Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8738 |
|---|---|
| ensemblid | ENSG00000169372.13 |
| hgncid | 2340 |
| symbol | CRADD |
| name | CASP2 and RIPK1 domain containing adaptor with death domain |
| refseq_nuc | NM_003805.5 |
| refseq_prot | NP_003796.1 |
| ensembl_nuc | ENST00000332896.8 |
| ensembl_prot | ENSP00000327647.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 93677375 |
| end | 93850756 |
| strand | + |
| ver | v1.2 |
| region | chr12:93677375-93850756 |
| region5000 | chr12:93672375-93855756 |
| regionname0 | CRADD_chr12_93677375_93850756 |
| regionname5000 | CRADD_chr12_93672375_93855756 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 199 | 243 | 75 | 49 | 86 | 2 | 29 | 74 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0002 | 0/0 | 199 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0003 | 0/0 | 199 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0004 | 0/0 | 199 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 600 | 193 | 74 | 36 | 55 | 1 | 25 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| c0002 | 0/0 | 600 | 49 | 1 | 13 | 30 | 1 | 4 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| c0003 | 0/0 | 600 | 3 | 3 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| c0004 | 0/0 | 600 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| c0005 | 0/0 | 600 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| c0006 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 590 | 239 | 76 | 49 | 82 | 2 | 28 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| t0002 | 0/0 | 590 | 3 | 2 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| t0003 | 0/0 | 590 | 3 | 0 | 0 | 2 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| t0004 | 0/0 | 590 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| t0005 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| t0006 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 600 | 193 | 74 | 36 | 55 | 1 | 25 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0002 | 0/0 | 600 | 49 | 1 | 13 | 30 | 1 | 4 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0005 | 0/0 | 600 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0002c0003 | 0/0 | 600 | 3 | 3 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0003c0004 | 0/0 | 600 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0004c0006 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1189 | 186 | 72 | 35 | 52 | 1 | 24 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0001t0002 | 0/0 | 1189 | 3 | 2 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0001t0003 | 0/0 | 1189 | 3 | 0 | 0 | 2 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0001t0006 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0002t0001 | 0/0 | 1189 | 48 | 1 | 13 | 29 | 1 | 4 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0002t0005 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0001c0005t0001 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0002c0003t0001 | 0/0 | 1189 | 3 | 3 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0003c0004t0004 | 0/0 | 1189 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| a0004c0006t0001 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | copy fasta | chr12 | 93672375 | 93855756 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0001c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0002c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0003c0004t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| a0004c0006t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01167 | hp1 | a0004 | c0006 | t0001 | g0195 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0125 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03704 | hp1 | a0003 | c0004 | t0004 | g0200 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0234 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CHB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0076 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19009 | hp1 | a0001 | c0005 | t0001 | g0042 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19009 | hp2 | a0001 | c0002 | t0005 | g0089 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0079 | AFR | YRI | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | USA | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0113 | REF | REF | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | CRADD_chr12_93672375_93855756 | CRADD | chr12 | 93672375 | 93855756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:93678877
|
A | G | 1 | a0004 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.103A>G | p.Ile35Val | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/3 | 207/1189 | 103/600 | 35/199 | chr12 | 93678877 | ||
| chr12:93850225
|
G | A | 1 | a0002 | 3 | HG02965.hp2 NA18906.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.554G>A | p.Arg185Gln | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 658/1189 | 554/600 | 185/199 | chr12 | 93850225 | ||
| chr12:93850251
|
C | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.580C>G | p.Leu194Val | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 684/1189 | 580/600 | 194/199 | chr12 | 93850251 | ||
| chr12:93850252
|
T | A | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.581T>A | p.Leu194His | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 685/1189 | 581/600 | 194/199 | chr12 | 93850252 | ||
| chr12:93850254
|
C | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.583C>G | p.Leu195Val | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 687/1189 | 583/600 | 195/199 | chr12 | 93850254 | ||
| chr12:93850255
|
T | A | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.584T>A | p.Leu195Gln | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 688/1189 | 584/600 | 195/199 | chr12 | 93850255 | ||
| chr12:93850257
|
C | A | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.586C>A | p.His196Asn | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 690/1189 | 586/600 | 196/199 | chr12 | 93850257 | ||
| chr12:93850259
|
C | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.588C>G | p.His196Gln | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 692/1189 | 588/600 | 196/199 | chr12 | 93850259 | ||
| chr12:93850261
|
T | A | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.590T>A | p.Met197Lys | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 694/1189 | 590/600 | 197/199 | chr12 | 93850261 | ||
| chr12:93850263
|
T | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.592T>G | p.Leu198Val | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 696/1189 | 592/600 | 198/199 | chr12 | 93850263 | ||
| chr12:93850264
|
T | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.593T>G | p.Leu198Trp | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 697/1189 | 593/600 | 198/199 | chr12 | 93850264 | ||
| chr12:93850270
|
G | A | 1 | a0003 | 1 | HG03704.hp1 | stop_retained_variant | LOW | c.599G>A | p.Ter200Ter | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 703/1189 | 599/600 | 200/199 | chr12 | 93850270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:93850013
|
C | T | 1 | a0001c0005 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.342C>T | p.Ser114Ser | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 446/1189 | 342/600 | 114/199 | chr12 | 93850013 | ||
| chr12:93850077
|
C | T | 3 | a0001c0002a0001c0005a0002c0003 | 53 | HG00544.hp1 HG00735.hp1 HG01071.hp2 others(50): Show |
synonymous_variant | LOW | c.406C>T | p.Leu136Leu | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 510/1189 | 406/600 | 136/199 | chr12 | 93850077 | ||
| chr12:93850250
|
G | A | 1 | a0003c0004 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.579G>A | p.Leu193Leu | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 683/1189 | 579/600 | 193/199 | chr12 | 93850250 | ||
| chr12:93850253
|
C | G | 1 | a0003c0004 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.582C>G | p.Leu194Leu | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 686/1189 | 582/600 | 194/199 | chr12 | 93850253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:93850275
|
T | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 4 | chr12 | 93850275 | |||||
| chr12:93850277
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 6 | chr12 | 93850277 | |||||
| chr12:93850278
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 7 | chr12 | 93850278 | |||||
| chr12:93850279
|
T | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 8 | chr12 | 93850279 | |||||
| chr12:93850280
|
C | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 9 | chr12 | 93850280 | |||||
| chr12:93850281
|
C | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 10 | chr12 | 93850281 | |||||
| chr12:93850284
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 13 | chr12 | 93850284 | |||||
| chr12:93850287
|
C | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 16 | chr12 | 93850287 | |||||
| chr12:93850288
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 17 | chr12 | 93850288 | |||||
| chr12:93850288
|
C | T | 1 | a0001c0001t0003 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 17 | chr12 | 93850288 | |||||
| chr12:93850290
|
C | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 19 | chr12 | 93850290 | |||||
| chr12:93850291
|
T | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 20 | chr12 | 93850291 | |||||
| chr12:93850294
|
G | C | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 23 | chr12 | 93850294 | |||||
| chr12:93850295
|
G | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 24 | chr12 | 93850295 | |||||
| chr12:93850297
|
G | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 26 | chr12 | 93850297 | |||||
| chr12:93850298
|
T | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 27 | chr12 | 93850298 | |||||
| chr12:93850300
|
T | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 29 | chr12 | 93850300 | |||||
| chr12:93850302
|
T | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 31 | chr12 | 93850302 | |||||
| chr12:93850303
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 32 | chr12 | 93850303 | |||||
| chr12:93850304
|
C | A | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 33 | chr12 | 93850304 | |||||
| chr12:93850310
|
T | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 39 | chr12 | 93850310 | |||||
| chr12:93850311
|
C | G | 1 | a0003c0004t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 40 | chr12 | 93850311 | |||||
| chr12:93850356
|
G | T | 1 | a0001c0001t0006 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 85 | chr12 | 93850356 | |||||
| chr12:93850451
|
A | C | 1 | a0001c0002t0005 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 180 | chr12 | 93850451 | |||||
| chr12:93850602
|
T | C | 1 | a0001c0001t0003 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*331T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 331 | chr12 | 93850602 | |||||
| chr12:93850721
|
G | A | 1 | a0001c0001t0002 | 3 | HG00639.hp2 HG02622.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*450G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 3/3 | 450 | chr12 | 93850721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:93677555
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-7+83C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677555 | ||||||
| chr12:93677605
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-7+133C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677605 | ||||||
| chr12:93677623
|
C | T | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+151C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677623 | ||||||
| chr12:93677644
|
G | T | 1 | a0001c0002t0001g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-7+172G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677644 | ||||||
| chr12:93677826
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-7+354G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677826 | ||||||
| chr12:93677881
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-7+409G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93677881 | ||||||
| chr12:93678109
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-7+637C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93678109 | ||||||
| chr12:93678280
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6-489C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 1/2 | chr12 | 93678280 | ||||||
| chr12:93679126
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.298+54C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93679126 | ||||||
| chr12:93679254
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01167.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+182G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93679254 | ||||||
| chr12:93679598
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0003g0007 | 2 | NA18981.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.298+526G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93679598 | ||||||
| chr12:93679653
|
A | G | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+581A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93679653 | ||||||
| chr12:93680016
|
G | T | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+944G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680016 | ||||||
| chr12:93680276
|
T | TA | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG01081.hp1 HG01109.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.298+1206dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93680276 | |||||
| chr12:93680283
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298+1211G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680283 | ||||||
| chr12:93680361
|
T | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG01081.hp1 HG01109.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.298+1289T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680361 | ||||||
| chr12:93680437
|
T | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.298+1365T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680437 | ||||||
| chr12:93680863
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1791A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680863 | ||||||
| chr12:93680877
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG01109.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+1805G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680877 | ||||||
| chr12:93680919
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | NA18942.hp1 NA18979.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1847T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680919 | ||||||
| chr12:93680946
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+1874G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680946 | ||||||
| chr12:93680984
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+1912A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93680984 | ||||||
| chr12:93681124
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.298+2052T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681124 | ||||||
| chr12:93681136
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.298+2064G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681136 | ||||||
| chr12:93681181
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.298+2109G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681181 | ||||||
| chr12:93681279
|
A | T | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+2207A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681279 | ||||||
| chr12:93681323
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.298+2251G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681323 | ||||||
| chr12:93681324
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+2252A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681324 | ||||||
| chr12:93681385
|
A | T | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+2313A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681385 | ||||||
| chr12:93681391
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298+2319G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681391 | ||||||
| chr12:93681638
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+2566C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681638 | ||||||
| chr12:93681694
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.298+2622C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681694 | ||||||
| chr12:93681734
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.298+2662C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681734 | ||||||
| chr12:93681753
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+2681T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681753 | ||||||
| chr12:93681852
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(75): Show | 78 | HG00597.hp1 HG01081.hp1 HG01167.hp2 others(75): Show |
intron_variant | MODIFIER | c.298+2780G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681852 | ||||||
| chr12:93681877
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0069others(3): Show | 6 | HG01167.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+2805G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681877 | ||||||
| chr12:93681877
|
G | GTA | 17 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(14): Show | 17 | HG01257.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+2809_298+2810d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93681877 | |||||
| chr12:93681879
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.298+2807A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681879 | ||||||
| chr12:93681904
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.298+2832G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681904 | ||||||
| chr12:93681920
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(116): Show | 119 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.298+2848G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681920 | ||||||
| chr12:93681937
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(81): Show | 84 | HG00544.hp2 HG00597.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.298+2865A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681937 | ||||||
| chr12:93681960
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+2888T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93681960 | ||||||
| chr12:93682207
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+3135T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93682207 | ||||||
| chr12:93682675
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+3603A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93682675 | ||||||
| chr12:93682683
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.298+3611G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93682683 | ||||||
| chr12:93682718
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0002g0147 | 2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.298+3646C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93682718 | ||||||
| chr12:93682813
|
GA | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.298+3752delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93682813 | |||||
| chr12:93682835
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.298+3763G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93682835 | ||||||
| chr12:93683212
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.298+4140A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683212 | ||||||
| chr12:93683296
|
G | A | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.298+4224G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683296 | ||||||
| chr12:93683364
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.298+4292C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683364 | ||||||
| chr12:93683442
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298+4370G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683442 | ||||||
| chr12:93683450
|
C | T | 16 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+4378C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683450 | ||||||
| chr12:93683504
|
A | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(78): Show | 81 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.298+4432A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683504 | ||||||
| chr12:93683557
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+4485T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683557 | ||||||
| chr12:93683706
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+4634C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683706 | ||||||
| chr12:93683993
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+4921T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93683993 | ||||||
| chr12:93684087
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298+5015G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684087 | ||||||
| chr12:93684151
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+5079G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684151 | ||||||
| chr12:93684310
|
C | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+5238C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684310 | ||||||
| chr12:93684337
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+5265A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684337 | ||||||
| chr12:93684352
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(55): Show | 58 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.298+5280G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684352 | ||||||
| chr12:93684353
|
C | T | 43 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(40): Show | 43 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+5281C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684353 | ||||||
| chr12:93684366
|
T | C | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 104 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.298+5294T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684366 | ||||||
| chr12:93684414
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.298+5342T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684414 | ||||||
| chr12:93684431
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+5359T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684431 | ||||||
| chr12:93684768
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+5696G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684768 | ||||||
| chr12:93684977
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+5905T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93684977 | ||||||
| chr12:93685006
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+5934C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685006 | ||||||
| chr12:93685355
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+6283A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685355 | ||||||
| chr12:93685440
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298+6368C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685440 | ||||||
| chr12:93685444
|
G | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.298+6372G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685444 | ||||||
| chr12:93685518
|
A | C | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+6446A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685518 | ||||||
| chr12:93685558
|
A | G | 1 | a0001c0002t0001g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.298+6486A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685558 | ||||||
| chr12:93685707
|
A | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+6635A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685707 | ||||||
| chr12:93685736
|
G | A | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 36 | HG00544.hp1 HG01109.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.298+6664G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685736 | ||||||
| chr12:93685787
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+6715T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685787 | ||||||
| chr12:93685866
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0141 | 2 | NA18522.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.298+6794G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685866 | ||||||
| chr12:93685972
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+6900G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685972 | ||||||
| chr12:93685989
|
G | A | 1 | a0004c0006t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.298+6917G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93685989 | ||||||
| chr12:93686043
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.298+6971T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686043 | ||||||
| chr12:93686070
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | NA18949.hp1 NA19004.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.298+6998C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686070 | ||||||
| chr12:93686094
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+7022G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686094 | ||||||
| chr12:93686302
|
C | CAAA | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+7230_298+7231i others(5): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686302 | ||||||
| chr12:93686302
|
C | CAAAA | 40 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0066others(37): Show | 40 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.298+7230_298+7231i others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686302 | ||||||
| chr12:93686302
|
C | CAAAAA | 7 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0001g0138others(4): Show | 7 | HG01255.hp1 HG01358.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+7230_298+7231i others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686302 | ||||||
| chr12:93686303
|
C | A | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(57): Show | 60 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.298+7231C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686303 | ||||||
| chr12:93686303
|
C | CA | 12 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00544.hp1 NA18906.hp1 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+7231_298+7232i others(3): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686303 | ||||||
| chr12:93686304
|
C | A | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(78): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.298+7232C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686304 | ||||||
| chr12:93686305
|
A | C | 14 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG01081.hp1 HG01106.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+7233A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686305 | ||||||
| chr12:93686306
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.298+7234A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686306 | ||||||
| chr12:93686361
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298+7289A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686361 | ||||||
| chr12:93686821
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0003g0083 | 2 | HG01257.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.298+7749C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686821 | ||||||
| chr12:93686904
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.298+7832G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686904 | ||||||
| chr12:93686914
|
A | AT | 22 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0063others(19): Show | 22 | HG00544.hp1 HG01257.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.298+7855dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93686914 | |||||
| chr12:93686914
|
AT | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0072a0001c0001t0001g0084others(7): Show | 10 | HG01192.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+7855delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93686914 | |||||
| chr12:93686980
|
T | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+7908T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93686980 | ||||||
| chr12:93687063
|
C | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(102): Show | 105 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.298+7991C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687063 | ||||||
| chr12:93687255
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298+8183G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687255 | ||||||
| chr12:93687294
|
T | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0188others(2): Show | 5 | HG01071.hp1 HG01106.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+8222T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687294 | ||||||
| chr12:93687368
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+8296T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687368 | ||||||
| chr12:93687387
|
A | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0241a0001c0001t0001g0242others(5): Show | 8 | HG01257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+8315A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687387 | ||||||
| chr12:93687510
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.298+8438G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687510 | ||||||
| chr12:93687551
|
C | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0220a0001c0001t0001g0222 | 3 | NA18945.hp1 NA18993.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.298+8479C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687551 | ||||||
| chr12:93687552
|
G | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG00544.hp1 HG02040.hp1 HG03669.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+8480G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687552 | ||||||
| chr12:93687601
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+8529C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687601 | ||||||
| chr12:93687733
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.298+8661G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687733 | ||||||
| chr12:93687734
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.298+8662T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687734 | ||||||
| chr12:93687784
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298+8712T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687784 | ||||||
| chr12:93687844
|
C | G | 1 | a0002c0003t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298+8772C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93687844 | ||||||
| chr12:93688055
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0002g0147 | 2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.298+8983C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688055 | ||||||
| chr12:93688257
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.298+9185G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688257 | ||||||
| chr12:93688271
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.298+9199G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688271 | ||||||
| chr12:93688445
|
A | G | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+9373A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688445 | ||||||
| chr12:93688494
|
C | CA | 9 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0069others(6): Show | 9 | HG02257.hp1 HG02602.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+9438dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93688494 | |||||
| chr12:93688494
|
C | CAA | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+9437_298+9438d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93688494 | |||||
| chr12:93688666
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.298+9594G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688666 | ||||||
| chr12:93688802
|
C | T | 17 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(14): Show | 17 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.298+9730C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688802 | ||||||
| chr12:93688889
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+9817T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93688889 | ||||||
| chr12:93689056
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+9984T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689056 | ||||||
| chr12:93689098
|
T | G | 63 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(60): Show | 63 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.298+10026T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689098 | ||||||
| chr12:93689113
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.298+10041A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689113 | ||||||
| chr12:93689264
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298+10192C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689264 | ||||||
| chr12:93689268
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0220a0001c0001t0001g0222 | 3 | NA18945.hp1 NA18993.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.298+10196A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689268 | ||||||
| chr12:93689329
|
T | C | 48 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(45): Show | 48 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.298+10257T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689329 | ||||||
| chr12:93689486
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+10414C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689486 | ||||||
| chr12:93689487
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.298+10415A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689487 | ||||||
| chr12:93689603
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.298+10531T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689603 | ||||||
| chr12:93689663
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+10591C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689663 | ||||||
| chr12:93689893
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+10821G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689893 | ||||||
| chr12:93689900
|
T | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(102): Show | 105 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.298+10828T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689900 | ||||||
| chr12:93689904
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+10832A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93689904 | ||||||
| chr12:93690030
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+10958A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690030 | ||||||
| chr12:93690355
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+11283G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690355 | ||||||
| chr12:93690642
|
T | C | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+11570T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690642 | ||||||
| chr12:93690702
|
G | A | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+11630G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690702 | ||||||
| chr12:93690745
|
C | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | NA18949.hp1 NA19004.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.298+11673C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690745 | ||||||
| chr12:93690891
|
C | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+11819C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690891 | ||||||
| chr12:93690980
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0220a0001c0001t0001g0222 | 3 | NA18945.hp1 NA18993.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.298+11908A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93690980 | ||||||
| chr12:93691032
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+11960T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691032 | ||||||
| chr12:93691070
|
C | T | 1 | a0001c0002t0001g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.298+11998C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691070 | ||||||
| chr12:93691102
|
T | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.298+12030T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691102 | ||||||
| chr12:93691113
|
G | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+12041G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691113 | ||||||
| chr12:93691218
|
T | C | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+12146T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691218 | ||||||
| chr12:93691249
|
TGTTTTC | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0062others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298+12178_298+1218 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691249 | ||||||
| chr12:93691250
|
G | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(14): Show | 17 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+12178G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691250 | ||||||
| chr12:93691255
|
C | CT | 19 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0072others(16): Show | 19 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.298+12198dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93691255 | |||||
| chr12:93691255
|
CT | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(57): Show | 60 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.298+12198delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93691255 | |||||
| chr12:93691256
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0062others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298+12184T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691256 | ||||||
| chr12:93691314
|
C | T | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+12242C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691314 | ||||||
| chr12:93691339
|
C | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01516.hp1 HG01928.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+12267C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691339 | ||||||
| chr12:93691449
|
T | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+12377T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691449 | ||||||
| chr12:93691450
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+12378C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691450 | ||||||
| chr12:93691800
|
A | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+12728A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691800 | ||||||
| chr12:93691930
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.298+12858T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93691930 | ||||||
| chr12:93692043
|
A | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+12971A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692043 | ||||||
| chr12:93692071
|
C | T | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298+12999C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692071 | ||||||
| chr12:93692083
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298+13011T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692083 | ||||||
| chr12:93692124
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+13052T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692124 | ||||||
| chr12:93692126
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+13054A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692126 | ||||||
| chr12:93692217
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+13145C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692217 | ||||||
| chr12:93692288
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+13216T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692288 | ||||||
| chr12:93692394
|
C | A | 43 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(40): Show | 43 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+13322C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692394 | ||||||
| chr12:93692403
|
C | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+13331C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692403 | ||||||
| chr12:93692618
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+13546T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692618 | ||||||
| chr12:93692636
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+13564T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692636 | ||||||
| chr12:93692661
|
T | A | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+13589T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692661 | ||||||
| chr12:93692975
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+13903A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93692975 | ||||||
| chr12:93693324
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+14252C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693324 | ||||||
| chr12:93693401
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+14329T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693401 | ||||||
| chr12:93693415
|
A | G | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+14343A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693415 | ||||||
| chr12:93693417
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+14345G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693417 | ||||||
| chr12:93693532
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298+14460A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693532 | ||||||
| chr12:93693551
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+14479C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693551 | ||||||
| chr12:93693552
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(102): Show | 105 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.298+14480A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693552 | ||||||
| chr12:93693566
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+14494A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693566 | ||||||
| chr12:93693634
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+14562A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693634 | ||||||
| chr12:93693767
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0062others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298+14695C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693767 | ||||||
| chr12:93693866
|
C | G | 1 | a0001c0002t0001g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298+14794C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693866 | ||||||
| chr12:93693906
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+14834C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93693906 | ||||||
| chr12:93694021
|
T | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0157 | 3 | NA18942.hp2 NA18957.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.298+14949T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694021 | ||||||
| chr12:93694250
|
CT | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+15181delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93694250 | |||||
| chr12:93694407
|
G | C | 1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.298+15335G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694407 | ||||||
| chr12:93694409
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.298+15337A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694409 | ||||||
| chr12:93694423
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+15351C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694423 | ||||||
| chr12:93694621
|
G | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(18): Show | 21 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.298+15549G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694621 | ||||||
| chr12:93694639
|
A | G | 44 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+15567A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694639 | ||||||
| chr12:93694658
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+15586C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694658 | ||||||
| chr12:93694694
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+15622A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694694 | ||||||
| chr12:93694807
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+15735T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694807 | ||||||
| chr12:93694879
|
C | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(12): Show | 15 | HG01109.hp2 HG01257.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.298+15807C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694879 | ||||||
| chr12:93694893
|
TGATTTAT others(1): Show |
T | 6 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG01192.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+15826_298+1583 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93694893 | |||||
| chr12:93694978
|
G | A | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+15906G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93694978 | ||||||
| chr12:93695048
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+15976A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695048 | ||||||
| chr12:93695202
|
A | G | 1 | a0001c0002t0001g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.298+16130A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695202 | ||||||
| chr12:93695422
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+16350C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695422 | ||||||
| chr12:93695471
|
T | G | 1 | a0002c0003t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298+16399T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695471 | ||||||
| chr12:93695474
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+16402T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695474 | ||||||
| chr12:93695626
|
A | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0002t0001g0041others(3): Show | 6 | HG02040.hp2 HG02071.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+16554A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695626 | ||||||
| chr12:93695668
|
C | T | 43 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(40): Show | 43 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+16596C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695668 | ||||||
| chr12:93695680
|
C | A | 164 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(161): Show | 164 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.298+16608C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695680 | ||||||
| chr12:93695820
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.298+16748C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695820 | ||||||
| chr12:93695865
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+16793G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695865 | ||||||
| chr12:93695867
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.298+16795A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695867 | ||||||
| chr12:93695897
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.298+16825C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93695897 | ||||||
| chr12:93696096
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+17024C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696096 | ||||||
| chr12:93696102
|
T | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 61 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.298+17030T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696102 | ||||||
| chr12:93696116
|
G | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0021others(19): Show | 22 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.298+17044G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696116 | ||||||
| chr12:93696158
|
T | C | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 61 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.298+17086T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696158 | ||||||
| chr12:93696223
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG01106.hp1 HG01975.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.298+17151C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696223 | ||||||
| chr12:93696235
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+17163T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696235 | ||||||
| chr12:93696368
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+17296A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696368 | ||||||
| chr12:93696498
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.298+17426A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93696498 | ||||||
| chr12:93696626
|
TAGAC | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0062others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298+17557_298+1756 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93696626 | |||||
| chr12:93696745
|
G | GA | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 62 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.298+17683dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93696745 | |||||
| chr12:93697091
|
A | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 193 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.298+18019A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697091 | ||||||
| chr12:93697108
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+18036C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697108 | ||||||
| chr12:93697145
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.298+18073A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697145 | ||||||
| chr12:93697248
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+18176G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697248 | ||||||
| chr12:93697532
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+18460G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697532 | ||||||
| chr12:93697543
|
C | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+18471C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697543 | ||||||
| chr12:93697558
|
G | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+18486G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697558 | ||||||
| chr12:93697593
|
TAATAAGT others(2): Show |
T | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 60 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.298+18532_298+1854 others(13): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93697593 | |||||
| chr12:93697596
|
TAAGTTAA others(4): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298+18525_298+1853 others(15): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93697596 | ||||||
| chr12:93698223
|
T | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0021others(26): Show | 29 | HG00544.hp1 HG01257.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.298+19151T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698223 | ||||||
| chr12:93698263
|
T | G | 2 | a0001c0001t0001g0078a0002c0003t0001g0079 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+19191T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698263 | ||||||
| chr12:93698322
|
A | G | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00597.hp1 HG01081.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.298+19250A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698322 | ||||||
| chr12:93698360
|
G | A | 1 | a0003c0004t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.298+19288G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698360 | ||||||
| chr12:93698390
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+19318T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698390 | ||||||
| chr12:93698469
|
G | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+19397G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698469 | ||||||
| chr12:93698583
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+19511T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698583 | ||||||
| chr12:93698648
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+19576G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698648 | ||||||
| chr12:93698816
|
C | T | 2 | a0001c0001t0001g0078a0002c0003t0001g0079 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+19744C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698816 | ||||||
| chr12:93698914
|
C | G | 72 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(69): Show | 72 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.298+19842C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698914 | ||||||
| chr12:93698921
|
G | A | 3 | a0001c0001t0001g0040a0001c0002t0001g0041a0001c0005t0001g0042 | 3 | NA18977.hp2 NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.298+19849G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698921 | ||||||
| chr12:93698947
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0124a0001c0001t0001g0126others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+19875C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93698947 | ||||||
| chr12:93699056
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298+19984G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699056 | ||||||
| chr12:93699230
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+20158A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699230 | ||||||
| chr12:93699366
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+20294C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699366 | ||||||
| chr12:93699589
|
T | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+20517T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699589 | ||||||
| chr12:93699591
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+20519T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699591 | ||||||
| chr12:93699618
|
C | A | 71 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(68): Show | 71 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.298+20546C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699618 | ||||||
| chr12:93699640
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(15): Show | 18 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+20568G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699640 | ||||||
| chr12:93699647
|
T | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+20575T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699647 | ||||||
| chr12:93699985
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.298+20913C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699985 | ||||||
| chr12:93699986
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+20914G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93699986 | ||||||
| chr12:93700186
|
C | T | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+21114C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93700186 | ||||||
| chr12:93700241
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+21169A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93700241 | ||||||
| chr12:93700433
|
A | AT | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+21371dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93700433 | |||||
| chr12:93700770
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+21698G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93700770 | ||||||
| chr12:93700784
|
T | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(15): Show | 18 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+21712T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93700784 | ||||||
| chr12:93701043
|
ATGT | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+21976_298+2197 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701043 | |||||
| chr12:93701295
|
G | GAC | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.298+22259_298+2226 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
G | GACAC | 20 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0105others(17): Show | 20 | HG01192.hp2 HG01934.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+22257_298+2226 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
G | GACACAC | 10 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0096others(7): Show | 10 | HG01928.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+22255_298+2226 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
G | GACACACA others(1): Show |
18 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0072others(15): Show | 18 | HG01071.hp1 HG01106.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+22253_298+2226 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
G | GACACACA others(3): Show |
2 | a0001c0001t0001g0092a0001c0002t0001g0115 | 2 | HG00544.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.298+22251_298+2226 others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
G | GACACACA others(11): Show |
1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+22243_298+2226 others(22): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
GAC | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0030others(11): Show | 14 | HG00597.hp1 HG01109.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+22259_298+2226 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701295
|
GACAC | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0137a0001c0001t0001g0223others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+22257_298+2226 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93701295 | |||||
| chr12:93701397
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+22325C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701397 | ||||||
| chr12:93701483
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+22411C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701483 | ||||||
| chr12:93701672
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0002t0001g0032 | 3 | HG01978.hp1 NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.298+22600G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701672 | ||||||
| chr12:93701673
|
A | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.298+22601A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701673 | ||||||
| chr12:93701697
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+22625A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701697 | ||||||
| chr12:93701851
|
C | T | 1 | a0001c0001t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.298+22779C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701851 | ||||||
| chr12:93701946
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.298+22874T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93701946 | ||||||
| chr12:93702026
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+22954C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702026 | ||||||
| chr12:93702067
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+22995C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702067 | ||||||
| chr12:93702259
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+23187G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702259 | ||||||
| chr12:93702266
|
T | C | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.298+23194T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702266 | ||||||
| chr12:93702360
|
A | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+23288A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702360 | ||||||
| chr12:93702397
|
A | T | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.298+23325A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702397 | ||||||
| chr12:93702512
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+23440T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702512 | ||||||
| chr12:93702799
|
G | T | 1 | a0001c0002t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.298+23727G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702799 | ||||||
| chr12:93702812
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.298+23740C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702812 | ||||||
| chr12:93702944
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298+23872T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702944 | ||||||
| chr12:93702997
|
T | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+23925T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93702997 | ||||||
| chr12:93703054
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+23982G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703054 | ||||||
| chr12:93703113
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.298+24041T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703113 | ||||||
| chr12:93703153
|
A | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+24081A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703153 | ||||||
| chr12:93703212
|
A | AT | 11 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+24148dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703212 | |||||
| chr12:93703220
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.298+24148T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703220 | ||||||
| chr12:93703288
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.298+24216A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703288 | ||||||
| chr12:93703359
|
C | CT | 15 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(12): Show | 15 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.298+24303dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703359 | |||||
| chr12:93703359
|
CT | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0124others(3): Show | 6 | HG02559.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+24303delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703359 | |||||
| chr12:93703506
|
G | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+24434G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703506 | ||||||
| chr12:93703550
|
C | T | 1 | a0001c0001t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.298+24478C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703550 | ||||||
| chr12:93703599
|
C | T | 72 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(69): Show | 72 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.298+24527C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703599 | ||||||
| chr12:93703829
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.298+24757A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93703829 | ||||||
| chr12:93703978
|
C | CT | 91 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0027others(88): Show | 91 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.298+24928dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703978 | |||||
| chr12:93703978
|
C | CTT | 9 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG01255.hp2 HG01257.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+24927_298+2492 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703978 | |||||
| chr12:93703978
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0117 | 3 | HG02965.hp1 HG03669.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298+24918_298+2492 others(15): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93703978 | |||||
| chr12:93704173
|
A | G | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+25101A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704173 | ||||||
| chr12:93704271
|
A | G | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+25199A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704271 | ||||||
| chr12:93704496
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+25424A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704496 | ||||||
| chr12:93704536
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.298+25464G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704536 | ||||||
| chr12:93704595
|
G | A | 2 | a0001c0001t0001g0078a0002c0003t0001g0079 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+25523G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704595 | ||||||
| chr12:93704716
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+25644A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704716 | ||||||
| chr12:93704737
|
C | T | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+25665C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704737 | ||||||
| chr12:93704853
|
C | T | 8 | a0001c0001t0001g0028a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 8 | NA18747.hp1 NA18942.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+25781C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704853 | ||||||
| chr12:93704866
|
C | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG00544.hp1 HG02040.hp1 HG03669.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+25794C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704866 | ||||||
| chr12:93704912
|
G | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.298+25840G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704912 | ||||||
| chr12:93704928
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+25856C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93704928 | ||||||
| chr12:93705031
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+25959C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705031 | ||||||
| chr12:93705034
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+25962A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705034 | ||||||
| chr12:93705107
|
C | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01516.hp1 HG01928.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+26035C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705107 | ||||||
| chr12:93705487
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298+26415C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705487 | ||||||
| chr12:93705500
|
T | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+26428T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705500 | ||||||
| chr12:93705678
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298+26606A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705678 | ||||||
| chr12:93705703
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+26631G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705703 | ||||||
| chr12:93705713
|
T | C | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.298+26641T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705713 | ||||||
| chr12:93705835
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.298+26763T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705835 | ||||||
| chr12:93705929
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+26857C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93705929 | ||||||
| chr12:93706050
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.298+26978T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706050 | ||||||
| chr12:93706073
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+27001A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706073 | ||||||
| chr12:93706124
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298+27052T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706124 | ||||||
| chr12:93706239
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+27167C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706239 | ||||||
| chr12:93706354
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+27282A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706354 | ||||||
| chr12:93706433
|
G | GT | 24 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(21): Show | 24 | HG00639.hp2 HG01192.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.298+27368dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93706433 | |||||
| chr12:93706441
|
G | T | 2 | a0001c0001t0001g0152a0001c0002t0001g0179 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.298+27369G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706441 | ||||||
| chr12:93706475
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+27403C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706475 | ||||||
| chr12:93706608
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+27536C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706608 | ||||||
| chr12:93706655
|
T | A | 1 | a0001c0002t0001g0204 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.298+27583T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706655 | ||||||
| chr12:93706735
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+27663A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706735 | ||||||
| chr12:93706740
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+27668G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706740 | ||||||
| chr12:93706803
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+27731A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706803 | ||||||
| chr12:93706850
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+27778C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706850 | ||||||
| chr12:93706954
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0220a0001c0001t0001g0222 | 3 | NA18945.hp1 NA18993.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.298+27882A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706954 | ||||||
| chr12:93706992
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.298+27920G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93706992 | ||||||
| chr12:93707447
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.298+28375G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93707447 | ||||||
| chr12:93707470
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+28398G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93707470 | ||||||
| chr12:93707766
|
G | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+28694G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93707766 | ||||||
| chr12:93707952
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+28880G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93707952 | ||||||
| chr12:93708023
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.298+28951A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708023 | ||||||
| chr12:93708085
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0215 | 2 | NA18953.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.298+29013G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708085 | ||||||
| chr12:93708099
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+29027T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708099 | ||||||
| chr12:93708115
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+29043G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708115 | ||||||
| chr12:93708258
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+29186A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708258 | ||||||
| chr12:93708328
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+29256A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708328 | ||||||
| chr12:93708353
|
C | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.298+29281C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708353 | ||||||
| chr12:93708375
|
G | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 61 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.298+29303G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708375 | ||||||
| chr12:93708678
|
A | G | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.298+29606A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708678 | ||||||
| chr12:93708733
|
C | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+29661C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708733 | ||||||
| chr12:93708743
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+29671T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708743 | ||||||
| chr12:93708892
|
G | C | 17 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(14): Show | 17 | HG00597.hp2 HG01928.hp2 HG03239.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+29820G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93708892 | ||||||
| chr12:93709139
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+30067G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93709139 | ||||||
| chr12:93709447
|
G | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+30375G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93709447 | ||||||
| chr12:93709532
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.298+30460G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93709532 | ||||||
| chr12:93709799
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+30727G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93709799 | ||||||
| chr12:93709872
|
G | A | 2 | a0001c0001t0001g0078a0002c0003t0001g0079 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+30800G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93709872 | ||||||
| chr12:93710232
|
A | C | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.298+31160A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710232 | ||||||
| chr12:93710248
|
A | G | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.298+31176A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710248 | ||||||
| chr12:93710264
|
T | C | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+31192T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710264 | ||||||
| chr12:93710286
|
G | A | 10 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | NA18945.hp2 NA18953.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+31214G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710286 | ||||||
| chr12:93710345
|
C | CT | 92 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(89): Show | 92 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.298+31291dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93710345 | |||||
| chr12:93710345
|
CT | C | 19 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(16): Show | 19 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.298+31291delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93710345 | |||||
| chr12:93710369
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.298+31297G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710369 | ||||||
| chr12:93710449
|
G | A | 3 | a0001c0001t0001g0202a0001c0002t0001g0022a0001c0002t0001g0205 | 3 | NA18977.hp1 NA18988.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.298+31377G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710449 | ||||||
| chr12:93710505
|
T | C | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.298+31433T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710505 | ||||||
| chr12:93710506
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.298+31434G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710506 | ||||||
| chr12:93710731
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+31659C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710731 | ||||||
| chr12:93710774
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+31702G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710774 | ||||||
| chr12:93710826
|
G | C | 1 | a0001c0002t0001g0100 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.298+31754G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93710826 | ||||||
| chr12:93711026
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.298+31954C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711026 | ||||||
| chr12:93711055
|
C | CT | 85 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0025others(82): Show | 85 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.298+32002dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93711055 | |||||
| chr12:93711055
|
C | CTT | 7 | a0001c0001t0001g0055a0001c0001t0001g0072a0001c0001t0001g0178others(4): Show | 7 | HG00735.hp1 HG02293.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+32001_298+3200 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93711055 | |||||
| chr12:93711055
|
CT | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0108a0001c0001t0001g0109others(11): Show | 14 | HG00544.hp1 HG02040.hp1 HG03669.hp2 others(11): Show |
intron_variant | MODIFIER | c.298+32002delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93711055 | |||||
| chr12:93711239
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.298+32167A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711239 | ||||||
| chr12:93711481
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+32409A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711481 | ||||||
| chr12:93711491
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+32419C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711491 | ||||||
| chr12:93711756
|
C | CT | 6 | a0001c0001t0001g0091a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+32698dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93711756 | |||||
| chr12:93711756
|
CT | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(203): Show |
intron_variant | MODIFIER | c.298+32698delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93711756 | |||||
| chr12:93711917
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.298+32845G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711917 | ||||||
| chr12:93711974
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.298+32902T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93711974 | ||||||
| chr12:93712190
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+33118C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712190 | ||||||
| chr12:93712197
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0194a0001c0001t0001g0226 | 3 | HG02886.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.298+33125T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712197 | ||||||
| chr12:93712236
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+33164T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712236 | ||||||
| chr12:93712238
|
T | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+33166T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712238 | ||||||
| chr12:93712361
|
C | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(15): Show | 18 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+33289C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712361 | ||||||
| chr12:93712403
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+33331G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712403 | ||||||
| chr12:93712580
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+33508T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712580 | ||||||
| chr12:93712590
|
A | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 185 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(182): Show |
intron_variant | MODIFIER | c.298+33518A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712590 | ||||||
| chr12:93712693
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.298+33621T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712693 | ||||||
| chr12:93712931
|
T | C | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+33859T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93712931 | ||||||
| chr12:93713238
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298+34166G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713238 | ||||||
| chr12:93713265
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+34193G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713265 | ||||||
| chr12:93713573
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+34501T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713573 | ||||||
| chr12:93713621
|
CG | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(20): Show | 23 | HG00544.hp1 HG00639.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.298+34550delG | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713621 | ||||||
| chr12:93713766
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.298+34694A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713766 | ||||||
| chr12:93713778
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.298+34706T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713778 | ||||||
| chr12:93713936
|
C | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.298+34864C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93713936 | ||||||
| chr12:93714262
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.298+35190C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714262 | ||||||
| chr12:93714337
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.298+35265G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714337 | ||||||
| chr12:93714396
|
A | G | 72 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(69): Show | 72 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.298+35324A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714396 | ||||||
| chr12:93714474
|
G | A | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+35402G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714474 | ||||||
| chr12:93714572
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+35500G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714572 | ||||||
| chr12:93714710
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.298+35638C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714710 | ||||||
| chr12:93714711
|
G | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+35639G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714711 | ||||||
| chr12:93714753
|
G | A | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.298+35681G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714753 | ||||||
| chr12:93714755
|
C | A | 2 | a0001c0002t0001g0164a0001c0002t0001g0165 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.298+35683C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714755 | ||||||
| chr12:93714778
|
A | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.298+35706A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93714778 | ||||||
| chr12:93715038
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+35966A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715038 | ||||||
| chr12:93715058
|
T | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+35986T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715058 | ||||||
| chr12:93715065
|
TA | T | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00544.hp1 HG01109.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.298+36003delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93715065 | |||||
| chr12:93715065
|
TAA | T | 20 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+36002_298+3600 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93715065 | |||||
| chr12:93715067
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+35995A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715067 | ||||||
| chr12:93715070
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+35998A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715070 | ||||||
| chr12:93715161
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+36089A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715161 | ||||||
| chr12:93715376
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.298+36304A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715376 | ||||||
| chr12:93715851
|
A | G | 1 | a0001c0001t0002g0001 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.298+36779A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715851 | ||||||
| chr12:93715913
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+36841G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715913 | ||||||
| chr12:93715922
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+36850G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715922 | ||||||
| chr12:93715943
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298+36871A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93715943 | ||||||
| chr12:93716118
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+37046C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716118 | ||||||
| chr12:93716131
|
C | CA | 8 | a0001c0001t0001g0062a0001c0001t0001g0117a0001c0001t0001g0241others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+37073dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93716131 | |||||
| chr12:93716131
|
C | CAA | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+37072_298+3707 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93716131 | |||||
| chr12:93716131
|
CA | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+37073delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93716131 | |||||
| chr12:93716483
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+37411C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716483 | ||||||
| chr12:93716614
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+37542G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716614 | ||||||
| chr12:93716664
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+37592C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716664 | ||||||
| chr12:93716712
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+37640G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716712 | ||||||
| chr12:93716824
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.298+37752G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93716824 | ||||||
| chr12:93717024
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+37952A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717024 | ||||||
| chr12:93717213
|
A | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0078others(17): Show | 20 | HG00544.hp1 HG02040.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.298+38141A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717213 | ||||||
| chr12:93717314
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+38242C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717314 | ||||||
| chr12:93717319
|
T | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+38247T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717319 | ||||||
| chr12:93717442
|
A | C | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+38370A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717442 | ||||||
| chr12:93717808
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0063 | 2 | HG02572.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.298+38736G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717808 | ||||||
| chr12:93717811
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.298+38739G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93717811 | ||||||
| chr12:93718060
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+38988C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718060 | ||||||
| chr12:93718064
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+38992C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718064 | ||||||
| chr12:93718132
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+39060T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718132 | ||||||
| chr12:93718226
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 53 | HG00544.hp1 HG01109.hp2 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.298+39154G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718226 | ||||||
| chr12:93718248
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0158others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+39176G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718248 | ||||||
| chr12:93718302
|
C | T | 29 | a0001c0001t0001g0113a0001c0001t0001g0134a0001c0001t0001g0146others(26): Show | 29 | HG00544.hp2 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.298+39230C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718302 | ||||||
| chr12:93718313
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+39241A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718313 | ||||||
| chr12:93718431
|
A | G | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00544.hp1 HG01109.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.298+39359A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718431 | ||||||
| chr12:93718578
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.298+39506A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718578 | ||||||
| chr12:93718805
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298+39733G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718805 | ||||||
| chr12:93718959
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+39887C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93718959 | ||||||
| chr12:93719107
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.298+40035T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719107 | ||||||
| chr12:93719192
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.298+40120A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719192 | ||||||
| chr12:93719282
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+40210C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719282 | ||||||
| chr12:93719392
|
A | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+40320A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719392 | ||||||
| chr12:93719410
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+40338C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719410 | ||||||
| chr12:93719533
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0158a0001c0001t0001g0166 | 3 | HG02258.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.298+40461C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719533 | ||||||
| chr12:93719534
|
T | G | 6 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG01192.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+40462T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719534 | ||||||
| chr12:93719760
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.298+40688A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719760 | ||||||
| chr12:93719801
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+40729T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719801 | ||||||
| chr12:93719909
|
T | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+40837T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719909 | ||||||
| chr12:93719931
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+40859G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93719931 | ||||||
| chr12:93720018
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+40946G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720018 | ||||||
| chr12:93720309
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+41237A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720309 | ||||||
| chr12:93720343
|
A | G | 1 | a0001c0001t0003g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.298+41271A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720343 | ||||||
| chr12:93720376
|
G | C | 1 | a0001c0002t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.298+41304G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720376 | ||||||
| chr12:93720448
|
T | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0107a0001c0001t0001g0138others(4): Show | 7 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+41376T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720448 | ||||||
| chr12:93720506
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+41434G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720506 | ||||||
| chr12:93720575
|
C | T | 1 | a0001c0002t0005g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.298+41503C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720575 | ||||||
| chr12:93720739
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+41667G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720739 | ||||||
| chr12:93720760
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+41688G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720760 | ||||||
| chr12:93720916
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00544.hp1 HG01109.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.298+41844G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720916 | ||||||
| chr12:93720962
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0158a0001c0001t0001g0166 | 3 | HG02258.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.298+41890T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93720962 | ||||||
| chr12:93721053
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+41981A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721053 | ||||||
| chr12:93721140
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+42068G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721140 | ||||||
| chr12:93721256
|
G | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0207others(1): Show | 4 | HG01928.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+42184G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721256 | ||||||
| chr12:93721413
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0158others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+42341G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721413 | ||||||
| chr12:93721444
|
T | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+42372T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721444 | ||||||
| chr12:93721460
|
C | CAT | 10 | a0001c0001t0001g0062a0001c0001t0001g0107a0001c0001t0001g0117others(7): Show | 10 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+42398_298+4239 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93721460 | |||||
| chr12:93721597
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0215 | 2 | NA18953.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.298+42525A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721597 | ||||||
| chr12:93721691
|
T | G | 2 | a0001c0001t0001g0152a0001c0002t0001g0179 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.298+42619T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721691 | ||||||
| chr12:93721864
|
A | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+42792A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721864 | ||||||
| chr12:93721896
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.298+42824A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93721896 | ||||||
| chr12:93722074
|
T | C | 3 | a0001c0001t0001g0150a0001c0002t0001g0115a0001c0002t0001g0149 | 3 | HG00544.hp1 NA18972.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.298+43002T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722074 | ||||||
| chr12:93722234
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.298+43162C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722234 | ||||||
| chr12:93722303
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+43231C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722303 | ||||||
| chr12:93722360
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.298+43288C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722360 | ||||||
| chr12:93722473
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+43401C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722473 | ||||||
| chr12:93722634
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0158a0001c0001t0001g0166 | 3 | HG02258.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.298+43562C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722634 | ||||||
| chr12:93722694
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+43622A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722694 | ||||||
| chr12:93722766
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0158a0001c0001t0001g0166 | 3 | HG02258.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.298+43694A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93722766 | ||||||
| chr12:93723030
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+43958T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723030 | ||||||
| chr12:93723322
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+44250A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723322 | ||||||
| chr12:93723442
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.298+44370G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723442 | ||||||
| chr12:93723708
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.298+44636A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723708 | ||||||
| chr12:93723743
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(7): Show | 10 | HG00639.hp2 HG01109.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+44671A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723743 | ||||||
| chr12:93723884
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0117 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+44812G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93723884 | ||||||
| chr12:93724098
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0002g0147 | 2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.298+45026G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724098 | ||||||
| chr12:93724333
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.298+45261C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724333 | ||||||
| chr12:93724378
|
C | CA | 9 | a0001c0001t0001g0091a0001c0001t0001g0241a0001c0001t0001g0242others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+45324dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93724378 | |||||
| chr12:93724378
|
CA | C | 103 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 103 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.298+45324delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93724378 | |||||
| chr12:93724378
|
CAA | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0117others(3): Show | 6 | HG01099.hp2 HG01168.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+45323_298+4532 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93724378 | |||||
| chr12:93724456
|
G | A | 74 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(71): Show | 74 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.298+45384G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724456 | ||||||
| chr12:93724559
|
T | G | 2 | a0001c0002t0001g0051a0001c0002t0001g0052 | 2 | NA18949.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.298+45487T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724559 | ||||||
| chr12:93724613
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298+45541T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724613 | ||||||
| chr12:93724639
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.298+45567T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724639 | ||||||
| chr12:93724827
|
C | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(14): Show | 17 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+45755C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724827 | ||||||
| chr12:93724827
|
C | T | 1 | a0001c0002t0001g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.298+45755C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93724827 | ||||||
| chr12:93724841
|
C | CTTA | 19 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(16): Show | 19 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.298+45786_298+4578 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93724841 | |||||
| chr12:93725010
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+45938G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725010 | ||||||
| chr12:93725021
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(79): Show | 82 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+45949T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725021 | ||||||
| chr12:93725070
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.298+45998C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725070 | ||||||
| chr12:93725107
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0241others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+46035G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725107 | ||||||
| chr12:93725272
|
A | G | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+46200A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725272 | ||||||
| chr12:93725323
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.298+46251A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93725323 | ||||||
| chr12:93725448
|
T | TGCTGTCT others(15): Show |
14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+46378_298+4637 others(26): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93725448 | |||||
| chr12:93726042
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+46970T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726042 | ||||||
| chr12:93726061
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+46989A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726061 | ||||||
| chr12:93726094
|
G | GT | 62 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0065others(59): Show | 62 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.298+47046dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93726094 | |||||
| chr12:93726094
|
GT | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01071.hp1 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.298+47046delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93726094 | |||||
| chr12:93726094
|
GTTTTTTT others(1): Show |
G | 17 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(14): Show | 17 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+47039_298+4704 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93726094 | |||||
| chr12:93726094
|
GTTTTTTT others(3): Show |
G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+47037_298+4704 others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93726094 | |||||
| chr12:93726105
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+47033T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726105 | ||||||
| chr12:93726141
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298+47069G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726141 | ||||||
| chr12:93726207
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+47135G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726207 | ||||||
| chr12:93726265
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+47193A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726265 | ||||||
| chr12:93726276
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01106.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.298+47204G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726276 | ||||||
| chr12:93726406
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+47334T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726406 | ||||||
| chr12:93726457
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.298+47385G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726457 | ||||||
| chr12:93726486
|
T | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0117 | 3 | HG02965.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+47414T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726486 | ||||||
| chr12:93726532
|
C | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(2): Show | 5 | NA18955.hp2 NA18975.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+47460C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726532 | ||||||
| chr12:93726563
|
C | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(79): Show | 82 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+47491C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726563 | ||||||
| chr12:93726702
|
T | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(79): Show | 82 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+47630T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726702 | ||||||
| chr12:93726748
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0107a0001c0001t0001g0138others(4): Show | 7 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+47676A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726748 | ||||||
| chr12:93726956
|
G | A | 122 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.298+47884G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726956 | ||||||
| chr12:93726961
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+47889C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93726961 | ||||||
| chr12:93727080
|
C | T | 1 | a0002c0003t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298+48008C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727080 | ||||||
| chr12:93727093
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.298+48021G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727093 | ||||||
| chr12:93727219
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+48147G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727219 | ||||||
| chr12:93727271
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.298+48199G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727271 | ||||||
| chr12:93727277
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298+48205T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727277 | ||||||
| chr12:93727499
|
T | C | 74 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(71): Show | 74 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.298+48427T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727499 | ||||||
| chr12:93727504
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+48432C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727504 | ||||||
| chr12:93727538
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(79): Show | 82 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+48466T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727538 | ||||||
| chr12:93727583
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.298+48511G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727583 | ||||||
| chr12:93727678
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.298+48606G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93727678 | ||||||
| chr12:93727847
|
TCTGGATG others(3): Show |
T | 3 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0117 | 3 | HG02965.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.298+48778_298+4878 others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93727847 | |||||
| chr12:93728001
|
G | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+48929G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728001 | ||||||
| chr12:93728121
|
T | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0107others(11): Show | 14 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.298+49049T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728121 | ||||||
| chr12:93728278
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+49206A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728278 | ||||||
| chr12:93728443
|
C | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(75): Show | 78 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+49371C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728443 | ||||||
| chr12:93728478
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+49406T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728478 | ||||||
| chr12:93728539
|
C | T | 74 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(71): Show | 74 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.298+49467C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728539 | ||||||
| chr12:93728666
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.298+49594T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728666 | ||||||
| chr12:93728795
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+49723G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93728795 | ||||||
| chr12:93729005
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+49933A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729005 | ||||||
| chr12:93729088
|
G | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+50016G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729088 | ||||||
| chr12:93729468
|
T | C | 1 | a0001c0002t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.298+50396T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729468 | ||||||
| chr12:93729515
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0241others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+50443G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729515 | ||||||
| chr12:93729677
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG00597.hp2 NA18747.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+50605C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729677 | ||||||
| chr12:93729700
|
G | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG00544.hp1 HG02040.hp1 HG03669.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+50628G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93729700 | ||||||
| chr12:93729785
|
C | CA | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(51): Show | 54 | HG00544.hp1 HG00639.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.298+50731dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93729785 | |||||
| chr12:93729785
|
CA | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0241a0001c0001t0001g0242others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+50731delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93729785 | |||||
| chr12:93730041
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+50969C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730041 | ||||||
| chr12:93730063
|
A | G | 1 | a0001c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.298+50991A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730063 | ||||||
| chr12:93730212
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+51140C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730212 | ||||||
| chr12:93730433
|
T | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+51361T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730433 | ||||||
| chr12:93730717
|
C | CT | 13 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0150others(10): Show | 13 | HG01109.hp2 HG01192.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+51663dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93730717 | |||||
| chr12:93730770
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG03688.hp1 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.298+51698C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730770 | ||||||
| chr12:93730775
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+51703G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730775 | ||||||
| chr12:93730784
|
C | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(75): Show | 78 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+51712C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730784 | ||||||
| chr12:93730996
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+51924G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93730996 | ||||||
| chr12:93731013
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+51941C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731013 | ||||||
| chr12:93731265
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.298+52193A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731265 | ||||||
| chr12:93731398
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01192.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+52326T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731398 | ||||||
| chr12:93731684
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(79): Show | 82 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+52612T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731684 | ||||||
| chr12:93731844
|
C | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+52772C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731844 | ||||||
| chr12:93731907
|
C | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0241others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+52835C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731907 | ||||||
| chr12:93731992
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.298+52920C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93731992 | ||||||
| chr12:93732009
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.298+52937G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732009 | ||||||
| chr12:93732031
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | NA18949.hp1 NA19004.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.298+52959G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732031 | ||||||
| chr12:93732076
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+53004C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732076 | ||||||
| chr12:93732077
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+53005G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732077 | ||||||
| chr12:93732139
|
G | GA | 33 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0062others(30): Show | 33 | HG00544.hp1 HG00639.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.298+53081dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93732139 | |||||
| chr12:93732209
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+53137T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732209 | ||||||
| chr12:93732286
|
TTCAGTG | T | 74 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(71): Show | 74 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.298+53217_298+5322 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93732286 | |||||
| chr12:93732322
|
G | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(69): Show | 72 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.298+53250G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732322 | ||||||
| chr12:93732401
|
G | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0158a0001c0001t0001g0166 | 3 | HG02258.hp1 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.298+53329G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732401 | ||||||
| chr12:93732451
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.298+53379A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732451 | ||||||
| chr12:93732565
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.298+53493A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732565 | ||||||
| chr12:93732929
|
T | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298+53857T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93732929 | ||||||
| chr12:93733079
|
G | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(69): Show | 72 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.298+54007G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733079 | ||||||
| chr12:93733103
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.298+54031A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733103 | ||||||
| chr12:93733149
|
T | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(77): Show | 80 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.298+54077T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733149 | ||||||
| chr12:93733201
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.298+54129C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733201 | ||||||
| chr12:93733226
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+54154G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733226 | ||||||
| chr12:93733403
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+54331G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733403 | ||||||
| chr12:93733466
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+54394C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733466 | ||||||
| chr12:93733529
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+54457C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733529 | ||||||
| chr12:93733538
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298+54466G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733538 | ||||||
| chr12:93733541
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0224others(1): Show | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+54469G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733541 | ||||||
| chr12:93733713
|
GATTC | G | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+54648_298+5465 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93733713 | |||||
| chr12:93733741
|
G | GT | 6 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0096others(3): Show | 6 | HG00597.hp1 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+54684dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93733741 | |||||
| chr12:93733888
|
A | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0241others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+54816A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733888 | ||||||
| chr12:93733943
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+54871C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733943 | ||||||
| chr12:93733998
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298+54926A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93733998 | ||||||
| chr12:93734005
|
C | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0241a0001c0001t0001g0242others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+54933C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93734005 | ||||||
| chr12:93734041
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0108others(15): Show | 18 | HG00544.hp1 HG02040.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+54969A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93734041 | ||||||
| chr12:93734155
|
C | T | 71 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0055others(68): Show | 71 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.298+55083C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93734155 | ||||||
| chr12:93734159
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298+55087C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93734159 | ||||||
| chr12:93734263
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+55191T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93734263 | ||||||
| chr12:93735049
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298+55977A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735049 | ||||||
| chr12:93735077
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298+56005T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735077 | ||||||
| chr12:93735090
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0117a0001c0001t0001g0208 | 3 | HG02965.hp1 NA18522.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.298+56018G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735090 | ||||||
| chr12:93735186
|
G | A | 1 | a0003c0004t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.298+56114G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735186 | ||||||
| chr12:93735194
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.298+56122C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735194 | ||||||
| chr12:93735287
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+56215G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735287 | ||||||
| chr12:93735377
|
T | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0063others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+56305T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735377 | ||||||
| chr12:93735421
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298+56349T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735421 | ||||||
| chr12:93735584
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.298+56512T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735584 | ||||||
| chr12:93735743
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0226 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.298+56671G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735743 | ||||||
| chr12:93735756
|
G | GA | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(2): Show | 5 | NA18968.hp1 NA18975.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+56687dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93735756 | |||||
| chr12:93735793
|
A | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00597.hp1 HG02257.hp1 HG02559.hp1 others(31): Show |
intron_variant | MODIFIER | c.298+56721A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735793 | ||||||
| chr12:93735795
|
C | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00597.hp1 HG02257.hp1 HG02559.hp1 others(31): Show |
intron_variant | MODIFIER | c.298+56723C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735795 | ||||||
| chr12:93735796
|
TAG | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00597.hp1 HG02257.hp1 HG02559.hp1 others(31): Show |
intron_variant | MODIFIER | c.298+56726_298+5672 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93735796 | |||||
| chr12:93735863
|
G | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0231others(1): Show | 4 | HG01516.hp1 HG01928.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+56791G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93735863 | ||||||
| chr12:93736037
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+56965A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736037 | ||||||
| chr12:93736444
|
C | T | 12 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0087others(9): Show | 12 | HG00597.hp1 NA18747.hp2 NA18977.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+57372C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736444 | ||||||
| chr12:93736493
|
T | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(29): Show | 32 | HG01081.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.298+57421T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736493 | ||||||
| chr12:93736558
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.298+57486G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736558 | ||||||
| chr12:93736581
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.298+57509T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736581 | ||||||
| chr12:93736937
|
T | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0124others(7): Show | 10 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+57865T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736937 | ||||||
| chr12:93736952
|
T | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+57880T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93736952 | ||||||
| chr12:93737191
|
T | A | 77 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(74): Show | 77 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.298+58119T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737191 | ||||||
| chr12:93737348
|
G | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0025others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.298+58276G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737348 | ||||||
| chr12:93737454
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.298+58382A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737454 | ||||||
| chr12:93737483
|
A | G | 57 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0025others(54): Show | 57 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.298+58411A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737483 | ||||||
| chr12:93737535
|
T | G | 77 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(74): Show | 77 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.298+58463T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737535 | ||||||
| chr12:93737633
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0075 | 3 | HG02809.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.298+58561T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93737633 | ||||||
| chr12:93738037
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0090others(3): Show | 6 | HG01884.hp1 HG02683.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+58965G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738037 | ||||||
| chr12:93738055
|
G | C | 1 | a0004c0006t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.298+58983G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738055 | ||||||
| chr12:93738281
|
G | T | 39 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG01081.hp1 HG01496.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.298+59209G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738281 | ||||||
| chr12:93738284
|
T | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0124others(7): Show | 10 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+59212T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738284 | ||||||
| chr12:93738410
|
T | A | 97 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(94): Show | 97 | HG00597.hp1 HG00639.hp2 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.298+59338T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738410 | ||||||
| chr12:93738442
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298+59370A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738442 | ||||||
| chr12:93738514
|
A | G | 51 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0025others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.298+59442A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738514 | ||||||
| chr12:93738576
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+59504A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738576 | ||||||
| chr12:93738801
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.298+59729A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738801 | ||||||
| chr12:93738837
|
AAG | A | 78 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(75): Show | 78 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+59770_298+5977 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93738837 | |||||
| chr12:93738842
|
A | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0025others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.298+59770A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738842 | ||||||
| chr12:93738937
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298+59865T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93738937 | ||||||
| chr12:93739045
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298+59973T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739045 | ||||||
| chr12:93739304
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+60232A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739304 | ||||||
| chr12:93739333
|
GAT | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(243): Show |
intron_variant | MODIFIER | c.298+60276_298+6027 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93739333 | |||||
| chr12:93739407
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.298+60335A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739407 | ||||||
| chr12:93739508
|
A | G | 77 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(74): Show | 77 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.298+60436A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739508 | ||||||
| chr12:93739550
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+60478T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739550 | ||||||
| chr12:93739647
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298+60575C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739647 | ||||||
| chr12:93739697
|
A | G | 51 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0025others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.298+60625A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739697 | ||||||
| chr12:93739953
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.298+60881T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93739953 | ||||||
| chr12:93740214
|
A | G | 2 | a0001c0002t0001g0164a0001c0002t0001g0165 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.298+61142A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93740214 | ||||||
| chr12:93740488
|
G | A | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(30): Show | 33 | HG00597.hp1 HG02257.hp1 HG02559.hp1 others(30): Show |
intron_variant | MODIFIER | c.298+61416G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93740488 | ||||||
| chr12:93740638
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+61566A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93740638 | ||||||
| chr12:93740774
|
A | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+61702A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93740774 | ||||||
| chr12:93740838
|
T | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0169 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+61766T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93740838 | ||||||
| chr12:93741162
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.298+62090C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741162 | ||||||
| chr12:93741290
|
T | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG02451.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+62218T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741290 | ||||||
| chr12:93741493
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+62421C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741493 | ||||||
| chr12:93741572
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+62500C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741572 | ||||||
| chr12:93741592
|
C | T | 39 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG01081.hp1 HG01496.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.298+62520C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741592 | ||||||
| chr12:93741689
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298+62617G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741689 | ||||||
| chr12:93741758
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+62686G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741758 | ||||||
| chr12:93741854
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+62782G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741854 | ||||||
| chr12:93741909
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.298+62837T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741909 | ||||||
| chr12:93741952
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0146 | 3 | HG00544.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.298+62880T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741952 | ||||||
| chr12:93741961
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.298+62889T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741961 | ||||||
| chr12:93741976
|
G | T | 12 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0178others(9): Show | 12 | HG01516.hp1 HG01928.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+62904G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93741976 | ||||||
| chr12:93742162
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+63090G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742162 | ||||||
| chr12:93742233
|
G | C | 189 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 189 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.298+63161G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742233 | ||||||
| chr12:93742440
|
G | GCCGGCTG others(12): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0158others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+63378_298+6339 others(23): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93742440 | |||||
| chr12:93742573
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.298+63501T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742573 | ||||||
| chr12:93742630
|
A | G | 31 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(28): Show | 31 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.298+63558A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742630 | ||||||
| chr12:93742760
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+63688C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742760 | ||||||
| chr12:93742778
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+63706A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93742778 | ||||||
| chr12:93743230
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298+64158G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743230 | ||||||
| chr12:93743310
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0124others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+64238C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743310 | ||||||
| chr12:93743336
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+64264T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743336 | ||||||
| chr12:93743729
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+64657G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743729 | ||||||
| chr12:93743767
|
G | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03041.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298+64695G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743767 | ||||||
| chr12:93743896
|
C | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0140others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+64824C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93743896 | ||||||
| chr12:93744144
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0098others(14): Show | 17 | HG00544.hp1 HG01106.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+65072G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744144 | ||||||
| chr12:93744286
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+65214T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744286 | ||||||
| chr12:93744303
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.298+65231T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744303 | ||||||
| chr12:93744340
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.298+65268T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744340 | ||||||
| chr12:93744420
|
A | C | 60 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(57): Show | 60 | HG01081.hp1 HG01257.hp2 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.298+65348A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744420 | ||||||
| chr12:93744586
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0242others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+65514T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744586 | ||||||
| chr12:93744622
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.298+65550C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744622 | ||||||
| chr12:93744656
|
T | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.298+65584T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744656 | ||||||
| chr12:93744822
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03041.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298+65750A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93744822 | ||||||
| chr12:93745009
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0223 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.298+65937A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745009 | ||||||
| chr12:93745036
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298+65964G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745036 | ||||||
| chr12:93745078
|
T | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0087others(8): Show | 11 | HG00597.hp1 NA18747.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+66006T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745078 | ||||||
| chr12:93745289
|
A | G | 1 | a0001c0002t0001g0191 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.298+66217A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745289 | ||||||
| chr12:93745438
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0116others(2): Show | 5 | HG02040.hp1 NA18967.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+66366T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745438 | ||||||
| chr12:93745607
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.298+66535C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745607 | ||||||
| chr12:93745642
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+66570T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745642 | ||||||
| chr12:93745746
|
T | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+66674T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93745746 | ||||||
| chr12:93746022
|
A | C | 1 | a0001c0002t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.298+66950A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93746022 | ||||||
| chr12:93746687
|
C | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(83): Show | 86 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.298+67615C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93746687 | ||||||
| chr12:93746782
|
A | AT | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 36 | HG00597.hp1 HG01081.hp2 HG02257.hp1 others(33): Show |
intron_variant | MODIFIER | c.298+67725dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93746782 | |||||
| chr12:93746916
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG02970.hp2 HG03195.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.298+67844C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93746916 | ||||||
| chr12:93747166
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.298+68094G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747166 | ||||||
| chr12:93747212
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0242others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+68140G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747212 | ||||||
| chr12:93747281
|
C | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0224others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+68209C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747281 | ||||||
| chr12:93747284
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0002t0001g0080others(1): Show | 4 | NA18612.hp1 NA19003.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+68212G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747284 | ||||||
| chr12:93747393
|
T | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0224others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+68321T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747393 | ||||||
| chr12:93747457
|
TTTC | T | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(3): Show | 6 | NA18955.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+68394_298+6839 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93747457 | |||||
| chr12:93747483
|
T | C | 188 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(185): Show | 188 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.298+68411T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747483 | ||||||
| chr12:93747523
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+68451C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747523 | ||||||
| chr12:93747680
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0223 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.298+68608C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747680 | ||||||
| chr12:93747724
|
C | T | 53 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(50): Show | 53 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(50): Show |
intron_variant | MODIFIER | c.298+68652C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747724 | ||||||
| chr12:93747760
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0001g0218others(1): Show | 4 | HG00639.hp1 HG00735.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+68688C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747760 | ||||||
| chr12:93747764
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | NA18942.hp1 NA18979.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.298+68692C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747764 | ||||||
| chr12:93747929
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298+68857T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747929 | ||||||
| chr12:93747988
|
G | GA | 7 | a0001c0001t0001g0096a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG02451.hp2 HG02647.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+68923dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93747988 | |||||
| chr12:93747995
|
AT | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02683.hp1 HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298+68924delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747995 | ||||||
| chr12:93747996
|
T | A | 142 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(139): Show | 142 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(139): Show |
intron_variant | MODIFIER | c.298+68924T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747996 | ||||||
| chr12:93747998
|
T | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+68926T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93747998 | ||||||
| chr12:93748276
|
G | A | 1 | a0001c0001t0003g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.298+69204G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748276 | ||||||
| chr12:93748287
|
G | A | 125 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(122): Show | 125 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.298+69215G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748287 | ||||||
| chr12:93748339
|
CTT | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0224others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+69268_298+6926 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748339 | ||||||
| chr12:93748410
|
A | AT | 122 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(119): Show | 122 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.298+69340dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93748410 | |||||
| chr12:93748505
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.298+69433C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748505 | ||||||
| chr12:93748553
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.298+69481C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748553 | ||||||
| chr12:93748662
|
C | CAA | 122 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(119): Show | 122 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.298+69593_298+6959 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93748662 | |||||
| chr12:93748703
|
T | C | 122 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(119): Show | 122 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.298+69631T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748703 | ||||||
| chr12:93748769
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+69697G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748769 | ||||||
| chr12:93748810
|
T | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.298+69738T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748810 | ||||||
| chr12:93748875
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298+69803C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748875 | ||||||
| chr12:93748904
|
C | G | 1 | a0001c0001t0003g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298+69832C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93748904 | ||||||
| chr12:93749035
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298+69963C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749035 | ||||||
| chr12:93749055
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.298+69983A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749055 | ||||||
| chr12:93749103
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.298+70031T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749103 | ||||||
| chr12:93749116
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.298+70044G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749116 | ||||||
| chr12:93749481
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.298+70409G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749481 | ||||||
| chr12:93749564
|
T | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+70492T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749564 | ||||||
| chr12:93749708
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.298+70636C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749708 | ||||||
| chr12:93749845
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+70773A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93749845 | ||||||
| chr12:93750206
|
CT | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0075 | 3 | HG02809.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.298+71139delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93750206 | |||||
| chr12:93750227
|
CA | C | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+71157delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93750227 | |||||
| chr12:93750241
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0140others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+71169G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93750241 | ||||||
| chr12:93750399
|
A | G | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+71327A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93750399 | ||||||
| chr12:93750404
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+71332A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93750404 | ||||||
| chr12:93750627
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+71555T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93750627 | ||||||
| chr12:93751099
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18962.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.298+72027A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751099 | ||||||
| chr12:93751242
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+72170T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751242 | ||||||
| chr12:93751344
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+72272G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751344 | ||||||
| chr12:93751460
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+72388A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751460 | ||||||
| chr12:93751496
|
T | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0026others(32): Show | 35 | HG00597.hp1 HG02257.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+72424T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751496 | ||||||
| chr12:93751756
|
C | T | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+72684C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93751756 | ||||||
| chr12:93752100
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.298+73028G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752100 | ||||||
| chr12:93752228
|
G | A | 28 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(25): Show | 28 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(25): Show |
intron_variant | MODIFIER | c.298+73156G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752228 | ||||||
| chr12:93752565
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.298+73493T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752565 | ||||||
| chr12:93752587
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+73515A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752587 | ||||||
| chr12:93752683
|
T | G | 122 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(119): Show | 122 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.298+73611T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752683 | ||||||
| chr12:93752778
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+73706G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752778 | ||||||
| chr12:93752890
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+73818G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752890 | ||||||
| chr12:93752926
|
A | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.298+73854A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93752926 | ||||||
| chr12:93753159
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+74087G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753159 | ||||||
| chr12:93753435
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+74363G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753435 | ||||||
| chr12:93753531
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0223 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.298+74459A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753531 | ||||||
| chr12:93753711
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.298+74639C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753711 | ||||||
| chr12:93753725
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0156 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.298+74653T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753725 | ||||||
| chr12:93753814
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0002c0003t0001g0125 | 3 | HG02922.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+74742C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753814 | ||||||
| chr12:93753899
|
C | G | 1 | a0001c0005t0001g0042 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.298+74827C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753899 | ||||||
| chr12:93753987
|
T | G | 186 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(183): Show | 186 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.298+74915T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93753987 | ||||||
| chr12:93754176
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+75104G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754176 | ||||||
| chr12:93754295
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0246 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+75223C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754295 | ||||||
| chr12:93754750
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.298+75678A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754750 | ||||||
| chr12:93754768
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0223 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.298+75696C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754768 | ||||||
| chr12:93754852
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.298+75780C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754852 | ||||||
| chr12:93754963
|
A | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+75891A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754963 | ||||||
| chr12:93754977
|
A | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0205 | 2 | NA18977.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.298+75905A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93754977 | ||||||
| chr12:93755175
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+76103G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93755175 | ||||||
| chr12:93755243
|
A | G | 2 | a0001c0002t0001g0029a0001c0002t0001g0036 | 2 | NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.298+76171A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93755243 | ||||||
| chr12:93755615
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+76543G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93755615 | ||||||
| chr12:93755757
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0045others(7): Show | 10 | HG01081.hp1 HG01496.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+76685C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93755757 | ||||||
| chr12:93755832
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298+76760C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93755832 | ||||||
| chr12:93756386
|
C | T | 121 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(118): Show | 121 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.298+77314C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756386 | ||||||
| chr12:93756544
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.298+77472T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756544 | ||||||
| chr12:93756545
|
T | G | 190 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(187): Show | 190 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.298+77473T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756545 | ||||||
| chr12:93756607
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.298+77535G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756607 | ||||||
| chr12:93756763
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0224others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+77691T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756763 | ||||||
| chr12:93756789
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+77717G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756789 | ||||||
| chr12:93756867
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.298+77795C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756867 | ||||||
| chr12:93756885
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+77813C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756885 | ||||||
| chr12:93756982
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0140others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+77910C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756982 | ||||||
| chr12:93756983
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0140others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+77911T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756983 | ||||||
| chr12:93756984
|
A | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0140others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+77912A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93756984 | ||||||
| chr12:93757178
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG03688.hp1 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.298+78106G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93757178 | ||||||
| chr12:93758007
|
G | T | 2 | a0001c0001t0001g0072a0002c0003t0001g0079 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.298+78935G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758007 | ||||||
| chr12:93758068
|
C | T | 182 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(179): Show | 182 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.298+78996C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758068 | ||||||
| chr12:93758468
|
C | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0116others(2): Show | 5 | HG02040.hp1 NA18967.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+79396C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758468 | ||||||
| chr12:93758594
|
T | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.298+79522T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758594 | ||||||
| chr12:93758700
|
T | C | 115 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(112): Show | 115 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.298+79628T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758700 | ||||||
| chr12:93758998
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+79926G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93758998 | ||||||
| chr12:93759028
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.298+79956T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759028 | ||||||
| chr12:93759078
|
T | C | 29 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 29 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(26): Show |
intron_variant | MODIFIER | c.298+80006T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759078 | ||||||
| chr12:93759179
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+80107G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759179 | ||||||
| chr12:93759350
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298+80278A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759350 | ||||||
| chr12:93759424
|
GA | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.298+80362delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93759424 | |||||
| chr12:93759482
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.298+80410C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759482 | ||||||
| chr12:93759486
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0224others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+80414G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759486 | ||||||
| chr12:93759530
|
A | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+80458A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759530 | ||||||
| chr12:93759738
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.298+80666C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759738 | ||||||
| chr12:93759809
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298+80737A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759809 | ||||||
| chr12:93759883
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+80811T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93759883 | ||||||
| chr12:93760049
|
A | G | 115 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(112): Show | 115 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.298+80977A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93760049 | ||||||
| chr12:93760349
|
T | C | 115 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(112): Show | 115 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.298+81277T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93760349 | ||||||
| chr12:93760374
|
T | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0127a0001c0001t0001g0130 | 3 | NA18949.hp2 NA18999.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.298+81302T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93760374 | ||||||
| chr12:93760427
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+81355A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93760427 | ||||||
| chr12:93760527
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0172 | 2 | HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.298+81455T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93760527 | ||||||
| chr12:93760680
|
C | CCATT | 3 | a0001c0001t0001g0116a0001c0001t0001g0236a0002c0003t0001g0079 | 3 | HG01099.hp2 HG02040.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+81635_298+8163 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93760680 | |||||
| chr12:93760757
|
GGGT | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+81687_298+8168 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93760757 | |||||
| chr12:93761508
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298+82436G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93761508 | ||||||
| chr12:93761777
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+82705T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93761777 | ||||||
| chr12:93761869
|
C | G | 112 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 112 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.298+82797C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93761869 | ||||||
| chr12:93762198
|
C | T | 2 | a0001c0001t0001g0206a0001c0002t0001g0122 | 2 | HG00597.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.298+83126C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762198 | ||||||
| chr12:93762351
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+83279G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762351 | ||||||
| chr12:93762374
|
C | T | 60 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(57): Show | 60 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(57): Show |
intron_variant | MODIFIER | c.298+83302C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762374 | ||||||
| chr12:93762385
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+83313C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762385 | ||||||
| chr12:93762758
|
A | T | 123 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(120): Show | 123 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.298+83686A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762758 | ||||||
| chr12:93762811
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.298+83739G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762811 | ||||||
| chr12:93762884
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.298+83812G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762884 | ||||||
| chr12:93762935
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.298+83863A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93762935 | ||||||
| chr12:93763035
|
G | T | 1 | a0001c0002t0001g0059 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.298+83963G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763035 | ||||||
| chr12:93763190
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298+84118C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763190 | ||||||
| chr12:93763199
|
G | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(5): Show | 8 | HG01106.hp1 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+84127G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763199 | ||||||
| chr12:93763253
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+84181T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763253 | ||||||
| chr12:93763372
|
T | TA | 123 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(120): Show | 123 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.298+84309dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93763372 | |||||
| chr12:93763452
|
C | CT | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG01081.hp1 HG01496.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.298+84391dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93763452 | |||||
| chr12:93763578
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+84506A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763578 | ||||||
| chr12:93763705
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.298+84633T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763705 | ||||||
| chr12:93763956
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(110): Show | 113 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.298+84884G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93763956 | ||||||
| chr12:93764180
|
C | CT | 11 | a0001c0001t0001g0015a0001c0001t0001g0109a0001c0001t0001g0110others(8): Show | 11 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+85126dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93764180 | |||||
| chr12:93764180
|
C | CTT | 84 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(81): Show | 84 | HG00544.hp2 HG00597.hp1 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.298+85125_298+8512 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93764180 | |||||
| chr12:93764180
|
C | CTTT | 28 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0093others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.298+85124_298+8512 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93764180 | |||||
| chr12:93764200
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+85128C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764200 | ||||||
| chr12:93764247
|
G | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(107): Show | 110 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.298+85175G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764247 | ||||||
| chr12:93764286
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.298+85214G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764286 | ||||||
| chr12:93764419
|
T | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0157 | 3 | NA18942.hp2 NA18957.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.298+85347T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764419 | ||||||
| chr12:93764507
|
T | C | 30 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(27): Show | 30 | HG00597.hp1 HG02257.hp1 HG02559.hp1 others(27): Show |
intron_variant | MODIFIER | c.298+85435T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764507 | ||||||
| chr12:93764560
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-85410A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764560 | ||||||
| chr12:93764711
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.299-85259G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764711 | ||||||
| chr12:93764732
|
GGT | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0171a0001c0001t0001g0186 | 3 | HG02602.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.299-85237_299-8523 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764732 | ||||||
| chr12:93764733
|
GTT | G | 178 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(175): Show | 178 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(175): Show |
intron_variant | MODIFIER | c.299-85226_299-8522 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93764733 | |||||
| chr12:93764736
|
T | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(5): Show | 8 | HG01106.hp1 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-85234T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764736 | ||||||
| chr12:93764891
|
G | T | 183 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.299-85079G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764891 | ||||||
| chr12:93764943
|
G | A | 182 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(179): Show | 182 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.299-85027G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764943 | ||||||
| chr12:93764970
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-85000C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93764970 | ||||||
| chr12:93765006
|
A | AT | 45 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 45 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-84952dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93765006 | |||||
| chr12:93765135
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-84835A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765135 | ||||||
| chr12:93765439
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.299-84531A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765439 | ||||||
| chr12:93765463
|
C | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-84507C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765463 | ||||||
| chr12:93765627
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-84343G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765627 | ||||||
| chr12:93765812
|
A | G | 113 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(110): Show | 113 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.299-84158A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765812 | ||||||
| chr12:93765848
|
G | GT | 110 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(107): Show | 110 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.299-84111dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93765848 | |||||
| chr12:93765893
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0156 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.299-84077T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93765893 | ||||||
| chr12:93766083
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0002g0244 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-83887C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93766083 | ||||||
| chr12:93766109
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-83861C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93766109 | ||||||
| chr12:93766238
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299-83732A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93766238 | ||||||
| chr12:93766383
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-83587T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93766383 | ||||||
| chr12:93766770
|
G | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-83200G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93766770 | ||||||
| chr12:93767083
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0002g0244 | 3 | HG02451.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-82887A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767083 | ||||||
| chr12:93767175
|
A | G | 142 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(139): Show | 142 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.299-82795A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767175 | ||||||
| chr12:93767219
|
G | A | 141 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(138): Show | 141 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.299-82751G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767219 | ||||||
| chr12:93767322
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-82648G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767322 | ||||||
| chr12:93767470
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0168 | 2 | HG01884.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.299-82500G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767470 | ||||||
| chr12:93767507
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | NA18945.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.299-82463T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767507 | ||||||
| chr12:93767720
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-82250C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767720 | ||||||
| chr12:93767943
|
C | T | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.299-82027C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93767943 | ||||||
| chr12:93768490
|
G | GT | 10 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0138others(7): Show | 10 | HG01106.hp1 HG01257.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-81467dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93768490 | |||||
| chr12:93768673
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(231): Show |
intron_variant | MODIFIER | c.299-81297G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93768673 | ||||||
| chr12:93768701
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0188 | 3 | HG01071.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.299-81269G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93768701 | ||||||
| chr12:93768780
|
T | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(140): Show | 143 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.299-81190T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93768780 | ||||||
| chr12:93768984
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299-80986T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93768984 | ||||||
| chr12:93769081
|
T | TA | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-80888dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93769081 | |||||
| chr12:93769086
|
A | T | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-80884A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769086 | ||||||
| chr12:93769225
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0002g0244 | 3 | HG02451.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-80745G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769225 | ||||||
| chr12:93769231
|
G | A | 1 | a0004c0006t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.299-80739G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769231 | ||||||
| chr12:93769232
|
T | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(140): Show | 143 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.299-80738T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769232 | ||||||
| chr12:93769311
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0210a0001c0002t0001g0149 | 3 | NA18962.hp2 NA18972.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.299-80659T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769311 | ||||||
| chr12:93769534
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-80436G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769534 | ||||||
| chr12:93769535
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-80435C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769535 | ||||||
| chr12:93769546
|
A | T | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-80424A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769546 | ||||||
| chr12:93769665
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-80305G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769665 | ||||||
| chr12:93769687
|
C | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(80): Show | 83 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.299-80283C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769687 | ||||||
| chr12:93769920
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.299-80050A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93769920 | ||||||
| chr12:93770096
|
C | CT | 25 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.299-79857dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93770096 | |||||
| chr12:93770096
|
C | CTT | 106 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(103): Show | 106 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.299-79858_299-7985 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93770096 | |||||
| chr12:93770096
|
C | CTTT | 13 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0150others(10): Show | 13 | HG02071.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-79859_299-7985 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93770096 | |||||
| chr12:93770134
|
G | C | 81 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(78): Show | 81 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.299-79836G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770134 | ||||||
| chr12:93770135
|
G | A | 81 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(78): Show | 81 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.299-79835G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770135 | ||||||
| chr12:93770138
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-79832C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770138 | ||||||
| chr12:93770142
|
T | C | 81 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(78): Show | 81 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.299-79828T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770142 | ||||||
| chr12:93770143
|
G | T | 81 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(78): Show | 81 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.299-79827G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770143 | ||||||
| chr12:93770214
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.299-79756G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770214 | ||||||
| chr12:93770241
|
G | A | 2 | a0001c0001t0001g0033a0001c0002t0001g0037 | 2 | NA19063.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.299-79729G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770241 | ||||||
| chr12:93770307
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.299-79663C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770307 | ||||||
| chr12:93770362
|
G | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(140): Show | 143 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.299-79608G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770362 | ||||||
| chr12:93770374
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03041.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.299-79596A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770374 | ||||||
| chr12:93770379
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-79591G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770379 | ||||||
| chr12:93770455
|
A | C | 112 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 112 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.299-79515A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770455 | ||||||
| chr12:93770689
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-79281C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93770689 | ||||||
| chr12:93771210
|
T | C | 3 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0002g0244 | 3 | HG02451.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-78760T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771210 | ||||||
| chr12:93771215
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-78755T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771215 | ||||||
| chr12:93771251
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.299-78719C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771251 | ||||||
| chr12:93771356
|
A | C | 1 | a0001c0002t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-78614A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771356 | ||||||
| chr12:93771557
|
G | T | 183 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(180): Show | 183 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.299-78413G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771557 | ||||||
| chr12:93771587
|
A | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG00544.hp1 NA18945.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-78383A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771587 | ||||||
| chr12:93771923
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-78047G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771923 | ||||||
| chr12:93771933
|
A | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-78037A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93771933 | ||||||
| chr12:93772030
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.299-77940A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772030 | ||||||
| chr12:93772215
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.299-77755T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772215 | ||||||
| chr12:93772249
|
C | T | 1 | a0002c0003t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-77721C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772249 | ||||||
| chr12:93772301
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.299-77669A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772301 | ||||||
| chr12:93772329
|
A | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-77641A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772329 | ||||||
| chr12:93772599
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-77371A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772599 | ||||||
| chr12:93772756
|
A | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(140): Show | 143 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.299-77214A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772756 | ||||||
| chr12:93772882
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0172 | 2 | HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.299-77088C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93772882 | ||||||
| chr12:93773142
|
G | A | 181 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(178): Show | 181 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.299-76828G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773142 | ||||||
| chr12:93773146
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.299-76824A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773146 | ||||||
| chr12:93773204
|
A | G | 181 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(178): Show | 181 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.299-76766A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773204 | ||||||
| chr12:93773232
|
T | C | 112 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 112 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.299-76738T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773232 | ||||||
| chr12:93773365
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-76605C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773365 | ||||||
| chr12:93773397
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18953.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.299-76573C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773397 | ||||||
| chr12:93773444
|
C | T | 142 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0019others(139): Show | 142 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.299-76526C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773444 | ||||||
| chr12:93773516
|
T | G | 184 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(181): Show | 184 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.299-76454T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773516 | ||||||
| chr12:93773547
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-76423G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773547 | ||||||
| chr12:93773567
|
T | C | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-76403T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773567 | ||||||
| chr12:93773595
|
C | T | 2 | a0001c0001t0001g0242a0002c0003t0001g0079 | 2 | HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.299-76375C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773595 | ||||||
| chr12:93773701
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-76269G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773701 | ||||||
| chr12:93773706
|
C | G | 184 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(181): Show | 184 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.299-76264C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773706 | ||||||
| chr12:93773737
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0002g0244 | 3 | HG02451.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-76233G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773737 | ||||||
| chr12:93773813
|
G | GT | 12 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0062others(9): Show | 12 | HG02451.hp2 HG02647.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-76135dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93773813 | |||||
| chr12:93773813
|
G | GTTT | 39 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0030others(36): Show | 39 | HG00597.hp1 HG00639.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.299-76137_299-7613 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93773813 | |||||
| chr12:93773813
|
G | GTTTT | 117 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0021others(114): Show | 117 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.299-76138_299-7613 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93773813 | |||||
| chr12:93773813
|
G | GTTTTT | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0050others(13): Show | 16 | HG01358.hp1 HG01928.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-76139_299-7613 others(9): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93773813 | |||||
| chr12:93773846
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-76124C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93773846 | ||||||
| chr12:93774000
|
A | AT | 137 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(134): Show | 137 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.299-75954dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93774000 | |||||
| chr12:93774000
|
A | ATT | 5 | a0001c0001t0001g0063a0001c0001t0001g0238a0001c0001t0003g0007others(2): Show | 5 | HG02572.hp1 HG04115.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-75955_299-7595 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93774000 | |||||
| chr12:93774451
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-75519C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93774451 | ||||||
| chr12:93774659
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.299-75311C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93774659 | ||||||
| chr12:93774910
|
G | T | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-75060G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93774910 | ||||||
| chr12:93775070
|
T | A | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-74900T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775070 | ||||||
| chr12:93775087
|
C | A | 1 | a0002c0003t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299-74883C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775087 | ||||||
| chr12:93775109
|
A | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-74861A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775109 | ||||||
| chr12:93775150
|
G | A | 116 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(113): Show | 116 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.299-74820G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775150 | ||||||
| chr12:93775233
|
A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-74737A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775233 | ||||||
| chr12:93775373
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0039others(2): Show | 5 | HG02257.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-74597C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775373 | ||||||
| chr12:93775408
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-74562C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775408 | ||||||
| chr12:93775576
|
A | AG | 159 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(156): Show | 159 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.299-74389dupG | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93775576 | |||||
| chr12:93775752
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0189others(3): Show | 6 | HG01106.hp1 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-74218G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775752 | ||||||
| chr12:93775787
|
T | A | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-74183T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775787 | ||||||
| chr12:93775861
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-74109G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775861 | ||||||
| chr12:93775876
|
A | G | 85 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(82): Show | 85 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.299-74094A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775876 | ||||||
| chr12:93775877
|
C | A | 85 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(82): Show | 85 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.299-74093C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775877 | ||||||
| chr12:93775994
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-73976T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93775994 | ||||||
| chr12:93776055
|
A | G | 84 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(81): Show | 84 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.299-73915A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776055 | ||||||
| chr12:93776345
|
T | TG | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-73624dupG | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93776345 | |||||
| chr12:93776472
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-73498G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776472 | ||||||
| chr12:93776501
|
G | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 247 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(244): Show |
intron_variant | MODIFIER | c.299-73469G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776501 | ||||||
| chr12:93776742
|
G | A | 153 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(150): Show | 153 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.299-73228G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776742 | ||||||
| chr12:93776763
|
A | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-73207A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776763 | ||||||
| chr12:93776953
|
T | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(30): Show | 33 | HG00597.hp1 HG02257.hp1 HG02572.hp1 others(30): Show |
intron_variant | MODIFIER | c.299-73017T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93776953 | ||||||
| chr12:93777016
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-72954G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777016 | ||||||
| chr12:93777175
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-72795G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777175 | ||||||
| chr12:93777241
|
C | A | 191 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(188): Show | 191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.299-72729C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777241 | ||||||
| chr12:93777420
|
T | G | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-72550T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777420 | ||||||
| chr12:93777492
|
G | A | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG02257.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-72478G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777492 | ||||||
| chr12:93777660
|
G | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0206others(1): Show | 4 | HG00597.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-72310G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93777660 | ||||||
| chr12:93778203
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-71767C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778203 | ||||||
| chr12:93778258
|
T | G | 24 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0023others(21): Show | 24 | HG01106.hp1 HG01257.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-71712T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778258 | ||||||
| chr12:93778514
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-71456A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778514 | ||||||
| chr12:93778723
|
G | GT | 9 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0135others(6): Show | 9 | HG00639.hp2 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-71232dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93778723 | |||||
| chr12:93778855
|
A | G | 38 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.299-71115A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778855 | ||||||
| chr12:93778909
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.299-71061A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778909 | ||||||
| chr12:93778972
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-70998A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93778972 | ||||||
| chr12:93779023
|
C | T | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-70947C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779023 | ||||||
| chr12:93779161
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-70809A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779161 | ||||||
| chr12:93779333
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-70637C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779333 | ||||||
| chr12:93779591
|
C | CT | 110 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(107): Show | 110 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.299-70363dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93779591 | |||||
| chr12:93779600
|
T | TG | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | NA18942.hp1 NA18979.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.299-70370_299-7036 others(5): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779600 | ||||||
| chr12:93779836
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-70134G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779836 | ||||||
| chr12:93779846
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-70124C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779846 | ||||||
| chr12:93779906
|
T | A | 155 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(152): Show | 155 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.299-70064T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93779906 | ||||||
| chr12:93780018
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-69952T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780018 | ||||||
| chr12:93780202
|
TTCTC | T | 57 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(54): Show | 57 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(54): Show |
intron_variant | MODIFIER | c.299-69766_299-6976 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93780202 | |||||
| chr12:93780241
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-69729A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780241 | ||||||
| chr12:93780252
|
A | G | 46 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-69718A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780252 | ||||||
| chr12:93780390
|
G | A | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-69580G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780390 | ||||||
| chr12:93780498
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-69472T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780498 | ||||||
| chr12:93780661
|
G | A | 40 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(37): Show | 40 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-69309G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780661 | ||||||
| chr12:93780741
|
C | CT | 7 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0138others(4): Show | 7 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-69215dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93780741 | |||||
| chr12:93780854
|
TCTCAGC | T | 158 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(155): Show | 158 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(155): Show |
intron_variant | MODIFIER | c.299-69106_299-6910 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93780854 | |||||
| chr12:93780877
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-69093G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780877 | ||||||
| chr12:93780912
|
A | AT | 89 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0024others(86): Show | 89 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.299-69043dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93780912 | |||||
| chr12:93780912
|
AT | A | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(56): Show | 59 | HG00597.hp2 HG01081.hp1 HG01257.hp2 others(56): Show |
intron_variant | MODIFIER | c.299-69043delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93780912 | |||||
| chr12:93780931
|
T | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-69039T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93780931 | ||||||
| chr12:93781002
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-68968C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781002 | ||||||
| chr12:93781061
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0156 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.299-68909G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781061 | ||||||
| chr12:93781212
|
A | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-68758A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781212 | ||||||
| chr12:93781273
|
G | A | 184 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(181): Show | 184 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.299-68697G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781273 | ||||||
| chr12:93781417
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-68553G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781417 | ||||||
| chr12:93781500
|
A | G | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-68470A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781500 | ||||||
| chr12:93781646
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-68324A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781646 | ||||||
| chr12:93781714
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-68256A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781714 | ||||||
| chr12:93781936
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.299-68034G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93781936 | ||||||
| chr12:93782028
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-67942A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782028 | ||||||
| chr12:93782093
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-67877C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782093 | ||||||
| chr12:93782098
|
A | G | 191 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(188): Show | 191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.299-67872A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782098 | ||||||
| chr12:93782148
|
G | A | 41 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(38): Show | 41 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.299-67822G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782148 | ||||||
| chr12:93782198
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.299-67772T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782198 | ||||||
| chr12:93782427
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-67543G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782427 | ||||||
| chr12:93782493
|
TA | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-67469delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93782493 | |||||
| chr12:93782495
|
A | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-67475A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93782495 | ||||||
| chr12:93782594
|
G | GA | 5 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0071others(2): Show | 5 | HG02683.hp1 HG03139.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-67360dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93782594 | |||||
| chr12:93782594
|
GA | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-67360delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93782594 | |||||
| chr12:93783002
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-66968A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783002 | ||||||
| chr12:93783199
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.299-66771A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783199 | ||||||
| chr12:93783228
|
G | GTAT | 31 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0024others(28): Show | 31 | HG01071.hp2 HG01258.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.299-66698_299-6669 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783228
|
G | GTATTAT | 5 | a0001c0001t0001g0068a0001c0001t0001g0130a0001c0001t0001g0156others(2): Show | 5 | HG02602.hp2 HG03710.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-66701_299-6669 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783228
|
GTAT | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 59 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.299-66698_299-6669 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783228
|
GTATTAT | G | 46 | a0001c0001t0001g0028a0001c0001t0001g0107a0001c0001t0001g0113others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-66701_299-6669 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783228
|
GTATTATT others(2): Show |
G | 18 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0040others(15): Show | 18 | HG02451.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-66704_299-6669 others(13): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783228
|
GTATTATT others(5): Show |
G | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-66707_299-6669 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783228 | |||||
| chr12:93783230
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0171 | 2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.299-66740A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783230 | ||||||
| chr12:93783276
|
T | G | 42 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(39): Show | 42 | HG00597.hp2 HG01081.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.299-66694T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783276 | ||||||
| chr12:93783759
|
TA | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-66207delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93783759 | |||||
| chr12:93783805
|
A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-66165A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783805 | ||||||
| chr12:93783951
|
G | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(111): Show | 114 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.299-66019G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93783951 | ||||||
| chr12:93784022
|
G | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-65948G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784022 | ||||||
| chr12:93784031
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-65939G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784031 | ||||||
| chr12:93784174
|
T | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-65796T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784174 | ||||||
| chr12:93784182
|
A | G | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-65788A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784182 | ||||||
| chr12:93784247
|
G | A | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-65723G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784247 | ||||||
| chr12:93784251
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0069others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-65719G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784251 | ||||||
| chr12:93784282
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-65688G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784282 | ||||||
| chr12:93784425
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-65545G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784425 | ||||||
| chr12:93784713
|
G | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03041.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.299-65257G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784713 | ||||||
| chr12:93784722
|
A | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(83): Show | 86 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.299-65248A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93784722 | ||||||
| chr12:93785098
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-64872T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785098 | ||||||
| chr12:93785099
|
A | T | 187 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(184): Show | 187 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.299-64871A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785099 | ||||||
| chr12:93785181
|
A | G | 2 | a0001c0001t0001g0124a0002c0003t0001g0125 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.299-64789A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785181 | ||||||
| chr12:93785187
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.299-64783C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785187 | ||||||
| chr12:93785397
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-64573T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785397 | ||||||
| chr12:93785491
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-64479T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785491 | ||||||
| chr12:93785538
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-64432C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93785538 | ||||||
| chr12:93786022
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0158a0001c0001t0001g0166others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-63948G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786022 | ||||||
| chr12:93786060
|
C | A | 86 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(83): Show | 86 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.299-63910C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786060 | ||||||
| chr12:93786093
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-63877A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786093 | ||||||
| chr12:93786130
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.299-63840C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786130 | ||||||
| chr12:93786138
|
T | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0023others(39): Show | 42 | HG00597.hp1 HG02257.hp1 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-63832T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786138 | ||||||
| chr12:93786186
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.299-63784C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786186 | ||||||
| chr12:93786262
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.299-63708C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786262 | ||||||
| chr12:93786321
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.299-63649G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786321 | ||||||
| chr12:93786509
|
T | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-63461T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786509 | ||||||
| chr12:93786534
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299-63436A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786534 | ||||||
| chr12:93786793
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-63177A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786793 | ||||||
| chr12:93786794
|
A | G | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-63176A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786794 | ||||||
| chr12:93786800
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-63170T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786800 | ||||||
| chr12:93786840
|
A | T | 85 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(82): Show | 85 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.299-63130A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786840 | ||||||
| chr12:93786850
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-63120C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786850 | ||||||
| chr12:93786851
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(133): Show | 136 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.299-63119A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786851 | ||||||
| chr12:93786872
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(51): Show | 54 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-63098A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786872 | ||||||
| chr12:93786916
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(51): Show | 54 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-63054G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786916 | ||||||
| chr12:93786922
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-63048T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786922 | ||||||
| chr12:93786926
|
A | G | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00597.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-63044A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786926 | ||||||
| chr12:93786962
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-63008G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786962 | ||||||
| chr12:93786975
|
A | G | 186 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(183): Show | 186 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.299-62995A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93786975 | ||||||
| chr12:93787128
|
A | AT | 11 | a0001c0001t0001g0005a0001c0001t0001g0078a0001c0001t0001g0082others(8): Show | 11 | HG02055.hp2 HG02071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-62818dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787128 | |||||
| chr12:93787128
|
AT | A | 71 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(68): Show | 71 | HG00639.hp1 HG01071.hp2 HG01099.hp2 others(68): Show |
intron_variant | MODIFIER | c.299-62818delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787128 | |||||
| chr12:93787128
|
ATT | A | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.299-62819_299-6281 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787128 | |||||
| chr12:93787128
|
ATTT | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-62820_299-6281 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787128 | |||||
| chr12:93787215
|
A | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-62755A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787215 | ||||||
| chr12:93787303
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299-62667G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787303 | ||||||
| chr12:93787305
|
G | GT | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0103others(9): Show | 12 | HG00544.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-62640dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787305 | |||||
| chr12:93787305
|
GT | G | 59 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0024others(56): Show | 59 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.299-62640delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787305 | |||||
| chr12:93787305
|
GTT | G | 104 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(101): Show | 104 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.299-62641_299-6264 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787305 | |||||
| chr12:93787305
|
GTTT | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0071others(12): Show | 15 | HG00639.hp2 HG01109.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-62642_299-6264 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93787305 | |||||
| chr12:93787314
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0150 | 2 | HG03017.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.299-62656T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787314 | ||||||
| chr12:93787315
|
T | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(80): Show | 83 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.299-62655T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787315 | ||||||
| chr12:93787325
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.299-62645T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787325 | ||||||
| chr12:93787403
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-62567C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787403 | ||||||
| chr12:93787485
|
C | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.299-62485C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787485 | ||||||
| chr12:93787552
|
G | A | 186 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(183): Show | 186 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.299-62418G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787552 | ||||||
| chr12:93787694
|
G | A | 85 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(82): Show | 85 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.299-62276G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787694 | ||||||
| chr12:93787710
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01106.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.299-62260C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787710 | ||||||
| chr12:93787789
|
C | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(50): Show | 53 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.299-62181C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787789 | ||||||
| chr12:93787810
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-62160C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93787810 | ||||||
| chr12:93788067
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-61903C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788067 | ||||||
| chr12:93788068
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(50): Show | 53 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.299-61902G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788068 | ||||||
| chr12:93788164
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.299-61806A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788164 | ||||||
| chr12:93788238
|
G | A | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-61732G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788238 | ||||||
| chr12:93788274
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-61696G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788274 | ||||||
| chr12:93788301
|
C | T | 1 | a0002c0003t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-61669C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788301 | ||||||
| chr12:93788302
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-61668G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788302 | ||||||
| chr12:93788389
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0170others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-61581G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788389 | ||||||
| chr12:93788970
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-61000G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93788970 | ||||||
| chr12:93789607
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-60363G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93789607 | ||||||
| chr12:93789627
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-60343G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93789627 | ||||||
| chr12:93789683
|
TCATGGTT others(29): Show |
T | 4 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0233others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-60282_299-6024 others(40): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93789683 | |||||
| chr12:93789715
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0075 | 3 | HG02809.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.299-60255A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93789715 | ||||||
| chr12:93790092
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.299-59878C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790092 | ||||||
| chr12:93790190
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03041.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.299-59780A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790190 | ||||||
| chr12:93790224
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-59746A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790224 | ||||||
| chr12:93790306
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 93 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(90): Show |
intron_variant | MODIFIER | c.299-59664C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790306 | ||||||
| chr12:93790492
|
A | ATAAC | 124 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 124 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.299-59478_299-5947 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790492 | ||||||
| chr12:93790526
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-59444G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790526 | ||||||
| chr12:93790554
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-59416G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790554 | ||||||
| chr12:93790642
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-59328G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790642 | ||||||
| chr12:93790729
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.299-59241A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790729 | ||||||
| chr12:93790770
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-59200G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790770 | ||||||
| chr12:93790777
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-59193T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93790777 | ||||||
| chr12:93790912
|
G | GAC | 8 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG01884.hp2 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-59031_299-5903 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACAC | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-59035_299-5903 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(1): Show |
7 | a0001c0001t0001g0021a0001c0001t0001g0107a0001c0001t0001g0138others(4): Show | 7 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-59037_299-5903 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(3): Show |
47 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0040others(44): Show | 47 | HG00597.hp2 HG01081.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.299-59039_299-5903 others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(5): Show |
19 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(16): Show | 19 | HG00544.hp2 HG00639.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-59041_299-5903 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(7): Show |
54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(51): Show | 54 | HG01071.hp2 HG01099.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.299-59043_299-5903 others(18): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(9): Show |
7 | a0001c0001t0001g0093a0001c0001t0001g0199a0001c0001t0001g0231others(4): Show | 7 | HG01934.hp2 HG02559.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-59045_299-5903 others(20): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(11): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0170others(5): Show | 8 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-59047_299-5903 others(22): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93790912
|
G | GACACACA others(13): Show |
2 | a0001c0001t0001g0243a0001c0001t0002g0244 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.299-59049_299-5903 others(24): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93790912 | |||||
| chr12:93791022
|
C | G | 1 | a0003c0004t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-58948C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791022 | ||||||
| chr12:93791139
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0156 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.299-58831A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791139 | ||||||
| chr12:93791358
|
A | T | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.299-58612A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791358 | ||||||
| chr12:93791467
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0090a0001c0001t0001g0117others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-58503A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791467 | ||||||
| chr12:93791469
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-58501A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791469 | ||||||
| chr12:93791594
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0146 | 3 | HG00544.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.299-58376A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791594 | ||||||
| chr12:93791603
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-58367G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791603 | ||||||
| chr12:93791614
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-58356C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791614 | ||||||
| chr12:93791628
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02647.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-58342A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791628 | ||||||
| chr12:93791640
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-58330T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791640 | ||||||
| chr12:93791878
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0090a0001c0001t0001g0117 | 3 | HG02965.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-58092G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791878 | ||||||
| chr12:93791885
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-58085G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791885 | ||||||
| chr12:93791895
|
AT | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.299-58055delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93791895 | |||||
| chr12:93791895
|
ATT | A | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(80): Show | 83 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.299-58056_299-5805 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93791895 | |||||
| chr12:93791967
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-58003A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93791967 | ||||||
| chr12:93792155
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-57815C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792155 | ||||||
| chr12:93792162
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-57808T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792162 | ||||||
| chr12:93792183
|
G | A | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-57787G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792183 | ||||||
| chr12:93792187
|
G | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-57783G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792187 | ||||||
| chr12:93792510
|
C | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 68 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.299-57460C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792510 | ||||||
| chr12:93792621
|
G | T | 1 | a0001c0002t0001g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-57349G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792621 | ||||||
| chr12:93792799
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-57171C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792799 | ||||||
| chr12:93792815
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-57155C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792815 | ||||||
| chr12:93792923
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-57047T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93792923 | ||||||
| chr12:93793127
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-56843A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793127 | ||||||
| chr12:93793142
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-56828C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793142 | ||||||
| chr12:93793203
|
C | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-56767C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793203 | ||||||
| chr12:93793313
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-56657C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793313 | ||||||
| chr12:93793575
|
A | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-56395A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793575 | ||||||
| chr12:93793731
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299-56239G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93793731 | ||||||
| chr12:93794249
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0156 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.299-55721T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794249 | ||||||
| chr12:93794406
|
A | AC | 50 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(47): Show | 50 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(47): Show |
intron_variant | MODIFIER | c.299-55559dupC | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93794406 | |||||
| chr12:93794535
|
C | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(14): Show | 17 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-55435C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794535 | ||||||
| chr12:93794711
|
C | T | 23 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(20): Show | 23 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.299-55259C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794711 | ||||||
| chr12:93794721
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-55249A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794721 | ||||||
| chr12:93794781
|
T | A | 25 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-55189T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794781 | ||||||
| chr12:93794871
|
G | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.299-55099G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93794871 | ||||||
| chr12:93795005
|
T | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0187a0001c0001t0001g0198others(1): Show | 4 | HG00639.hp1 HG01168.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-54965T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795005 | ||||||
| chr12:93795063
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0112 | 2 | NA18981.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.299-54907T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795063 | ||||||
| chr12:93795071
|
A | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-54899A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795071 | ||||||
| chr12:93795379
|
G | T | 25 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-54591G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795379 | ||||||
| chr12:93795392
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-54578C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795392 | ||||||
| chr12:93795409
|
T | C | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-54561T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795409 | ||||||
| chr12:93795484
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-54486G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795484 | ||||||
| chr12:93795521
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.299-54449C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795521 | ||||||
| chr12:93795663
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-54307G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795663 | ||||||
| chr12:93795725
|
C | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-54245C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795725 | ||||||
| chr12:93795968
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-54002G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93795968 | ||||||
| chr12:93796147
|
G | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(86): Show | 89 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.299-53823G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796147 | ||||||
| chr12:93796334
|
A | C | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-53636A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796334 | ||||||
| chr12:93796387
|
T | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 174 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.299-53583T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796387 | ||||||
| chr12:93796479
|
C | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(13): Show | 16 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-53491C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796479 | ||||||
| chr12:93796554
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-53416G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796554 | ||||||
| chr12:93796567
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02647.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-53403T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796567 | ||||||
| chr12:93796600
|
C | CA | 149 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(146): Show | 149 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.299-53354dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93796600 | |||||
| chr12:93796600
|
C | CAA | 6 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0146others(3): Show | 6 | HG00544.hp2 NA18612.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-53355_299-5335 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93796600 | |||||
| chr12:93796600
|
CA | C | 11 | a0001c0001t0001g0063a0001c0001t0001g0107a0001c0001t0001g0156others(8): Show | 11 | HG01257.hp2 HG01516.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-53354delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93796600 | |||||
| chr12:93796727
|
T | C | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(79): Show | 82 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.299-53243T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796727 | ||||||
| chr12:93796762
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.299-53208C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796762 | ||||||
| chr12:93796775
|
G | C | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-53195G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93796775 | ||||||
| chr12:93797126
|
C | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-52844C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797126 | ||||||
| chr12:93797402
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0232 | 3 | HG02280.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299-52568C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797402 | ||||||
| chr12:93797595
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-52375G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797595 | ||||||
| chr12:93797688
|
T | A | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-52282T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797688 | ||||||
| chr12:93797799
|
G | A | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-52171G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797799 | ||||||
| chr12:93797807
|
G | A | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-52163G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797807 | ||||||
| chr12:93797807
|
G | T | 1 | a0001c0001t0001g0130 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.299-52163G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93797807 | ||||||
| chr12:93798028
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0071others(5): Show | 8 | HG01109.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-51942A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798028 | ||||||
| chr12:93798111
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.299-51859C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798111 | ||||||
| chr12:93798144
|
T | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.299-51826T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798144 | ||||||
| chr12:93798189
|
C | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-51781C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798189 | ||||||
| chr12:93798192
|
T | TG | 122 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(119): Show | 122 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.299-51778_299-5177 others(5): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798192 | ||||||
| chr12:93798234
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-51736G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798234 | ||||||
| chr12:93798299
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.299-51671C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798299 | ||||||
| chr12:93798449
|
A | G | 45 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(42): Show | 45 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-51521A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798449 | ||||||
| chr12:93798476
|
A | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-51494A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798476 | ||||||
| chr12:93798868
|
C | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(46): Show | 49 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-51102C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93798868 | ||||||
| chr12:93799013
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.299-50957G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799013 | ||||||
| chr12:93799093
|
C | T | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00544.hp1 NA18953.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-50877C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799093 | ||||||
| chr12:93799137
|
A | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(13): Show | 16 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-50833A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799137 | ||||||
| chr12:93799194
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-50776G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799194 | ||||||
| chr12:93799347
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.299-50623A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799347 | ||||||
| chr12:93799378
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-50592C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799378 | ||||||
| chr12:93799515
|
A | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02647.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-50455A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799515 | ||||||
| chr12:93799572
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-50398G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799572 | ||||||
| chr12:93799690
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-50280T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93799690 | ||||||
| chr12:93800111
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-49859G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800111 | ||||||
| chr12:93800114
|
T | C | 25 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-49856T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800114 | ||||||
| chr12:93800242
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-49728C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800242 | ||||||
| chr12:93800394
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(56): Show | 59 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.299-49576T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800394 | ||||||
| chr12:93800407
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-49563T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800407 | ||||||
| chr12:93800476
|
G | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(86): Show | 89 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.299-49494G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800476 | ||||||
| chr12:93800502
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.299-49468C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93800502 | ||||||
| chr12:93801114
|
A | G | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-48856A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801114 | ||||||
| chr12:93801146
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0097others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-48824C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801146 | ||||||
| chr12:93801228
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02647.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-48742T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801228 | ||||||
| chr12:93801531
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.299-48439T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801531 | ||||||
| chr12:93801707
|
A | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0090 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-48263A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801707 | ||||||
| chr12:93801814
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-48156C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801814 | ||||||
| chr12:93801847
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.299-48123C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801847 | ||||||
| chr12:93801905
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01071.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.299-48065C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801905 | ||||||
| chr12:93801940
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-48030A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93801940 | ||||||
| chr12:93802069
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-47901C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802069 | ||||||
| chr12:93802102
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-47868C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802102 | ||||||
| chr12:93802118
|
C | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(112): Show | 115 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.299-47852C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802118 | ||||||
| chr12:93802280
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0097others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-47690T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802280 | ||||||
| chr12:93802399
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.299-47571G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802399 | ||||||
| chr12:93802495
|
TGGGCCAG | T | 186 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 186 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.299-47466_299-4746 others(11): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93802495 | |||||
| chr12:93802655
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-47315C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802655 | ||||||
| chr12:93802677
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-47293G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802677 | ||||||
| chr12:93802818
|
A | T | 4 | a0001c0001t0001g0040a0001c0002t0001g0051a0001c0002t0001g0052others(1): Show | 4 | NA18949.hp1 NA19003.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-47152A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802818 | ||||||
| chr12:93802997
|
A | G | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(86): Show | 89 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.299-46973A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93802997 | ||||||
| chr12:93803488
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0001 | 3 | HG00639.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-46482A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93803488 | ||||||
| chr12:93803646
|
ACTTCCAG others(5261): Show |
A | 2 | a0001c0001t0001g0238a0001c0001t0003g0007 | 2 | NA18981.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-46320_299-4105 others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93803646 | |||||
| chr12:93803697
|
G | A | 75 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(72): Show | 75 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.299-46273G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93803697 | ||||||
| chr12:93803903
|
C | G | 123 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.299-46067C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93803903 | ||||||
| chr12:93803946
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(11): Show | 14 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-46024A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93803946 | ||||||
| chr12:93804165
|
A | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.299-45805A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804165 | ||||||
| chr12:93804353
|
G | A | 1 | a0004c0006t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.299-45617G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804353 | ||||||
| chr12:93804499
|
A | G | 1 | a0002c0003t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-45471A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804499 | ||||||
| chr12:93804800
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-45170A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804800 | ||||||
| chr12:93804836
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 26 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-45134A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804836 | ||||||
| chr12:93804885
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-45085T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804885 | ||||||
| chr12:93804991
|
T | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0036 | 2 | NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.299-44979T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93804991 | ||||||
| chr12:93805290
|
T | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-44680T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805290 | ||||||
| chr12:93805515
|
G | T | 1 | a0001c0001t0001g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-44455G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805515 | ||||||
| chr12:93805575
|
T | TATAA | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0071others(5): Show | 8 | HG01109.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-44373_299-4437 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93805575 | |||||
| chr12:93805575
|
T | TATAAATA others(1): Show |
73 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(70): Show | 73 | HG00597.hp2 HG01192.hp1 HG01257.hp2 others(70): Show |
intron_variant | MODIFIER | c.299-44377_299-4437 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93805575 | |||||
| chr12:93805575
|
T | TATAAATA others(5): Show |
10 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(7): Show | 10 | HG00597.hp1 HG01081.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-44381_299-4437 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93805575 | |||||
| chr12:93805575
|
TATAAATA others(5): Show |
T | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.299-44381_299-4437 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93805575 | |||||
| chr12:93805737
|
T | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(102): Show | 105 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.299-44233T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805737 | ||||||
| chr12:93805771
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-44199G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805771 | ||||||
| chr12:93805836
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0155 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.299-44134G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805836 | ||||||
| chr12:93805879
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-44091T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805879 | ||||||
| chr12:93805901
|
A | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 21 | HG00597.hp1 HG01192.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.299-44069A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805901 | ||||||
| chr12:93805927
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-44043G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805927 | ||||||
| chr12:93805938
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.299-44032A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93805938 | ||||||
| chr12:93806001
|
A | C | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(78): Show | 81 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.299-43969A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806001 | ||||||
| chr12:93806174
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-43796C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806174 | ||||||
| chr12:93806235
|
A | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.299-43735A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806235 | ||||||
| chr12:93806250
|
G | A | 45 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0044others(42): Show | 45 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-43720G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806250 | ||||||
| chr12:93806321
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.299-43649G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806321 | ||||||
| chr12:93806451
|
C | CA | 6 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0183others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-43498dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806451 | |||||
| chr12:93806451
|
CA | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0063others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-43498delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806451 | |||||
| chr12:93806451
|
CAA | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0206a0001c0001t0001g0242others(3): Show | 6 | HG00597.hp2 HG02559.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-43499_299-4349 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806451 | |||||
| chr12:93806451
|
CAAA | C | 68 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(65): Show | 68 | HG00597.hp1 HG01081.hp1 HG01192.hp1 others(65): Show |
intron_variant | MODIFIER | c.299-43500_299-4349 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806451 | |||||
| chr12:93806467
|
A | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.299-43503A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806467 | ||||||
| chr12:93806468
|
AAAAAC | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0071others(4): Show | 7 | HG01109.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-43497_299-4349 others(9): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806468 | |||||
| chr12:93806469
|
AAAAC | A | 71 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(68): Show | 71 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.299-43497_299-4349 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806469 | |||||
| chr12:93806471
|
AAC | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(9): Show | 12 | HG01257.hp2 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-43497_299-4349 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93806471 | |||||
| chr12:93806473
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-43497C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806473 | ||||||
| chr12:93806476
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0245 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.299-43494A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806476 | ||||||
| chr12:93806505
|
G | A | 1 | a0001c0001t0003g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.299-43465G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806505 | ||||||
| chr12:93806779
|
G | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(99): Show | 102 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.299-43191G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806779 | ||||||
| chr12:93806781
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0018others(62): Show | 65 | HG00597.hp2 HG01081.hp1 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.299-43189A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93806781 | ||||||
| chr12:93807141
|
A | G | 1 | a0001c0001t0006g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-42829A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807141 | ||||||
| chr12:93807444
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0137 | 2 | HG02683.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-42526C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807444 | ||||||
| chr12:93807503
|
A | G | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 108 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.299-42467A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807503 | ||||||
| chr12:93807788
|
A | G | 73 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0028others(70): Show | 73 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.299-42182A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807788 | ||||||
| chr12:93807800
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.299-42170A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807800 | ||||||
| chr12:93807837
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-42133C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807837 | ||||||
| chr12:93807855
|
C | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0246 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-42115C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93807855 | ||||||
| chr12:93807981
|
C | CA | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0117others(3): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-41969dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
C | CAAA | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG01081.hp1 HG01081.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.299-41971_299-4196 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
C | CAAAA | 42 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(39): Show | 42 | HG00639.hp2 HG01106.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-41972_299-4196 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
C | CAAAAA | 20 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0075others(17): Show | 20 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-41973_299-4196 others(9): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
C | CAAAAAA | 41 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0038others(38): Show | 41 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.299-41974_299-4196 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
C | CAAAAAAA | 6 | a0001c0001t0001g0050a0001c0002t0001g0041a0001c0002t0001g0059others(3): Show | 6 | HG01943.hp1 HG03704.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-41975_299-4196 others(11): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93807981
|
CA | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(13): Show | 16 | HG01099.hp2 HG01109.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-41969delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93807981 | |||||
| chr12:93808127
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0095 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.299-41843G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808127 | ||||||
| chr12:93808168
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(142): Show | 145 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.299-41802C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808168 | ||||||
| chr12:93808293
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0002t0001g0011 | 3 | HG02976.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.299-41677A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808293 | ||||||
| chr12:93808706
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0061others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-41264A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808706 | ||||||
| chr12:93808746
|
C | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.299-41224C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808746 | ||||||
| chr12:93808876
|
G | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 17 | HG01168.hp1 HG01255.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-41094G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808876 | ||||||
| chr12:93808908
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.299-41062T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808908 | ||||||
| chr12:93808979
|
T | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.299-40991T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93808979 | ||||||
| chr12:93809088
|
ATTTTTAA others(12): Show |
A | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0055others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-40879_299-4086 others(23): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93809088 | |||||
| chr12:93809265
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0246 | 3 | HG02559.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-40705G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809265 | ||||||
| chr12:93809502
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-40468G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809502 | ||||||
| chr12:93809538
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-40432C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809538 | ||||||
| chr12:93809542
|
C | T | 2 | a0001c0001t0001g0237a0001c0002t0001g0054 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299-40428C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809542 | ||||||
| chr12:93809629
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.299-40341G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809629 | ||||||
| chr12:93809884
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-40086C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809884 | ||||||
| chr12:93809893
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0246 | 3 | HG02559.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-40077G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93809893 | ||||||
| chr12:93810087
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-39883T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810087 | ||||||
| chr12:93810225
|
AG | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-39743delG | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810225 | |||||
| chr12:93810286
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.299-39684C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810286 | ||||||
| chr12:93810539
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-39431G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810539 | ||||||
| chr12:93810551
|
C | CA | 5 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0126others(2): Show | 5 | HG02559.hp2 HG03942.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-39379dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CA | C | 40 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0024others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-39379delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAA | C | 21 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0030others(18): Show | 21 | HG01071.hp2 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.299-39380_299-3937 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAA | C | 9 | a0001c0001t0001g0166a0001c0001t0001g0189a0001c0001t0001g0196others(6): Show | 9 | HG01167.hp1 HG01975.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-39381_299-3937 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAA | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0060a0001c0001t0001g0072others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-39382_299-3937 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAA | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0101others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-39383_299-3937 others(9): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAA | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0038others(12): Show | 15 | HG01109.hp1 HG01496.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-39384_299-3937 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0048others(36): Show | 39 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.299-39385_299-3937 others(11): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(1): Show |
C | 23 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.299-39386_299-3937 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(3): Show |
C | 19 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0056others(16): Show | 19 | HG01255.hp1 HG01258.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-39388_299-3937 others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0071others(5): Show | 8 | HG01168.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-39389_299-3937 others(15): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0090a0001c0001t0001g0171 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-39390_299-3937 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0001g0088 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.299-39392_299-3937 others(18): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(8): Show |
C | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-39393_299-3937 others(19): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-39394_299-3937 others(20): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0001g0010a0001c0001t0001g0150a0001c0001t0001g0246 | 3 | HG03209.hp1 NA18972.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-39395_299-3937 others(21): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0070a0001c0001t0001g0199 | 2 | HG03540.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.299-39397_299-3937 others(23): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810551
|
CAAAAAAA others(13): Show |
C | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 15 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-39398_299-3937 others(24): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93810551 | |||||
| chr12:93810614
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0246 | 3 | HG02559.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-39356C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810614 | ||||||
| chr12:93810622
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-39348A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810622 | ||||||
| chr12:93810726
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.299-39244C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810726 | ||||||
| chr12:93810760
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-39210G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810760 | ||||||
| chr12:93810955
|
C | A | 1 | a0001c0002t0001g0177 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-39015C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93810955 | ||||||
| chr12:93811050
|
GC | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.299-38913delC | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93811050 | |||||
| chr12:93811055
|
C | G | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 15 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-38915C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811055 | ||||||
| chr12:93811056
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-38914C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811056 | ||||||
| chr12:93811312
|
A | G | 3 | a0001c0002t0001g0121a0001c0002t0001g0149a0001c0002t0001g0205 | 3 | NA18747.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.299-38658A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811312 | ||||||
| chr12:93811355
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(132): Show | 135 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(132): Show |
intron_variant | MODIFIER | c.299-38615C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811355 | ||||||
| chr12:93811373
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-38597A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811373 | ||||||
| chr12:93811430
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(86): Show | 89 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.299-38540G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811430 | ||||||
| chr12:93811467
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | NA18945.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.299-38503C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811467 | ||||||
| chr12:93811664
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.299-38306C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811664 | ||||||
| chr12:93811802
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-38168T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811802 | ||||||
| chr12:93811954
|
A | G | 2 | a0001c0001t0001g0237a0001c0002t0001g0054 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299-38016A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93811954 | ||||||
| chr12:93812023
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.299-37947G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812023 | ||||||
| chr12:93812081
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-37889G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812081 | ||||||
| chr12:93812115
|
A | G | 5 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0159others(2): Show | 5 | HG02055.hp2 HG02300.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-37855A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812115 | ||||||
| chr12:93812200
|
C | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0140others(2): Show | 5 | HG00597.hp1 HG01099.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-37770C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812200 | ||||||
| chr12:93812290
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0050others(23): Show | 26 | HG00597.hp1 HG01099.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.299-37680G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812290 | ||||||
| chr12:93812393
|
A | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-37577A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812393 | ||||||
| chr12:93812432
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0087others(16): Show | 19 | HG00597.hp1 HG01099.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-37538T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812432 | ||||||
| chr12:93812450
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-37520G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812450 | ||||||
| chr12:93812500
|
C | A | 2 | a0001c0001t0001g0237a0001c0002t0001g0054 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299-37470C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812500 | ||||||
| chr12:93812522
|
C | CA | 11 | a0001c0001t0001g0124a0001c0001t0001g0144a0001c0001t0001g0148others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-37433dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93812522 | |||||
| chr12:93812522
|
CA | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0070others(29): Show | 32 | HG00597.hp1 HG01099.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-37433delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93812522 | |||||
| chr12:93812784
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-37186G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812784 | ||||||
| chr12:93812789
|
T | G | 1 | a0001c0002t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-37181T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812789 | ||||||
| chr12:93812804
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.299-37166T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812804 | ||||||
| chr12:93812869
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG02258.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-37101G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812869 | ||||||
| chr12:93812878
|
G | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0143others(6): Show | 9 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-37092G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93812878 | ||||||
| chr12:93813089
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0123others(1): Show | 4 | NA18942.hp2 NA18957.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-36881A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813089 | ||||||
| chr12:93813418
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.299-36552A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813418 | ||||||
| chr12:93813518
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(135): Show | 138 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.299-36452A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813518 | ||||||
| chr12:93813756
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(135): Show | 138 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.299-36214G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813756 | ||||||
| chr12:93813793
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.299-36177G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813793 | ||||||
| chr12:93813816
|
G | A | 1 | a0003c0004t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-36154G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813816 | ||||||
| chr12:93813953
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 247 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(244): Show |
intron_variant | MODIFIER | c.299-36017G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93813953 | ||||||
| chr12:93814004
|
G | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0245 | 2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.299-35966G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814004 | ||||||
| chr12:93814026
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(132): Show | 135 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.299-35944G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814026 | ||||||
| chr12:93814051
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | NA18953.hp1 NA18967.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-35919G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814051 | ||||||
| chr12:93814097
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-35873T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814097 | ||||||
| chr12:93814219
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-35751C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814219 | ||||||
| chr12:93814283
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.299-35687G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814283 | ||||||
| chr12:93814322
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-35648C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814322 | ||||||
| chr12:93814537
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.299-35433G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814537 | ||||||
| chr12:93814620
|
A | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0154a0001c0002t0001g0180 | 3 | HG00597.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.299-35350A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814620 | ||||||
| chr12:93814673
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-35297A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814673 | ||||||
| chr12:93814849
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0177a0001c0002t0001g0229 | 3 | HG01071.hp2 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.299-35121T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814849 | ||||||
| chr12:93814896
|
A | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0159others(1): Show | 4 | HG02055.hp2 HG02300.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-35074A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814896 | ||||||
| chr12:93814980
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0246 | 3 | HG02559.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-34990C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93814980 | ||||||
| chr12:93815146
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-34824G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815146 | ||||||
| chr12:93815149
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.299-34821G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815149 | ||||||
| chr12:93815166
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-34804G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815166 | ||||||
| chr12:93815325
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0242 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.299-34645C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815325 | ||||||
| chr12:93815359
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-34611T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815359 | ||||||
| chr12:93815462
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-34508T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815462 | ||||||
| chr12:93815463
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-34507G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815463 | ||||||
| chr12:93815577
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0246 | 3 | HG02559.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-34393A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815577 | ||||||
| chr12:93815607
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-34363G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815607 | ||||||
| chr12:93815833
|
A | G | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(3): Show | 6 | HG00544.hp1 NA18953.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-34137A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815833 | ||||||
| chr12:93815880
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0193 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.299-34090C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815880 | ||||||
| chr12:93815998
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-33972G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93815998 | ||||||
| chr12:93816008
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-33962A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816008 | ||||||
| chr12:93816115
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.299-33855A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816115 | ||||||
| chr12:93816167
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-33803A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816167 | ||||||
| chr12:93816279
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0143others(8): Show | 11 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-33691C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816279 | ||||||
| chr12:93816341
|
C | G | 25 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(22): Show | 25 | HG00597.hp2 HG02040.hp1 HG03017.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-33629C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816341 | ||||||
| chr12:93816369
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-33601G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816369 | ||||||
| chr12:93816383
|
A | ATTTTTT | 11 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0143others(8): Show | 11 | HG01516.hp1 HG01934.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-33577_299-3357 others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93816383 | |||||
| chr12:93816383
|
A | ATTTTTTT | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.299-33578_299-3357 others(11): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93816383 | |||||
| chr12:93816383
|
A | ATTTTTTT others(1): Show |
43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0023others(40): Show | 43 | HG01106.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.299-33579_299-3357 others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93816383 | |||||
| chr12:93816383
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-33583_299-3357 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93816383 | |||||
| chr12:93816400
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-33570G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816400 | ||||||
| chr12:93816433
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-33537G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816433 | ||||||
| chr12:93816461
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-33509A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816461 | ||||||
| chr12:93816648
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-33322G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816648 | ||||||
| chr12:93816654
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0006g0133 | 2 | NA18747.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-33316C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816654 | ||||||
| chr12:93816729
|
GT | G | 13 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0143others(10): Show | 13 | HG00544.hp2 HG01928.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-33239delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93816729 | |||||
| chr12:93816870
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.299-33100C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816870 | ||||||
| chr12:93816899
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(20): Show | 23 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.299-33071C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816899 | ||||||
| chr12:93816904
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-33066G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93816904 | ||||||
| chr12:93817193
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-32777A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817193 | ||||||
| chr12:93817532
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.299-32438C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817532 | ||||||
| chr12:93817602
|
A | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0028others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-32368A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817602 | ||||||
| chr12:93817655
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-32315G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817655 | ||||||
| chr12:93817689
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(175): Show |
intron_variant | MODIFIER | c.299-32281C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817689 | ||||||
| chr12:93817719
|
T | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.299-32251T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93817719 | ||||||
| chr12:93818314
|
G | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.299-31656G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818314 | ||||||
| chr12:93818540
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.299-31430C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818540 | ||||||
| chr12:93818569
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0168 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.299-31401G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818569 | ||||||
| chr12:93818570
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-31400T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818570 | ||||||
| chr12:93818856
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0168others(1): Show | 4 | HG01192.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-31114C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818856 | ||||||
| chr12:93818992
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0003g0083 | 2 | HG03942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.299-30978C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93818992 | ||||||
| chr12:93819140
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0169a0001c0001t0001g0193 | 3 | HG02886.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.299-30830G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819140 | ||||||
| chr12:93819142
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(14): Show | 17 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-30828C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819142 | ||||||
| chr12:93819357
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-30613G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819357 | ||||||
| chr12:93819363
|
GTAT | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0110others(2): Show | 5 | NA18962.hp2 NA18972.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-30605_299-3060 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93819363 | |||||
| chr12:93819446
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-30524G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819446 | ||||||
| chr12:93819616
|
T | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0071others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-30354T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819616 | ||||||
| chr12:93819676
|
C | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(11): Show | 14 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-30294C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819676 | ||||||
| chr12:93819867
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0071others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-30103C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93819867 | ||||||
| chr12:93820193
|
C | G | 15 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0061others(12): Show | 15 | HG00597.hp2 HG02683.hp1 HG03492.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-29777C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820193 | ||||||
| chr12:93820287
|
C | A | 17 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0061others(14): Show | 17 | HG00597.hp2 HG02622.hp2 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-29683C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820287 | ||||||
| chr12:93820336
|
T | C | 67 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(64): Show | 67 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.299-29634T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820336 | ||||||
| chr12:93820450
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0159 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.299-29520G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820450 | ||||||
| chr12:93820461
|
A | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(18): Show | 21 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-29509A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820461 | ||||||
| chr12:93820521
|
G | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.299-29449G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820521 | ||||||
| chr12:93820526
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-29444G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820526 | ||||||
| chr12:93820576
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0159 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.299-29394G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820576 | ||||||
| chr12:93820748
|
T | A | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-29222T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820748 | ||||||
| chr12:93820781
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-29189T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820781 | ||||||
| chr12:93820819
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0159 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.299-29151C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820819 | ||||||
| chr12:93820826
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0002g0244 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.299-29144C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93820826 | ||||||
| chr12:93821303
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0159 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.299-28667G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821303 | ||||||
| chr12:93821372
|
G | A | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-28598G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821372 | ||||||
| chr12:93821394
|
T | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(18): Show | 21 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.299-28576T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821394 | ||||||
| chr12:93821409
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-28561T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821409 | ||||||
| chr12:93821792
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-28178G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821792 | ||||||
| chr12:93821842
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-28128G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821842 | ||||||
| chr12:93821952
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-28018T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93821952 | ||||||
| chr12:93822001
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-27969C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93822001 | ||||||
| chr12:93822072
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-27898T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93822072 | ||||||
| chr12:93822117
|
C | CAA | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(107): Show | 110 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.299-27842_299-2784 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93822117 | |||||
| chr12:93822729
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-27241G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93822729 | ||||||
| chr12:93822868
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-27102T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93822868 | ||||||
| chr12:93822908
|
A | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 115 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(112): Show |
intron_variant | MODIFIER | c.299-27062A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93822908 | ||||||
| chr12:93823169
|
G | A | 19 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(16): Show | 19 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-26801G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823169 | ||||||
| chr12:93823206
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0221others(2): Show | 5 | HG02257.hp2 HG03225.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-26764C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823206 | ||||||
| chr12:93823294
|
A | AAAAC | 10 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(7): Show | 10 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-26672_299-2666 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93823294 | |||||
| chr12:93823298
|
C | CAAACA | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0171others(7): Show | 10 | HG00597.hp1 HG00735.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-26669_299-2666 others(9): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93823298 | |||||
| chr12:93823298
|
CA | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.299-26657delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93823298 | |||||
| chr12:93823426
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-26544G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823426 | ||||||
| chr12:93823439
|
C | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(18): Show | 21 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-26531C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823439 | ||||||
| chr12:93823753
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0110 | 3 | NA18981.hp1 NA19003.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-26217G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823753 | ||||||
| chr12:93823856
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.299-26114C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823856 | ||||||
| chr12:93823870
|
A | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 158 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(155): Show |
intron_variant | MODIFIER | c.299-26100A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823870 | ||||||
| chr12:93823996
|
T | G | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-25974T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93823996 | ||||||
| chr12:93824056
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.299-25914T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93824056 | ||||||
| chr12:93824065
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.299-25905A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93824065 | ||||||
| chr12:93824252
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0243 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.299-25718A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93824252 | ||||||
| chr12:93824421
|
T | TAC | 113 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(110): Show | 113 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.299-25530_299-2552 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93824421 | |||||
| chr12:93824421
|
T | TACAC | 21 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(18): Show | 21 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-25532_299-2552 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93824421 | |||||
| chr12:93824861
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.299-25109C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93824861 | ||||||
| chr12:93825084
|
G | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0033others(16): Show | 19 | HG00597.hp2 HG01109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-24886G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825084 | ||||||
| chr12:93825124
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0110 | 3 | NA18981.hp1 NA19003.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-24846G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825124 | ||||||
| chr12:93825125
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | NA18945.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.299-24845C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825125 | ||||||
| chr12:93825317
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.299-24653A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825317 | ||||||
| chr12:93825549
|
G | A | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-24421G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825549 | ||||||
| chr12:93825624
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.299-24346T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825624 | ||||||
| chr12:93825667
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(8): Show | 11 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-24303T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825667 | ||||||
| chr12:93825713
|
G | T | 1 | a0001c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-24257G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825713 | ||||||
| chr12:93825947
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-24023C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93825947 | ||||||
| chr12:93826087
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-23883A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93826087 | ||||||
| chr12:93826369
|
G | C | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-23601G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93826369 | ||||||
| chr12:93826412
|
A | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-23558A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93826412 | ||||||
| chr12:93826521
|
A | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-23449A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93826521 | ||||||
| chr12:93826625
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0003g0007a0001c0001t0003g0083 | 3 | HG03041.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-23345C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93826625 | ||||||
| chr12:93827201
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-22769C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827201 | ||||||
| chr12:93827207
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0159 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.299-22763C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827207 | ||||||
| chr12:93827212
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(15): Show | 18 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-22758A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827212 | ||||||
| chr12:93827224
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-22746T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827224 | ||||||
| chr12:93827253
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(14): Show | 17 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-22717G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827253 | ||||||
| chr12:93827302
|
A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.299-22668A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827302 | ||||||
| chr12:93827318
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.299-22652A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827318 | ||||||
| chr12:93827407
|
T | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0066others(10): Show | 13 | HG00597.hp2 HG03704.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-22563T>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827407 | ||||||
| chr12:93827509
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.299-22461C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93827509 | ||||||
| chr12:93828224
|
T | C | 1 | a0001c0002t0001g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.299-21746T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828224 | ||||||
| chr12:93828227
|
T | C | 65 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(62): Show | 65 | HG00544.hp2 HG01081.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.299-21743T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828227 | ||||||
| chr12:93828584
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-21386G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828584 | ||||||
| chr12:93828707
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083 | 3 | HG03942.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-21263C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828707 | ||||||
| chr12:93828729
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-21241A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828729 | ||||||
| chr12:93828807
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-21163A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828807 | ||||||
| chr12:93828846
|
G | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(9): Show | 12 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-21124G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828846 | ||||||
| chr12:93828881
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-21089G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828881 | ||||||
| chr12:93828914
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-21056C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93828914 | ||||||
| chr12:93829125
|
CT | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(11): Show | 14 | HG01109.hp2 HG01168.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-20831delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93829125 | |||||
| chr12:93829215
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0134 | 2 | HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.299-20755G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829215 | ||||||
| chr12:93829241
|
A | G | 1 | a0001c0002t0001g0142 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.299-20729A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829241 | ||||||
| chr12:93829462
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-20508G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829462 | ||||||
| chr12:93829689
|
T | TTTG | 11 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(8): Show | 11 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-20263_299-2026 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93829689 | |||||
| chr12:93829715
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-20255T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829715 | ||||||
| chr12:93829880
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0113 | 2 | HG03688.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.299-20090A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829880 | ||||||
| chr12:93829900
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-20070C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829900 | ||||||
| chr12:93829988
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-19982G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93829988 | ||||||
| chr12:93830003
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0138 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.299-19967A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93830003 | ||||||
| chr12:93830109
|
G | T | 1 | a0001c0002t0001g0122 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.299-19861G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93830109 | ||||||
| chr12:93830117
|
C | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(16): Show | 19 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-19853C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93830117 | ||||||
| chr12:93830861
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.299-19109T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93830861 | ||||||
| chr12:93830933
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18962.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.299-19037A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93830933 | ||||||
| chr12:93831198
|
G | A | 1 | a0001c0001t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.299-18772G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831198 | ||||||
| chr12:93831224
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083 | 3 | HG03942.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-18746G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831224 | ||||||
| chr12:93831548
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0174 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.299-18422G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831548 | ||||||
| chr12:93831551
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-18419G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831551 | ||||||
| chr12:93831567
|
C | CA | 5 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0221others(2): Show | 5 | HG02257.hp2 HG03225.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-18399dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93831567 | |||||
| chr12:93831651
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0239 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.299-18319A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831651 | ||||||
| chr12:93831716
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.299-18254A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831716 | ||||||
| chr12:93831761
|
A | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(29): Show | 32 | HG00597.hp1 HG00735.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-18209A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831761 | ||||||
| chr12:93831815
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(12): Show | 15 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-18155A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831815 | ||||||
| chr12:93831817
|
G | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(17): Show | 20 | HG00597.hp1 HG00735.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-18153G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831817 | ||||||
| chr12:93831838
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0243 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.299-18132A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831838 | ||||||
| chr12:93831961
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0096 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.299-18009C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831961 | ||||||
| chr12:93831974
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0070others(6): Show | 9 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-17996G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93831974 | ||||||
| chr12:93832043
|
G | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(12): Show | 15 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-17927G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832043 | ||||||
| chr12:93832060
|
A | AT | 15 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(12): Show | 15 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-17903dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93832060 | |||||
| chr12:93832179
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(12): Show | 15 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-17791C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832179 | ||||||
| chr12:93832315
|
G | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(9): Show | 12 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-17655G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832315 | ||||||
| chr12:93832325
|
T | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(9): Show | 12 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-17645T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832325 | ||||||
| chr12:93832482
|
TAA | T | 3 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083 | 3 | HG03942.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-17487_299-1748 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832482 | ||||||
| chr12:93832552
|
CTT | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(9): Show | 12 | HG01168.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-17416_299-1741 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93832552 | |||||
| chr12:93832555
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0241 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.299-17415T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832555 | ||||||
| chr12:93832572
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-17398C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832572 | ||||||
| chr12:93832683
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-17287T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832683 | ||||||
| chr12:93832772
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(11): Show | 14 | HG01168.hp1 HG01192.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-17198G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832772 | ||||||
| chr12:93832795
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 99 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.299-17175T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832795 | ||||||
| chr12:93832810
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-17160C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93832810 | ||||||
| chr12:93833085
|
C | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 103 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.299-16885C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833085 | ||||||
| chr12:93833089
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.299-16881G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833089 | ||||||
| chr12:93833225
|
A | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(167): Show |
intron_variant | MODIFIER | c.299-16745A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833225 | ||||||
| chr12:93833405
|
C | T | 14 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(11): Show | 14 | HG00544.hp2 HG01928.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-16565C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833405 | ||||||
| chr12:93833661
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-16309A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833661 | ||||||
| chr12:93833743
|
A | AT | 126 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(123): Show | 126 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.299-16221dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93833743 | |||||
| chr12:93833771
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-16199C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93833771 | ||||||
| chr12:93833822
|
G | GT | 156 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 156 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.299-16139dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93833822 | |||||
| chr12:93834074
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-15896G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834074 | ||||||
| chr12:93834370
|
CAT | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-15598_299-1559 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93834370 | |||||
| chr12:93834444
|
A | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 60 | HG00597.hp1 HG01109.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.299-15526A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834444 | ||||||
| chr12:93834634
|
C | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.299-15336C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834634 | ||||||
| chr12:93834637
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0071others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-15333C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834637 | ||||||
| chr12:93834649
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0168 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-15321C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834649 | ||||||
| chr12:93834697
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG00597.hp1 HG01109.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-15273A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93834697 | ||||||
| chr12:93835045
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-14925C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835045 | ||||||
| chr12:93835208
|
T | C | 15 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0066others(12): Show | 15 | HG00597.hp2 HG00639.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-14762T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835208 | ||||||
| chr12:93835482
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-14488T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835482 | ||||||
| chr12:93835543
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0243 | 2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.299-14427C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835543 | ||||||
| chr12:93835598
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.299-14372A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835598 | ||||||
| chr12:93835952
|
G | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 58 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.299-14018G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835952 | ||||||
| chr12:93835980
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-13990T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93835980 | ||||||
| chr12:93836047
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-13923G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836047 | ||||||
| chr12:93836051
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.299-13919G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836051 | ||||||
| chr12:93836143
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.299-13827C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836143 | ||||||
| chr12:93836352
|
T | C | 1 | a0001c0001t0003g0007 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.299-13618T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836352 | ||||||
| chr12:93836358
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0168 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-13612C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836358 | ||||||
| chr12:93836379
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0168 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-13591G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836379 | ||||||
| chr12:93836396
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.299-13574C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836396 | ||||||
| chr12:93836526
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0074a0001c0001t0001g0166others(1): Show | 4 | HG01192.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-13444G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836526 | ||||||
| chr12:93836600
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-13370C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836600 | ||||||
| chr12:93836674
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-13296T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836674 | ||||||
| chr12:93836712
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-13258T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836712 | ||||||
| chr12:93836895
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0168 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-13075C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93836895 | ||||||
| chr12:93837157
|
CATGTGAG others(4): Show |
C | 10 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0098others(7): Show | 10 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-12809_299-1279 others(15): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93837157 | |||||
| chr12:93837182
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-12788C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837182 | ||||||
| chr12:93837245
|
GTTTTTGT others(5): Show |
G | 11 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0064others(8): Show | 11 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-12723_299-1271 others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93837245 | |||||
| chr12:93837247
|
TTTTG | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0016others(16): Show | 19 | HG00597.hp1 HG01167.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-12699_299-1269 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93837247 | |||||
| chr12:93837273
|
TTTTG | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-12693_299-1269 others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93837273 | |||||
| chr12:93837279
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-12691T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837279 | ||||||
| chr12:93837283
|
T | G | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(11): Show | 14 | HG01071.hp2 HG01943.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-12687T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837283 | ||||||
| chr12:93837301
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-12669G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837301 | ||||||
| chr12:93837460
|
T | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(243): Show |
intron_variant | MODIFIER | c.299-12510T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837460 | ||||||
| chr12:93837506
|
G | C | 42 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(39): Show | 42 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.299-12464G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837506 | ||||||
| chr12:93837563
|
G | GTT | 68 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0033others(65): Show | 68 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.299-12405_299-1240 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93837563 | |||||
| chr12:93837629
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG02922.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-12341G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837629 | ||||||
| chr12:93837639
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0126 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.299-12331A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837639 | ||||||
| chr12:93837682
|
T | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0034others(64): Show | 67 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.299-12288T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837682 | ||||||
| chr12:93837755
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG01167.hp1 HG01167.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.299-12215G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837755 | ||||||
| chr12:93837886
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-12084C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837886 | ||||||
| chr12:93837948
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.299-12022C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837948 | ||||||
| chr12:93837966
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0168 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-12004A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837966 | ||||||
| chr12:93837981
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG02280.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-11989A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93837981 | ||||||
| chr12:93838201
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(131): Show | 134 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.299-11769T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838201 | ||||||
| chr12:93838214
|
G | GT | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(32): Show | 35 | HG00597.hp1 HG01106.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.299-11737dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838214 | |||||
| chr12:93838214
|
G | GTT | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(114): Show | 117 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.299-11738_299-1173 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838214 | |||||
| chr12:93838214
|
G | GTTT | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0063others(8): Show | 11 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-11739_299-1173 others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838214 | |||||
| chr12:93838214
|
GT | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0040others(13): Show | 16 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-11737delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838214 | |||||
| chr12:93838214
|
GTT | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0020others(26): Show | 29 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.299-11738_299-1173 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838214 | |||||
| chr12:93838442
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 167 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.299-11528G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838442 | ||||||
| chr12:93838556
|
TTC | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(128): Show | 131 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.299-11406_299-1140 others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838556 | |||||
| chr12:93838563
|
TC | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0025others(31): Show | 34 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(31): Show |
intron_variant | MODIFIER | c.299-11406delC | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838563 | ||||||
| chr12:93838564
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-11406C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838564 | ||||||
| chr12:93838564
|
CT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(8): Show | 11 | HG01884.hp2 HG01975.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-11392delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93838564 | |||||
| chr12:93838599
|
T | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-11371T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838599 | ||||||
| chr12:93838662
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-11308G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838662 | ||||||
| chr12:93838665
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0025others(19): Show | 22 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-11305C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838665 | ||||||
| chr12:93838671
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | NA18942.hp2 NA18957.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-11299C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838671 | ||||||
| chr12:93838855
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-11115C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838855 | ||||||
| chr12:93838858
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG01109.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-11112A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93838858 | ||||||
| chr12:93839053
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0038 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.299-10917G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839053 | ||||||
| chr12:93839201
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.299-10769A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839201 | ||||||
| chr12:93839202
|
T | C | 1 | a0004c0006t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.299-10768T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839202 | ||||||
| chr12:93839219
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-10751A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839219 | ||||||
| chr12:93839346
|
A | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(14): Show | 17 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-10624A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839346 | ||||||
| chr12:93839385
|
G | A | 13 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(10): Show | 13 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-10585G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839385 | ||||||
| chr12:93839474
|
G | A | 13 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(10): Show | 13 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-10496G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839474 | ||||||
| chr12:93839591
|
G | C | 1 | a0001c0002t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-10379G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839591 | ||||||
| chr12:93839625
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-10345A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839625 | ||||||
| chr12:93839896
|
G | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 97 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(94): Show |
intron_variant | MODIFIER | c.299-10074G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839896 | ||||||
| chr12:93839977
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 180 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.299-9993C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93839977 | ||||||
| chr12:93840210
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.299-9760G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840210 | ||||||
| chr12:93840273
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(207): Show |
intron_variant | MODIFIER | c.299-9697G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840273 | ||||||
| chr12:93840283
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-9687T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840283 | ||||||
| chr12:93840473
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-9497T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840473 | ||||||
| chr12:93840560
|
CTT | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 209 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(206): Show |
intron_variant | MODIFIER | c.299-9399_299-9398d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93840560 | |||||
| chr12:93840588
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.299-9382T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840588 | ||||||
| chr12:93840591
|
A | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-9379A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840591 | ||||||
| chr12:93840749
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-9221G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840749 | ||||||
| chr12:93840758
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(31): Show | 34 | HG01109.hp1 HG01978.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.299-9212G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93840758 | ||||||
| chr12:93841102
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-8868T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841102 | ||||||
| chr12:93841106
|
C | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(10): Show | 13 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-8864C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841106 | ||||||
| chr12:93841276
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-8694C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841276 | ||||||
| chr12:93841359
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-8611G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841359 | ||||||
| chr12:93841389
|
A | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(14): Show | 17 | HG01884.hp1 HG01928.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-8581A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841389 | ||||||
| chr12:93841439
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0071others(4): Show | 7 | HG02970.hp2 HG03139.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-8531A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841439 | ||||||
| chr12:93841463
|
A | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0083 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-8507A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841463 | ||||||
| chr12:93841652
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-8318C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841652 | ||||||
| chr12:93841701
|
A | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-8269A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841701 | ||||||
| chr12:93841724
|
CA | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0169others(1): Show | 4 | HG02886.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-8245delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841724 | ||||||
| chr12:93841839
|
T | C | 22 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(19): Show | 22 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-8131T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841839 | ||||||
| chr12:93841877
|
A | G | 22 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(19): Show | 22 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-8093A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93841877 | ||||||
| chr12:93842009
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 203 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(200): Show |
intron_variant | MODIFIER | c.299-7961C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842009 | ||||||
| chr12:93842070
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 127 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.299-7900G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842070 | ||||||
| chr12:93842109
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.299-7861T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842109 | ||||||
| chr12:93842126
|
C | CT | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.299-7842dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93842126 | |||||
| chr12:93842267
|
C | G | 4 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083others(1): Show | 4 | HG03654.hp1 HG03942.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-7703C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842267 | ||||||
| chr12:93842356
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.299-7614G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842356 | ||||||
| chr12:93842485
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-7485C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842485 | ||||||
| chr12:93842679
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.299-7291A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842679 | ||||||
| chr12:93842716
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(190): Show |
intron_variant | MODIFIER | c.299-7254G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842716 | ||||||
| chr12:93842809
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.299-7161A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842809 | ||||||
| chr12:93842843
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-7127T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842843 | ||||||
| chr12:93842953
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(14): Show | 17 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-7017G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93842953 | ||||||
| chr12:93843017
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.299-6953A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843017 | ||||||
| chr12:93843201
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.299-6769G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843201 | ||||||
| chr12:93843305
|
C | G | 53 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0056others(50): Show | 53 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.299-6665C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843305 | ||||||
| chr12:93843319
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG01884.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-6651T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843319 | ||||||
| chr12:93843322
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.299-6648C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843322 | ||||||
| chr12:93843384
|
C | CT | 41 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0104others(38): Show | 41 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.299-6570dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93843384 | |||||
| chr12:93843384
|
C | CTT | 12 | a0001c0001t0001g0019a0001c0002t0001g0036a0001c0002t0001g0051others(9): Show | 12 | HG02602.hp1 HG03239.hp2 HG04228.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-6571_299-6570d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93843384 | |||||
| chr12:93843466
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-6504G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843466 | ||||||
| chr12:93843529
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083others(1): Show | 4 | HG03654.hp1 HG03942.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-6441G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843529 | ||||||
| chr12:93843766
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.299-6204G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843766 | ||||||
| chr12:93843780
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(207): Show |
intron_variant | MODIFIER | c.299-6190A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843780 | ||||||
| chr12:93843793
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0124others(3): Show | 6 | HG01192.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-6177T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843793 | ||||||
| chr12:93843799
|
C | A | 1 | a0001c0002t0001g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-6171C>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843799 | ||||||
| chr12:93843813
|
C | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0064others(9): Show | 12 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-6157C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843813 | ||||||
| chr12:93843865
|
C | T | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-6105C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843865 | ||||||
| chr12:93843964
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG01884.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-6006C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843964 | ||||||
| chr12:93843968
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0201 | 2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.299-6002C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843968 | ||||||
| chr12:93843989
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(15): Show | 18 | HG01167.hp1 HG01168.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-5981T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93843989 | ||||||
| chr12:93844583
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-5387A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93844583 | ||||||
| chr12:93844669
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 139 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(136): Show |
intron_variant | MODIFIER | c.299-5301A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93844669 | ||||||
| chr12:93844939
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-5031C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93844939 | ||||||
| chr12:93845012
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0156 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.299-4958G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845012 | ||||||
| chr12:93845028
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 211 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.299-4942T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845028 | ||||||
| chr12:93845188
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00639.hp2 HG01109.hp2 HG01192.hp2 others(79): Show |
intron_variant | MODIFIER | c.299-4782G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845188 | ||||||
| chr12:93845258
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-4712C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845258 | ||||||
| chr12:93845267
|
G | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-4703G>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845267 | ||||||
| chr12:93845351
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.299-4619C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845351 | ||||||
| chr12:93845362
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.299-4608T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845362 | ||||||
| chr12:93845380
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0028others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-4590G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845380 | ||||||
| chr12:93845493
|
T | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(173): Show |
intron_variant | MODIFIER | c.299-4477T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845493 | ||||||
| chr12:93845563
|
A | AAT | 3 | a0001c0001t0001g0102a0001c0001t0001g0238a0001c0002t0001g0088 | 3 | NA18981.hp2 NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.299-4392_299-4391d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845563 | |||||
| chr12:93845576
|
A | ATTT | 4 | a0001c0001t0001g0126a0001c0001t0002g0001a0001c0001t0002g0147others(1): Show | 4 | HG00639.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-4393_299-4392i others(5): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845576 | |||||
| chr12:93845576
|
A | ATTTT | 4 | a0001c0001t0001g0017a0001c0001t0001g0124a0001c0001t0001g0166others(1): Show | 4 | HG01192.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-4393_299-4392i others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845576 | |||||
| chr12:93845577
|
TA | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(87): Show | 90 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.299-4392delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845577 | ||||||
| chr12:93845578
|
A | ATATATT | 6 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-4391_299-4390i others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845578 | |||||
| chr12:93845578
|
A | ATATT | 53 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0030others(50): Show | 53 | HG01361.hp1 HG01928.hp1 HG01978.hp2 others(50): Show |
intron_variant | MODIFIER | c.299-4391_299-4390i others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845578 | |||||
| chr12:93845578
|
A | ATATTTT | 4 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0072others(1): Show | 4 | HG02572.hp2 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-4391_299-4390i others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845578 | |||||
| chr12:93845578
|
A | ATTTT | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0026others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-4390_299-4387d others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93845578 | |||||
| chr12:93845578
|
A | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0124a0001c0001t0001g0126others(5): Show | 8 | HG00639.hp2 HG01192.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-4392A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845578 | ||||||
| chr12:93845669
|
A | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0031 | 2 | NA18977.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.299-4301A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845669 | ||||||
| chr12:93845890
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.299-4080G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845890 | ||||||
| chr12:93845962
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0083others(1): Show | 4 | HG03654.hp1 HG03942.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-4008T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845962 | ||||||
| chr12:93845997
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0123a0001c0001t0001g0215 | 3 | HG03704.hp2 NA18953.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.299-3973G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93845997 | ||||||
| chr12:93846119
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.299-3851A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846119 | ||||||
| chr12:93846227
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-3743G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846227 | ||||||
| chr12:93846249
|
G | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(39): Show | 42 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.299-3721G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846249 | ||||||
| chr12:93846384
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(42): Show | 45 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-3586T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846384 | ||||||
| chr12:93846394
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0110 | 3 | NA18981.hp1 NA19003.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-3576C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846394 | ||||||
| chr12:93846416
|
A | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0064others(10): Show | 13 | HG01167.hp1 HG01168.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-3554A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846416 | ||||||
| chr12:93846454
|
T | TTTTTG | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 125 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(122): Show |
intron_variant | MODIFIER | c.299-3495_299-3491d others(7): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846454 | |||||
| chr12:93846510
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-3460A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846510 | ||||||
| chr12:93846581
|
A | AAC | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0107others(6): Show | 9 | HG01168.hp1 HG01257.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-3346_299-3345d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACAC | 4 | a0001c0001t0001g0018a0001c0001t0001g0102a0001c0001t0001g0154others(1): Show | 4 | HG01071.hp1 HG01106.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-3348_299-3345d others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACACAC | 2 | a0001c0001t0001g0087a0001c0001t0001g0233 | 2 | HG00597.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.299-3350_299-3345d others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0225a0001c0001t0001g0245others(2): Show | 5 | HG02280.hp2 HG02451.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-3352_299-3345d others(10): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACACACA others(3): Show |
5 | a0001c0001t0001g0066a0001c0001t0001g0085a0001c0001t0001g0104others(2): Show | 5 | HG01255.hp1 HG03688.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-3354_299-3345d others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACACACA others(5): Show |
4 | a0001c0001t0001g0034a0001c0001t0001g0099a0001c0001t0001g0113others(1): Show | 4 | HG03654.hp1 NA18962.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-3356_299-3345d others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
A | AACACACA others(7): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0247 | 3 | NA18971.hp1 NA18978.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.299-3358_299-3345d others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
AAC | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0073others(14): Show | 17 | HG01167.hp1 HG01168.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-3346_299-3345d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-3354_299-3345d others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846581
|
AACACACA others(5): Show |
A | 3 | a0001c0001t0001g0019a0001c0001t0001g0153a0001c0001t0001g0186 | 3 | HG02602.hp1 HG02602.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.299-3356_299-3345d others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846581 | |||||
| chr12:93846586
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-3373_299-3372i others(18): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846586 | |||||
| chr12:93846588
|
A | ACACACAC others(7): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0072others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-3373_299-3372i others(16): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846588 | |||||
| chr12:93846590
|
A | ACACACAC others(5): Show |
4 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0110others(1): Show | 4 | HG02698.hp2 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-3373_299-3372i others(14): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846590 | |||||
| chr12:93846592
|
A | ACACACGC others(3): Show |
1 | a0001c0001t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-3373_299-3372i others(12): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846592 | |||||
| chr12:93846594
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 126 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(123): Show |
intron_variant | MODIFIER | c.299-3376A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846594 | ||||||
| chr12:93846610
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 126 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(123): Show |
intron_variant | MODIFIER | c.299-3360A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846610 | ||||||
| chr12:93846617
|
C | CACACAT | 9 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0043others(6): Show | 9 | HG01081.hp1 HG02683.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-3348_299-3347i others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846617 | |||||
| chr12:93846617
|
C | CACAT | 5 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0101others(2): Show | 5 | HG00544.hp2 HG02257.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-3350_299-3349i others(6): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846617 | |||||
| chr12:93846617
|
C | CAT | 7 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0050others(4): Show | 7 | HG01928.hp2 HG01943.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-3352_299-3351i others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846617 | |||||
| chr12:93846635
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(25): Show | 28 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.299-3335A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846635 | ||||||
| chr12:93846855
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(19): Show | 22 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-3115C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846855 | ||||||
| chr12:93846944
|
CA | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.299-3017delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93846944 | |||||
| chr12:93846953
|
A | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0095a0001c0001t0001g0224 | 3 | HG02109.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.299-3017A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846953 | ||||||
| chr12:93846957
|
G | A | 3 | a0001c0002t0001g0052a0001c0002t0001g0080a0001c0002t0001g0149 | 3 | NA18949.hp1 NA19004.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.299-3013G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846957 | ||||||
| chr12:93846997
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.299-2973G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93846997 | ||||||
| chr12:93847020
|
A | G | 3 | a0001c0002t0001g0052a0001c0002t0001g0080a0001c0002t0001g0149 | 3 | NA18949.hp1 NA19004.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.299-2950A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847020 | ||||||
| chr12:93847126
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.299-2844A>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847126 | ||||||
| chr12:93847165
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299-2805C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847165 | ||||||
| chr12:93847370
|
A | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0020others(18): Show | 21 | HG01081.hp1 HG01928.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-2600A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847370 | ||||||
| chr12:93847498
|
G | GA | 102 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(99): Show | 102 | HG00544.hp1 HG00735.hp1 HG01071.hp2 others(99): Show |
intron_variant | MODIFIER | c.299-2449dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93847498 | |||||
| chr12:93847498
|
G | GAA | 14 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0095others(11): Show | 14 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-2450_299-2449d others(4): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93847498 | |||||
| chr12:93847498
|
GA | G | 10 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0064others(7): Show | 10 | HG01168.hp2 HG01261.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2449delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93847498 | |||||
| chr12:93847516
|
A | AC | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(12): Show | 15 | HG00735.hp2 HG01192.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-2454_299-2453i others(3): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847516 | ||||||
| chr12:93847516
|
A | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(33): Show | 36 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-2454A>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93847516 | ||||||
| chr12:93847605
|
ACAACAG | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0020others(18): Show | 21 | HG01081.hp1 HG01928.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-2359_299-2354d others(8): Show |
CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93847605 | |||||
| chr12:93848080
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-1890C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848080 | ||||||
| chr12:93848151
|
A | AT | 6 | a0001c0001t0001g0126a0001c0002t0001g0032a0001c0002t0001g0129others(3): Show | 6 | HG01071.hp2 HG01934.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1809dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93848151 | |||||
| chr12:93848151
|
AT | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(10): Show | 13 | HG00735.hp2 HG01192.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-1809delT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93848151 | |||||
| chr12:93848248
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0126others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1722G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848248 | ||||||
| chr12:93848357
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-1613G>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848357 | ||||||
| chr12:93848454
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(19): Show | 22 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-1516A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848454 | ||||||
| chr12:93848494
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-1476G>A | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848494 | ||||||
| chr12:93848770
|
C | CT | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 207 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(204): Show |
intron_variant | MODIFIER | c.299-1199dupT | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93848770 | |||||
| chr12:93848993
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-977C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93848993 | ||||||
| chr12:93849024
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00544.hp1 HG00735.hp1 HG01071.hp2 others(106): Show |
intron_variant | MODIFIER | c.299-946T>C | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849024 | ||||||
| chr12:93849120
|
C | T | 4 | a0001c0002t0001g0011a0002c0003t0001g0076a0002c0003t0001g0079others(1): Show | 4 | HG02965.hp2 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-850C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849120 | ||||||
| chr12:93849142
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(31): Show | 34 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.299-828C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849142 | ||||||
| chr12:93849246
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0156 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.299-724T>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849246 | ||||||
| chr12:93849255
|
A | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0156others(3): Show | 6 | HG03654.hp1 HG03942.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-715A>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849255 | ||||||
| chr12:93849339
|
C | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0083a0001c0001t0003g0131 | 3 | HG03654.hp1 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.299-631C>G | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849339 | ||||||
| chr12:93849740
|
C | CA | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(11): Show | 14 | HG00735.hp2 HG01928.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-211dupA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93849740 | |||||
| chr12:93849740
|
CA | C | 13 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0055others(10): Show | 13 | HG00639.hp2 HG02622.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-211delA | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 93849740 | |||||
| chr12:93849895
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(10): Show | 13 | HG00735.hp2 HG01192.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-75C>T | CRADD | ENSG00000169372.13 | transcript | ENST00000332896.8 | protein_coding | 2/2 | chr12 | 93849895 |