | 27 | a0003c0002t0001g0014a0003c0002t0001g0015a0003c0002t0001g0016others(24): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+8764C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97852025 | ||||||
| chr3:97852909
|
A | C | 26 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0116others(23): Show | 28 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.216+9648A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97852909 | ||||||
| chr3:97853148
|
A | G | 28 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0116others(25): Show | 30 | HG01175.hp1 HG01256.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.216+9887A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853148 | ||||||
| chr3:97853324
|
G | A | 1 | a0005c0006t0004g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.216+10063G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853324 | ||||||
| chr3:97853331
|
C | T | 1 | a0001c0004t0002g0238 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.216+10070C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853331 | ||||||
| chr3:97853392
|
A | C | 1 | a0002c0018t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.216+10131A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853392 | ||||||
| chr3:97853406
|
T | TAC | 11 | a0003c0002t0001g0067a0004c0005t0001g0027a0004c0005t0001g0161others(8): Show | 12 | HG00642.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.216+10176_216+1017 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
T | TACAC | 42 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(39): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.216+10174_216+1017 others(8): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
T | TACACAC | 5 | a0003c0002t0001g0037a0003c0002t0001g0053a0003c0002t0001g0069others(2): Show | 5 | HG00741.hp2 HG02055.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+10172_216+1017 others(10): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
TAC | T | 24 | a0001c0004t0002g0188a0001c0004t0002g0243a0002c0001t0001g0023others(21): Show | 26 | HG00423.hp2 HG00733.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.216+10176_216+1017 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
TACAC | T | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.216+10174_216+1017 others(8): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
TACACAC | T | 3 | a0001c0003t0002g0222a0002c0001t0001g0108a0002c0001t0001g0109 | 3 | HG02572.hp1 HG02622.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.216+10172_216+1017 others(10): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853406
|
TACACACA others(3): Show |
T | 1 | a0006c0008t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.216+10168_216+1017 others(14): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97853406 | |||||
| chr3:97853517
|
A | C | 1 | a0025c0035t0002g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.216+10256A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853517 | ||||||
| chr3:97853523
|
G | A | 1 | a0001c0003t0002g0209 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.216+10262G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853523 | ||||||
| chr3:97853588
|
T | C | 23 | a0002c0001t0001g0108a0002c0001t0001g0109a0002c0007t0001g0100others(20): Show | 23 | HG00423.hp2 HG00733.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.216+10327T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853588 | ||||||
| chr3:97853703
|
A | C | 169 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.216+10442A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853703 | ||||||
| chr3:97853707
|
C | T | 7 | a0006c0008t0001g0151a0006c0008t0001g0152a0006c0008t0001g0153others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+10446C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853707 | ||||||
| chr3:97853851
|
C | CAT | 192 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(189): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.217-10366_217-1036 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97853851 | ||||||
| chr3:97854264
|
A | G | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.217-9953A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97854264 | ||||||
| chr3:97854591
|
A | AT | 14 | a0001c0003t0002g0220a0001c0003t0002g0242a0001c0004t0002g0237others(11): Show | 15 | HG00558.hp1 HG00642.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.217-9611dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97854591 | |||||
| chr3:97854591
|
AT | A | 69 | a0001c0004t0002g0238a0002c0001t0001g0108a0002c0001t0001g0109others(66): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.217-9611delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97854591 | |||||
| chr3:97854850
|
C | A | 1 | a0001c0003t0002g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.217-9367C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97854850 | ||||||
| chr3:97854893
|
G | C | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-9324G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97854893 | ||||||
| chr3:97855195
|
T | C | 1 | a0003c0002t0001g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.217-9022T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855195 | ||||||
| chr3:97855215
|
T | A | 1 | a0002c0007t0001g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217-9002T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855215 | ||||||
| chr3:97855245
|
T | C | 1 | a0002c0007t0001g0100 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.217-8972T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855245 | ||||||
| chr3:97855310
|
T | G | 1 | a0007c0009t0005g0035 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.217-8907T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855310 | ||||||
| chr3:97855646
|
G | T | 1 | a0020c0050t0001g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.217-8571G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855646 | ||||||
| chr3:97855702
|
G | A | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.217-8515G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855702 | ||||||
| chr3:97855871
|
C | T | 9 | a0002c0018t0001g0158a0006c0008t0001g0151a0006c0008t0001g0152others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-8346C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855871 | ||||||
| chr3:97855939
|
T | C | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.217-8278T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855939 | ||||||
| chr3:97855980
|
G | A | 1 | a0001c0004t0002g0188 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.217-8237G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97855980 | ||||||
| chr3:97856152
|
T | A | 1 | a0001c0003t0002g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.217-8065T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856152 | ||||||
| chr3:97856168
|
A | G | 2 | a0006c0008t0001g0151a0006c0008t0001g0152 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.217-8049A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856168 | ||||||
| chr3:97856354
|
G | T | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.217-7863G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856354 | ||||||
| chr3:97856390
|
G | C | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.217-7827G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856390 | ||||||
| chr3:97856579
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-7638G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856579 | ||||||
| chr3:97856628
|
C | T | 1 | a0028c0027t0002g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.217-7589C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856628 | ||||||
| chr3:97856755
|
C | T | 3 | a0003c0002t0001g0043a0003c0002t0001g0052a0003c0002t0001g0147 | 3 | HG00597.hp2 HG02129.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.217-7462C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856755 | ||||||
| chr3:97856850
|
G | A | 2 | a0005c0006t0004g0201a0005c0006t0004g0225 | 2 | NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.217-7367G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97856850 | ||||||
| chr3:97857094
|
T | A | 5 | a0001c0004t0002g0181a0001c0004t0002g0182a0001c0004t0002g0183others(2): Show | 5 | NA18943.hp2 NA18990.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-7123T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857094 | ||||||
| chr3:97857184
|
A | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-7033A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857184 | ||||||
| chr3:97857298
|
G | A | 1 | a0002c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.217-6919G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857298 | ||||||
| chr3:97857332
|
A | T | 1 | a0001c0003t0002g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.217-6885A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857332 | ||||||
| chr3:97857740
|
C | T | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.217-6477C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857740 | ||||||
| chr3:97857741
|
A | G | 2 | a0001c0003t0002g0235a0001c0003t0002g0240 | 2 | HG00735.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.217-6476A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97857741 | ||||||
| chr3:97858038
|
C | T | 1 | a0020c0050t0001g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.217-6179C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858038 | ||||||
| chr3:97858165
|
GT | G | 238 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.217-6037delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97858165 | |||||
| chr3:97858165
|
GTT | G | 5 | a0002c0001t0001g0005a0002c0001t0001g0023a0002c0001t0001g0084others(2): Show | 9 | HG00558.hp2 HG00597.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-6038_217-6037d others(4): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97858165 | |||||
| chr3:97858186
|
G | A | 162 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(159): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.217-6031G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858186 | ||||||
| chr3:97858268
|
C | T | 1 | a0001c0004t0002g0195 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.217-5949C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858268 | ||||||
| chr3:97858275
|
T | C | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.217-5942T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858275 | ||||||
| chr3:97858549
|
A | T | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-5668A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858549 | ||||||
| chr3:97858844
|
A | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-5373A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97858844 | ||||||
| chr3:97858971
|
A | AT | 51 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(48): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.217-5240dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97858971 | |||||
| chr3:97859035
|
G | A | 1 | a0001c0004t0002g0250 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.217-5182G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97859035 | ||||||
| chr3:97859288
|
G | A | 1 | a0003c0002t0001g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.217-4929G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97859288 | ||||||
| chr3:97859549
|
A | G | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-4668A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97859549 | ||||||
| chr3:97859709
|
T | C | 4 | a0001c0003t0002g0227a0001c0003t0002g0247a0001c0003t0002g0248others(1): Show | 4 | HG02004.hp1 HG02602.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-4508T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97859709 | ||||||
| chr3:97859734
|
T | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-4483T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97859734 | ||||||
| chr3:97860132
|
A | G | 3 | a0002c0001t0001g0125a0002c0001t0001g0126a0002c0001t0001g0127 | 3 | HG01175.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.217-4085A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97860132 | ||||||
| chr3:97860806
|
A | C | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.217-3411A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97860806 | ||||||
| chr3:97860927
|
T | C | 1 | a0001c0004t0002g0185 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.217-3290T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97860927 | ||||||
| chr3:97860976
|
T | C | 2 | a0002c0001t0001g0025a0002c0001t0001g0132 | 3 | HG01884.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.217-3241T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97860976 | ||||||
| chr3:97861037
|
A | AT | 8 | a0002c0001t0001g0116a0002c0001t0001g0117a0002c0001t0001g0118others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.217-3172dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97861037 | |||||
| chr3:97861390
|
A | C | 1 | a0024c0034t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.217-2827A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861390 | ||||||
| chr3:97861539
|
A | C | 3 | a0002c0026t0007g0114a0008c0015t0003g0115a0008c0015t0003g0139 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.217-2678A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861539 | ||||||
| chr3:97861647
|
A | C | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.217-2570A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861647 | ||||||
| chr3:97861740
|
G | A | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-2477G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861740 | ||||||
| chr3:97861747
|
G | A | 1 | a0013c0021t0002g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.217-2470G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861747 | ||||||
| chr3:97861945
|
A | G | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.217-2272A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861945 | ||||||
| chr3:97861951
|
G | A | 8 | a0001c0003t0002g0171a0004c0005t0001g0027a0004c0005t0001g0161others(5): Show | 10 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-2266G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97861951 | ||||||
| chr3:97862027
|
T | C | 1 | a0038c0047t0001g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.217-2190T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862027 | ||||||
| chr3:97862090
|
G | GT | 168 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(165): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.217-2117dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 97862090 | |||||
| chr3:97862099
|
T | A | 1 | a0002c0018t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.217-2118T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862099 | ||||||
| chr3:97862100
|
T | A | 12 | a0002c0001t0001g0079a0002c0018t0001g0158a0002c0018t0001g0159others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-2117T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862100 | ||||||
| chr3:97862101
|
A | T | 19 | a0001c0004t0002g0194a0002c0007t0001g0100a0002c0007t0001g0103others(16): Show | 21 | HG00423.hp2 HG00733.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.217-2116A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862101 | ||||||
| chr3:97862164
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-2053A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862164 | ||||||
| chr3:97862459
|
G | T | 4 | a0002c0001t0001g0116a0002c0001t0001g0117a0002c0001t0001g0118others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-1758G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862459 | ||||||
| chr3:97862500
|
A | G | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.217-1717A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862500 | ||||||
| chr3:97862675
|
C | T | 1 | a0004c0005t0001g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.217-1542C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862675 | ||||||
| chr3:97862778
|
ATCT | A | 221 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.217-1438_217-1436d others(5): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862778 | ||||||
| chr3:97862842
|
A | G | 49 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(46): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.217-1375A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97862842 | ||||||
| chr3:97863028
|
T | C | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.217-1189T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863028 | ||||||
| chr3:97863136
|
T | C | 1 | a0001c0003t0002g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.217-1081T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863136 | ||||||
| chr3:97863545
|
T | C | 1 | a0001c0003t0002g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.217-672T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863545 | ||||||
| chr3:97863579
|
C | T | 1 | a0001c0003t0002g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.217-638C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863579 | ||||||
| chr3:97863843
|
T | G | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-374T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863843 | ||||||
| chr3:97863984
|
G | A | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-233G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97863984 | ||||||
| chr3:97864020
|
A | G | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.217-197A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97864020 | ||||||
| chr3:97864026
|
C | T | 1 | a0003c0002t0001g0051 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.217-191C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97864026 | ||||||
| chr3:97864027
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-190G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97864027 | ||||||
| chr3:97864042
|
G | A | 2 | a0002c0007t0001g0103a0002c0007t0001g0111 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.217-175G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97864042 | ||||||
| chr3:97864173
|
T | A | 1 | a0001c0003t0002g0191 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.217-44T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 2/21 | chr3 | 97864173 | ||||||
| chr3:97864680
|
T | C | 13 | a0002c0001t0001g0121a0002c0001t0001g0122a0002c0001t0001g0125others(10): Show | 14 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.647+33T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97864680 | ||||||
| chr3:97864759
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.647+112T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97864759 | ||||||
| chr3:97864826
|
A | T | 3 | a0006c0008t0001g0153a0006c0008t0001g0154a0006c0008t0001g0157 | 3 | HG02886.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.647+179A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97864826 | ||||||
| chr3:97864832
|
A | G | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.647+185A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97864832 | ||||||
| chr3:97865247
|
T | C | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.647+600T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865247 | ||||||
| chr3:97865291
|
A | G | 1 | a0002c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.647+644A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865291 | ||||||
| chr3:97865399
|
A | G | 2 | a0003c0002t0001g0004a0003c0002t0001g0041 | 5 | NA18945.hp2 NA18984.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+752A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865399 | ||||||
| chr3:97865424
|
G | A | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+777G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865424 | ||||||
| chr3:97865495
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.647+848T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865495 | ||||||
| chr3:97865552
|
A | G | 2 | a0001c0003t0002g0032a0001c0003t0002g0234 | 3 | HG03139.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.647+905A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865552 | ||||||
| chr3:97865611
|
A | G | 1 | a0026c0033t0002g0170 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.647+964A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865611 | ||||||
| chr3:97865661
|
G | A | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.647+1014G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865661 | ||||||
| chr3:97865917
|
A | G | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.647+1270A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97865917 | ||||||
| chr3:97866050
|
A | G | 2 | a0001c0004t0002g0033a0001c0004t0002g0239 | 3 | NA18939.hp2 NA18945.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.647+1403A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866050 | ||||||
| chr3:97866080
|
A | G | 1 | a0003c0002t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.647+1433A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866080 | ||||||
| chr3:97866126
|
G | C | 2 | a0009c0014t0003g0013a0009c0014t0003g0055 | 3 | NA18970.hp1 NA18989.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.647+1479G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866126 | ||||||
| chr3:97866358
|
G | A | 221 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.647+1711G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866358 | ||||||
| chr3:97866451
|
G | A | 1 | a0003c0002t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.647+1804G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866451 | ||||||
| chr3:97866548
|
A | T | 1 | a0002c0001t0001g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.647+1901A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866548 | ||||||
| chr3:97866585
|
C | T | 1 | a0001c0004t0002g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.647+1938C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866585 | ||||||
| chr3:97866588
|
G | A | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.647+1941G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866588 | ||||||
| chr3:97866602
|
G | A | 10 | a0002c0001t0001g0121a0002c0001t0001g0122a0002c0001t0001g0125others(7): Show | 10 | HG01175.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.647+1955G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866602 | ||||||
| chr3:97866703
|
G | A | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.647+2056G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866703 | ||||||
| chr3:97866764
|
T | C | 4 | a0003c0002t0001g0074a0009c0014t0003g0013a0009c0014t0003g0055others(1): Show | 5 | HG02135.hp2 NA18970.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+2117T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97866764 | ||||||
| chr3:97867127
|
A | G | 1 | a0001c0004t0002g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.647+2480A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867127 | ||||||
| chr3:97867187
|
C | A | 5 | a0003c0002t0001g0014a0003c0002t0001g0057a0003c0002t0001g0058others(2): Show | 6 | HG01243.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+2540C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867187 | ||||||
| chr3:97867189
|
G | A | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.647+2542G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867189 | ||||||
| chr3:97867217
|
A | AT | 49 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(46): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.647+2579dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 97867217 | |||||
| chr3:97867388
|
A | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+2741A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867388 | ||||||
| chr3:97867403
|
T | C | 109 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(106): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.647+2756T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867403 | ||||||
| chr3:97867611
|
A | G | 1 | a0003c0002t0001g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.647+2964A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867611 | ||||||
| chr3:97867672
|
T | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.647+3025T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97867672 | ||||||
| chr3:97868000
|
G | T | 1 | a0002c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.647+3353G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868000 | ||||||
| chr3:97868058
|
C | T | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+3411C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868058 | ||||||
| chr3:97868201
|
G | A | 1 | a0033c0037t0001g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.647+3554G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868201 | ||||||
| chr3:97868233
|
G | A | 1 | a0001c0003t0002g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.647+3586G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868233 | ||||||
| chr3:97868283
|
C | CA | 103 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(100): Show | 122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.648-3542dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 97868283 | |||||
| chr3:97868283
|
CA | C | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.648-3542delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 97868283 | |||||
| chr3:97868301
|
T | A | 2 | a0001c0003t0002g0211a0020c0050t0001g0044 | 2 | HG00099.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.648-3541T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868301 | ||||||
| chr3:97868715
|
A | G | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.648-3127A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868715 | ||||||
| chr3:97868795
|
A | G | 1 | a0001c0003t0002g0166 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.648-3047A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97868795 | ||||||
| chr3:97869007
|
G | GA | 14 | a0002c0001t0001g0121a0002c0001t0001g0122a0002c0001t0001g0125others(11): Show | 14 | HG01175.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.648-2824dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 97869007 | |||||
| chr3:97869213
|
C | T | 3 | a0002c0001t0001g0024a0002c0001t0001g0120a0002c0001t0001g0150 | 4 | HG02976.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-2629C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97869213 | ||||||
| chr3:97869244
|
T | A | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.648-2598T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97869244 | ||||||
| chr3:97869636
|
A | C | 1 | a0039c0048t0002g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.648-2206A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97869636 | ||||||
| chr3:97869871
|
T | C | 1 | a0001c0003t0002g0212 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.648-1971T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97869871 | ||||||
| chr3:97869887
|
T | C | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.648-1955T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97869887 | ||||||
| chr3:97870607
|
A | G | 1 | a0001c0003t0002g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.648-1235A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97870607 | ||||||
| chr3:97870670
|
T | G | 2 | a0032c0038t0003g0138a0033c0037t0001g0137 | 2 | HG01256.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.648-1172T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97870670 | ||||||
| chr3:97870906
|
ATGT | A | 49 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(46): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.648-932_648-930del others(3): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 97870906 | |||||
| chr3:97871115
|
C | A | 1 | a0001c0003t0002g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.648-727C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97871115 | ||||||
| chr3:97871161
|
T | G | 2 | a0003c0002t0001g0015a0003c0002t0001g0053 | 3 | HG01109.hp1 HG01257.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.648-681T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97871161 | ||||||
| chr3:97871196
|
T | A | 2 | a0001c0003t0002g0010a0036c0030t0002g0010 | 3 | NA19004.hp2 NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.648-646T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97871196 | ||||||
| chr3:97871558
|
A | G | 3 | a0002c0026t0007g0114a0008c0015t0003g0115a0008c0015t0003g0139 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.648-284A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 3/21 | chr3 | 97871558 | ||||||
| chr3:97878182
|
A | T | 1 | a0042c0023t0001g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6843+145A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878182 | ||||||
| chr3:97878331
|
A | G | 1 | a0003c0002t0001g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6843+294A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878331 | ||||||
| chr3:97878404
|
C | G | 1 | a0003c0002t0001g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6843+367C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878404 | ||||||
| chr3:97878528
|
C | G | 1 | a0003c0002t0001g0018 | 2 | HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.6843+491C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878528 | ||||||
| chr3:97878585
|
G | T | 1 | a0002c0001t0001g0091 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6843+548G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878585 | ||||||
| chr3:97878987
|
A | G | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.6844-717A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97878987 | ||||||
| chr3:97879132
|
C | T | 1 | a0001c0004t0002g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6844-572C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 4/21 | chr3 | 97879132 | ||||||
| chr3:97879757
|
A | G | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.6888+9A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 5/21 | chr3 | 97879757 | ||||||
| chr3:97879901
|
C | T | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6889-84C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 5/21 | chr3 | 97879901 | ||||||
| chr3:97879976
|
G | A | 2 | a0003c0002t0001g0045a0003c0002t0001g0046 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.6889-9G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 5/21 | chr3 | 97879976 | ||||||
| chr3:97880121
|
T | C | 2 | a0003c0002t0001g0074a0018c0051t0001g0056 | 2 | HG02135.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.7004+21T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880121 | ||||||
| chr3:97880126
|
G | A | 1 | a0003c0002t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.7004+26G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880126 | ||||||
| chr3:97880660
|
T | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7005-412T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880660 | ||||||
| chr3:97880667
|
G | A | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7005-405G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880667 | ||||||
| chr3:97880750
|
A | G | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7005-322A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880750 | ||||||
| chr3:97880902
|
C | T | 1 | a0001c0003t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7005-170C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 6/21 | chr3 | 97880902 | ||||||
| chr3:97881355
|
C | A | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7152+136C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97881355 | ||||||
| chr3:97881365
|
T | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7152+146T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97881365 | ||||||
| chr3:97881522
|
C | CCTGGCCA others(486): Show |
1 | a0015c0020t0009g0029 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7152+350_7152+842d others(495): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 97881522 | |||||
| chr3:97881669
|
TCACGCCA others(3): Show |
T | 1 | a0001c0003t0002g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7152+454_7152+463d others(12): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 97881669 | |||||
| chr3:97881731
|
A | G | 1 | a0001c0003t0002g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.7152+512A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97881731 | ||||||
| chr3:97881823
|
C | CCTATAAT others(18): Show |
3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.7152+621_7152+645d others(27): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 97881823 | |||||
| chr3:97882199
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.7152+980C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97882199 | ||||||
| chr3:97882205
|
CTAA | C | 192 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(189): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.7152+1010_7152+101 others(7): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 97882205 | |||||
| chr3:97882616
|
T | C | 39 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(36): Show | 46 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.7152+1397T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97882616 | ||||||
| chr3:97882641
|
C | T | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.7152+1422C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97882641 | ||||||
| chr3:97882656
|
G | A | 1 | a0001c0004t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7152+1437G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97882656 | ||||||
| chr3:97883484
|
C | G | 1 | a0002c0001t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7152+2265C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97883484 | ||||||
| chr3:97883560
|
G | A | 1 | a0002c0001t0001g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7152+2341G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97883560 | ||||||
| chr3:97883861
|
G | A | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.7152+2642G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97883861 | ||||||
| chr3:97883893
|
A | G | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7152+2674A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97883893 | ||||||
| chr3:97883962
|
A | G | 1 | a0037c0046t0002g0172 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7153-2669A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97883962 | ||||||
| chr3:97884029
|
G | A | 1 | a0002c0001t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7153-2602G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884029 | ||||||
| chr3:97884095
|
C | T | 1 | a0002c0001t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7153-2536C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884095 | ||||||
| chr3:97884152
|
A | G | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.7153-2479A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884152 | ||||||
| chr3:97884192
|
A | G | 11 | a0003c0002t0001g0014a0003c0002t0001g0016a0003c0002t0001g0017others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.7153-2439A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884192 | ||||||
| chr3:97884272
|
G | A | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.7153-2359G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884272 | ||||||
| chr3:97884417
|
G | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.7153-2214G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884417 | ||||||
| chr3:97884628
|
A | G | 1 | a0002c0001t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7153-2003A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97884628 | ||||||
| chr3:97885293
|
G | A | 2 | a0001c0004t0002g0009a0001c0004t0002g0243 | 4 | NA18944.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7153-1338G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885293 | ||||||
| chr3:97885330
|
T | C | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.7153-1301T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885330 | ||||||
| chr3:97885369
|
G | T | 1 | a0001c0003t0002g0219 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.7153-1262G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885369 | ||||||
| chr3:97885428
|
T | A | 1 | a0003c0002t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.7153-1203T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885428 | ||||||
| chr3:97885446
|
A | G | 3 | a0002c0001t0007g0113a0002c0001t0007g0123a0008c0039t0003g0124 | 3 | HG02615.hp1 HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7153-1185A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885446 | ||||||
| chr3:97885460
|
G | A | 3 | a0002c0026t0007g0114a0008c0015t0003g0115a0008c0015t0003g0139 | 3 | HG02615.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7153-1171G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885460 | ||||||
| chr3:97885574
|
A | G | 182 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(179): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.7153-1057A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885574 | ||||||
| chr3:97885810
|
T | C | 59 | a0002c0001t0001g0148a0002c0007t0001g0100a0002c0007t0001g0103others(56): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.7153-821T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885810 | ||||||
| chr3:97885845
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7153-786A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885845 | ||||||
| chr3:97885914
|
T | A | 1 | a0002c0001t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7153-717T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885914 | ||||||
| chr3:97885947
|
C | T | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.7153-684C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885947 | ||||||
| chr3:97885961
|
A | G | 1 | a0002c0001t0001g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.7153-670A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97885961 | ||||||
| chr3:97886106
|
C | T | 1 | a0016c0019t0001g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7153-525C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97886106 | ||||||
| chr3:97886314
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7153-317G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97886314 | ||||||
| chr3:97886469
|
A | T | 176 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(173): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.7153-162A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97886469 | ||||||
| chr3:97886470
|
A | T | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7153-161A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97886470 | ||||||
| chr3:97886614
|
T | G | 1 | a0001c0003t0002g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7153-17T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 7/21 | chr3 | 97886614 | ||||||
| chr3:97886833
|
A | G | 112 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(109): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.7289+66A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97886833 | ||||||
| chr3:97886865
|
A | T | 2 | a0007c0009t0005g0254a0007c0009t0005g0255 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.7289+98A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97886865 | ||||||
| chr3:97887187
|
T | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7289+420T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887187 | ||||||
| chr3:97887245
|
C | T | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.7289+478C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887245 | ||||||
| chr3:97887319
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7289+552C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887319 | ||||||
| chr3:97887436
|
C | T | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7289+669C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887436 | ||||||
| chr3:97887494
|
G | A | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7289+727G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887494 | ||||||
| chr3:97887507
|
T | C | 2 | a0002c0001t0001g0081a0002c0001t0001g0093 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.7289+740T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887507 | ||||||
| chr3:97887536
|
G | A | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.7289+769G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887536 | ||||||
| chr3:97887732
|
G | A | 1 | a0027c0029t0002g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7290-609G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887732 | ||||||
| chr3:97887828
|
A | G | 11 | a0001c0003t0002g0175a0001c0003t0002g0197a0001c0003t0002g0227others(8): Show | 12 | HG01256.hp1 HG01257.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.7290-513A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887828 | ||||||
| chr3:97887877
|
C | T | 4 | a0001c0003t0002g0227a0001c0003t0002g0247a0001c0003t0002g0248others(1): Show | 4 | HG02004.hp1 HG02602.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.7290-464C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97887877 | ||||||
| chr3:97888015
|
T | G | 181 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(178): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.7290-326T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 8/21 | chr3 | 97888015 | ||||||
| chr3:97888757
|
G | A | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7404+302G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/21 | chr3 | 97888757 | ||||||
| chr3:97888776
|
A | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7404+321A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/21 | chr3 | 97888776 | ||||||
| chr3:97889149
|
A | G | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.7405-206A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/21 | chr3 | 97889149 | ||||||
| chr3:97889184
|
A | G | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7405-171A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/21 | chr3 | 97889184 | ||||||
| chr3:97889187
|
A | G | 1 | a0001c0003t0002g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.7405-168A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 9/21 | chr3 | 97889187 | ||||||
| chr3:97890014
|
C | T | 1 | a0003c0002t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.7440+624C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890014 | ||||||
| chr3:97890072
|
A | G | 1 | a0001c0003t0002g0036 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.7440+682A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890072 | ||||||
| chr3:97890365
|
T | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7440+975T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890365 | ||||||
| chr3:97890404
|
T | G | 1 | a0024c0034t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7440+1014T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890404 | ||||||
| chr3:97890615
|
G | C | 12 | a0001c0003t0002g0166a0001c0003t0002g0211a0001c0003t0002g0212others(9): Show | 12 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.7440+1225G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890615 | ||||||
| chr3:97890709
|
C | T | 1 | a0025c0035t0002g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7440+1319C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890709 | ||||||
| chr3:97890737
|
G | A | 1 | a0042c0023t0001g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7440+1347G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890737 | ||||||
| chr3:97890806
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7440+1416G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890806 | ||||||
| chr3:97890989
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7440+1599A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97890989 | ||||||
| chr3:97891090
|
C | T | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.7440+1700C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891090 | ||||||
| chr3:97891107
|
A | G | 181 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(178): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.7440+1717A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891107 | ||||||
| chr3:97891520
|
G | A | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.7441-1340G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891520 | ||||||
| chr3:97891561
|
C | T | 1 | a0003c0002t0001g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.7441-1299C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891561 | ||||||
| chr3:97891562
|
G | A | 2 | a0006c0008t0001g0151a0006c0008t0001g0152 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.7441-1298G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891562 | ||||||
| chr3:97891607
|
G | T | 1 | a0001c0003t0002g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7441-1253G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891607 | ||||||
| chr3:97891622
|
T | C | 1 | a0009c0014t0003g0055 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.7441-1238T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891622 | ||||||
| chr3:97891947
|
A | G | 1 | a0005c0006t0004g0230 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.7441-913A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97891947 | ||||||
| chr3:97892018
|
A | T | 1 | a0002c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.7441-842A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892018 | ||||||
| chr3:97892054
|
C | T | 7 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112others(4): Show | 7 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.7441-806C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892054 | ||||||
| chr3:97892131
|
C | A | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7441-729C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892131 | ||||||
| chr3:97892176
|
T | C | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.7441-684T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892176 | ||||||
| chr3:97892205
|
G | C | 1 | a0002c0007t0001g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7441-655G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892205 | ||||||
| chr3:97892369
|
C | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7441-491C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892369 | ||||||
| chr3:97892445
|
C | G | 1 | a0001c0003t0002g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.7441-415C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892445 | ||||||
| chr3:97892612
|
C | T | 1 | a0001c0003t0002g0036 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.7441-248C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892612 | ||||||
| chr3:97892623
|
G | A | 1 | a0028c0027t0002g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7441-237G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892623 | ||||||
| chr3:97892716
|
C | T | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7441-144C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892716 | ||||||
| chr3:97892829
|
T | G | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.7441-31T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 10/21 | chr3 | 97892829 | ||||||
| chr3:97893072
|
A | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.7574+79A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97893072 | ||||||
| chr3:97893229
|
T | C | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.7574+236T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97893229 | ||||||
| chr3:97893630
|
C | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7574+637C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97893630 | ||||||
| chr3:97893687
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7574+694G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97893687 | ||||||
| chr3:97894109
|
G | T | 3 | a0002c0001t0001g0116a0002c0001t0001g0118a0002c0001t0001g0129 | 3 | HG02280.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7574+1116G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894109 | ||||||
| chr3:97894241
|
T | C | 2 | a0003c0002t0001g0016a0003c0002t0001g0072 | 3 | HG00280.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.7574+1248T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894241 | ||||||
| chr3:97894311
|
C | T | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.7574+1318C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894311 | ||||||
| chr3:97894373
|
G | GAA | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.7574+1382_7574+138 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 97894373 | |||||
| chr3:97894705
|
T | C | 4 | a0001c0003t0002g0203a0002c0011t0001g0106a0002c0011t0001g0107others(1): Show | 4 | HG00423.hp2 HG01070.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.7575-1254T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894705 | ||||||
| chr3:97894741
|
G | A | 4 | a0003c0002t0001g0004a0003c0002t0001g0007a0003c0002t0001g0040others(1): Show | 9 | NA18944.hp1 NA18945.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.7575-1218G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894741 | ||||||
| chr3:97894865
|
A | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.7575-1094A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97894865 | ||||||
| chr3:97895332
|
A | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7575-627A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 11/21 | chr3 | 97895332 | ||||||
| chr3:97896094
|
G | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7701+9G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896094 | ||||||
| chr3:97896345
|
C | G | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7701+260C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896345 | ||||||
| chr3:97896486
|
A | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7701+401A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896486 | ||||||
| chr3:97896486
|
A | G | 1 | a0001c0003t0002g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.7701+401A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896486 | ||||||
| chr3:97896692
|
G | T | 1 | a0001c0004t0002g0190 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7701+607G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896692 | ||||||
| chr3:97896716
|
T | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7701+631T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896716 | ||||||
| chr3:97896814
|
G | A | 1 | a0001c0004t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7701+729G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97896814 | ||||||
| chr3:97897238
|
C | T | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.7701+1153C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897238 | ||||||
| chr3:97897239
|
G | A | 109 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(106): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.7701+1154G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897239 | ||||||
| chr3:97897394
|
C | G | 1 | a0003c0002t0001g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7701+1309C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897394 | ||||||
| chr3:97897404
|
G | T | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7701+1319G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897404 | ||||||
| chr3:97897423
|
A | G | 1 | a0030c0041t0001g0089 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.7701+1338A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897423 | ||||||
| chr3:97897605
|
T | G | 3 | a0011c0010t0002g0200a0011c0010t0002g0216a0011c0010t0002g0217 | 3 | HG00280.hp2 HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.7702-1278T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897605 | ||||||
| chr3:97897626
|
T | C | 1 | a0002c0001t0001g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7702-1257T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897626 | ||||||
| chr3:97897676
|
T | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7702-1207T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897676 | ||||||
| chr3:97897769
|
A | C | 1 | a0007c0009t0005g0035 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7702-1114A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897769 | ||||||
| chr3:97897866
|
A | G | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.7702-1017A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897866 | ||||||
| chr3:97897948
|
C | T | 9 | a0003c0002t0001g0012a0003c0002t0001g0042a0003c0002t0001g0047others(6): Show | 10 | HG01123.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.7702-935C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97897948 | ||||||
| chr3:97898003
|
G | A | 1 | a0003c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7702-880G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898003 | ||||||
| chr3:97898088
|
T | C | 109 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(106): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.7702-795T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898088 | ||||||
| chr3:97898089
|
G | A | 1 | a0042c0023t0001g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7702-794G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898089 | ||||||
| chr3:97898143
|
C | G | 1 | a0001c0003t0002g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.7702-740C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898143 | ||||||
| chr3:97898160
|
C | T | 1 | a0002c0001t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7702-723C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898160 | ||||||
| chr3:97898282
|
A | G | 1 | a0002c0001t0001g0078 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.7702-601A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898282 | ||||||
| chr3:97898348
|
G | A | 2 | a0001c0003t0002g0032a0001c0003t0002g0234 | 3 | HG03139.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.7702-535G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898348 | ||||||
| chr3:97898479
|
T | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7702-404T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898479 | ||||||
| chr3:97898671
|
T | C | 1 | a0008c0015t0003g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7702-212T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 12/21 | chr3 | 97898671 | ||||||
| chr3:97899322
|
G | A | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7971+59G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899322 | ||||||
| chr3:97899445
|
GAGATGGC others(23): Show |
G | 2 | a0002c0001t0001g0121a0002c0018t0001g0158 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7971+184_7971+213d others(32): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 97899445 | |||||
| chr3:97899467
|
A | G | 1 | a0027c0029t0002g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7971+204A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899467 | ||||||
| chr3:97899534
|
A | G | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.7971+271A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899534 | ||||||
| chr3:97899622
|
A | C | 3 | a0006c0008t0001g0153a0006c0008t0001g0154a0006c0008t0001g0157 | 3 | HG02886.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7971+359A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899622 | ||||||
| chr3:97899718
|
T | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.7971+455T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899718 | ||||||
| chr3:97899806
|
A | G | 1 | a0001c0004t0002g0243 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.7971+543A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899806 | ||||||
| chr3:97899898
|
T | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7972-555T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97899898 | ||||||
| chr3:97900039
|
T | C | 1 | a0003c0002t0001g0070 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7972-414T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900039 | ||||||
| chr3:97900060
|
T | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7972-393T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900060 | ||||||
| chr3:97900153
|
G | C | 1 | a0002c0001t0001g0099 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.7972-300G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900153 | ||||||
| chr3:97900153
|
GC | G | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.7972-298delC | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 97900153 | |||||
| chr3:97900179
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7972-274C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900179 | ||||||
| chr3:97900404
|
G | A | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7972-49G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900404 | ||||||
| chr3:97900406
|
C | CAACTA | 111 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(108): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.7972-46_7972-45ins others(5): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 97900406 | |||||
| chr3:97900417
|
A | T | 1 | a0001c0003t0002g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7972-36A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 14/21 | chr3 | 97900417 | ||||||
| chr3:97900587
|
C | T | 4 | a0001c0003t0002g0032a0001c0003t0002g0234a0001c0003t0002g0235others(1): Show | 5 | HG00735.hp2 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.8004+102C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97900587 | ||||||
| chr3:97900920
|
A | G | 1 | a0024c0034t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8004+435A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97900920 | ||||||
| chr3:97900990
|
C | G | 6 | a0001c0003t0002g0030a0001c0003t0002g0202a0001c0003t0002g0203others(3): Show | 7 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.8004+505C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97900990 | ||||||
| chr3:97901000
|
A | G | 1 | a0031c0031t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.8004+515A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901000 | ||||||
| chr3:97901017
|
G | C | 1 | a0002c0001t0001g0099 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.8004+532G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901017 | ||||||
| chr3:97901242
|
A | T | 1 | a0015c0020t0009g0029 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.8004+757A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901242 | ||||||
| chr3:97901264
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8004+779G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901264 | ||||||
| chr3:97901328
|
T | A | 1 | a0003c0002t0001g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.8004+843T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901328 | ||||||
| chr3:97901452
|
T | C | 1 | a0003c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8004+967T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901452 | ||||||
| chr3:97901684
|
A | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.8004+1199A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901684 | ||||||
| chr3:97901991
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8004+1506T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97901991 | ||||||
| chr3:97902041
|
G | T | 1 | a0002c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8004+1556G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902041 | ||||||
| chr3:97902079
|
G | A | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8004+1594G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902079 | ||||||
| chr3:97902116
|
G | A | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.8004+1631G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902116 | ||||||
| chr3:97902142
|
C | T | 2 | a0001c0003t0002g0219a0025c0035t0002g0221 | 2 | NA18957.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.8004+1657C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902142 | ||||||
| chr3:97902285
|
G | A | 3 | a0002c0001t0001g0116a0002c0001t0001g0118a0002c0001t0001g0129 | 3 | HG02280.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8004+1800G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902285 | ||||||
| chr3:97902312
|
A | C | 1 | a0002c0001t0001g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.8004+1827A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902312 | ||||||
| chr3:97902494
|
TA | T | 59 | a0002c0001t0001g0109a0002c0007t0001g0100a0002c0007t0001g0103others(56): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.8004+2020delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97902494 | |||||
| chr3:97902525
|
C | G | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.8004+2040C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902525 | ||||||
| chr3:97902529
|
C | G | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8004+2044C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902529 | ||||||
| chr3:97902738
|
T | C | 1 | a0003c0002t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.8004+2253T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902738 | ||||||
| chr3:97902950
|
T | C | 5 | a0002c0007t0001g0100a0002c0007t0001g0104a0002c0007t0001g0110others(2): Show | 5 | HG00733.hp2 HG02165.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.8004+2465T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97902950 | ||||||
| chr3:97903069
|
C | A | 1 | a0001c0004t0002g0033 | 2 | NA18939.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.8004+2584C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903069 | ||||||
| chr3:97903226
|
T | G | 3 | a0001c0003t0002g0171a0001c0003t0002g0257a0040c0025t0002g0218 | 3 | HG00639.hp1 HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.8004+2741T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903226 | ||||||
| chr3:97903405
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8004+2920G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903405 | ||||||
| chr3:97903418
|
A | G | 1 | a0002c0001t0001g0022 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.8004+2933A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903418 | ||||||
| chr3:97903630
|
A | G | 3 | a0002c0001t0001g0116a0002c0001t0001g0118a0002c0001t0001g0129 | 3 | HG02280.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8004+3145A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903630 | ||||||
| chr3:97903739
|
G | T | 1 | a0001c0003t0002g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.8004+3254G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903739 | ||||||
| chr3:97903746
|
T | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8004+3261T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903746 | ||||||
| chr3:97903790
|
C | T | 7 | a0001c0004t0002g0033a0001c0004t0002g0229a0001c0004t0002g0239others(4): Show | 9 | HG00738.hp1 HG01175.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.8004+3305C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903790 | ||||||
| chr3:97903853
|
C | A | 104 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(101): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.8004+3368C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903853 | ||||||
| chr3:97903999
|
C | T | 1 | a0001c0003t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8004+3514C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97903999 | ||||||
| chr3:97904000
|
G | T | 2 | a0001c0004t0002g0245a0039c0048t0002g0246 | 2 | HG01168.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.8004+3515G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904000 | ||||||
| chr3:97904024
|
T | C | 1 | a0002c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.8004+3539T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904024 | ||||||
| chr3:97904215
|
G | T | 1 | a0033c0037t0001g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.8004+3730G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904215 | ||||||
| chr3:97904251
|
A | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8004+3766A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904251 | ||||||
| chr3:97904326
|
A | C | 1 | a0001c0003t0002g0222 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.8004+3841A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904326 | ||||||
| chr3:97904390
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8004+3905C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904390 | ||||||
| chr3:97904652
|
G | A | 1 | a0007c0009t0005g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.8004+4167G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904652 | ||||||
| chr3:97904680
|
TTTTTTAT others(7): Show |
T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8004+4209_8004+422 others(18): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97904680 | |||||
| chr3:97904708
|
T | G | 6 | a0001c0003t0002g0212a0001c0003t0002g0213a0001c0003t0002g0219others(3): Show | 6 | NA18957.hp1 NA18980.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.8004+4223T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904708 | ||||||
| chr3:97904872
|
A | G | 1 | a0001c0004t0002g0243 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.8004+4387A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904872 | ||||||
| chr3:97904984
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8004+4499C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97904984 | ||||||
| chr3:97905007
|
C | T | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8004+4522C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905007 | ||||||
| chr3:97905027
|
AATG | A | 2 | a0001c0003t0002g0036a0001c0003t0002g0252 | 3 | HG02723.hp2 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8004+4548_8004+455 others(7): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97905027 | |||||
| chr3:97905039
|
C | T | 1 | a0001c0003t0002g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.8004+4554C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905039 | ||||||
| chr3:97905078
|
A | C | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8004+4593A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905078 | ||||||
| chr3:97905247
|
G | C | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8004+4762G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905247 | ||||||
| chr3:97905284
|
A | T | 180 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(177): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.8004+4799A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905284 | ||||||
| chr3:97905385
|
T | C | 1 | a0007c0009t0005g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.8004+4900T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905385 | ||||||
| chr3:97905394
|
C | G | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8004+4909C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905394 | ||||||
| chr3:97905403
|
C | T | 1 | a0007c0009t0005g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.8004+4918C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905403 | ||||||
| chr3:97905532
|
T | A | 1 | a0005c0006t0004g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8004+5047T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905532 | ||||||
| chr3:97905778
|
A | G | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.8004+5293A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905778 | ||||||
| chr3:97905841
|
T | A | 192 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(189): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.8004+5356T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905841 | ||||||
| chr3:97905884
|
C | T | 1 | a0001c0003t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8004+5399C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905884 | ||||||
| chr3:97905921
|
A | G | 1 | a0002c0001t0001g0091 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8004+5436A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905921 | ||||||
| chr3:97905936
|
G | A | 1 | a0002c0001t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8004+5451G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97905936 | ||||||
| chr3:97906060
|
T | G | 3 | a0002c0001t0001g0116a0002c0001t0001g0118a0002c0001t0001g0129 | 3 | HG02280.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8004+5575T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906060 | ||||||
| chr3:97906063
|
G | A | 11 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(8): Show | 13 | HG00642.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.8004+5578G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906063 | ||||||
| chr3:97906170
|
AG | A | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.8004+5687delG | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97906170 | |||||
| chr3:97906218
|
C | G | 173 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(170): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.8004+5733C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906218 | ||||||
| chr3:97906296
|
C | G | 1 | a0001c0003t0002g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.8004+5811C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906296 | ||||||
| chr3:97906347
|
T | G | 221 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.8005-5820T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906347 | ||||||
| chr3:97906515
|
T | G | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8005-5652T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906515 | ||||||
| chr3:97906537
|
T | C | 1 | a0001c0022t0002g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.8005-5630T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906537 | ||||||
| chr3:97906694
|
G | A | 22 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(19): Show | 32 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.8005-5473G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906694 | ||||||
| chr3:97906780
|
G | A | 1 | a0001c0003t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8005-5387G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906780 | ||||||
| chr3:97906885
|
T | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8005-5282T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906885 | ||||||
| chr3:97906935
|
A | C | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-5232A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97906935 | ||||||
| chr3:97907018
|
C | G | 1 | a0037c0046t0002g0172 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8005-5149C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907018 | ||||||
| chr3:97907236
|
G | T | 1 | a0003c0002t0001g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8005-4931G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907236 | ||||||
| chr3:97907279
|
T | C | 1 | a0041c0024t0002g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8005-4888T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907279 | ||||||
| chr3:97907324
|
C | T | 3 | a0002c0001t0001g0090a0002c0001t0001g0092a0002c0036t0001g0088 | 3 | HG02027.hp2 HG02056.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.8005-4843C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907324 | ||||||
| chr3:97907490
|
A | G | 2 | a0001c0004t0002g0245a0039c0048t0002g0246 | 2 | HG01168.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.8005-4677A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907490 | ||||||
| chr3:97907657
|
C | T | 26 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0116others(23): Show | 28 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.8005-4510C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907657 | ||||||
| chr3:97907665
|
C | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8005-4502C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907665 | ||||||
| chr3:97907679
|
G | C | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8005-4488G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907679 | ||||||
| chr3:97907754
|
T | G | 2 | a0003c0002t0001g0004a0003c0002t0001g0041 | 5 | NA18945.hp2 NA18984.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.8005-4413T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97907754 | ||||||
| chr3:97908264
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8005-3903C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908264 | ||||||
| chr3:97908265
|
G | T | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8005-3902G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908265 | ||||||
| chr3:97908370
|
A | G | 1 | a0001c0004t0002g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.8005-3797A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908370 | ||||||
| chr3:97908423
|
T | G | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.8005-3744T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908423 | ||||||
| chr3:97908675
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8005-3492C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908675 | ||||||
| chr3:97908691
|
C | T | 2 | a0001c0004t0002g0193a0001c0004t0002g0194 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.8005-3476C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908691 | ||||||
| chr3:97908766
|
A | G | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-3401A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908766 | ||||||
| chr3:97908877
|
G | A | 1 | a0001c0003t0002g0036 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8005-3290G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908877 | ||||||
| chr3:97908910
|
G | A | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8005-3257G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97908910 | ||||||
| chr3:97909074
|
C | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-3093C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909074 | ||||||
| chr3:97909179
|
C | G | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8005-2988C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909179 | ||||||
| chr3:97909198
|
A | T | 1 | a0030c0041t0001g0089 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.8005-2969A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909198 | ||||||
| chr3:97909231
|
G | C | 1 | a0001c0003t0002g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8005-2936G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909231 | ||||||
| chr3:97909293
|
C | T | 1 | a0005c0006t0004g0253 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.8005-2874C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909293 | ||||||
| chr3:97909384
|
C | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-2783C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909384 | ||||||
| chr3:97909494
|
C | A | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8005-2673C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909494 | ||||||
| chr3:97909540
|
T | C | 8 | a0001c0003t0002g0197a0004c0005t0001g0027a0004c0005t0001g0161others(5): Show | 10 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.8005-2627T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909540 | ||||||
| chr3:97909594
|
T | C | 1 | a0001c0003t0002g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8005-2573T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909594 | ||||||
| chr3:97909702
|
C | T | 1 | a0002c0001t0001g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8005-2465C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909702 | ||||||
| chr3:97909749
|
G | A | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-2418G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909749 | ||||||
| chr3:97909799
|
G | A | 3 | a0002c0001t0001g0125a0002c0001t0001g0126a0002c0001t0001g0127 | 3 | HG01175.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8005-2368G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909799 | ||||||
| chr3:97909870
|
T | C | 7 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112others(4): Show | 7 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.8005-2297T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97909870 | ||||||
| chr3:97910032
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-2135C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910032 | ||||||
| chr3:97910033
|
T | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-2134T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910033 | ||||||
| chr3:97910060
|
A | G | 5 | a0003c0002t0001g0042a0003c0002t0001g0064a0007c0009t0005g0035others(2): Show | 6 | HG01123.hp1 HG01496.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.8005-2107A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910060 | ||||||
| chr3:97910077
|
G | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-2090G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910077 | ||||||
| chr3:97910087
|
A | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8005-2080A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910087 | ||||||
| chr3:97910122
|
C | T | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8005-2045C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910122 | ||||||
| chr3:97910197
|
TTTTG | T | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8005-1964_8005-196 others(8): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97910197 | |||||
| chr3:97910205
|
G | T | 1 | a0002c0011t0001g0107 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.8005-1962G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910205 | ||||||
| chr3:97910220
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8005-1947C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910220 | ||||||
| chr3:97910355
|
C | A | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-1812C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910355 | ||||||
| chr3:97910400
|
ACTCTGTG others(11): Show |
A | 3 | a0003c0002t0001g0014a0003c0002t0001g0057a0003c0002t0001g0068 | 4 | HG02257.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8005-1763_8005-174 others(22): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 97910400 | |||||
| chr3:97910421
|
C | A | 3 | a0003c0002t0001g0014a0003c0002t0001g0057a0003c0002t0001g0068 | 4 | HG02257.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8005-1746C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910421 | ||||||
| chr3:97910469
|
C | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-1698C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910469 | ||||||
| chr3:97910594
|
T | G | 223 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(220): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.8005-1573T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910594 | ||||||
| chr3:97910610
|
C | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8005-1557C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910610 | ||||||
| chr3:97910621
|
C | G | 7 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112others(4): Show | 7 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.8005-1546C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910621 | ||||||
| chr3:97910763
|
G | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8005-1404G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910763 | ||||||
| chr3:97910857
|
C | G | 1 | a0034c0043t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.8005-1310C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910857 | ||||||
| chr3:97910882
|
A | T | 2 | a0005c0006t0004g0201a0005c0006t0004g0225 | 2 | NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.8005-1285A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97910882 | ||||||
| chr3:97911030
|
A | G | 5 | a0002c0001t0001g0025a0002c0001t0001g0127a0002c0001t0001g0130others(2): Show | 6 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.8005-1137A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911030 | ||||||
| chr3:97911154
|
C | T | 2 | a0002c0001t0001g0024a0002c0001t0001g0120 | 3 | HG02976.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.8005-1013C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911154 | ||||||
| chr3:97911531
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8005-636C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911531 | ||||||
| chr3:97911553
|
A | G | 3 | a0003c0002t0001g0043a0003c0002t0001g0052a0003c0002t0001g0147 | 3 | HG00597.hp2 HG02129.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.8005-614A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911553 | ||||||
| chr3:97911582
|
G | T | 192 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(189): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.8005-585G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911582 | ||||||
| chr3:97911677
|
G | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8005-490G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911677 | ||||||
| chr3:97911900
|
A | T | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.8005-267A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 15/21 | chr3 | 97911900 | ||||||
| chr3:97912287
|
T | C | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.8114+11T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97912287 | ||||||
| chr3:97912330
|
A | C | 8 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(5): Show | 8 | HG00733.hp2 HG02165.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.8114+54A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97912330 | ||||||
| chr3:97912643
|
C | T | 1 | a0003c0002t0001g0015 | 2 | HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.8114+367C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97912643 | ||||||
| chr3:97912658
|
T | A | 1 | a0025c0035t0002g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8114+382T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97912658 | ||||||
| chr3:97912846
|
T | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8114+570T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97912846 | ||||||
| chr3:97913262
|
A | G | 1 | a0001c0003t0002g0031 | 2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.8114+986A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913262 | ||||||
| chr3:97913270
|
G | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8114+994G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913270 | ||||||
| chr3:97913330
|
C | T | 1 | a0034c0043t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.8114+1054C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913330 | ||||||
| chr3:97913447
|
T | C | 181 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(178): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.8114+1171T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913447 | ||||||
| chr3:97913627
|
G | A | 1 | a0001c0003t0002g0166 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.8114+1351G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913627 | ||||||
| chr3:97913664
|
G | C | 1 | a0033c0037t0001g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.8114+1388G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913664 | ||||||
| chr3:97913772
|
T | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8114+1496T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913772 | ||||||
| chr3:97913872
|
G | A | 193 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(190): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.8114+1596G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913872 | ||||||
| chr3:97913916
|
A | G | 1 | a0003c0002t0001g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.8114+1640A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97913916 | ||||||
| chr3:97914000
|
T | C | 1 | a0003c0002t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.8115-1610T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914000 | ||||||
| chr3:97914055
|
C | T | 1 | a0001c0004t0002g0183 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.8115-1555C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914055 | ||||||
| chr3:97914321
|
T | G | 3 | a0002c0001t0001g0125a0002c0001t0001g0126a0002c0001t0001g0127 | 3 | HG01175.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8115-1289T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914321 | ||||||
| chr3:97914343
|
GA | G | 10 | a0002c0001t0001g0021a0002c0001t0001g0082a0002c0001t0001g0086others(7): Show | 10 | HG02027.hp2 HG02056.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.8115-1263delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 97914343 | |||||
| chr3:97914515
|
G | A | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8115-1095G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914515 | ||||||
| chr3:97914538
|
G | T | 2 | a0002c0001t0001g0081a0002c0001t0001g0093 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.8115-1072G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914538 | ||||||
| chr3:97914634
|
AG | A | 3 | a0001c0004t0002g0033a0001c0004t0002g0239a0001c0004t0002g0250 | 4 | NA18939.hp2 NA18945.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.8115-972delG | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 97914634 | |||||
| chr3:97914637
|
G | A | 5 | a0006c0008t0001g0151a0006c0008t0001g0152a0006c0008t0001g0153others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.8115-973G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914637 | ||||||
| chr3:97914799
|
A | C | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.8115-811A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914799 | ||||||
| chr3:97914893
|
T | C | 105 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(102): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.8115-717T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97914893 | ||||||
| chr3:97915119
|
A | G | 1 | a0002c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.8115-491A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97915119 | ||||||
| chr3:97915338
|
C | T | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8115-272C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97915338 | ||||||
| chr3:97915409
|
C | T | 180 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(177): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.8115-201C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 16/21 | chr3 | 97915409 | ||||||
| chr3:97915878
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8241+142C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97915878 | ||||||
| chr3:97916190
|
G | A | 2 | a0002c0001t0001g0121a0002c0001t0001g0128 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8241+454G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916190 | ||||||
| chr3:97916241
|
C | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8241+505C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916241 | ||||||
| chr3:97916487
|
G | A | 109 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(106): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.8241+751G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916487 | ||||||
| chr3:97916536
|
A | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+800A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916536 | ||||||
| chr3:97916796
|
T | C | 1 | a0030c0041t0001g0089 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.8241+1060T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916796 | ||||||
| chr3:97916907
|
T | C | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8241+1171T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97916907 | ||||||
| chr3:97917122
|
C | T | 3 | a0002c0001t0001g0133a0002c0001t0001g0134a0002c0001t0001g0135 | 3 | HG03130.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.8241+1386C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97917122 | ||||||
| chr3:97917245
|
CAG | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+1513_8241+151 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97917245 | |||||
| chr3:97917475
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+1739C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97917475 | ||||||
| chr3:97917617
|
A | G | 1 | a0003c0002t0001g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8241+1881A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97917617 | ||||||
| chr3:97918220
|
A | G | 1 | a0020c0050t0001g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.8241+2484A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918220 | ||||||
| chr3:97918327
|
G | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+2591G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918327 | ||||||
| chr3:97918412
|
C | T | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8241+2676C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918412 | ||||||
| chr3:97918432
|
T | C | 1 | a0001c0003t0002g0231 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.8241+2696T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918432 | ||||||
| chr3:97918447
|
G | A | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.8241+2711G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918447 | ||||||
| chr3:97918466
|
T | C | 65 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(62): Show | 76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.8241+2730T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918466 | ||||||
| chr3:97918613
|
T | C | 1 | a0003c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8241+2877T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918613 | ||||||
| chr3:97918792
|
C | T | 110 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(107): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.8241+3056C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97918792 | ||||||
| chr3:97919252
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8241+3516G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919252 | ||||||
| chr3:97919282
|
GA | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8241+3548delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97919282 | |||||
| chr3:97919348
|
T | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+3612T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919348 | ||||||
| chr3:97919355
|
A | C | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+3619A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919355 | ||||||
| chr3:97919680
|
A | C | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8241+3944A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919680 | ||||||
| chr3:97919714
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8241+3978T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919714 | ||||||
| chr3:97919714
|
T | TA | 19 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(16): Show | 19 | HG00423.hp2 HG00597.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.8241+3995dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97919714 | |||||
| chr3:97919714
|
T | TAA | 42 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(39): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.8241+3994_8241+399 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97919714 | |||||
| chr3:97919714
|
TA | T | 17 | a0001c0003t0002g0191a0001c0003t0002g0231a0001c0003t0002g0242others(14): Show | 19 | HG01106.hp1 HG01257.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.8241+3995delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97919714 | |||||
| chr3:97919734
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8241+3998C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919734 | ||||||
| chr3:97919760
|
G | A | 50 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(47): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.8241+4024G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919760 | ||||||
| chr3:97919830
|
T | A | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.8241+4094T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919830 | ||||||
| chr3:97919938
|
G | A | 2 | a0007c0009t0005g0254a0007c0009t0005g0255 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.8241+4202G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919938 | ||||||
| chr3:97919955
|
A | G | 1 | a0002c0001t0001g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8241+4219A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97919955 | ||||||
| chr3:97920014
|
C | G | 1 | a0001c0003t0002g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8241+4278C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920014 | ||||||
| chr3:97920092
|
C | A | 1 | a0002c0001t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8241+4356C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920092 | ||||||
| chr3:97920102
|
G | A | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+4366G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920102 | ||||||
| chr3:97920112
|
A | G | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8241+4376A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920112 | ||||||
| chr3:97920238
|
A | G | 1 | a0006c0008t0001g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.8241+4502A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920238 | ||||||
| chr3:97920334
|
A | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8241+4598A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920334 | ||||||
| chr3:97920531
|
C | A | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8241+4795C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920531 | ||||||
| chr3:97920615
|
C | T | 110 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(107): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.8241+4879C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97920615 | ||||||
| chr3:97921000
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+5264C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921000 | ||||||
| chr3:97921025
|
A | T | 1 | a0001c0003t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8241+5289A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921025 | ||||||
| chr3:97921099
|
A | T | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+5363A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921099 | ||||||
| chr3:97921383
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8241+5647T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921383 | ||||||
| chr3:97921468
|
C | A | 1 | a0002c0007t0001g0100 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.8241+5732C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921468 | ||||||
| chr3:97921468
|
C | CT | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8241+5733dupT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97921468 | |||||
| chr3:97921486
|
T | G | 1 | a0001c0004t0002g0181 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.8241+5750T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921486 | ||||||
| chr3:97921521
|
C | T | 3 | a0003c0002t0001g0069a0003c0002t0001g0073a0019c0049t0001g0059 | 3 | HG02735.hp2 HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.8241+5785C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97921521 | ||||||
| chr3:97922002
|
A | T | 2 | a0001c0004t0002g0229a0023c0028t0002g0176 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.8241+6266A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922002 | ||||||
| chr3:97922151
|
G | A | 1 | a0011c0010t0002g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8241+6415G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922151 | ||||||
| chr3:97922575
|
A | G | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.8241+6839A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922575 | ||||||
| chr3:97922692
|
G | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8241+6956G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922692 | ||||||
| chr3:97922828
|
T | C | 196 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(193): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.8241+7092T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922828 | ||||||
| chr3:97922924
|
AC | A | 58 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(55): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8241+7189delC | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922924 | ||||||
| chr3:97922959
|
C | T | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+7223C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922959 | ||||||
| chr3:97922960
|
G | A | 2 | a0002c0001t0001g0143a0002c0001t0001g0145 | 2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.8241+7224G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922960 | ||||||
| chr3:97922960
|
G | T | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8241+7224G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97922960 | ||||||
| chr3:97923040
|
G | A | 2 | a0001c0003t0002g0231a0001c0003t0002g0232 | 2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.8241+7304G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923040 | ||||||
| chr3:97923051
|
A | C | 1 | a0001c0004t0002g0185 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.8241+7315A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923051 | ||||||
| chr3:97923137
|
A | G | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8241+7401A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923137 | ||||||
| chr3:97923498
|
C | T | 1 | a0001c0003t0002g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8241+7762C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923498 | ||||||
| chr3:97923552
|
G | A | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8241+7816G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923552 | ||||||
| chr3:97923578
|
A | G | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8241+7842A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923578 | ||||||
| chr3:97923993
|
G | A | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8241+8257G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97923993 | ||||||
| chr3:97924016
|
C | A | 111 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(108): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.8241+8280C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97924016 | ||||||
| chr3:97924109
|
G | A | 1 | a0023c0028t0002g0176 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.8241+8373G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97924109 | ||||||
| chr3:97924867
|
G | C | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.8242-8827G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97924867 | ||||||
| chr3:97924947
|
C | T | 3 | a0001c0004t0002g0188a0001c0022t0002g0178a0001c0022t0002g0187 | 3 | HG00423.hp1 HG02129.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.8242-8747C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97924947 | ||||||
| chr3:97925425
|
G | A | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.8242-8269G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925425 | ||||||
| chr3:97925723
|
C | A | 1 | a0001c0003t0002g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8242-7971C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925723 | ||||||
| chr3:97925772
|
G | A | 1 | a0002c0001t0001g0022 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.8242-7922G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925772 | ||||||
| chr3:97925804
|
G | C | 1 | a0001c0003t0002g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8242-7890G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925804 | ||||||
| chr3:97925808
|
T | C | 254 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(251): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.8242-7886T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925808 | ||||||
| chr3:97925846
|
AT | A | 12 | a0001c0003t0002g0175a0001c0003t0002g0197a0001c0003t0002g0227others(9): Show | 13 | HG01256.hp1 HG01257.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.8242-7839delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97925846 | |||||
| chr3:97925848
|
T | C | 2 | a0001c0003t0002g0231a0001c0003t0002g0232 | 2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.8242-7846T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925848 | ||||||
| chr3:97925988
|
A | G | 1 | a0002c0001t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8242-7706A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97925988 | ||||||
| chr3:97926181
|
G | A | 4 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.8242-7513G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926181 | ||||||
| chr3:97926241
|
C | T | 1 | a0027c0029t0002g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.8242-7453C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926241 | ||||||
| chr3:97926263
|
A | G | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.8242-7431A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926263 | ||||||
| chr3:97926525
|
A | G | 1 | a0001c0003t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.8242-7169A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926525 | ||||||
| chr3:97926545
|
G | A | 4 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.8242-7149G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926545 | ||||||
| chr3:97926547
|
A | G | 7 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(4): Show | 9 | HG00642.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.8242-7147A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926547 | ||||||
| chr3:97926771
|
C | T | 1 | a0022c0044t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.8242-6923C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926771 | ||||||
| chr3:97926869
|
A | G | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8242-6825A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926869 | ||||||
| chr3:97926882
|
A | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8242-6812A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926882 | ||||||
| chr3:97926892
|
C | A | 1 | a0001c0003t0002g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.8242-6802C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926892 | ||||||
| chr3:97926913
|
C | G | 1 | a0002c0001t0001g0020 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.8242-6781C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97926913 | ||||||
| chr3:97927154
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8242-6540C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97927154 | ||||||
| chr3:97927454
|
CTG | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8242-6238_8242-623 others(6): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97927454 | |||||
| chr3:97928200
|
C | G | 2 | a0001c0004t0002g0033a0001c0004t0002g0239 | 3 | NA18939.hp2 NA18945.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.8242-5494C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928200 | ||||||
| chr3:97928220
|
T | TA | 10 | a0001c0004t0002g0033a0001c0004t0002g0229a0001c0004t0002g0237others(7): Show | 12 | HG00738.hp1 HG01168.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.8242-5467dupA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 97928220 | |||||
| chr3:97928335
|
A | T | 1 | a0001c0003t0002g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8242-5359A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928335 | ||||||
| chr3:97928410
|
A | G | 1 | a0024c0034t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8242-5284A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928410 | ||||||
| chr3:97928564
|
G | T | 65 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(62): Show | 76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.8242-5130G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928564 | ||||||
| chr3:97928812
|
G | A | 1 | a0001c0003t0002g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.8242-4882G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928812 | ||||||
| chr3:97928831
|
G | T | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.8242-4863G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928831 | ||||||
| chr3:97928876
|
A | G | 184 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(181): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.8242-4818A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97928876 | ||||||
| chr3:97929032
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8242-4662G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97929032 | ||||||
| chr3:97929075
|
C | T | 1 | a0001c0004t0002g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8242-4619C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97929075 | ||||||
| chr3:97929150
|
C | T | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8242-4544C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97929150 | ||||||
| chr3:97929631
|
A | C | 1 | a0010c0013t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8242-4063A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97929631 | ||||||
| chr3:97930294
|
T | C | 1 | a0001c0003t0002g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8242-3400T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97930294 | ||||||
| chr3:97930416
|
A | G | 1 | a0001c0004t0002g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8242-3278A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97930416 | ||||||
| chr3:97930511
|
T | A | 4 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.8242-3183T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97930511 | ||||||
| chr3:97930705
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8242-2989C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97930705 | ||||||
| chr3:97931087
|
C | G | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8242-2607C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931087 | ||||||
| chr3:97931294
|
G | A | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8242-2400G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931294 | ||||||
| chr3:97931297
|
A | G | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8242-2397A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931297 | ||||||
| chr3:97931458
|
T | C | 2 | a0001c0003t0002g0235a0001c0003t0002g0240 | 2 | HG00735.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.8242-2236T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931458 | ||||||
| chr3:97931560
|
C | T | 196 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(193): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.8242-2134C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931560 | ||||||
| chr3:97931642
|
A | T | 5 | a0002c0001t0001g0020a0002c0001t0001g0022a0002c0001t0001g0083others(2): Show | 7 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.8242-2052A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931642 | ||||||
| chr3:97931807
|
T | C | 8 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(5): Show | 8 | HG00733.hp2 HG02165.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.8242-1887T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931807 | ||||||
| chr3:97931817
|
C | G | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8242-1877C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931817 | ||||||
| chr3:97931859
|
C | G | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8242-1835C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931859 | ||||||
| chr3:97931871
|
A | G | 37 | a0003c0002t0001g0003a0003c0002t0001g0004a0003c0002t0001g0007others(34): Show | 52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.8242-1823A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931871 | ||||||
| chr3:97931971
|
A | G | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8242-1723A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97931971 | ||||||
| chr3:97932114
|
C | T | 10 | a0002c0001t0001g0021a0002c0001t0001g0082a0002c0001t0001g0086others(7): Show | 10 | HG02027.hp2 HG02056.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.8242-1580C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932114 | ||||||
| chr3:97932209
|
G | A | 8 | a0002c0007t0001g0100a0002c0007t0001g0103a0002c0007t0001g0104others(5): Show | 8 | HG00733.hp2 HG02165.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.8242-1485G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932209 | ||||||
| chr3:97932400
|
G | A | 1 | a0001c0003t0002g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8242-1294G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932400 | ||||||
| chr3:97932874
|
T | C | 1 | a0001c0004t0002g0239 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.8242-820T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932874 | ||||||
| chr3:97932910
|
C | A | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8242-784C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932910 | ||||||
| chr3:97932930
|
A | T | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.8242-764A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97932930 | ||||||
| chr3:97933004
|
C | G | 2 | a0002c0001t0001g0082a0002c0001t0001g0086 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.8242-690C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933004 | ||||||
| chr3:97933040
|
A | C | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8242-654A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933040 | ||||||
| chr3:97933146
|
C | T | 1 | a0001c0003t0002g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8242-548C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933146 | ||||||
| chr3:97933192
|
C | G | 2 | a0003c0002t0001g0016a0003c0002t0001g0072 | 3 | HG00280.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.8242-502C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933192 | ||||||
| chr3:97933320
|
T | A | 1 | a0025c0035t0002g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8242-374T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933320 | ||||||
| chr3:97933372
|
A | C | 3 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112 | 3 | HG00423.hp2 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.8242-322A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933372 | ||||||
| chr3:97933437
|
T | C | 1 | a0010c0013t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8242-257T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933437 | ||||||
| chr3:97933614
|
T | G | 1 | a0001c0003t0002g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.8242-80T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 17/21 | chr3 | 97933614 | ||||||
| chr3:97933917
|
G | C | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8381+84G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97933917 | ||||||
| chr3:97933976
|
G | A | 1 | a0002c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8381+143G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97933976 | ||||||
| chr3:97933993
|
T | C | 1 | a0017c0017t0008g0011 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8381+160T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97933993 | ||||||
| chr3:97934308
|
T | A | 40 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(37): Show | 47 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.8381+475T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97934308 | ||||||
| chr3:97934592
|
A | G | 2 | a0003c0002t0001g0057a0003c0002t0001g0068 | 2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.8381+759A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97934592 | ||||||
| chr3:97934700
|
TA | T | 119 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(116): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.8381+870delA | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 97934700 | |||||
| chr3:97934723
|
C | T | 1 | a0014c0016t0002g0034 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.8381+890C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97934723 | ||||||
| chr3:97935433
|
C | T | 2 | a0003c0002t0001g0015a0003c0002t0001g0053 | 3 | HG01109.hp1 HG01257.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.8382-1352C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935433 | ||||||
| chr3:97935535
|
C | T | 1 | a0002c0001t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8382-1250C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935535 | ||||||
| chr3:97935680
|
A | G | 1 | a0003c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.8382-1105A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935680 | ||||||
| chr3:97935762
|
C | G | 1 | a0001c0004t0002g0182 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.8382-1023C>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935762 | ||||||
| chr3:97935873
|
A | G | 1 | a0002c0018t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8382-912A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935873 | ||||||
| chr3:97935913
|
C | T | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8382-872C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97935913 | ||||||
| chr3:97936163
|
A | G | 1 | a0012c0012t0006g0008 | 3 | HG01106.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8382-622A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936163 | ||||||
| chr3:97936355
|
G | A | 1 | a0005c0006t0004g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.8382-430G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936355 | ||||||
| chr3:97936408
|
T | C | 1 | a0001c0003t0002g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.8382-377T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936408 | ||||||
| chr3:97936523
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8382-262T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936523 | ||||||
| chr3:97936619
|
G | A | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8382-166G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936619 | ||||||
| chr3:97936687
|
G | A | 2 | a0002c0001t0001g0108a0002c0001t0001g0109 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.8382-98G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936687 | ||||||
| chr3:97936725
|
T | C | 6 | a0004c0005t0001g0027a0004c0005t0001g0161a0004c0005t0001g0162others(3): Show | 7 | HG00642.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.8382-60T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 18/21 | chr3 | 97936725 | ||||||
| chr3:97937278
|
A | C | 2 | a0002c0001t0001g0130a0002c0001t0001g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.8505+370A>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97937278 | ||||||
| chr3:97937368
|
C | T | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.8505+460C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97937368 | ||||||
| chr3:97937771
|
G | A | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8505+863G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97937771 | ||||||
| chr3:97938076
|
C | T | 2 | a0001c0004t0002g0193a0001c0004t0002g0194 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.8505+1168C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938076 | ||||||
| chr3:97938179
|
GT | G | 108 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(105): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.8505+1273delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 97938179 | |||||
| chr3:97938356
|
G | C | 4 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.8505+1448G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938356 | ||||||
| chr3:97938450
|
C | T | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8505+1542C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938450 | ||||||
| chr3:97938528
|
TCACATGC others(1): Show |
T | 4 | a0001c0003t0002g0036a0001c0003t0002g0252a0001c0004t0002g0183others(1): Show | 5 | HG01975.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.8505+1641_8505+164 others(12): Show |
CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 97938528 | |||||
| chr3:97938632
|
G | A | 62 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(59): Show | 71 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.8505+1724G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938632 | ||||||
| chr3:97938704
|
T | C | 1 | a0032c0038t0003g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8505+1796T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938704 | ||||||
| chr3:97938769
|
A | G | 1 | a0001c0003t0002g0244 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.8505+1861A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938769 | ||||||
| chr3:97938796
|
T | A | 58 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(55): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.8505+1888T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938796 | ||||||
| chr3:97938819
|
T | C | 3 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255 | 4 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.8505+1911T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938819 | ||||||
| chr3:97938925
|
C | A | 4 | a0007c0009t0005g0035a0007c0009t0005g0254a0007c0009t0005g0255others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.8505+2017C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97938925 | ||||||
| chr3:97939146
|
G | C | 197 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(194): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.8506-2002G>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97939146 | ||||||
| chr3:97939402
|
GT | G | 10 | a0002c0018t0001g0158a0002c0018t0001g0159a0006c0008t0001g0151others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.8506-1744delT | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 97939402 | |||||
| chr3:97939859
|
T | C | 1 | a0001c0003t0002g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.8506-1289T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97939859 | ||||||
| chr3:97939974
|
C | A | 3 | a0010c0013t0001g0140a0010c0013t0001g0141a0010c0013t0001g0142 | 3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8506-1174C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97939974 | ||||||
| chr3:97940687
|
C | T | 1 | a0001c0004t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8506-461C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97940687 | ||||||
| chr3:97940709
|
C | T | 7 | a0002c0011t0001g0106a0002c0011t0001g0107a0002c0011t0001g0112others(4): Show | 7 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.8506-439C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97940709 | ||||||
| chr3:97941021
|
G | T | 107 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(104): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.8506-127G>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 19/21 | chr3 | 97941021 | ||||||
| chr3:97941354
|
A | G | 196 | a0001c0003t0002g0001a0001c0003t0002g0010a0001c0003t0002g0030others(193): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.8664+48A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941354 | ||||||
| chr3:97941415
|
A | G | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+109A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941415 | ||||||
| chr3:97941425
|
G | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+119G>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941425 | ||||||
| chr3:97941426
|
A | G | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+120A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941426 | ||||||
| chr3:97941431
|
A | T | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+125A>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941431 | ||||||
| chr3:97941436
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+130T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941436 | ||||||
| chr3:97941437
|
A | G | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+131A>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941437 | ||||||
| chr3:97941457
|
C | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+151C>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941457 | ||||||
| chr3:97941470
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+164T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941470 | ||||||
| chr3:97941475
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+169T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941475 | ||||||
| chr3:97941480
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+174T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941480 | ||||||
| chr3:97941507
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+201T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941507 | ||||||
| chr3:97941528
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+222T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941528 | ||||||
| chr3:97941530
|
T | A | 1 | a0001c0004t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8664+224T>A | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97941530 | ||||||
| chr3:97942280
|
T | G | 1 | a0002c0001t0001g0085 | 1 | HG00323.hp1 | splice_region_variant&intron_variant | LOW | c.8665-4T>G | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 20/21 | chr3 | 97942280 | ||||||
| chr3:97942563
|
T | C | 1 | a0029c0053t0011g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8824+120T>C | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 21/21 | chr3 | 97942563 | ||||||
| chr3:97942988
|
C | T | 1 | a0005c0006t0004g0241 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.8825-238C>T | CRYBG3 | ENSG00000080200.10 | transcript | ENST00000389622.7 | protein_coding | 21/21 | chr3 | 97942988 |