| geneid | 4703 |
|---|---|
| ensemblid | ENSG00000183091.21 |
| hgncid | 7720 |
| symbol | NEB |
| name | nebulin |
| refseq_nuc | NM_001164508.2 |
| refseq_prot | NP_001157980.2 |
| ensembl_nuc | ENST00000397345.8 |
| ensembl_prot | ENSP00000380505.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 151485339 |
| end | 151734476 |
| strand | - |
| ver | v1.2 |
| region | chr2:151485339-151734476 |
| region5000 | chr2:151480339-151739476 |
| regionname0 | NEB_chr2_151485339_151734476 |
| regionname5000 | NEB_chr2_151480339_151739476 |
| 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 | 0/0 | 8525 | 9 | 0 | 0 | 8 | 1 | 0 | 6 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0002 | 0/0 | 8525 | 8 | 0 | 2 | 6 | 0 | 0 | 5 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003 | 0/0 | 8525 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004 | 0/0 | 8525 | 5 | 3 | 0 | 2 | 0 | 0 | 2 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005 | 0/0 | 8525 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0006 | 0/0 | 8525 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0007 | 0/1 | 8525 | 3 | 0 | 1 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0008 | 0/0 | 8525 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0009 | 0/0 | 8525 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010 | 0/0 | 8525 | 3 | 0 | 1 | 2 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0011 | 0/0 | 8525 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0012 | 0/0 | 8525 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0013 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0014 | 0/0 | 8525 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0015 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0016 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0017 | 0/0 | 8525 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0018 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0019 | 0/0 | 8525 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0020 | 0/0 | 8525 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0021 | 0/0 | 8039 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0022 | 0/0 | 8525 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0023 | 0/0 | 8525 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0024 | 0/0 | 8525 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0025 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0026 | 0/0 | 8525 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0027 | 0/0 | 8525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0028 | 0/0 | 8520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0029 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0030 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0031 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0032 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0033 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0034 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0035 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0036 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0037 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0038 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0039 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0040 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0041 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0042 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0043 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0044 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0045 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0046 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0047 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0048 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0049 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0050 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0051 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0052 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0053 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0054 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0055 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0056 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0057 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0058 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0059 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0060 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0061 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0062 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0063 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0064 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0065 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0066 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0067 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0068 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0069 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0070 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0071 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0072 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0073 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0074 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0075 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0076 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0077 | 1/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0078 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0079 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0080 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0081 | 0/0 | 7553 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0082 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0083 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0084 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0085 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0086 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0087 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0088 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0089 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0090 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0091 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0092 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0093 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0094 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0095 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0096 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0097 | 0/0 | 8039 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0098 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0099 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0100 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0101 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0102 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0103 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0104 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0105 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0106 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0107 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0108 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0109 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0110 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0111 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0112 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0113 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0114 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0115 | 0/0 | 8039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0116 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0117 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0118 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0119 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0120 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0121 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0122 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0123 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0124 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0125 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0126 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0127 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0128 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0129 | 0/0 | 8525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0130 | 0/0 | 8520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0131 | 0/0 | 8520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0132 | 0/0 | 8520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0133 | 0/0 | 8520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| 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 | 0/0 | 25578 | 8 | 0 | 0 | 7 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0002 | 0/0 | 25578 | 7 | 0 | 2 | 5 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0003 | 0/1 | 25578 | 3 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0004 | 0/0 | 25578 | 3 | 2 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0005 | 0/0 | 25578 | 3 | 0 | 0 | 3 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0006 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0007 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0008 | 0/0 | 25578 | 2 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0009 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0010 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0011 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0012 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0013 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0014 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0015 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0016 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0017 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0018 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0019 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0020 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0021 | 0/0 | 25563 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0022 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0023 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0024 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0025 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0026 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0027 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0028 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0029 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0030 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0031 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0032 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0033 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0034 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0035 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0036 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0037 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0038 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0039 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0040 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0041 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0042 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0043 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0044 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0045 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0046 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0047 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0048 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0049 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0050 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0051 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0052 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0053 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0054 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0055 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0056 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0057 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0058 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0059 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0060 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0061 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0062 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0063 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0064 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0065 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0066 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0067 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0068 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0069 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0070 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0071 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0072 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0073 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0074 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0075 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0076 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0077 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0078 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0079 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0080 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0081 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0082 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0083 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0084 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0085 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0086 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0087 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0088 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0089 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0090 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0091 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0092 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0093 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0094 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0095 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0096 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0097 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0098 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0099 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0100 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0101 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0102 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0103 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0104 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0105 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0106 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0107 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0108 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0109 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0110 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0111 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0112 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0113 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0114 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0115 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0116 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0117 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0118 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0119 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0120 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0121 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0122 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0123 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0124 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0125 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0126 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0127 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0128 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0129 | 1/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0130 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0131 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0132 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0133 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0134 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0135 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0136 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0137 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0138 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0139 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0140 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0141 | 0/0 | 22662 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0142 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0143 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0144 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0145 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0146 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0147 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0148 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0149 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0150 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0151 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0152 | 0/0 | 25563 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| c0153 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| 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 | 614 | 180 | 51 | 18 | 79 | 8 | 22 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| t0002 | 0/0 | 612 | 7 | 7 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| t0003 | 0/0 | 614 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| 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 | 0/0 | 25578 | 8 | 0 | 0 | 7 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0001c0082 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0002c0002 | 0/0 | 25578 | 7 | 0 | 2 | 5 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0002c0048 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0005 | 0/0 | 25578 | 3 | 0 | 0 | 3 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0083 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0094 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0018 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0019 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0126 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0008 | 0/0 | 25578 | 2 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0063 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0064 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0006c0012 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0006c0079 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0007c0003 | 0/1 | 25578 | 3 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0008c0004 | 0/0 | 25578 | 3 | 2 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0009c0017 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0009c0109 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0137 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0138 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0139 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0011c0009 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0011c0070 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0012c0088 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0012c0090 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0013c0014 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0014c0112 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0014c0113 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0015c0108 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0015c0111 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0016c0016 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0017c0015 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0018c0020 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0019c0010 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0020c0007 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0021c0056 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0021c0057 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0022c0026 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0022c0054 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0023c0043 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0023c0044 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0024c0038 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0024c0040 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0025c0011 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0026c0006 | 0/0 | 25578 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0027c0013 | 0/0 | 25578 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0028c0021 | 0/0 | 25563 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0029c0081 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0030c0076 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0031c0078 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0032c0077 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0033c0024 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0034c0147 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0035c0146 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0036c0029 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0037c0087 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0038c0086 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0039c0153 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0040c0093 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0041c0085 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0042c0095 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0043c0084 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0044c0092 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0045c0089 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0046c0091 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0047c0097 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0048c0098 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0049c0096 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0050c0099 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0051c0131 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0052c0100 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0053c0127 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0054c0104 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0055c0116 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0056c0145 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0057c0114 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0058c0110 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0059c0143 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0060c0107 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0061c0115 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0062c0106 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0063c0105 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0064c0025 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0065c0119 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0066c0118 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0067c0117 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0068c0125 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0069c0120 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0070c0123 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0071c0124 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0072c0121 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0073c0122 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0074c0103 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0075c0102 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0076c0101 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0077c0129 | 1/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0078c0128 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0079c0130 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0080c0030 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0081c0141 | 0/0 | 22662 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0082c0140 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0083c0134 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0084c0133 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0085c0031 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0086c0032 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0087c0132 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0088c0037 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0089c0036 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0090c0035 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0091c0142 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0092c0135 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0093c0058 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0094c0061 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0095c0062 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0096c0060 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0097c0065 | 0/0 | 24120 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0098c0071 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0099c0067 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0100c0072 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0101c0068 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0102c0069 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0103c0066 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0104c0059 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0105c0080 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0106c0050 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0107c0045 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0108c0047 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0109c0046 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0110c0041 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0111c0049 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0112c0051 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0113c0042 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0114c0055 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0115c0053 | 0/0 | 24120 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0116c0052 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0117c0039 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0118c0073 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0119c0136 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0120c0023 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0121c0074 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0122c0033 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0123c0034 | 0/0 | 25578 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0124c0075 | 0/0 | 25578 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0125c0028 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0126c0027 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0127c0144 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0128c0148 | 0/0 | 25578 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0129c0022 | 0/0 | 25578 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0130c0150 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0131c0149 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0132c0151 | 0/0 | 25563 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0133c0152 | 0/0 | 25563 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 26191 | 8 | 0 | 0 | 7 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0001c0082t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0002c0002t0001 | 0/0 | 26191 | 7 | 0 | 2 | 5 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0002c0048t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0005t0001 | 0/0 | 26191 | 3 | 0 | 0 | 3 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0083t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0003c0094t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0018t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0019t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0004c0126t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0008t0001 | 0/0 | 26191 | 2 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0063t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0005c0064t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0006c0012t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0006c0079t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0007c0003t0001 | 0/1 | 26191 | 3 | 0 | 1 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0008c0004t0001 | 0/0 | 26191 | 3 | 2 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0009c0017t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0009c0109t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0137t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0138t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0010c0139t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0011c0009t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0011c0070t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0012c0088t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0012c0090t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0013c0014t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0014c0112t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0014c0113t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0015c0108t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0015c0111t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0016c0016t0002 | 0/0 | 26189 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0017c0015t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0018c0020t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0019c0010t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0019c0010t0003 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0020c0007t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0021c0056t0001 | 0/0 | 24733 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0021c0057t0001 | 0/0 | 24733 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0022c0026t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0022c0054t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0023c0043t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0023c0044t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0024c0038t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0024c0040t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0025c0011t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0026c0006t0001 | 0/0 | 26191 | 2 | 0 | 0 | 2 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0027c0013t0001 | 0/0 | 26191 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0028c0021t0001 | 0/0 | 26176 | 2 | 2 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0029c0081t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0030c0076t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0031c0078t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0032c0077t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0033c0024t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0034c0147t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0035c0146t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0036c0029t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0037c0087t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0038c0086t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0039c0153t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0040c0093t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0041c0085t0002 | 0/0 | 26189 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0042c0095t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0043c0084t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0044c0092t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0045c0089t0002 | 0/0 | 26189 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0046c0091t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0047c0097t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0048c0098t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0049c0096t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0050c0099t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0051c0131t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0052c0100t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0053c0127t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0054c0104t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0055c0116t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0056c0145t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0057c0114t0002 | 0/0 | 26189 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0058c0110t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0059c0143t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0060c0107t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0061c0115t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0062c0106t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0063c0105t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0064c0025t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0065c0119t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0066c0118t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0067c0117t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0068c0125t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0069c0120t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0070c0123t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0071c0124t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0072c0121t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0073c0122t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0074c0103t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0075c0102t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0076c0101t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0077c0129t0001 | 1/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0078c0128t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0079c0130t0002 | 0/0 | 26189 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0080c0030t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0081c0141t0001 | 0/0 | 23275 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0082c0140t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0083c0134t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0084c0133t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0085c0031t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0086c0032t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0087c0132t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0088c0037t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0089c0036t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0090c0035t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0091c0142t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0092c0135t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0093c0058t0002 | 0/0 | 26189 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0094c0061t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0095c0062t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0096c0060t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0097c0065t0001 | 0/0 | 24733 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0098c0071t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0099c0067t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0100c0072t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0101c0068t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0102c0069t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0103c0066t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0104c0059t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0105c0080t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0106c0050t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0107c0045t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0108c0047t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0109c0046t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0110c0041t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0111c0049t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0112c0051t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0113c0042t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0114c0055t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0115c0053t0001 | 0/0 | 24733 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0116c0052t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0117c0039t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0118c0073t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0119c0136t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0120c0023t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0121c0074t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0122c0033t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0123c0034t0001 | 0/0 | 26191 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0124c0075t0001 | 0/0 | 26191 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0125c0028t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0126c0027t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0127c0144t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0128c0148t0001 | 0/0 | 26191 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0129c0022t0001 | 0/0 | 26191 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0130c0150t0001 | 0/0 | 26176 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0131c0149t0001 | 0/0 | 26176 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0132c0151t0001 | 0/0 | 26176 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| a0133c0152t0001 | 0/0 | 26176 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | copy fasta | chr2 | 151480339 | 151739476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0001c0082t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0002c0048t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0003c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0003c0005t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0003c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0003c0083t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0003c0094t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0004c0018t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0004c0018t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0004c0019t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0004c0019t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0004c0126t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0005c0008t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0005c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0005c0063t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0005c0064t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0006c0012t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0006c0012t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0006c0079t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0007c0003t0001g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0007c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0007c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0008c0004t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0008c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0008c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0009c0017t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0009c0017t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0009c0109t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0010c0137t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0010c0138t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0010c0139t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0011c0009t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0011c0009t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0011c0070t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0012c0088t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0012c0090t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0013c0014t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0013c0014t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0014c0112t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0014c0113t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0015c0108t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0015c0111t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0016c0016t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0016c0016t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0017c0015t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0017c0015t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0018c0020t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0018c0020t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0019c0010t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0019c0010t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0020c0007t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0020c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0021c0056t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0021c0057t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0022c0026t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0022c0054t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0023c0043t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0023c0044t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0024c0038t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0024c0040t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0025c0011t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0025c0011t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0026c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0026c0006t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0027c0013t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0027c0013t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0028c0021t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0028c0021t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0029c0081t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0030c0076t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0031c0078t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0032c0077t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0033c0024t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0034c0147t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0035c0146t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0036c0029t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0037c0087t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0038c0086t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0039c0153t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0040c0093t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0041c0085t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0042c0095t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0043c0084t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0044c0092t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0045c0089t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0046c0091t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0047c0097t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0048c0098t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0049c0096t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0050c0099t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0051c0131t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0052c0100t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0053c0127t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0054c0104t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0055c0116t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0056c0145t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0057c0114t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0058c0110t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0059c0143t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0060c0107t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0061c0115t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0062c0106t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0063c0105t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0064c0025t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0065c0119t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0066c0118t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0067c0117t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0068c0125t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0069c0120t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0070c0123t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0071c0124t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0072c0121t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0073c0122t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0074c0103t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0075c0102t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0076c0101t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0077c0129t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0078c0128t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0079c0130t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0080c0030t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0081c0141t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0082c0140t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0083c0134t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0084c0133t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0085c0031t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0086c0032t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0087c0132t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0088c0037t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0089c0036t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0090c0035t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0091c0142t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0092c0135t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0093c0058t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0094c0061t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0095c0062t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0096c0060t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0097c0065t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0098c0071t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0099c0067t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0100c0072t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0101c0068t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0102c0069t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0103c0066t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0104c0059t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0105c0080t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0106c0050t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0107c0045t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0108c0047t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0109c0046t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0110c0041t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0111c0049t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0112c0051t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0113c0042t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0114c0055t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0115c0053t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0116c0052t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0117c0039t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0118c0073t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0119c0136t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0120c0023t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0121c0074t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0122c0033t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0123c0034t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0124c0075t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0125c0028t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0126c0027t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0127c0144t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0128c0148t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0129c0022t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0130c0150t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0131c0149t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0132c0151t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| a0133c0152t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0012 | c0090 | t0001 | g0005 | EUR | GBR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00099 | hp2 | a0112 | c0051 | t0001 | g0072 | EUR | GBR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00280 | hp2 | a0097 | c0065 | t0001 | g0066 | EUR | FIN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00423 | hp2 | a0010 | c0139 | t0001 | g0106 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00544 | hp1 | a0106 | c0050 | t0001 | g0045 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00544 | hp2 | a0043 | c0084 | t0001 | g0018 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00558 | hp1 | a0052 | c0100 | t0001 | g0142 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00558 | hp2 | a0082 | c0140 | t0001 | g0094 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00597 | hp1 | a0020 | c0007 | t0001 | g0042 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00597 | hp2 | a0009 | c0017 | t0001 | g0159 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00609 | hp1 | a0127 | c0144 | t0001 | g0129 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00609 | hp2 | a0113 | c0042 | t0001 | g0035 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00621 | hp1 | a0001 | c0082 | t0001 | g0147 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00639 | hp1 | a0035 | c0146 | t0001 | g0103 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00639 | hp2 | a0080 | c0030 | t0001 | g0074 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00673 | hp1 | a0023 | c0044 | t0001 | g0068 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00673 | hp2 | a0039 | c0153 | t0001 | g0021 | EAS | CHS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00741 | hp1 | a0088 | c0037 | t0001 | g0061 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG00741 | hp2 | a0107 | c0045 | t0001 | g0028 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01074 | hp1 | a0003 | c0094 | t0001 | g0014 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01074 | hp2 | a0005 | c0008 | t0001 | g0077 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01099 | hp1 | a0003 | c0083 | t0001 | g0003 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01099 | hp2 | a0005 | c0063 | t0001 | g0052 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01175 | hp1 | a0102 | c0069 | t0001 | g0033 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01192 | hp1 | a0008 | c0004 | t0001 | g0009 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01192 | hp2 | a0133 | c0152 | t0001 | g0169 | AMR | PUR | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01258 | hp1 | a0129 | c0022 | t0001 | g0114 | AMR | CLM | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01258 | hp2 | a0007 | c0003 | t0001 | g0029 | AMR | CLM | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01358 | hp1 | a0011 | c0070 | t0001 | g0055 | AMR | CLM | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01358 | hp2 | a0005 | c0064 | t0001 | g0083 | AMR | CLM | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01515 | hp1 | a0038 | c0086 | t0001 | g0007 | EUR | IBS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01515 | hp2 | a0114 | c0055 | t0001 | g0044 | EUR | IBS | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01884 | hp1 | a0036 | c0029 | t0001 | g0176 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01884 | hp2 | a0011 | c0009 | t0001 | g0040 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01891 | hp1 | a0121 | c0074 | t0001 | g0058 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01891 | hp2 | a0025 | c0011 | t0001 | g0089 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01993 | hp1 | a0010 | c0137 | t0001 | g0093 | AMR | PEL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02040 | hp1 | a0047 | c0097 | t0001 | g0185 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02040 | hp2 | a0010 | c0138 | t0001 | g0091 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02074 | hp1 | a0094 | c0061 | t0001 | g0080 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02074 | hp2 | a0059 | c0143 | t0001 | g0161 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02080 | hp1 | a0072 | c0121 | t0001 | g0143 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02080 | hp2 | a0006 | c0079 | t0001 | g0170 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02165 | hp1 | a0060 | c0107 | t0001 | g0157 | EAS | CDX | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02165 | hp2 | a0031 | c0078 | t0001 | g0171 | EAS | CDX | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02257 | hp1 | a0015 | c0108 | t0001 | g0136 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02257 | hp2 | a0027 | c0013 | t0001 | g0070 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02258 | hp1 | a0132 | c0151 | t0001 | g0179 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02258 | hp2 | a0099 | c0067 | t0001 | g0023 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02280 | hp1 | a0018 | c0020 | t0001 | g0122 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02280 | hp2 | a0056 | c0145 | t0001 | g0177 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02451 | hp1 | a0055 | c0116 | t0001 | g0150 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02451 | hp2 | a0085 | c0031 | t0001 | g0108 | AFR | ACB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02523 | hp1 | a0024 | c0040 | t0001 | g0062 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02523 | hp2 | a0069 | c0120 | t0001 | g0104 | EAS | KHV | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02572 | hp1 | a0119 | c0136 | t0001 | g0132 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02572 | hp2 | a0086 | c0032 | t0001 | g0109 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02622 | hp1 | a0083 | c0134 | t0001 | g0153 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02622 | hp2 | a0011 | c0009 | t0001 | g0078 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02630 | hp1 | a0033 | c0024 | t0001 | g0096 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02630 | hp2 | a0051 | c0131 | t0001 | g0187 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02647 | hp1 | a0084 | c0133 | t0001 | g0154 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02647 | hp2 | a0013 | c0014 | t0001 | g0099 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02683 | hp1 | a0110 | c0041 | t0001 | g0075 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02683 | hp2 | a0048 | c0098 | t0001 | g0186 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02735 | hp1 | a0021 | c0057 | t0001 | g0037 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02735 | hp2 | a0009 | c0109 | t0001 | g0130 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02809 | hp1 | a0018 | c0020 | t0001 | g0131 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02809 | hp2 | a0122 | c0033 | t0001 | g0087 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02818 | hp1 | a0042 | c0095 | t0001 | g0020 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02818 | hp2 | a0053 | c0127 | t0001 | g0152 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02886 | hp1 | a0130 | c0150 | t0001 | g0180 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02886 | hp2 | a0046 | c0091 | t0001 | g0017 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02895 | hp1 | a0004 | c0126 | t0001 | g0118 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02895 | hp2 | a0028 | c0021 | t0001 | g0183 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02897 | hp1 | a0092 | c0135 | t0001 | g0133 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02897 | hp2 | a0028 | c0021 | t0001 | g0182 | AFR | GWD | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02965 | hp1 | a0016 | c0016 | t0002 | g0100 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02965 | hp2 | a0037 | c0087 | t0001 | g0107 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02976 | hp1 | a0027 | c0013 | t0001 | g0071 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG02976 | hp2 | a0058 | c0110 | t0001 | g0149 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03098 | hp1 | a0013 | c0014 | t0001 | g0102 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03098 | hp2 | a0079 | c0130 | t0002 | g0105 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03139 | hp1 | a0004 | c0019 | t0001 | g0151 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03139 | hp2 | a0123 | c0034 | t0001 | g0082 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03195 | hp1 | a0045 | c0089 | t0002 | g0138 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03195 | hp2 | a0025 | c0011 | t0001 | g0090 | AFR | ESN | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03225 | hp1 | a0057 | c0114 | t0002 | g0115 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03225 | hp2 | a0008 | c0004 | t0001 | g0011 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03239 | hp1 | a0095 | c0062 | t0001 | g0081 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03239 | hp2 | a0098 | c0071 | t0001 | g0056 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03453 | hp1 | a0008 | c0004 | t0001 | g0012 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03453 | hp2 | a0064 | c0025 | t0001 | g0095 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03486 | hp1 | a0091 | c0142 | t0001 | g0119 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03486 | hp2 | a0041 | c0085 | t0002 | g0010 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03491 | hp1 | a0066 | c0118 | t0001 | g0146 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03491 | hp2 | a0021 | c0056 | t0001 | g0041 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03579 | hp1 | a0131 | c0149 | t0001 | g0181 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03579 | hp2 | a0004 | c0019 | t0001 | g0148 | AFR | MSL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03654 | hp1 | a0103 | c0066 | t0001 | g0065 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03654 | hp2 | a0096 | c0060 | t0001 | g0022 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03669 | hp1 | a0049 | c0096 | t0001 | g0184 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03669 | hp2 | a0100 | c0072 | t0001 | g0076 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03688 | hp1 | a0062 | c0106 | t0001 | g0140 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03688 | hp2 | a0005 | c0008 | t0001 | g0038 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03704 | hp1 | a0022 | c0054 | t0001 | g0030 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03704 | hp2 | a0067 | c0117 | t0001 | g0144 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03710 | hp1 | a0065 | c0119 | t0001 | g0145 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG03710 | hp2 | a0111 | c0049 | t0001 | g0073 | SAS | PJL | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG04115 | hp1 | a0007 | c0003 | t0001 | g0002 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG04115 | hp2 | a0101 | c0068 | t0001 | g0024 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG04204 | hp1 | a0014 | c0112 | t0001 | g0141 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG04204 | hp2 | a0023 | c0043 | t0001 | g0047 | SAS | STU | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18747 | hp1 | a0081 | c0141 | t0001 | g0092 | EAS | CHB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18747 | hp2 | a0117 | c0039 | t0001 | g0063 | EAS | CHB | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18906 | hp1 | a0087 | c0132 | t0001 | g0101 | AFR | YRI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18906 | hp2 | a0078 | c0128 | t0001 | g0163 | AFR | YRI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18942 | hp1 | a0022 | c0026 | t0001 | g0032 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18942 | hp2 | a0012 | c0088 | t0001 | g0016 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18943 | hp1 | a0003 | c0005 | t0001 | g0013 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18943 | hp2 | a0061 | c0115 | t0001 | g0158 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18945 | hp1 | a0076 | c0101 | t0001 | g0167 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18946 | hp1 | a0054 | c0104 | t0001 | g0162 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18946 | hp2 | a0116 | c0052 | t0001 | g0069 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18947 | hp1 | a0074 | c0103 | t0001 | g0168 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18947 | hp2 | a0118 | c0073 | t0001 | g0051 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18948 | hp1 | a0063 | c0105 | t0001 | g0160 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18950 | hp1 | a0104 | c0059 | t0001 | g0019 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18950 | hp2 | a0006 | c0012 | t0001 | g0172 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18952 | hp2 | a0019 | c0010 | t0001 | g0059 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18953 | hp1 | a0009 | c0017 | t0001 | g0121 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18960 | hp1 | a0125 | c0028 | t0001 | g0031 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18960 | hp2 | a0006 | c0012 | t0001 | g0173 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18962 | hp1 | a0002 | c0048 | t0001 | g0086 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18962 | hp2 | a0004 | c0018 | t0001 | g0135 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18966 | hp2 | a0070 | c0123 | t0001 | g0116 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18971 | hp1 | a0075 | c0102 | t0001 | g0166 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18971 | hp2 | a0109 | c0046 | t0001 | g0048 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18980 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18984 | hp1 | a0071 | c0124 | t0001 | g0128 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18984 | hp2 | a0108 | c0047 | t0001 | g0064 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA18991 | hp2 | a0126 | c0027 | t0001 | g0067 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19000 | hp1 | a0115 | c0053 | t0001 | g0084 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19000 | hp2 | a0014 | c0113 | t0001 | g0120 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19005 | hp1 | a0020 | c0007 | t0001 | g0043 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19005 | hp2 | a0030 | c0076 | t0001 | g0174 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19010 | hp1 | a0004 | c0018 | t0001 | g0134 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19010 | hp2 | a0026 | c0006 | t0001 | g0079 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19043 | hp1 | a0105 | c0080 | t0001 | g0034 | AFR | LWK | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19043 | hp2 | a0029 | c0081 | t0001 | g0123 | AFR | LWK | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19060 | hp1 | a0073 | c0122 | t0001 | g0113 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19060 | hp2 | a0019 | c0010 | t0003 | g0188 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19062 | hp1 | a0068 | c0125 | t0001 | g0111 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19062 | hp2 | a0090 | c0035 | t0001 | g0054 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19065 | hp1 | a0040 | c0093 | t0001 | g0015 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19066 | hp2 | a0026 | c0006 | t0001 | g0027 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19079 | hp1 | a0032 | c0077 | t0001 | g0175 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19080 | hp1 | a0017 | c0015 | t0001 | g0165 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19080 | hp2 | a0024 | c0038 | t0001 | g0085 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19084 | hp1 | a0128 | c0148 | t0001 | g0110 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0006 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19088 | hp1 | a0089 | c0036 | t0001 | g0053 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19088 | hp2 | a0017 | c0015 | t0001 | g0164 | EAS | JPT | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19240 | hp1 | a0093 | c0058 | t0002 | g0025 | AFR | YRI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA19240 | hp2 | a0120 | c0023 | t0001 | g0088 | AFR | YRI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA20129 | hp1 | a0050 | c0099 | t0001 | g0098 | AFR | ASW | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA20129 | hp2 | a0015 | c0111 | t0001 | g0139 | AFR | ASW | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA20805 | hp1 | a0044 | c0092 | t0001 | g0008 | EUR | TSI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| NA20805 | hp2 | a0124 | c0075 | t0001 | g0057 | EUR | TSI | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG06807 | hp1 | a0016 | c0016 | t0002 | g0137 | AFR | USA | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| HG06807 | hp2 | a0034 | c0147 | t0001 | g0178 | AFR | USA | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0003 | t0001 | g0001 | REF | REF | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| homoSapiens_grch38 | hp1 | a0077 | c0129 | t0001 | g0155 | REF | REF | NEB_chr2_151480339_151739476 | NEB | chr2 | 151480339 | 151739476 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:151485773
|
A | G | 1 | a0072 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.25565T>C | p.Val8522Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 182/182 | 25757/26191 | 25565/25578 | 8522/8525 | chr2 | 151485773 | ||
| chr2:151490465
|
T | C | 48 | a0002a0007a0013others(45): Show | 65 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
missense_variant | MODERATE | c.25204A>G | p.Ile8402Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 180/182 | 25396/26191 | 25204/25578 | 8402/8525 | chr2 | 151490465 | ||
| chr2:151490506
|
C | T | 2 | a0075a0076 | 2 | NA18945.hp1 NA18971.hp1 |
missense_variant | MODERATE | c.25163G>A | p.Arg8388His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 180/182 | 25355/26191 | 25163/25578 | 8388/8525 | chr2 | 151490506 | ||
| chr2:151494166
|
T | C | 2 | a0019a0074 | 3 | NA18947.hp1 NA18952.hp2 NA19060.hp2 |
missense_variant | MODERATE | c.24574A>G | p.Ser8192Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 174/182 | 24766/26191 | 24574/25578 | 8192/8525 | chr2 | 151494166 | ||
| chr2:151496329
|
C | G | 91 | a0001a0002a0005others(88): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
missense_variant | MODERATE | c.24433G>C | p.Ala8145Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/182 | 24625/26191 | 24433/25578 | 8145/8525 | chr2 | 151496329 | ||
| chr2:151496984
|
G | A | 1 | a0035 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.24350C>T | p.Pro8117Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/182 | 24542/26191 | 24350/25578 | 8117/8525 | chr2 | 151496984 | ||
| chr2:151497651
|
T | C | 1 | a0073 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.24275A>G | p.Lys8092Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/182 | 24467/26191 | 24275/25578 | 8092/8525 | chr2 | 151497651 | ||
| chr2:151499372
|
C | T | 1 | a0039 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.24040G>A | p.Val8014Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/182 | 24232/26191 | 24040/25578 | 8014/8525 | chr2 | 151499372 | ||
| chr2:151501435
|
G | A | 1 | a0074 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.23977C>T | p.Pro7993Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/182 | 24169/26191 | 23977/25578 | 7993/8525 | chr2 | 151501435 | ||
| chr2:151506216
|
T | G | 2 | a0010a0113 | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
missense_variant | MODERATE | c.23599A>C | p.Lys7867Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/182 | 23791/26191 | 23599/25578 | 7867/8525 | chr2 | 151506216 | ||
| chr2:151506970
|
G | A | 2 | a0008a0058 | 4 | HG01192.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.23495C>T | p.Thr7832Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 163/182 | 23687/26191 | 23495/25578 | 7832/8525 | chr2 | 151506970 | ||
| chr2:151506988
|
T | C | 1 | a0050 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.23477A>G | p.Asn7826Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 163/182 | 23669/26191 | 23477/25578 | 7826/8525 | chr2 | 151506988 | ||
| chr2:151508075
|
G | A | 1 | a0111 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.23381C>T | p.Ser7794Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/182 | 23573/26191 | 23381/25578 | 7794/8525 | chr2 | 151508075 | ||
| chr2:151516460
|
C | T | 2 | a0010a0113 | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
missense_variant | MODERATE | c.22904G>A | p.Gly7635Glu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/182 | 23096/26191 | 22904/25578 | 7635/8525 | chr2 | 151516460 | ||
| chr2:151526241
|
C | T | 1 | a0028 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.21967G>A | p.Val7323Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 149/182 | 22159/26191 | 21967/25578 | 7323/8525 | chr2 | 151526241 | ||
| chr2:151527007
|
C | T | 1 | a0100 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.21856G>A | p.Asp7286Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/182 | 22048/26191 | 21856/25578 | 7286/8525 | chr2 | 151527007 | ||
| chr2:151533503
|
C | T | 2 | a0109a0118 | 2 | NA18947.hp2 NA18971.hp2 |
missense_variant | MODERATE | c.21356G>A | p.Cys7119Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/182 | 21548/26191 | 21356/25578 | 7119/8525 | chr2 | 151533503 | ||
| chr2:151538196
|
C | T | 1 | a0046 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.20941G>A | p.Val6981Met | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 139/182 | 21133/26191 | 20941/25578 | 6981/8525 | chr2 | 151538196 | ||
| chr2:151547704
|
T | A | 17 | a0009a0013a0016others(14): Show | 22 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(19): Show |
missense_variant | MODERATE | c.20192A>T | p.Asp6731Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 132/182 | 20384/26191 | 20192/25578 | 6731/8525 | chr2 | 151547704 | ||
| chr2:151552707
|
C | T | 1 | a0098 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.19801G>A | p.Val6601Met | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/182 | 19993/26191 | 19801/25578 | 6601/8525 | chr2 | 151552707 | ||
| chr2:151554007
|
A | G | 1 | a0076 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.19447T>C | p.Tyr6483His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 126/182 | 19639/26191 | 19447/25578 | 6483/8525 | chr2 | 151554007 | ||
| chr2:151560611
|
T | C | 1 | a0059 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.19295A>G | p.Gln6432Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/182 | 19487/26191 | 19295/25578 | 6432/8525 | chr2 | 151560611 | ||
| chr2:151560620
|
G | T | 2 | a0010a0113 | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
missense_variant | MODERATE | c.19286C>A | p.Ala6429Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/182 | 19478/26191 | 19286/25578 | 6429/8525 | chr2 | 151560620 | ||
| chr2:151560621
|
C | T | 2 | a0010a0113 | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
missense_variant | MODERATE | c.19285G>A | p.Ala6429Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/182 | 19477/26191 | 19285/25578 | 6429/8525 | chr2 | 151560621 | ||
| chr2:151563872
|
C | T | 1 | a0115 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.18530G>A | p.Arg6177His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 118/182 | 18722/26191 | 18530/25578 | 6177/8525 | chr2 | 151563872 | ||
| chr2:151565051
|
T | G | 1 | a0033 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.18464A>C | p.Tyr6155Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/182 | 18656/26191 | 18464/25578 | 6155/8525 | chr2 | 151565051 | ||
| chr2:151565084
|
T | C | 1 | a0102 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.18431A>G | p.His6144Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/182 | 18623/26191 | 18431/25578 | 6144/8525 | chr2 | 151565084 | ||
| chr2:151565562
|
C | G | 97 | a0001a0002a0005others(94): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
missense_variant | MODERATE | c.18305G>C | p.Arg6102Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 116/182 | 18497/26191 | 18305/25578 | 6102/8525 | chr2 | 151565562 | ||
| chr2:151567211
|
T | C | 5 | a0033a0036a0046others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
missense_variant | MODERATE | c.18113A>G | p.Asn6038Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/182 | 18305/26191 | 18113/25578 | 6038/8525 | chr2 | 151567211 | ||
| chr2:151568082
|
C | T | 1 | a0061 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.17833G>A | p.Val5945Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/182 | 18025/26191 | 17833/25578 | 5945/8525 | chr2 | 151568082 | ||
| chr2:151568168
|
T | C | 1 | a0045 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.17747A>G | p.Lys5916Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/182 | 17939/26191 | 17747/25578 | 5916/8525 | chr2 | 151568168 | ||
| chr2:151576297
|
A | T | 14 | a0009a0016a0023others(11): Show | 18 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
missense_variant | MODERATE | c.16762T>A | p.Ser5588Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 106/182 | 16954/26191 | 16762/25578 | 5588/8525 | chr2 | 151576297 | ||
| chr2:151579372
|
A | G | 3 | a0013a0121a0122 | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
missense_variant | MODERATE | c.16670T>C | p.Ile5557Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16862/26191 | 16670/25578 | 5557/8525 | chr2 | 151579372 | ||
| chr2:151579405
|
C | T | 9 | a0020a0024a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp1 HG01884.hp1 others(8): Show |
missense_variant | MODERATE | c.16637G>A | p.Arg5546His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16829/26191 | 16637/25578 | 5546/8525 | chr2 | 151579405 | ||
| chr2:151579420
|
C | T | 1 | a0042 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.16622G>A | p.Arg5541His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16814/26191 | 16622/25578 | 5541/8525 | chr2 | 151579420 | ||
| chr2:151579498
|
T | G | 21 | a0001a0005a0012others(18): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(30): Show |
missense_variant | MODERATE | c.16544A>C | p.Lys5515Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16736/26191 | 16544/25578 | 5515/8525 | chr2 | 151579498 | ||
| chr2:151579592
|
C | T | 10 | a0017a0025a0042others(7): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
missense_variant | MODERATE | c.16450G>A | p.Ala5484Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16642/26191 | 16450/25578 | 5484/8525 | chr2 | 151579592 | ||
| chr2:151581575
|
C | T | 2 | a0075a0076 | 2 | NA18945.hp1 NA18971.hp1 |
missense_variant | MODERATE | c.16192G>A | p.Asp5398Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/182 | 16384/26191 | 16192/25578 | 5398/8525 | chr2 | 151581575 | ||
| chr2:151583609
|
T | A | 2 | a0129a0133 | 2 | HG01192.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.15821A>T | p.Asn5274Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/182 | 16013/26191 | 15821/25578 | 5274/8525 | chr2 | 151583609 | ||
| chr2:151584872
|
GTTTGTTT others(21093): Show |
G | 1 | a0081 | 1 | NA18747.hp1 | exon_loss_variant | HIGH | c.12747+634_15663+63 others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/182 | chr2 | 151584872 | ||||||
| chr2:151589956
|
T | C | 6 | a0027a0035a0078others(3): Show | 7 | HG00639.hp1 HG00741.hp1 HG01515.hp2 others(4): Show |
missense_variant | MODERATE | c.15179A>G | p.His5060Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/182 | 15371/26191 | 15179/25578 | 5060/8525 | chr2 | 151589956 | ||
| chr2:151591368
|
A | T | 3 | a0049a0066a0067 | 3 | HG03491.hp1 HG03669.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.14914T>A | p.Ser4972Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/182 | 15106/26191 | 14914/25578 | 4972/8525 | chr2 | 151591368 | ||
| chr2:151592053
|
T | C | 1 | a0121 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.14807A>G | p.Asn4936Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/182 | 14999/26191 | 14807/25578 | 4936/8525 | chr2 | 151592053 | ||
| chr2:151592126
|
T | C | 3 | a0094a0095a0112 | 3 | HG00099.hp2 HG02074.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.14734A>G | p.Asn4912Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/182 | 14926/26191 | 14734/25578 | 4912/8525 | chr2 | 151592126 | ||
| chr2:151593635
|
TCCTGCCC others(10546): Show |
T | 4 | a0021a0054a0074others(1): Show | 5 | HG00280.hp2 HG02735.hp1 HG03491.hp2 others(2): Show |
exon_loss_variant | HIGH | c.13059+372_14517+37 others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/182 | chr2 | 151593635 | ||||||
| chr2:151596140
|
T | C | 1 | a0082 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.14125A>G | p.Thr4709Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/182 | 14317/26191 | 14125/25578 | 4709/8525 | chr2 | 151596140 | ||
| chr2:151598359
|
CAAAAAAA others(10547): Show |
C | 4 | a0070a0071a0089others(1): Show | 4 | NA18966.hp2 NA18984.hp1 NA19000.hp1 others(1): Show |
exon_loss_variant | HIGH | c.12331-237_13789-23 others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | chr2 | 151598359 | ||||||
| chr2:151600509
|
T | C | 1 | a0027 | 2 | HG02257.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.13721A>G | p.His4574Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | 13913/26191 | 13721/25578 | 4574/8525 | chr2 | 151600509 | ||
| chr2:151600550
|
C | G | 1 | a0107 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.13680G>C | p.Gln4560His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | 13872/26191 | 13680/25578 | 4560/8525 | chr2 | 151600550 | ||
| chr2:151600602
|
T | G | 5 | a0036a0037a0046others(2): Show | 5 | HG01884.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.13628A>C | p.Lys4543Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | 13820/26191 | 13628/25578 | 4543/8525 | chr2 | 151600602 | ||
| chr2:151601921
|
A | T | 1 | a0067 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.13456T>A | p.Ser4486Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/182 | 13648/26191 | 13456/25578 | 4486/8525 | chr2 | 151601921 | ||
| chr2:151602606
|
T | C | 1 | a0121 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.13349A>G | p.Asn4450Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/182 | 13541/26191 | 13349/25578 | 4450/8525 | chr2 | 151602606 | ||
| chr2:151602679
|
C | T | 101 | a0001a0003a0004others(98): Show | 142 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(139): Show |
missense_variant | MODERATE | c.13276G>A | p.Asp4426Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/182 | 13468/26191 | 13276/25578 | 4426/8525 | chr2 | 151602679 | ||
| chr2:151604849
|
C | T | 1 | a0084 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.12770G>A | p.Arg4257His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/182 | 12962/26191 | 12770/25578 | 4257/8525 | chr2 | 151604849 | ||
| chr2:151606686
|
C | T | 48 | a0001a0002a0005others(45): Show | 73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
missense_variant | MODERATE | c.12667G>A | p.Ala4223Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/182 | 12859/26191 | 12667/25578 | 4223/8525 | chr2 | 151606686 | ||
| chr2:151608560
|
C | G | 1 | a0033 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.12447G>C | p.Arg4149Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/182 | 12639/26191 | 12447/25578 | 4149/8525 | chr2 | 151608560 | ||
| chr2:151610620
|
G | C | 1 | a0125 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.11914C>G | p.Leu3972Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 80/182 | 12106/26191 | 11914/25578 | 3972/8525 | chr2 | 151610620 | ||
| chr2:151612262
|
T | C | 1 | a0112 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.11729A>G | p.Asp3910Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/182 | 11921/26191 | 11729/25578 | 3910/8525 | chr2 | 151612262 | ||
| chr2:151617364
|
A | T | 1 | a0062 | 1 | HG03688.hp1 | missense_variant&splice_region_variant | MODERATE | c.11181T>A | p.Asp3727Glu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/182 | 11373/26191 | 11181/25578 | 3727/8525 | chr2 | 151617364 | ||
| chr2:151617397
|
C | G | 1 | a0097 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.11148G>C | p.Met3716Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/182 | 11340/26191 | 11148/25578 | 3716/8525 | chr2 | 151617397 | ||
| chr2:151619514
|
C | G | 27 | a0002a0007a0014others(24): Show | 40 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
missense_variant | MODERATE | c.10809G>C | p.Trp3603Cys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/182 | 11001/26191 | 10809/25578 | 3603/8525 | chr2 | 151619514 | ||
| chr2:151619579
|
C | T | 3 | a0056a0085a0130 | 3 | HG02280.hp2 HG02451.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.10744G>A | p.Val3582Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/182 | 10936/26191 | 10744/25578 | 3582/8525 | chr2 | 151619579 | ||
| chr2:151621016
|
C | T | 3 | a0065a0066a0067 | 3 | HG03491.hp1 HG03704.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.10463G>A | p.Arg3488His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/182 | 10655/26191 | 10463/25578 | 3488/8525 | chr2 | 151621016 | ||
| chr2:151625593
|
T | C | 1 | a0049 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.10393A>G | p.Ile3465Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/182 | 10585/26191 | 10393/25578 | 3465/8525 | chr2 | 151625593 | ||
| chr2:151627640
|
C | G | 1 | a0063 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.10026G>C | p.Lys3342Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 69/182 | 10218/26191 | 10026/25578 | 3342/8525 | chr2 | 151627640 | ||
| chr2:151631273
|
T | C | 1 | a0046 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.9488A>G | p.Lys3163Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/182 | 9680/26191 | 9488/25578 | 3163/8525 | chr2 | 151631273 | ||
| chr2:151633887
|
T | A | 1 | a0050 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.9181A>T | p.Met3061Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/182 | 9373/26191 | 9181/25578 | 3061/8525 | chr2 | 151633887 | ||
| chr2:151633944
|
A | G | 127 | a0001a0002a0003others(124): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
missense_variant | MODERATE | c.9124T>C | p.Cys3042Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/182 | 9316/26191 | 9124/25578 | 3042/8525 | chr2 | 151633944 | ||
| chr2:151636277
|
C | T | 4 | a0020a0024a0117others(1): Show | 6 | HG00597.hp1 HG00609.hp1 HG02523.hp1 others(3): Show |
missense_variant | MODERATE | c.9052G>A | p.Asp3018Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/182 | 9244/26191 | 9052/25578 | 3018/8525 | chr2 | 151636277 | ||
| chr2:151636282
|
C | T | 2 | a0030a0054 | 2 | NA18946.hp1 NA19005.hp2 |
missense_variant | MODERATE | c.9047G>A | p.Arg3016Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/182 | 9239/26191 | 9047/25578 | 3016/8525 | chr2 | 151636282 | ||
| chr2:151640012
|
A | G | 85 | a0001a0003a0004others(82): Show | 118 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(115): Show |
missense_variant | MODERATE | c.8734T>C | p.Ser2912Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 62/182 | 8926/26191 | 8734/25578 | 2912/8525 | chr2 | 151640012 | ||
| chr2:151640027
|
C | T | 1 | a0033 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.8719G>A | p.Gly2907Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 62/182 | 8911/26191 | 8719/25578 | 2907/8525 | chr2 | 151640027 | ||
| chr2:151640458
|
A | G | 1 | a0064 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.8582T>C | p.Leu2861Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8774/26191 | 8582/25578 | 2861/8525 | chr2 | 151640458 | ||
| chr2:151642612
|
T | C | 1 | a0079 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.8335A>G | p.Ile2779Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/182 | 8527/26191 | 8335/25578 | 2779/8525 | chr2 | 151642612 | ||
| chr2:151642629
|
C | T | 7 | a0020a0047a0048others(4): Show | 8 | HG00597.hp1 HG02040.hp1 HG02683.hp2 others(5): Show |
missense_variant | MODERATE | c.8318G>A | p.Arg2773Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/182 | 8510/26191 | 8318/25578 | 2773/8525 | chr2 | 151642629 | ||
| chr2:151642841
|
T | C | 3 | a0010a0081a0082 | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
missense_variant | MODERATE | c.8189A>G | p.Asp2730Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 59/182 | 8381/26191 | 8189/25578 | 2730/8525 | chr2 | 151642841 | ||
| chr2:151643935
|
C | G | 24 | a0002a0007a0020others(21): Show | 39 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
missense_variant | MODERATE | c.7839G>C | p.Lys2613Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/182 | 8031/26191 | 7839/25578 | 2613/8525 | chr2 | 151643935 | ||
| chr2:151643936
|
T | C | 1 | a0118 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.7838A>G | p.Lys2613Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/182 | 8030/26191 | 7838/25578 | 2613/8525 | chr2 | 151643936 | ||
| chr2:151644077
|
C | T | 1 | a0033 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.7697G>A | p.Arg2566Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/182 | 7889/26191 | 7697/25578 | 2566/8525 | chr2 | 151644077 | ||
| chr2:151650297
|
C | T | 3 | a0088a0089a0090 | 3 | HG00741.hp1 NA19062.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.7310G>A | p.Arg2437Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/182 | 7502/26191 | 7310/25578 | 2437/8525 | chr2 | 151650297 | ||
| chr2:151655360
|
A | C | 6 | a0006a0030a0031others(3): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
missense_variant | MODERATE | c.6717T>G | p.Ile2239Met | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/182 | 6909/26191 | 6717/25578 | 2239/8525 | chr2 | 151655360 | ||
| chr2:151656370
|
A | G | 2 | a0085a0086 | 2 | HG02451.hp2 HG02572.hp2 |
missense_variant | MODERATE | c.6278T>C | p.Val2093Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 49/182 | 6470/26191 | 6278/25578 | 2093/8525 | chr2 | 151656370 | ||
| chr2:151658000
|
T | C | 2 | a0083a0084 | 2 | HG02622.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.6166A>G | p.Arg2056Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/182 | 6358/26191 | 6166/25578 | 2056/8525 | chr2 | 151658000 | ||
| chr2:151659169
|
G | A | 14 | a0001a0052a0065others(11): Show | 22 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
missense_variant&splice_region_variant | MODERATE | c.5971C>T | p.His1991Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/182 | 6163/26191 | 5971/25578 | 1991/8525 | chr2 | 151659169 | ||
| chr2:151662137
|
C | T | 1 | a0051 | 1 | HG02630.hp2 | missense_variant&splice_region_variant | MODERATE | c.5968G>A | p.Glu1990Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/182 | 6160/26191 | 5968/25578 | 1990/8525 | chr2 | 151662137 | ||
| chr2:151662200
|
A | G | 4 | a0028a0130a0131others(1): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.5905T>C | p.Tyr1969His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/182 | 6097/26191 | 5905/25578 | 1969/8525 | chr2 | 151662200 | ||
| chr2:151664541
|
G | T | 3 | a0074a0075a0076 | 3 | NA18945.hp1 NA18947.hp1 NA18971.hp1 |
missense_variant | MODERATE | c.5411C>A | p.Ala1804Glu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/182 | 5603/26191 | 5411/25578 | 1804/8525 | chr2 | 151664541 | ||
| chr2:151665469
|
A | G | 3 | a0010a0081a0082 | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
missense_variant | MODERATE | c.5102T>C | p.Val1701Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/182 | 5294/26191 | 5102/25578 | 1701/8525 | chr2 | 151665469 | ||
| chr2:151666287
|
G | A | 1 | a0053 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.4834C>T | p.Arg1612Cys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/182 | 5026/26191 | 4834/25578 | 1612/8525 | chr2 | 151666287 | ||
| chr2:151669031
|
C | T | 1 | a0052 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.4607G>A | p.Ser1536Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/182 | 4799/26191 | 4607/25578 | 1536/8525 | chr2 | 151669031 | ||
| chr2:151671058
|
C | T | 47 | a0002a0005a0007others(44): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(66): Show |
missense_variant | MODERATE | c.4471G>A | p.Val1491Met | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/182 | 4663/26191 | 4471/25578 | 1491/8525 | chr2 | 151671058 | ||
| chr2:151671094
|
C | T | 66 | a0001a0004a0006others(63): Show | 90 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
missense_variant | MODERATE | c.4435G>A | p.Val1479Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/182 | 4627/26191 | 4435/25578 | 1479/8525 | chr2 | 151671094 | ||
| chr2:151671122
|
C | G | 6 | a0013a0047a0048others(3): Show | 7 | HG02040.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.4407G>C | p.Glu1469Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/182 | 4599/26191 | 4407/25578 | 1469/8525 | chr2 | 151671122 | ||
| chr2:151672622
|
A | G | 1 | a0080 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.4046T>C | p.Leu1349Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/182 | 4238/26191 | 4046/25578 | 1349/8525 | chr2 | 151672622 | ||
| chr2:151674563
|
A | G | 85 | a0002a0003a0005others(82): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
missense_variant | MODERATE | c.3901T>C | p.Tyr1301His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/182 | 4093/26191 | 3901/25578 | 1301/8525 | chr2 | 151674563 | ||
| chr2:151675340
|
G | T | 2 | a0122a0123 | 2 | HG02809.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.3826C>A | p.Pro1276Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/182 | 4018/26191 | 3826/25578 | 1276/8525 | chr2 | 151675340 | ||
| chr2:151677746
|
T | C | 1 | a0124 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.3593A>G | p.Asn1198Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/182 | 3785/26191 | 3593/25578 | 1198/8525 | chr2 | 151677746 | ||
| chr2:151678031
|
T | C | 3 | a0010a0081a0082 | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
missense_variant | MODERATE | c.3412A>G | p.Asn1138Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 33/182 | 3604/26191 | 3412/25578 | 1138/8525 | chr2 | 151678031 | ||
| chr2:151679765
|
T | G | 1 | a0132 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3211A>C | p.Ile1071Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/182 | 3403/26191 | 3211/25578 | 1071/8525 | chr2 | 151679765 | ||
| chr2:151679984
|
T | A | 63 | a0002a0005a0010others(60): Show | 87 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(84): Show |
missense_variant | MODERATE | c.3081A>T | p.Lys1027Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 31/182 | 3273/26191 | 3081/25578 | 1027/8525 | chr2 | 151679984 | ||
| chr2:151687453
|
A | G | 2 | a0026a0125 | 3 | NA18960.hp1 NA19010.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.2603T>C | p.Leu868Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/182 | 2795/26191 | 2603/25578 | 868/8525 | chr2 | 151687453 | ||
| chr2:151687718
|
C | T | 1 | a0126 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2431G>A | p.Asp811Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 26/182 | 2623/26191 | 2431/25578 | 811/8525 | chr2 | 151687718 | ||
| chr2:151688389
|
T | C | 4 | a0006a0030a0031others(1): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
missense_variant | MODERATE | c.2318A>G | p.Tyr773Cys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/182 | 2510/26191 | 2318/25578 | 773/8525 | chr2 | 151688389 | ||
| chr2:151692360
|
T | A | 1 | a0127 | 1 | HG00609.hp1 | missense_variant&splice_region_variant | MODERATE | c.1899A>T | p.Arg633Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 21/182 | 2091/26191 | 1899/25578 | 633/8525 | chr2 | 151692360 | ||
| chr2:151694363
|
T | C | 1 | a0027 | 2 | HG02257.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1856A>G | p.Lys619Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/182 | 2048/26191 | 1856/25578 | 619/8525 | chr2 | 151694363 | ||
| chr2:151710447
|
T | C | 1 | a0128 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.914A>G | p.Asp305Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/182 | 1106/26191 | 914/25578 | 305/8525 | chr2 | 151710447 | ||
| chr2:151710458
|
T | A | 1 | a0029 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.903A>T | p.Arg301Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/182 | 1095/26191 | 903/25578 | 301/8525 | chr2 | 151710458 | ||
| chr2:151710459
|
C | T | 1 | a0029 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.902G>A | p.Arg301Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/182 | 1094/26191 | 902/25578 | 301/8525 | chr2 | 151710459 | ||
| chr2:151724301
|
C | G | 2 | a0129a0133 | 2 | HG01192.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.571G>C | p.Glu191Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/182 | 763/26191 | 571/25578 | 191/8525 | chr2 | 151724301 | ||
| chr2:151727801
|
ATGCTGGC others(8): Show |
A | 5 | a0028a0130a0131others(2): Show | 6 | HG01192.hp2 HG02258.hp1 HG02886.hp1 others(3): Show |
conservative_inframe_deletion | MODERATE | c.169_183delCTGGCACA others(7): Show |
p.Leu57_Ala61del | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/182 | 375/26191 | 169/25578 | 57/8525 | chr2 | 151727801 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:151485796
|
G | A | 3 | a0010c0138a0010c0139a0113c0042 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
synonymous_variant | LOW | c.25542C>T | p.Thr8514Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 182/182 | 25734/26191 | 25542/25578 | 8514/8525 | chr2 | 151485796 | ||
| chr2:151506954
|
C | T | 1 | a0080c0030 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.23511G>A | p.Thr7837Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 163/182 | 23703/26191 | 23511/25578 | 7837/8525 | chr2 | 151506954 | ||
| chr2:151514390
|
C | T | 1 | a0021c0056 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.23055G>A | p.Gly7685Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 159/182 | 23247/26191 | 23055/25578 | 7685/8525 | chr2 | 151514390 | ||
| chr2:151514848
|
A | G | 1 | a0017c0015 | 2 | NA19080.hp1 NA19088.hp2 |
synonymous_variant | LOW | c.22986T>C | p.His7662His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 158/182 | 23178/26191 | 22986/25578 | 7662/8525 | chr2 | 151514848 | ||
| chr2:151518998
|
A | G | 1 | a0051c0131 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.22662T>C | p.Asn7554Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 155/182 | 22854/26191 | 22662/25578 | 7554/8525 | chr2 | 151518998 | ||
| chr2:151526245
|
T | C | 4 | a0025c0011a0042c0095a0044c0092others(1): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.21963A>G | p.Lys7321Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 149/182 | 22155/26191 | 21963/25578 | 7321/8525 | chr2 | 151526245 | ||
| chr2:151529210
|
A | G | 1 | a0065c0119 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.21735T>C | p.Asn7245Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/182 | 21927/26191 | 21735/25578 | 7245/8525 | chr2 | 151529210 | ||
| chr2:151529225
|
G | A | 1 | a0009c0109 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.21720C>T | p.Tyr7240Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/182 | 21912/26191 | 21720/25578 | 7240/8525 | chr2 | 151529225 | ||
| chr2:151531039
|
T | C | 67 | a0001c0001a0001c0082a0002c0002others(64): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
synonymous_variant | LOW | c.21585A>G | p.Thr7195Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/182 | 21777/26191 | 21585/25578 | 7195/8525 | chr2 | 151531039 | ||
| chr2:151531042
|
G | A | 1 | a0031c0078 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.21582C>T | p.Asp7194Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/182 | 21774/26191 | 21582/25578 | 7194/8525 | chr2 | 151531042 | ||
| chr2:151531078
|
G | A | 5 | a0002c0048a0014c0113a0026c0006others(2): Show | 6 | NA18960.hp1 NA18962.hp1 NA18984.hp1 others(3): Show |
synonymous_variant | LOW | c.21546C>T | p.Asn7182Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/182 | 21738/26191 | 21546/25578 | 7182/8525 | chr2 | 151531078 | ||
| chr2:151531795
|
G | A | 9 | a0017c0015a0036c0029a0046c0091others(6): Show | 10 | HG01884.hp1 HG02886.hp2 HG03491.hp1 others(7): Show |
synonymous_variant | LOW | c.21519C>T | p.Ser7173Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/182 | 21711/26191 | 21519/25578 | 7173/8525 | chr2 | 151531795 | ||
| chr2:151531828
|
G | A | 1 | a0010c0139 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.21486C>T | p.His7162His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/182 | 21678/26191 | 21486/25578 | 7162/8525 | chr2 | 151531828 | ||
| chr2:151533477
|
A | G | 4 | a0025c0011a0042c0095a0044c0092others(1): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.21382T>C | p.Leu7128Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/182 | 21574/26191 | 21382/25578 | 7128/8525 | chr2 | 151533477 | ||
| chr2:151541531
|
G | C | 18 | a0009c0017a0009c0109a0013c0014others(15): Show | 21 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(18): Show |
synonymous_variant | LOW | c.20598C>G | p.Gly6866Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 136/182 | 20790/26191 | 20598/25578 | 6866/8525 | chr2 | 151541531 | ||
| chr2:151553464
|
A | G | 1 | a0050c0099 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.19665T>C | p.Ile6555Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 127/182 | 19857/26191 | 19665/25578 | 6555/8525 | chr2 | 151553464 | ||
| chr2:151553828
|
A | G | 1 | a0005c0063 | 1 | HG01099.hp2 | splice_region_variant&synonymous_variant | LOW | c.19626T>C | p.Asp6542Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 126/182 | 19818/26191 | 19626/25578 | 6542/8525 | chr2 | 151553828 | ||
| chr2:151554982
|
G | A | 1 | a0083c0134 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.19377C>T | p.Asp6459Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 125/182 | 19569/26191 | 19377/25578 | 6459/8525 | chr2 | 151554982 | ||
| chr2:151560595
|
G | A | 4 | a0036c0029a0046c0091a0087c0132others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.19311C>T | p.Ser6437Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/182 | 19503/26191 | 19311/25578 | 6437/8525 | chr2 | 151560595 | ||
| chr2:151560622
|
G | A | 1 | a0035c0146 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.19284C>T | p.His6428His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/182 | 19476/26191 | 19284/25578 | 6428/8525 | chr2 | 151560622 | ||
| chr2:151561253
|
C | A | 1 | a0011c0070 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.19056G>T | p.Thr6352Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 122/182 | 19248/26191 | 19056/25578 | 6352/8525 | chr2 | 151561253 | ||
| chr2:151562617
|
C | T | 1 | a0004c0018 | 2 | NA18962.hp2 NA19010.hp1 |
synonymous_variant | LOW | c.18885G>A | p.Leu6295Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/182 | 19077/26191 | 18885/25578 | 6295/8525 | chr2 | 151562617 | ||
| chr2:151562641
|
G | A | 1 | a0050c0099 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.18861C>T | p.Arg6287Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/182 | 19053/26191 | 18861/25578 | 6287/8525 | chr2 | 151562641 | ||
| chr2:151562719
|
C | T | 4 | a0049c0096a0065c0119a0066c0118others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
synonymous_variant | LOW | c.18783G>A | p.Gln6261Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/182 | 18975/26191 | 18783/25578 | 6261/8525 | chr2 | 151562719 | ||
| chr2:151563606
|
C | G | 5 | a0010c0137a0010c0138a0010c0139others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
synonymous_variant | LOW | c.18693G>C | p.Ala6231Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/182 | 18885/26191 | 18693/25578 | 6231/8525 | chr2 | 151563606 | ||
| chr2:151565573
|
A | G | 26 | a0001c0001a0001c0082a0005c0008others(23): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
synonymous_variant | LOW | c.18294T>C | p.Tyr6098Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 116/182 | 18486/26191 | 18294/25578 | 6098/8525 | chr2 | 151565573 | ||
| chr2:151568651
|
C | T | 1 | a0029c0081 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.17601G>A | p.Val5867Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 111/182 | 17793/26191 | 17601/25578 | 5867/8525 | chr2 | 151568651 | ||
| chr2:151570207
|
C | T | 2 | a0091c0142a0131c0149 | 2 | HG03486.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.17304G>A | p.Leu5768Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 109/182 | 17496/26191 | 17304/25578 | 5768/8525 | chr2 | 151570207 | ||
| chr2:151575797
|
T | C | 9 | a0003c0083a0003c0094a0021c0057others(6): Show | 9 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.16911A>G | p.Pro5637Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/182 | 17103/26191 | 16911/25578 | 5637/8525 | chr2 | 151575797 | ||
| chr2:151579389
|
G | A | 2 | a0023c0043a0096c0060 | 2 | HG03654.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.16653C>T | p.Pro5551Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16845/26191 | 16653/25578 | 5551/8525 | chr2 | 151579389 | ||
| chr2:151579500
|
G | C | 10 | a0009c0017a0009c0109a0023c0044others(7): Show | 11 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(8): Show |
synonymous_variant | LOW | c.16542C>G | p.Ala5514Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16734/26191 | 16542/25578 | 5514/8525 | chr2 | 151579500 | ||
| chr2:151579593
|
G | A | 4 | a0010c0137a0010c0138a0010c0139others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
synonymous_variant | LOW | c.16449C>T | p.Ser5483Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/182 | 16641/26191 | 16449/25578 | 5483/8525 | chr2 | 151579593 | ||
| chr2:151580797
|
G | A | 6 | a0010c0137a0010c0138a0010c0139others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.16392C>T | p.Asp5464Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/182 | 16584/26191 | 16392/25578 | 5464/8525 | chr2 | 151580797 | ||
| chr2:151581498
|
G | A | 2 | a0075c0102a0076c0101 | 2 | NA18945.hp1 NA18971.hp1 |
synonymous_variant | LOW | c.16269C>T | p.Ala5423Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/182 | 16461/26191 | 16269/25578 | 5423/8525 | chr2 | 151581498 | ||
| chr2:151582622
|
A | G | 59 | a0002c0002a0002c0048a0005c0063others(56): Show | 75 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.16021T>C | p.Leu5341Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/182 | 16213/26191 | 16021/25578 | 5341/8525 | chr2 | 151582622 | ||
| chr2:151583470
|
G | A | 1 | a0084c0133 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.15960C>T | p.Tyr5320Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/182 | 16152/26191 | 15960/25578 | 5320/8525 | chr2 | 151583470 | ||
| chr2:151583521
|
C | T | 1 | a0096c0060 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.15909G>A | p.Gln5303Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/182 | 16101/26191 | 15909/25578 | 5303/8525 | chr2 | 151583521 | ||
| chr2:151583707
|
T | A | 1 | a0062c0106 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.15723A>T | p.Leu5241Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/182 | 15915/26191 | 15723/25578 | 5241/8525 | chr2 | 151583707 | ||
| chr2:151586447
|
C | T | 1 | a0049c0096 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.15513G>A | p.Pro5171Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/182 | 15705/26191 | 15513/25578 | 5171/8525 | chr2 | 151586447 | ||
| chr2:151589898
|
T | C | 1 | a0121c0074 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.15237A>G | p.Leu5079Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/182 | 15429/26191 | 15237/25578 | 5079/8525 | chr2 | 151589898 | ||
| chr2:151591348
|
A | G | 2 | a0025c0011a0042c0095 | 3 | HG01891.hp2 HG02818.hp1 HG03195.hp2 |
splice_region_variant&synonymous_variant | LOW | c.14934T>C | p.Asp4978Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/182 | 15126/26191 | 14934/25578 | 4978/8525 | chr2 | 151591348 | ||
| chr2:151592049
|
A | G | 4 | a0010c0137a0010c0138a0010c0139others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
synonymous_variant | LOW | c.14811T>C | p.Ala4937Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/182 | 15003/26191 | 14811/25578 | 4937/8525 | chr2 | 151592049 | ||
| chr2:151593174
|
A | G | 141 | a0001c0001a0001c0082a0002c0002others(138): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
synonymous_variant | LOW | c.14563T>C | p.Leu4855Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/182 | 14755/26191 | 14563/25578 | 4855/8525 | chr2 | 151593174 | ||
| chr2:151594010
|
G | A | 1 | a0084c0133 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.14514C>T | p.Ser4838Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/182 | 14706/26191 | 14514/25578 | 4838/8525 | chr2 | 151594010 | ||
| chr2:151597978
|
G | A | 3 | a0008c0004a0015c0111a0058c0110 | 5 | HG01192.hp1 HG02976.hp2 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.13941C>T | p.Val4647Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/182 | 14133/26191 | 13941/25578 | 4647/8525 | chr2 | 151597978 | ||
| chr2:151600451
|
T | C | 1 | a0121c0074 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.13779A>G | p.Leu4593Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | 13971/26191 | 13779/25578 | 4593/8525 | chr2 | 151600451 | ||
| chr2:151600697
|
G | A | 1 | a0113c0042 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.13533C>T | p.Ser4511Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/182 | 13725/26191 | 13533/25578 | 4511/8525 | chr2 | 151600697 | ||
| chr2:151601901
|
G | A | 134 | a0001c0001a0001c0082a0002c0002others(131): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
splice_region_variant&synonymous_variant | LOW | c.13476C>T | p.Asp4492Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/182 | 13668/26191 | 13476/25578 | 4492/8525 | chr2 | 151601901 | ||
| chr2:151602602
|
G | A | 138 | a0001c0001a0001c0082a0002c0002others(135): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
synonymous_variant | LOW | c.13353C>T | p.Ala4451Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/182 | 13545/26191 | 13353/25578 | 4451/8525 | chr2 | 151602602 | ||
| chr2:151603727
|
G | A | 9 | a0012c0090a0036c0029a0037c0087others(6): Show | 9 | HG00099.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
synonymous_variant | LOW | c.13105C>T | p.Leu4369Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/182 | 13297/26191 | 13105/25578 | 4369/8525 | chr2 | 151603727 | ||
| chr2:151609992
|
C | T | 2 | a0091c0142a0131c0149 | 2 | HG03486.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.12147G>A | p.Lys4049Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/182 | 12339/26191 | 12147/25578 | 4049/8525 | chr2 | 151609992 | ||
| chr2:151612222
|
A | G | 5 | a0033c0024a0036c0029a0046c0091others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.11769T>C | p.Ile3923Ile | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/182 | 11961/26191 | 11769/25578 | 3923/8525 | chr2 | 151612222 | ||
| chr2:151618347
|
C | T | 5 | a0010c0137a0010c0138a0010c0139others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
synonymous_variant | LOW | c.11004G>A | p.Thr3668Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/182 | 11196/26191 | 11004/25578 | 3668/8525 | chr2 | 151618347 | ||
| chr2:151619616
|
C | T | 33 | a0008c0004a0009c0017a0009c0109others(30): Show | 41 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
synonymous_variant | LOW | c.10707G>A | p.Lys3569Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/182 | 10899/26191 | 10707/25578 | 3569/8525 | chr2 | 151619616 | ||
| chr2:151625609
|
G | A | 1 | a0121c0074 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.10377C>T | p.Asp3459Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/182 | 10569/26191 | 10377/25578 | 3459/8525 | chr2 | 151625609 | ||
| chr2:151627005
|
G | A | 6 | a0010c0137a0010c0138a0010c0139others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
synonymous_variant | LOW | c.10344C>T | p.Asn3448Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/182 | 10536/26191 | 10344/25578 | 3448/8525 | chr2 | 151627005 | ||
| chr2:151627011
|
A | G | 6 | a0010c0137a0010c0138a0010c0139others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
synonymous_variant | LOW | c.10338T>C | p.Asn3446Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/182 | 10530/26191 | 10338/25578 | 3446/8525 | chr2 | 151627011 | ||
| chr2:151631227
|
C | T | 1 | a0010c0137 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.9534G>A | p.Gln3178Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/182 | 9726/26191 | 9534/25578 | 3178/8525 | chr2 | 151631227 | ||
| chr2:151633705
|
A | G | 103 | a0001c0001a0001c0082a0002c0002others(100): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
synonymous_variant | LOW | c.9363T>C | p.Pro3121Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/182 | 9555/26191 | 9363/25578 | 3121/8525 | chr2 | 151633705 | ||
| chr2:151636257
|
C | T | 1 | a0110c0041 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.9072G>A | p.Ala3024Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/182 | 9264/26191 | 9072/25578 | 3024/8525 | chr2 | 151636257 | ||
| chr2:151640394
|
G | A | 2 | a0042c0095a0121c0074 | 2 | HG01891.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.8646C>T | p.Asp2882Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8838/26191 | 8646/25578 | 2882/8525 | chr2 | 151640394 | ||
| chr2:151640415
|
T | C | 1 | a0081c0141 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.8625A>G | p.Thr2875Thr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8817/26191 | 8625/25578 | 2875/8525 | chr2 | 151640415 | ||
| chr2:151640448
|
A | G | 2 | a0013c0014a0064c0025 | 3 | HG02647.hp2 HG03098.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.8592T>C | p.Asp2864Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8784/26191 | 8592/25578 | 2864/8525 | chr2 | 151640448 | ||
| chr2:151640487
|
C | T | 2 | a0034c0147a0035c0146 | 2 | HG00639.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.8553G>A | p.Gly2851Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8745/26191 | 8553/25578 | 2851/8525 | chr2 | 151640487 | ||
| chr2:151640541
|
C | T | 1 | a0024c0038 | 1 | NA19080.hp2 | synonymous_variant | LOW | c.8499G>A | p.Lys2833Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8691/26191 | 8499/25578 | 2833/8525 | chr2 | 151640541 | ||
| chr2:151640574
|
G | A | 13 | a0028c0021a0033c0024a0047c0097others(10): Show | 14 | HG02040.hp1 HG02258.hp1 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.8466C>T | p.His2822His | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/182 | 8658/26191 | 8466/25578 | 2822/8525 | chr2 | 151640574 | ||
| chr2:151642828
|
G | A | 2 | a0034c0147a0035c0146 | 2 | HG00639.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.8202C>T | p.Val2734Val | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 59/182 | 8394/26191 | 8202/25578 | 2734/8525 | chr2 | 151642828 | ||
| chr2:151655904
|
G | C | 2 | a0083c0134a0084c0133 | 2 | HG02622.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.6615C>G | p.Arg2205Arg | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 50/182 | 6807/26191 | 6615/25578 | 2205/8525 | chr2 | 151655904 | ||
| chr2:151658007
|
C | T | 1 | a0003c0083 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.6159G>A | p.Lys2053Lys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/182 | 6351/26191 | 6159/25578 | 2053/8525 | chr2 | 151658007 | ||
| chr2:151662303
|
G | A | 3 | a0004c0126a0053c0127a0092c0135 | 3 | HG02818.hp2 HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.5802C>T | p.Gly1934Gly | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/182 | 5994/26191 | 5802/25578 | 1934/8525 | chr2 | 151662303 | ||
| chr2:151662333
|
G | A | 7 | a0006c0012a0006c0079a0030c0076others(4): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
synonymous_variant | LOW | c.5772C>T | p.Tyr1924Tyr | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/182 | 5964/26191 | 5772/25578 | 1924/8525 | chr2 | 151662333 | ||
| chr2:151664582
|
C | T | 92 | a0001c0001a0001c0082a0003c0005others(89): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
synonymous_variant | LOW | c.5370G>A | p.Glu1790Glu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/182 | 5562/26191 | 5370/25578 | 1790/8525 | chr2 | 151664582 | ||
| chr2:151666141
|
G | A | 1 | a0051c0131 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.4980C>T | p.Pro1660Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/182 | 5172/26191 | 4980/25578 | 1660/8525 | chr2 | 151666141 | ||
| chr2:151672447
|
C | T | 2 | a0034c0147a0035c0146 | 2 | HG00639.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.4221G>A | p.Gln1407Gln | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/182 | 4413/26191 | 4221/25578 | 1407/8525 | chr2 | 151672447 | ||
| chr2:151675365
|
A | G | 2 | a0085c0031a0086c0032 | 2 | HG02451.hp2 HG02572.hp2 |
synonymous_variant | LOW | c.3801T>C | p.Asp1267Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/182 | 3993/26191 | 3801/25578 | 1267/8525 | chr2 | 151675365 | ||
| chr2:151677703
|
G | A | 1 | a0051c0131 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.3636C>T | p.Asp1212Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/182 | 3828/26191 | 3636/25578 | 1212/8525 | chr2 | 151677703 | ||
| chr2:151679721
|
G | A | 1 | a0091c0142 | 1 | HG03486.hp1 | splice_region_variant&synonymous_variant | LOW | c.3255C>T | p.Asp1085Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/182 | 3447/26191 | 3255/25578 | 1085/8525 | chr2 | 151679721 | ||
| chr2:151684874
|
G | A | 1 | a0059c0143 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.2739C>T | p.Ser913Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/182 | 2931/26191 | 2739/25578 | 913/8525 | chr2 | 151684874 | ||
| chr2:151692062
|
A | G | 1 | a0001c0082 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.2103T>C | p.Ser701Ser | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 22/182 | 2295/26191 | 2103/25578 | 701/8525 | chr2 | 151692062 | ||
| chr2:151692278
|
G | A | 1 | a0105c0080 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1981C>T | p.Leu661Leu | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 21/182 | 2173/26191 | 1981/25578 | 661/8525 | chr2 | 151692278 | ||
| chr2:151697205
|
G | A | 1 | a0056c0145 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1413C>T | p.Phe471Phe | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 16/182 | 1605/26191 | 1413/25578 | 471/8525 | chr2 | 151697205 | ||
| chr2:151697595
|
G | A | 2 | a0034c0147a0035c0146 | 2 | HG00639.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1206C>T | p.Cys402Cys | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 14/182 | 1398/26191 | 1206/25578 | 402/8525 | chr2 | 151697595 | ||
| chr2:151717455
|
A | G | 1 | a0022c0026 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.783T>C | p.Asp261Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/182 | 975/26191 | 783/25578 | 261/8525 | chr2 | 151717455 | ||
| chr2:151717467
|
A | G | 65 | a0002c0002a0002c0048a0005c0008others(62): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
synonymous_variant | LOW | c.771T>C | p.Ala257Ala | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/182 | 963/26191 | 771/25578 | 257/8525 | chr2 | 151717467 | ||
| chr2:151723424
|
C | T | 2 | a0033c0024a0064c0025 | 2 | HG02630.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.675G>A | p.Pro225Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/182 | 867/26191 | 675/25578 | 225/8525 | chr2 | 151723424 | ||
| chr2:151723433
|
A | G | 1 | a0120c0023 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.666T>C | p.Asn222Asn | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/182 | 858/26191 | 666/25578 | 222/8525 | chr2 | 151723433 | ||
| chr2:151727790
|
C | T | 4 | a0028c0021a0130c0150a0131c0149others(1): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.195G>A | p.Pro65Pro | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/182 | 387/26191 | 195/25578 | 65/8525 | chr2 | 151727790 | ||
| chr2:151733145
|
G | A | 1 | a0039c0153 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.12C>T | p.Asp4Asp | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/182 | 204/26191 | 12/25578 | 4/8525 | chr2 | 151733145 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:151485494
|
CCT | C | 6 | a0016c0016t0002a0041c0085t0002a0045c0089t0002others(3): Show | 7 | HG02965.hp1 HG03098.hp2 HG03195.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*264_*265delAG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 182/182 | 264 | chr2 | 151485494 | |||||
| chr2:151734433
|
G | A | 1 | a0019c0010t0003 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 1/182 | 1277 | chr2 | 151734433 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:151485949
|
G | GA | 3 | a0010c0138t0001g0091a0010c0139t0001g0106a0113c0042t0001g0035 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.25405-17dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151485949 | ||||||
| chr2:151485967
|
A | G | 47 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.25405-34T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151485967 | ||||||
| chr2:151486036
|
G | A | 5 | a0016c0016t0002g0100a0016c0016t0002g0137a0041c0085t0002g0010others(2): Show | 5 | HG02965.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.25405-103C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486036 | ||||||
| chr2:151486160
|
C | T | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.25405-227G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486160 | ||||||
| chr2:151486182
|
A | C | 1 | a0010c0138t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.25405-249T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486182 | ||||||
| chr2:151486243
|
A | G | 3 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.25405-310T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486243 | ||||||
| chr2:151486651
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25405-718C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486651 | ||||||
| chr2:151486656
|
A | G | 17 | a0015c0108t0001g0136a0015c0111t0001g0139a0016c0016t0002g0100others(14): Show | 17 | HG00639.hp2 HG01175.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.25405-723T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486656 | ||||||
| chr2:151486661
|
TGGGTAGT others(10): Show |
T | 3 | a0010c0138t0001g0091a0010c0139t0001g0106a0113c0042t0001g0035 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.25405-745_25405-72 others(21): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486661 | ||||||
| chr2:151486680
|
G | A | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25405-747C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486680 | ||||||
| chr2:151486698
|
G | A | 1 | a0017c0015t0001g0164 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.25405-765C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486698 | ||||||
| chr2:151486782
|
A | T | 1 | a0086c0032t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.25405-849T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486782 | ||||||
| chr2:151486812
|
T | C | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.25405-879A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151486812 | ||||||
| chr2:151487046
|
TGTG | T | 15 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(12): Show | 15 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.25405-1116_25405-1 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487046 | ||||||
| chr2:151487058
|
C | T | 1 | a0086c0032t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.25405-1125G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487058 | ||||||
| chr2:151487089
|
G | A | 1 | a0002c0048t0001g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.25405-1156C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487089 | ||||||
| chr2:151487127
|
T | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.25405-1194A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487127 | ||||||
| chr2:151487304
|
T | C | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25405-1371A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487304 | ||||||
| chr2:151487431
|
T | C | 3 | a0003c0005t0001g0004a0003c0005t0001g0006a0039c0153t0001g0021 | 3 | HG00673.hp2 NA18980.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.25405-1498A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487431 | ||||||
| chr2:151487743
|
TAA | T | 3 | a0010c0138t0001g0091a0010c0139t0001g0106a0113c0042t0001g0035 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.25405-1812_25405-1 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487743 | ||||||
| chr2:151487766
|
C | CAT | 15 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(12): Show | 15 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.25405-1835_25405-1 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487766 | ||||||
| chr2:151487850
|
C | T | 1 | a0008c0004t0001g0009 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.25405-1917G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487850 | ||||||
| chr2:151487968
|
C | G | 1 | a0015c0111t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.25404+2003G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151487968 | ||||||
| chr2:151488081
|
C | T | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.25404+1890G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488081 | ||||||
| chr2:151488143
|
G | A | 2 | a0005c0063t0001g0052a0005c0064t0001g0083 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.25404+1828C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488143 | ||||||
| chr2:151488297
|
A | C | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.25404+1674T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488297 | ||||||
| chr2:151488379
|
G | T | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.25404+1592C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488379 | ||||||
| chr2:151488436
|
T | C | 3 | a0010c0138t0001g0091a0010c0139t0001g0106a0113c0042t0001g0035 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.25404+1535A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488436 | ||||||
| chr2:151488478
|
C | CA | 10 | a0001c0001t0001g0097a0003c0005t0001g0004a0014c0113t0001g0120others(7): Show | 10 | HG00558.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.25404+1492dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488478 | ||||||
| chr2:151488652
|
TA | T | 46 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.25404+1318delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488652 | ||||||
| chr2:151488660
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25404+1311T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488660 | ||||||
| chr2:151488692
|
A | G | 42 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.25404+1279T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488692 | ||||||
| chr2:151488998
|
A | G | 4 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(1): Show | 4 | HG01192.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.25404+973T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151488998 | ||||||
| chr2:151489049
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25404+922C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489049 | ||||||
| chr2:151489236
|
A | G | 2 | a0060c0107t0001g0157a0104c0059t0001g0019 | 2 | HG02165.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.25404+735T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489236 | ||||||
| chr2:151489357
|
C | G | 65 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.25404+614G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489357 | ||||||
| chr2:151489380
|
TG | T | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.25404+590delC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489380 | ||||||
| chr2:151489556
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.25404+415G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489556 | ||||||
| chr2:151489604
|
C | A | 61 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.25404+367G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489604 | ||||||
| chr2:151489758
|
T | G | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.25404+213A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489758 | ||||||
| chr2:151489887
|
A | C | 4 | a0002c0002t0001g0026a0007c0003t0001g0001a0007c0003t0001g0002others(1): Show | 4 | HG01175.hp2 HG01258.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.25404+84T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 181/181 | chr2 | 151489887 | ||||||
| chr2:151490199
|
C | A | 5 | a0002c0002t0001g0039a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG00621.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.25298-122G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 180/181 | chr2 | 151490199 | ||||||
| chr2:151490287
|
G | C | 5 | a0002c0002t0001g0039a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG00621.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.25297+85C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 180/181 | chr2 | 151490287 | ||||||
| chr2:151490633
|
CT | C | 3 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170 | 3 | HG02080.hp2 NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25151-116delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151490633 | ||||||
| chr2:151490757
|
A | C | 1 | a0071c0124t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25151-239T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151490757 | ||||||
| chr2:151491037
|
CT | C | 119 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.25151-520delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491037 | ||||||
| chr2:151491058
|
G | GGGGT | 16 | a0015c0108t0001g0136a0015c0111t0001g0139a0016c0016t0002g0100others(13): Show | 16 | HG00639.hp2 HG01175.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.25151-544_25151-54 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491058 | ||||||
| chr2:151491086
|
A | G | 65 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(62): Show | 65 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.25151-568T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491086 | ||||||
| chr2:151491189
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25150+494G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491189 | ||||||
| chr2:151491421
|
CT | C | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.25150+261delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491421 | ||||||
| chr2:151491542
|
C | G | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.25150+141G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491542 | ||||||
| chr2:151491629
|
T | C | 4 | a0028c0021t0001g0182a0028c0021t0001g0183a0119c0136t0001g0132others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.25150+54A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491629 | ||||||
| chr2:151491671
|
C | T | 17 | a0015c0108t0001g0136a0015c0111t0001g0139a0016c0016t0002g0100others(14): Show | 17 | HG00639.hp2 HG01175.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.25150+12G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 179/181 | chr2 | 151491671 | ||||||
| chr2:151491971
|
C | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25057+127G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 178/181 | chr2 | 151491971 | ||||||
| chr2:151492289
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.24874-8C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 177/181 | chr2 | 151492289 | ||||||
| chr2:151492328
|
T | A | 37 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(34): Show | 37 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.24874-47A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 177/181 | chr2 | 151492328 | ||||||
| chr2:151492333
|
C | T | 3 | a0010c0138t0001g0091a0010c0139t0001g0106a0113c0042t0001g0035 | 3 | HG00423.hp2 HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.24874-52G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 177/181 | chr2 | 151492333 | ||||||
| chr2:151492512
|
G | A | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.24766-18C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151492512 | ||||||
| chr2:151492560
|
C | T | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.24766-66G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151492560 | ||||||
| chr2:151492591
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.24766-97G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151492591 | ||||||
| chr2:151492874
|
T | C | 1 | a0014c0112t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.24766-380A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151492874 | ||||||
| chr2:151492880
|
G | A | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.24766-386C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151492880 | ||||||
| chr2:151493208
|
T | C | 1 | a0026c0006t0001g0027 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.24765+145A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151493208 | ||||||
| chr2:151493284
|
G | A | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.24765+69C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 176/181 | chr2 | 151493284 | ||||||
| chr2:151493948
|
T | C | 130 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.24580-81A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 174/181 | chr2 | 151493948 | ||||||
| chr2:151494388
|
A | T | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.24487-135T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494388 | ||||||
| chr2:151494389
|
G | GTA | 67 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(64): Show | 67 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.24487-138_24487-13 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494389 | ||||||
| chr2:151494448
|
G | A | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.24487-195C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494448 | ||||||
| chr2:151494532
|
C | T | 1 | a0086c0032t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.24487-279G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494532 | ||||||
| chr2:151494585
|
T | G | 1 | a0004c0018t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.24487-332A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494585 | ||||||
| chr2:151494612
|
T | C | 130 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.24487-359A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494612 | ||||||
| chr2:151494634
|
T | G | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24487-381A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494634 | ||||||
| chr2:151494705
|
A | G | 1 | a0038c0086t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.24487-452T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494705 | ||||||
| chr2:151494741
|
C | T | 2 | a0025c0011t0001g0090a0070c0123t0001g0116 | 2 | HG03195.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.24487-488G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494741 | ||||||
| chr2:151494784
|
G | C | 4 | a0028c0021t0001g0182a0028c0021t0001g0183a0119c0136t0001g0132others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.24487-531C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494784 | ||||||
| chr2:151494933
|
C | A | 48 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0125others(45): Show | 48 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.24487-680G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151494933 | ||||||
| chr2:151495006
|
C | G | 1 | a0078c0128t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.24487-753G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495006 | ||||||
| chr2:151495011
|
A | G | 1 | a0078c0128t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.24487-758T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495011 | ||||||
| chr2:151495214
|
G | A | 14 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(11): Show | 14 | HG00280.hp1 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.24487-961C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495214 | ||||||
| chr2:151495283
|
C | G | 36 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(33): Show | 36 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.24486+993G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495283 | ||||||
| chr2:151495306
|
G | A | 1 | a0008c0004t0001g0009 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.24486+970C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495306 | ||||||
| chr2:151495447
|
G | GATGCGTG others(3): Show |
99 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.24486+819_24486+82 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495447 | ||||||
| chr2:151495657
|
A | T | 1 | a0024c0040t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.24486+619T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495657 | ||||||
| chr2:151495692
|
C | T | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.24486+584G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495692 | ||||||
| chr2:151495693
|
G | A | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.24486+583C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495693 | ||||||
| chr2:151495737
|
TTAAG | T | 126 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.24486+535_24486+53 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495737 | ||||||
| chr2:151495905
|
A | G | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24486+371T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495905 | ||||||
| chr2:151495948
|
C | G | 15 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(12): Show | 15 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.24486+328G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495948 | ||||||
| chr2:151495950
|
C | T | 2 | a0046c0091t0001g0017a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.24486+326G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151495950 | ||||||
| chr2:151496076
|
T | G | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24486+200A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151496076 | ||||||
| chr2:151496144
|
A | G | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24486+132T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151496144 | ||||||
| chr2:151496246
|
A | G | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.24486+30T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 173/181 | chr2 | 151496246 | ||||||
| chr2:151496564
|
A | C | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.24394-196T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496564 | ||||||
| chr2:151496572
|
C | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.24394-204G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496572 | ||||||
| chr2:151496636
|
G | A | 14 | a0015c0111t0001g0139a0016c0016t0002g0100a0016c0016t0002g0137others(11): Show | 14 | HG00639.hp2 HG01175.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.24394-268C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496636 | ||||||
| chr2:151496814
|
A | T | 1 | a0003c0005t0001g0013 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.24393+127T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496814 | ||||||
| chr2:151496862
|
G | T | 2 | a0004c0019t0001g0148a0004c0019t0001g0151 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.24393+79C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496862 | ||||||
| chr2:151496881
|
T | G | 36 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(33): Show | 36 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.24393+60A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 172/181 | chr2 | 151496881 | ||||||
| chr2:151497067
|
A | ATGAG | 3 | a0036c0029t0001g0176a0087c0132t0001g0101a0105c0080t0001g0034 | 3 | HG01884.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.24301-38_24301-35d others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497067 | ||||||
| chr2:151497126
|
C | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.24301-93G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497126 | ||||||
| chr2:151497191
|
T | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.24301-158A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497191 | ||||||
| chr2:151497214
|
A | C | 2 | a0030c0076t0001g0174a0054c0104t0001g0162 | 2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.24301-181T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497214 | ||||||
| chr2:151497278
|
G | GTTATT | 4 | a0034c0147t0001g0178a0036c0029t0001g0176a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.24301-250_24301-24 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497278 | ||||||
| chr2:151497281
|
A | AT | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.24301-249dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497281 | ||||||
| chr2:151497319
|
A | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.24301-286T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497319 | ||||||
| chr2:151497398
|
A | AAAAG | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.24300+224_24300+22 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 171/181 | chr2 | 151497398 | ||||||
| chr2:151497725
|
G | A | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.24208-7C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 170/181 | chr2 | 151497725 | ||||||
| chr2:151498472
|
A | G | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24115-120T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498472 | ||||||
| chr2:151498669
|
A | G | 16 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.24115-317T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498669 | ||||||
| chr2:151498701
|
T | C | 16 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.24115-349A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498701 | ||||||
| chr2:151498744
|
T | C | 35 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(32): Show | 35 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.24115-392A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498744 | ||||||
| chr2:151498891
|
T | TAAA | 17 | a0015c0111t0001g0139a0016c0016t0002g0100a0016c0016t0002g0137others(14): Show | 17 | HG00639.hp2 HG01175.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.24114+404_24114+40 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498891 | ||||||
| chr2:151498891
|
T | TAAAA | 101 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.24114+403_24114+40 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498891 | ||||||
| chr2:151498891
|
T | TAAAAA | 7 | a0013c0014t0001g0099a0013c0014t0001g0102a0034c0147t0001g0178others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.24114+402_24114+40 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498891 | ||||||
| chr2:151498920
|
C | CAAAT | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.24114+374_24114+37 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498920 | ||||||
| chr2:151498951
|
T | TAA | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.24114+345_24114+34 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498951 | ||||||
| chr2:151498958
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24114+340G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151498958 | ||||||
| chr2:151499031
|
T | TATAA | 100 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.24114+263_24114+26 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151499031 | ||||||
| chr2:151499043
|
T | C | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.24114+255A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 169/181 | chr2 | 151499043 | ||||||
| chr2:151499811
|
C | T | 2 | a0004c0018t0001g0134a0004c0018t0001g0135 | 2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.24022-421G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151499811 | ||||||
| chr2:151499847
|
A | G | 100 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.24022-457T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151499847 | ||||||
| chr2:151500064
|
G | A | 1 | a0120c0023t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.24022-674C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500064 | ||||||
| chr2:151500106
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.24022-716T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500106 | ||||||
| chr2:151500143
|
T | TAAC | 12 | a0009c0017t0001g0121a0009c0017t0001g0159a0023c0043t0001g0047others(9): Show | 12 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.24022-756_24022-75 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500143 | ||||||
| chr2:151500288
|
A | C | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24022-898T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500288 | ||||||
| chr2:151500403
|
A | C | 1 | a0125c0028t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24021+988T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500403 | ||||||
| chr2:151500423
|
T | TAGAC | 100 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.24021+967_24021+96 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500423 | ||||||
| chr2:151500425
|
C | G | 100 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.24021+966G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500425 | ||||||
| chr2:151500444
|
A | AGAG | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.24021+944_24021+94 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500444 | ||||||
| chr2:151500593
|
C | CT | 99 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.24021+797dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500593 | ||||||
| chr2:151500644
|
T | C | 1 | a0067c0117t0001g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.24021+747A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500644 | ||||||
| chr2:151500754
|
C | T | 8 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0126others(5): Show | 8 | HG00423.hp1 HG02074.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.24021+637G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500754 | ||||||
| chr2:151500786
|
A | G | 1 | a0104c0059t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.24021+605T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500786 | ||||||
| chr2:151500851
|
G | A | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.24021+540C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500851 | ||||||
| chr2:151500870
|
G | A | 185 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.24021+521C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151500870 | ||||||
| chr2:151501088
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.24021+303C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151501088 | ||||||
| chr2:151501144
|
A | C | 2 | a0046c0091t0001g0017a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.24021+247T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151501144 | ||||||
| chr2:151501289
|
T | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.24021+102A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 168/181 | chr2 | 151501289 | ||||||
| chr2:151501528
|
T | C | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.23929-45A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501528 | ||||||
| chr2:151501721
|
C | T | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23929-238G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501721 | ||||||
| chr2:151501731
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23929-248C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501731 | ||||||
| chr2:151501772
|
A | G | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23929-289T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501772 | ||||||
| chr2:151501826
|
A | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23929-343T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501826 | ||||||
| chr2:151501836
|
A | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23929-353T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151501836 | ||||||
| chr2:151502097
|
T | C | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.23929-614A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502097 | ||||||
| chr2:151502209
|
G | GC | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23928+583_23928+58 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502209 | ||||||
| chr2:151502229
|
A | G | 127 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.23928+564T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502229 | ||||||
| chr2:151502293
|
C | A | 1 | a0003c0094t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.23928+500G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502293 | ||||||
| chr2:151502387
|
T | TA | 18 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(15): Show | 18 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.23928+405dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502387 | ||||||
| chr2:151502387
|
TA | T | 98 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.23928+405delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502387 | ||||||
| chr2:151502418
|
T | C | 127 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.23928+375A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502418 | ||||||
| chr2:151502521
|
T | C | 1 | a0038c0086t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.23928+272A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502521 | ||||||
| chr2:151502636
|
C | T | 1 | a0062c0106t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.23928+157G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502636 | ||||||
| chr2:151502762
|
A | AT | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.23928+30dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502762 | ||||||
| chr2:151502762
|
AT | A | 6 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(3): Show | 6 | HG02080.hp1 HG03491.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.23928+30delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 167/181 | chr2 | 151502762 | ||||||
| chr2:151503051
|
A | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23836-166T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 166/181 | chr2 | 151503051 | ||||||
| chr2:151503061
|
T | A | 1 | a0057c0114t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.23836-176A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 166/181 | chr2 | 151503061 | ||||||
| chr2:151503248
|
C | A | 4 | a0034c0147t0001g0178a0036c0029t0001g0176a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.23835+101G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 166/181 | chr2 | 151503248 | ||||||
| chr2:151503248
|
C | T | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23835+101G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 166/181 | chr2 | 151503248 | ||||||
| chr2:151503622
|
AT | A | 126 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.23743-182delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151503622 | ||||||
| chr2:151503707
|
T | C | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.23743-266A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151503707 | ||||||
| chr2:151503724
|
T | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23743-283A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151503724 | ||||||
| chr2:151503736
|
G | T | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23743-295C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151503736 | ||||||
| chr2:151503774
|
G | C | 1 | a0123c0034t0001g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.23743-333C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151503774 | ||||||
| chr2:151504053
|
G | A | 94 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.23743-612C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504053 | ||||||
| chr2:151504160
|
A | G | 21 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.23743-719T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504160 | ||||||
| chr2:151504208
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23743-767C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504208 | ||||||
| chr2:151504296
|
T | C | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23743-855A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504296 | ||||||
| chr2:151504531
|
G | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23742+947C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504531 | ||||||
| chr2:151504669
|
A | T | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23742+809T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504669 | ||||||
| chr2:151504741
|
A | G | 1 | a0120c0023t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23742+737T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151504741 | ||||||
| chr2:151505037
|
C | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.23742+441G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151505037 | ||||||
| chr2:151505270
|
C | T | 1 | a0113c0042t0001g0035 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.23742+208G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 165/181 | chr2 | 151505270 | ||||||
| chr2:151505822
|
C | T | 2 | a0046c0091t0001g0017a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.23650-252G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/181 | chr2 | 151505822 | ||||||
| chr2:151505884
|
G | C | 112 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.23649+282C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/181 | chr2 | 151505884 | ||||||
| chr2:151505909
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23649+257C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/181 | chr2 | 151505909 | ||||||
| chr2:151505971
|
T | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23649+195A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/181 | chr2 | 151505971 | ||||||
| chr2:151506074
|
T | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23649+92A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 164/181 | chr2 | 151506074 | ||||||
| chr2:151506369
|
T | C | 1 | a0099c0067t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.23557-111A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 163/181 | chr2 | 151506369 | ||||||
| chr2:151506687
|
A | G | 1 | a0083c0134t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.23556+222T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 163/181 | chr2 | 151506687 | ||||||
| chr2:151507143
|
C | T | 1 | a0043c0084t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.23452-130G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507143 | ||||||
| chr2:151507153
|
A | G | 2 | a0016c0016t0002g0137a0079c0130t0002g0105 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.23452-140T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507153 | ||||||
| chr2:151507449
|
T | G | 1 | a0075c0102t0001g0166 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23452-436A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507449 | ||||||
| chr2:151507529
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23451+476T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507529 | ||||||
| chr2:151507622
|
T | G | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.23451+383A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507622 | ||||||
| chr2:151507685
|
G | A | 122 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.23451+320C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507685 | ||||||
| chr2:151507786
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23451+219T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507786 | ||||||
| chr2:151507796
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23451+209G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507796 | ||||||
| chr2:151507991
|
T | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23451+14A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 162/181 | chr2 | 151507991 | ||||||
| chr2:151508171
|
C | G | 4 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123others(1): Show | 4 | HG03139.hp1 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23347-62G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508171 | ||||||
| chr2:151508400
|
C | G | 1 | a0001c0001t0001g0156 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.23347-291G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508400 | ||||||
| chr2:151508448
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23347-339C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508448 | ||||||
| chr2:151508457
|
G | A | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.23347-348C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508457 | ||||||
| chr2:151508474
|
T | A | 1 | a0039c0153t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.23347-365A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508474 | ||||||
| chr2:151508528
|
C | CAAAG | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23347-423_23347-42 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508528 | ||||||
| chr2:151508592
|
C | T | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.23347-483G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508592 | ||||||
| chr2:151508623
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23347-514C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508623 | ||||||
| chr2:151508628
|
T | G | 18 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(15): Show | 18 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.23347-519A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508628 | ||||||
| chr2:151508798
|
G | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23347-689C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508798 | ||||||
| chr2:151508826
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23347-717G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151508826 | ||||||
| chr2:151509151
|
C | A | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.23347-1042G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509151 | ||||||
| chr2:151509261
|
T | C | 123 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.23347-1152A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509261 | ||||||
| chr2:151509325
|
G | A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23347-1216C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509325 | ||||||
| chr2:151509327
|
A | AAAAC | 39 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.23347-1222_23347-1 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509327 | ||||||
| chr2:151509342
|
G | T | 6 | a0003c0094t0001g0014a0021c0057t0001g0037a0022c0054t0001g0030others(3): Show | 6 | HG00280.hp2 HG01074.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.23347-1233C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509342 | ||||||
| chr2:151509359
|
G | GAAAC | 18 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(15): Show | 18 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.23347-1254_23347-1 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509359 | ||||||
| chr2:151509427
|
A | G | 18 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(15): Show | 18 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.23347-1318T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509427 | ||||||
| chr2:151509570
|
G | A | 98 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.23347-1461C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509570 | ||||||
| chr2:151509570
|
G | C | 1 | a0123c0034t0001g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.23347-1461C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509570 | ||||||
| chr2:151509629
|
T | G | 1 | a0104c0059t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.23347-1520A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509629 | ||||||
| chr2:151509899
|
C | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.23347-1790G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151509899 | ||||||
| chr2:151510015
|
C | T | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23347-1906G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510015 | ||||||
| chr2:151510060
|
C | A | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00544.hp2 HG00673.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.23347-1951G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510060 | ||||||
| chr2:151510316
|
T | C | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.23347-2207A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510316 | ||||||
| chr2:151510485
|
A | G | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23346+2248T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510485 | ||||||
| chr2:151510614
|
A | G | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23346+2119T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510614 | ||||||
| chr2:151510645
|
T | G | 3 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.23346+2088A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510645 | ||||||
| chr2:151510826
|
T | C | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.23346+1907A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510826 | ||||||
| chr2:151510848
|
T | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23346+1885A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510848 | ||||||
| chr2:151510849
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23346+1884G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510849 | ||||||
| chr2:151510877
|
A | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23346+1856T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151510877 | ||||||
| chr2:151511119
|
C | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23346+1614G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511119 | ||||||
| chr2:151511174
|
A | G | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23346+1559T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511174 | ||||||
| chr2:151511271
|
C | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23346+1462G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511271 | ||||||
| chr2:151511348
|
C | T | 4 | a0028c0021t0001g0182a0028c0021t0001g0183a0119c0136t0001g0132others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.23346+1385G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511348 | ||||||
| chr2:151511392
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23346+1341G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511392 | ||||||
| chr2:151511541
|
C | G | 126 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.23346+1192G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511541 | ||||||
| chr2:151511558
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23346+1175C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511558 | ||||||
| chr2:151511564
|
A | G | 1 | a0132c0151t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.23346+1169T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511564 | ||||||
| chr2:151511707
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23346+1026G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511707 | ||||||
| chr2:151511877
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23346+856T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151511877 | ||||||
| chr2:151512019
|
C | CT | 11 | a0003c0005t0001g0006a0004c0019t0001g0148a0004c0019t0001g0151others(8): Show | 11 | HG00544.hp2 HG01891.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.23346+713dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
C | CTTTTTTT others(3): Show |
1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23346+704_23346+71 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
C | CTTTTTTT others(4): Show |
1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.23346+703_23346+71 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
CT | C | 5 | a0010c0137t0001g0093a0021c0056t0001g0041a0027c0013t0001g0071others(2): Show | 5 | HG01993.hp1 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.23346+713delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
CTTTTTTT others(1): Show |
C | 38 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.23346+706_23346+71 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
CTTTTTTT others(2): Show |
C | 57 | a0001c0001t0001g0125a0002c0002t0001g0026a0002c0002t0001g0036others(54): Show | 57 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.23346+705_23346+71 others(13): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512019
|
CTTTTTTT others(3): Show |
C | 3 | a0002c0002t0001g0060a0028c0021t0001g0182a0125c0028t0001g0031 | 3 | HG01993.hp2 HG02897.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.23346+704_23346+71 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512019 | ||||||
| chr2:151512030
|
T | C | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.23346+703A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512030 | ||||||
| chr2:151512082
|
G | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.23346+651C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512082 | ||||||
| chr2:151512192
|
G | A | 1 | a0059c0143t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.23346+541C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512192 | ||||||
| chr2:151512328
|
C | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.23346+405G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512328 | ||||||
| chr2:151512350
|
A | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.23346+383T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512350 | ||||||
| chr2:151512351
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23346+382T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512351 | ||||||
| chr2:151512415
|
G | A | 2 | a0028c0021t0001g0182a0028c0021t0001g0183 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.23346+318C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512415 | ||||||
| chr2:151512603
|
T | C | 186 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.23346+130A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512603 | ||||||
| chr2:151512708
|
G | T | 2 | a0046c0091t0001g0017a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.23346+25C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 161/181 | chr2 | 151512708 | ||||||
| chr2:151512852
|
C | T | 1 | a0047c0097t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.23242-15G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151512852 | ||||||
| chr2:151512883
|
C | CAACA | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23242-50_23242-47d others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151512883 | ||||||
| chr2:151513156
|
A | G | 1 | a0010c0139t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.23242-319T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151513156 | ||||||
| chr2:151513277
|
C | T | 127 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.23241+303G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151513277 | ||||||
| chr2:151513413
|
A | G | 3 | a0015c0108t0001g0136a0091c0142t0001g0119a0131c0149t0001g0181 | 3 | HG02257.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.23241+167T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151513413 | ||||||
| chr2:151513537
|
C | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.23241+43G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151513537 | ||||||
| chr2:151513538
|
A | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.23241+42T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 160/181 | chr2 | 151513538 | ||||||
| chr2:151513885
|
A | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.23128-192T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 159/181 | chr2 | 151513885 | ||||||
| chr2:151514295
|
C | T | 1 | a0065c0119t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.23127+23G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 159/181 | chr2 | 151514295 | ||||||
| chr2:151514487
|
G | A | 1 | a0057c0114t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.23017-59C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 158/181 | chr2 | 151514487 | ||||||
| chr2:151514548
|
A | G | 1 | a0031c0078t0001g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.23017-120T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 158/181 | chr2 | 151514548 | ||||||
| chr2:151515012
|
A | C | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.22906-84T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515012 | ||||||
| chr2:151515034
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22906-106A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515034 | ||||||
| chr2:151515070
|
CAT | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22906-144_22906-14 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515070 | ||||||
| chr2:151515219
|
G | A | 121 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.22906-291C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515219 | ||||||
| chr2:151515280
|
G | A | 13 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.22906-352C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515280 | ||||||
| chr2:151515413
|
A | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.22906-485T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515413 | ||||||
| chr2:151515515
|
G | T | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.22906-587C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515515 | ||||||
| chr2:151515630
|
G | A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.22906-702C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515630 | ||||||
| chr2:151515710
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.22905+749G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515710 | ||||||
| chr2:151515906
|
A | G | 36 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(33): Show | 36 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.22905+553T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151515906 | ||||||
| chr2:151516393
|
A | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.22905+66T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 157/181 | chr2 | 151516393 | ||||||
| chr2:151516871
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.22801-308G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151516871 | ||||||
| chr2:151517012
|
G | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22801-449C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517012 | ||||||
| chr2:151517277
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.22801-714C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517277 | ||||||
| chr2:151517293
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.22801-730C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517293 | ||||||
| chr2:151517587
|
TCA | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22800+729_22800+73 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517587 | ||||||
| chr2:151517833
|
A | G | 3 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.22800+485T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517833 | ||||||
| chr2:151517842
|
C | T | 1 | a0088c0037t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.22800+476G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151517842 | ||||||
| chr2:151518128
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22800+190T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151518128 | ||||||
| chr2:151518280
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22800+38T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151518280 | ||||||
| chr2:151518286
|
G | A | 98 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.22800+32C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151518286 | ||||||
| chr2:151518309
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.22800+9A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 156/181 | chr2 | 151518309 | ||||||
| chr2:151518478
|
A | G | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.22696-56T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 155/181 | chr2 | 151518478 | ||||||
| chr2:151518517
|
G | C | 2 | a0052c0100t0001g0142a0069c0120t0001g0104 | 2 | HG00558.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.22696-95C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 155/181 | chr2 | 151518517 | ||||||
| chr2:151518704
|
T | C | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.22695+261A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 155/181 | chr2 | 151518704 | ||||||
| chr2:151518725
|
A | T | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.22695+240T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 155/181 | chr2 | 151518725 | ||||||
| chr2:151519136
|
AAGTGAGA others(1): Show |
A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.22591-75_22591-68d others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 154/181 | chr2 | 151519136 | ||||||
| chr2:151519421
|
C | T | 125 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.22590+237G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 154/181 | chr2 | 151519421 | ||||||
| chr2:151519468
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22590+190A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 154/181 | chr2 | 151519468 | ||||||
| chr2:151519533
|
T | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22590+125A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 154/181 | chr2 | 151519533 | ||||||
| chr2:151520018
|
T | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22480-250A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520018 | ||||||
| chr2:151520037
|
AAC | A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.22480-271_22480-27 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520037 | ||||||
| chr2:151520039
|
CA | C | 93 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.22480-272delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520039 | ||||||
| chr2:151520039
|
CAA | C | 23 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.22480-273_22480-27 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520039 | ||||||
| chr2:151520167
|
G | T | 1 | a0112c0051t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22480-399C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520167 | ||||||
| chr2:151520224
|
A | C | 1 | a0069c0120t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.22480-456T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520224 | ||||||
| chr2:151520225
|
T | A | 4 | a0002c0002t0001g0026a0007c0003t0001g0001a0007c0003t0001g0002others(1): Show | 4 | HG01175.hp2 HG01258.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.22480-457A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520225 | ||||||
| chr2:151520291
|
G | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22480-523C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520291 | ||||||
| chr2:151520335
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22480-567C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520335 | ||||||
| chr2:151520443
|
G | A | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.22480-675C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520443 | ||||||
| chr2:151520571
|
A | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22480-803T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520571 | ||||||
| chr2:151520596
|
G | A | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.22480-828C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520596 | ||||||
| chr2:151520742
|
T | TA | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.22480-975dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520742 | ||||||
| chr2:151520865
|
CAAAA | C | 19 | a0015c0111t0001g0139a0016c0016t0002g0100a0016c0016t0002g0137others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.22480-1101_22480-1 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151520865 | ||||||
| chr2:151521339
|
C | T | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22480-1571G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521339 | ||||||
| chr2:151521385
|
C | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22480-1617G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521385 | ||||||
| chr2:151521645
|
T | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.22480-1877A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521645 | ||||||
| chr2:151521658
|
A | G | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.22480-1890T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521658 | ||||||
| chr2:151521792
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22480-2024T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521792 | ||||||
| chr2:151521893
|
A | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.22480-2125T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151521893 | ||||||
| chr2:151522192
|
G | T | 2 | a0011c0009t0001g0040a0011c0070t0001g0055 | 2 | HG01358.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.22479+2119C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151522192 | ||||||
| chr2:151522440
|
C | T | 98 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.22479+1871G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151522440 | ||||||
| chr2:151522441
|
A | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.22479+1870T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151522441 | ||||||
| chr2:151522492
|
A | C | 1 | a0002c0048t0001g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.22479+1819T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151522492 | ||||||
| chr2:151522771
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.22479+1540G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151522771 | ||||||
| chr2:151523046
|
G | A | 1 | a0059c0143t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.22479+1265C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523046 | ||||||
| chr2:151523343
|
C | T | 22 | a0015c0111t0001g0139a0016c0016t0002g0100a0016c0016t0002g0137others(19): Show | 22 | HG00639.hp2 HG01175.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.22479+968G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523343 | ||||||
| chr2:151523350
|
T | C | 1 | a0043c0084t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.22479+961A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523350 | ||||||
| chr2:151523510
|
T | C | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.22479+801A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523510 | ||||||
| chr2:151523692
|
A | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22479+619T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523692 | ||||||
| chr2:151523792
|
A | C | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.22479+519T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523792 | ||||||
| chr2:151523858
|
GC | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.22479+452delG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151523858 | ||||||
| chr2:151524020
|
A | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.22479+291T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 153/181 | chr2 | 151524020 | ||||||
| chr2:151524654
|
C | CT | 7 | a0010c0139t0001g0106a0069c0120t0001g0104a0079c0130t0002g0105others(4): Show | 7 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.22273-39dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 151/181 | chr2 | 151524654 | ||||||
| chr2:151524654
|
C | CTT | 7 | a0009c0017t0001g0159a0023c0043t0001g0047a0060c0107t0001g0157others(4): Show | 7 | HG00544.hp1 HG00597.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.22273-40_22273-39d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 151/181 | chr2 | 151524654 | ||||||
| chr2:151524654
|
CT | C | 63 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.22273-39delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 151/181 | chr2 | 151524654 | ||||||
| chr2:151524654
|
CTT | C | 35 | a0002c0002t0001g0036a0002c0002t0001g0039a0002c0002t0001g0046others(32): Show | 35 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.22273-40_22273-39d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 151/181 | chr2 | 151524654 | ||||||
| chr2:151525133
|
C | T | 1 | a0010c0139t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.22272+30G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 151/181 | chr2 | 151525133 | ||||||
| chr2:151525330
|
T | C | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.22162-57A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525330 | ||||||
| chr2:151525381
|
G | A | 102 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.22162-108C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525381 | ||||||
| chr2:151525472
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.22162-199C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525472 | ||||||
| chr2:151525562
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0112a0059c0143t0001g0161others(2): Show | 5 | HG00423.hp1 HG02074.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.22162-289G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525562 | ||||||
| chr2:151525660
|
T | TAATA | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.22161+294_22161+29 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525660 | ||||||
| chr2:151525685
|
A | G | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.22161+273T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525685 | ||||||
| chr2:151525815
|
G | A | 116 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.22161+143C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525815 | ||||||
| chr2:151525940
|
C | G | 102 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.22161+18G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 150/181 | chr2 | 151525940 | ||||||
| chr2:151526113
|
G | A | 1 | a0086c0032t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.22050+45C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 149/181 | chr2 | 151526113 | ||||||
| chr2:151526114
|
T | C | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.22050+44A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 149/181 | chr2 | 151526114 | ||||||
| chr2:151526145
|
G | A | 2 | a0046c0091t0001g0017a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.22050+13C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 149/181 | chr2 | 151526145 | ||||||
| chr2:151526345
|
A | G | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.21946-83T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526345 | ||||||
| chr2:151526497
|
C | T | 9 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.21946-235G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526497 | ||||||
| chr2:151526508
|
C | T | 2 | a0035c0146t0001g0103a0112c0051t0001g0072 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.21946-246G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526508 | ||||||
| chr2:151526548
|
G | A | 24 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(21): Show | 24 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.21946-286C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526548 | ||||||
| chr2:151526635
|
A | G | 1 | a0015c0111t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.21945+283T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526635 | ||||||
| chr2:151526701
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21945+217A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526701 | ||||||
| chr2:151526768
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.21945+150G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526768 | ||||||
| chr2:151526786
|
A | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.21945+132T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526786 | ||||||
| chr2:151526834
|
T | G | 8 | a0036c0029t0001g0176a0046c0091t0001g0017a0049c0096t0001g0184others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.21945+84A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 148/181 | chr2 | 151526834 | ||||||
| chr2:151527040
|
C | T | 1 | a0090c0035t0001g0054 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.21841-18G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 147/181 | chr2 | 151527040 | ||||||
| chr2:151527399
|
T | C | 123 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.21840+82A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 147/181 | chr2 | 151527399 | ||||||
| chr2:151527448
|
C | T | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.21840+33G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 147/181 | chr2 | 151527448 | ||||||
| chr2:151527468
|
T | G | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.21840+13A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 147/181 | chr2 | 151527468 | ||||||
| chr2:151527749
|
C | T | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.21736-164G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151527749 | ||||||
| chr2:151527837
|
A | G | 3 | a0004c0018t0001g0134a0004c0018t0001g0135a0047c0097t0001g0185 | 3 | HG02040.hp1 NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.21736-252T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151527837 | ||||||
| chr2:151527852
|
C | T | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.21736-267G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151527852 | ||||||
| chr2:151527863
|
T | C | 122 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.21736-278A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151527863 | ||||||
| chr2:151527956
|
C | G | 1 | a0052c0100t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.21736-371G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151527956 | ||||||
| chr2:151528009
|
A | T | 1 | a0069c0120t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.21736-424T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151528009 | ||||||
| chr2:151528363
|
T | C | 1 | a0010c0138t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.21736-778A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151528363 | ||||||
| chr2:151528547
|
G | A | 2 | a0051c0131t0001g0187a0083c0134t0001g0153 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.21735+663C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151528547 | ||||||
| chr2:151528703
|
C | T | 37 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(34): Show | 37 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.21735+507G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151528703 | ||||||
| chr2:151528775
|
C | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.21735+435G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151528775 | ||||||
| chr2:151529066
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.21735+144G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 146/181 | chr2 | 151529066 | ||||||
| chr2:151529521
|
G | A | 5 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.21631-207C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529521 | ||||||
| chr2:151529534
|
A | AT | 39 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.21631-221dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529534 | ||||||
| chr2:151529534
|
AT | A | 13 | a0022c0054t0001g0030a0033c0024t0001g0096a0036c0029t0001g0176others(10): Show | 13 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.21631-221delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529534 | ||||||
| chr2:151529655
|
T | C | 1 | a0088c0037t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.21631-341A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529655 | ||||||
| chr2:151529676
|
A | G | 122 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.21631-362T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529676 | ||||||
| chr2:151529773
|
G | A | 1 | a0009c0109t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.21631-459C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529773 | ||||||
| chr2:151529878
|
A | C | 126 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.21631-564T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151529878 | ||||||
| chr2:151530414
|
C | T | 6 | a0002c0002t0001g0039a0002c0002t0001g0049a0002c0002t0001g0050others(3): Show | 6 | HG00558.hp2 HG00621.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.21630+580G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151530414 | ||||||
| chr2:151530427
|
T | C | 1 | a0014c0113t0001g0120 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.21630+567A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151530427 | ||||||
| chr2:151530578
|
G | A | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.21630+416C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151530578 | ||||||
| chr2:151530598
|
A | C | 33 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(30): Show | 33 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.21630+396T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 145/181 | chr2 | 151530598 | ||||||
| chr2:151531248
|
T | C | 122 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.21523-147A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531248 | ||||||
| chr2:151531251
|
A | C | 6 | a0015c0108t0001g0136a0015c0111t0001g0139a0057c0114t0002g0115others(3): Show | 6 | HG01175.hp1 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.21523-150T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531251 | ||||||
| chr2:151531300
|
T | TTTTC | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.21523-203_21523-20 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531300 | ||||||
| chr2:151531308
|
C | CT | 8 | a0003c0083t0001g0003a0004c0019t0001g0148a0008c0004t0001g0009others(5): Show | 8 | HG01099.hp1 HG01192.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.21523-208dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531308 | ||||||
| chr2:151531308
|
CT | C | 16 | a0001c0001t0001g0097a0003c0005t0001g0004a0005c0008t0001g0038others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.21523-208delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531308 | ||||||
| chr2:151531308
|
CTT | C | 47 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.21523-209_21523-20 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531308 | ||||||
| chr2:151531308
|
CTTT | C | 33 | a0002c0002t0001g0036a0002c0002t0001g0039a0002c0002t0001g0046others(30): Show | 33 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.21523-210_21523-20 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531308 | ||||||
| chr2:151531360
|
A | C | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.21523-259T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531360 | ||||||
| chr2:151531444
|
G | C | 1 | a0045c0089t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.21523-343C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531444 | ||||||
| chr2:151531570
|
G | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.21522+222C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531570 | ||||||
| chr2:151531631
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.21522+161A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531631 | ||||||
| chr2:151531667
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.21522+125C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531667 | ||||||
| chr2:151531678
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.21522+114A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531678 | ||||||
| chr2:151531714
|
G | C | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.21522+78C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 144/181 | chr2 | 151531714 | ||||||
| chr2:151531901
|
AT | A | 86 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
splice_region_variant&intron_variant | LOW | c.21418-6delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151531901 | ||||||
| chr2:151531943
|
G | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.21418-47C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151531943 | ||||||
| chr2:151531985
|
A | G | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.21418-89T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151531985 | ||||||
| chr2:151532139
|
C | T | 2 | a0011c0009t0001g0040a0011c0070t0001g0055 | 2 | HG01358.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.21418-243G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532139 | ||||||
| chr2:151532192
|
A | G | 134 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.21418-296T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532192 | ||||||
| chr2:151532253
|
G | A | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.21418-357C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532253 | ||||||
| chr2:151532732
|
G | A | 3 | a0016c0016t0002g0100a0016c0016t0002g0137a0079c0130t0002g0105 | 3 | HG02965.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.21417+710C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532732 | ||||||
| chr2:151532746
|
CT | C | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.21417+695delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532746 | ||||||
| chr2:151532976
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.21417+466G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151532976 | ||||||
| chr2:151533028
|
T | C | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.21417+414A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 143/181 | chr2 | 151533028 | ||||||
| chr2:151533736
|
C | T | 5 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.21313-190G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151533736 | ||||||
| chr2:151533864
|
C | T | 4 | a0028c0021t0001g0182a0028c0021t0001g0183a0119c0136t0001g0132others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.21313-318G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151533864 | ||||||
| chr2:151533935
|
T | C | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.21313-389A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151533935 | ||||||
| chr2:151534061
|
C | T | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.21313-515G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534061 | ||||||
| chr2:151534284
|
A | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.21313-738T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534284 | ||||||
| chr2:151534520
|
T | C | 9 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.21313-974A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534520 | ||||||
| chr2:151534663
|
A | G | 105 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.21312+1028T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534663 | ||||||
| chr2:151534745
|
C | T | 181 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.21312+946G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534745 | ||||||
| chr2:151534861
|
G | T | 2 | a0009c0017t0001g0121a0032c0077t0001g0175 | 2 | NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.21312+830C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534861 | ||||||
| chr2:151534983
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.21312+708C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151534983 | ||||||
| chr2:151535078
|
G | A | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.21312+613C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 142/181 | chr2 | 151535078 | ||||||
| chr2:151535883
|
A | G | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.21208-88T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151535883 | ||||||
| chr2:151535993
|
G | A | 25 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.21208-198C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151535993 | ||||||
| chr2:151536151
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.21208-356C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536151 | ||||||
| chr2:151536273
|
T | C | 25 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.21208-478A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536273 | ||||||
| chr2:151536463
|
G | A | 4 | a0002c0002t0001g0026a0007c0003t0001g0001a0007c0003t0001g0002others(1): Show | 4 | HG01175.hp2 HG01258.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.21208-668C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536463 | ||||||
| chr2:151536540
|
T | A | 95 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.21207+592A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536540 | ||||||
| chr2:151536782
|
C | T | 105 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.21207+350G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536782 | ||||||
| chr2:151536785
|
C | T | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.21207+347G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536785 | ||||||
| chr2:151536908
|
T | C | 32 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(29): Show | 32 | HG00280.hp2 HG00673.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.21207+224A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 141/181 | chr2 | 151536908 | ||||||
| chr2:151537313
|
A | T | 15 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(12): Show | 15 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.21103-77T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 140/181 | chr2 | 151537313 | ||||||
| chr2:151537328
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.21103-92T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 140/181 | chr2 | 151537328 | ||||||
| chr2:151537491
|
A | G | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.21103-255T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 140/181 | chr2 | 151537491 | ||||||
| chr2:151537592
|
G | C | 104 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.21102+280C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 140/181 | chr2 | 151537592 | ||||||
| chr2:151538020
|
T | G | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.20998-44A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 139/181 | chr2 | 151538020 | ||||||
| chr2:151538255
|
A | G | 2 | a0109c0046t0001g0048a0118c0073t0001g0051 | 2 | NA18947.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.20893-11T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151538255 | ||||||
| chr2:151538268
|
A | G | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20893-24T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151538268 | ||||||
| chr2:151538718
|
T | TA | 3 | a0008c0004t0001g0011a0008c0004t0001g0012a0058c0110t0001g0149 | 3 | HG02976.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.20893-475dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151538718 | ||||||
| chr2:151539455
|
C | T | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20892+889G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151539455 | ||||||
| chr2:151539826
|
A | G | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20892+518T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151539826 | ||||||
| chr2:151539877
|
C | T | 2 | a0001c0001t0001g0125a0070c0123t0001g0116 | 2 | NA18966.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.20892+467G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151539877 | ||||||
| chr2:151539927
|
A | G | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20892+417T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151539927 | ||||||
| chr2:151540000
|
C | T | 1 | a0031c0078t0001g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.20892+344G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540000 | ||||||
| chr2:151540093
|
C | T | 25 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.20892+251G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540093 | ||||||
| chr2:151540131
|
A | G | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.20892+213T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540131 | ||||||
| chr2:151540187
|
T | C | 1 | a0088c0037t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20892+157A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540187 | ||||||
| chr2:151540212
|
T | TA | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20892+131dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540212 | ||||||
| chr2:151540222
|
T | C | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.20892+122A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 138/181 | chr2 | 151540222 | ||||||
| chr2:151540611
|
G | T | 1 | a0081c0141t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.20787+86C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 137/181 | chr2 | 151540611 | ||||||
| chr2:151540680
|
C | G | 1 | a0069c0120t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.20787+17G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 137/181 | chr2 | 151540680 | ||||||
| chr2:151540920
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.20683-119A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 136/181 | chr2 | 151540920 | ||||||
| chr2:151540950
|
G | A | 3 | a0036c0029t0001g0176a0087c0132t0001g0101a0105c0080t0001g0034 | 3 | HG01884.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.20683-149C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 136/181 | chr2 | 151540950 | ||||||
| chr2:151541100
|
C | G | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.20683-299G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 136/181 | chr2 | 151541100 | ||||||
| chr2:151541404
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.20682+43G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 136/181 | chr2 | 151541404 | ||||||
| chr2:151541889
|
T | C | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20578-338A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151541889 | ||||||
| chr2:151542058
|
G | A | 131 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.20578-507C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151542058 | ||||||
| chr2:151543223
|
G | A | 1 | a0045c0089t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20578-1672C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151543223 | ||||||
| chr2:151543300
|
A | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20578-1749T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151543300 | ||||||
| chr2:151543675
|
C | T | 1 | a0009c0017t0001g0121 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20578-2124G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151543675 | ||||||
| chr2:151543712
|
C | G | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20578-2161G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151543712 | ||||||
| chr2:151543716
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.20578-2165G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151543716 | ||||||
| chr2:151544033
|
T | C | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.20577+1855A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544033 | ||||||
| chr2:151544101
|
T | G | 16 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(13): Show | 16 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.20577+1787A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544101 | ||||||
| chr2:151544191
|
A | G | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.20577+1697T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544191 | ||||||
| chr2:151544218
|
C | T | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.20577+1670G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544218 | ||||||
| chr2:151544368
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.20577+1520G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544368 | ||||||
| chr2:151544571
|
G | A | 5 | a0035c0146t0001g0103a0049c0096t0001g0184a0065c0119t0001g0145others(2): Show | 5 | HG00639.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.20577+1317C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544571 | ||||||
| chr2:151544797
|
C | A | 99 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.20577+1091G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544797 | ||||||
| chr2:151544827
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.20577+1061A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544827 | ||||||
| chr2:151544853
|
A | T | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.20577+1035T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544853 | ||||||
| chr2:151544955
|
G | A | 2 | a0005c0063t0001g0052a0005c0064t0001g0083 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.20577+933C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544955 | ||||||
| chr2:151544981
|
C | T | 1 | a0005c0063t0001g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20577+907G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151544981 | ||||||
| chr2:151545045
|
C | G | 2 | a0009c0017t0001g0121a0032c0077t0001g0175 | 2 | NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.20577+843G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545045 | ||||||
| chr2:151545165
|
G | A | 104 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.20577+723C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545165 | ||||||
| chr2:151545211
|
C | G | 5 | a0035c0146t0001g0103a0049c0096t0001g0184a0065c0119t0001g0145others(2): Show | 5 | HG00639.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.20577+677G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545211 | ||||||
| chr2:151545280
|
AATT | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.20577+605_20577+60 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545280 | ||||||
| chr2:151545305
|
G | A | 25 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.20577+583C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545305 | ||||||
| chr2:151545375
|
A | C | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.20577+513T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545375 | ||||||
| chr2:151545431
|
C | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.20577+457G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545431 | ||||||
| chr2:151545657
|
C | A | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.20577+231G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 135/181 | chr2 | 151545657 | ||||||
| chr2:151546001
|
T | TA | 45 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(42): Show | 45 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.20467-4dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546001 | ||||||
| chr2:151546001
|
T | TAA | 39 | a0001c0001t0001g0097a0001c0001t0001g0125a0001c0082t0001g0147others(36): Show | 39 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.20467-5_20467-4dup others(2): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546001 | ||||||
| chr2:151546001
|
T | TAAA | 5 | a0002c0002t0001g0049a0036c0029t0001g0176a0046c0091t0001g0017others(2): Show | 5 | HG00621.hp2 HG01884.hp1 HG02886.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.20467-6_20467-4dup others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546001 | ||||||
| chr2:151546001
|
TA | T | 9 | a0004c0018t0001g0134a0004c0018t0001g0135a0004c0019t0001g0148others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.20467-4delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546001 | ||||||
| chr2:151546002
|
A | T | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.20467-4T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546002 | ||||||
| chr2:151546149
|
C | T | 5 | a0036c0029t0001g0176a0037c0087t0001g0107a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.20467-151G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546149 | ||||||
| chr2:151546197
|
A | G | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.20466+148T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 134/181 | chr2 | 151546197 | ||||||
| chr2:151546500
|
C | T | 103 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.20368-57G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546500 | ||||||
| chr2:151546557
|
C | CT | 91 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.20368-115dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546557 | ||||||
| chr2:151546557
|
C | CTT | 21 | a0009c0017t0001g0121a0009c0017t0001g0159a0010c0137t0001g0093others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.20368-116_20368-11 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546557 | ||||||
| chr2:151546637
|
C | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.20368-194G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546637 | ||||||
| chr2:151546892
|
A | T | 1 | a0062c0106t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.20368-449T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546892 | ||||||
| chr2:151546933
|
C | G | 4 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(1): Show | 4 | HG01192.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.20368-490G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151546933 | ||||||
| chr2:151547067
|
C | G | 25 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.20367+362G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151547067 | ||||||
| chr2:151547168
|
A | G | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.20367+261T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151547168 | ||||||
| chr2:151547344
|
C | T | 1 | a0132c0151t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20367+85G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151547344 | ||||||
| chr2:151547350
|
C | T | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20367+79G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151547350 | ||||||
| chr2:151547413
|
C | G | 2 | a0023c0044t0001g0068a0126c0027t0001g0067 | 2 | HG00673.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.20367+16G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 133/181 | chr2 | 151547413 | ||||||
| chr2:151547551
|
C | T | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20263-18G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 132/181 | chr2 | 151547551 | ||||||
| chr2:151547780
|
C | T | 128 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.20158-42G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 131/181 | chr2 | 151547780 | ||||||
| chr2:151547866
|
G | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.20158-128C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 131/181 | chr2 | 151547866 | ||||||
| chr2:151547942
|
T | C | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.20158-204A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 131/181 | chr2 | 151547942 | ||||||
| chr2:151548261
|
G | A | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.20157+47C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 131/181 | chr2 | 151548261 | ||||||
| chr2:151548774
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20050-359C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151548774 | ||||||
| chr2:151548955
|
G | A | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20050-540C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151548955 | ||||||
| chr2:151549299
|
T | C | 94 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.20049+337A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151549299 | ||||||
| chr2:151549351
|
G | A | 1 | a0132c0151t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20049+285C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151549351 | ||||||
| chr2:151549479
|
C | A | 18 | a0004c0019t0001g0148a0009c0017t0001g0121a0009c0017t0001g0159others(15): Show | 18 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.20049+157G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151549479 | ||||||
| chr2:151549533
|
A | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.20049+103T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 130/181 | chr2 | 151549533 | ||||||
| chr2:151549881
|
G | T | 2 | a0004c0018t0001g0134a0004c0018t0001g0135 | 2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.19945-141C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151549881 | ||||||
| chr2:151549985
|
T | G | 1 | a0009c0109t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.19945-245A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151549985 | ||||||
| chr2:151550096
|
A | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.19945-356T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550096 | ||||||
| chr2:151550103
|
T | C | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.19945-363A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550103 | ||||||
| chr2:151550188
|
G | T | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.19945-448C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550188 | ||||||
| chr2:151550227
|
G | A | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19945-487C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550227 | ||||||
| chr2:151550266
|
CA | C | 88 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.19945-527delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550266 | ||||||
| chr2:151550266
|
CAA | C | 49 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0046others(46): Show | 49 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.19945-528_19945-52 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550266 | ||||||
| chr2:151550266
|
CAAAA | C | 22 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(19): Show | 22 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.19945-530_19945-52 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550266 | ||||||
| chr2:151550287
|
A | C | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19945-547T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550287 | ||||||
| chr2:151550433
|
C | T | 2 | a0091c0142t0001g0119a0114c0055t0001g0044 | 2 | HG01515.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.19945-693G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550433 | ||||||
| chr2:151550713
|
C | T | 99 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.19945-973G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550713 | ||||||
| chr2:151550716
|
C | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.19945-976G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550716 | ||||||
| chr2:151550853
|
T | C | 94 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.19944+885A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550853 | ||||||
| chr2:151550947
|
A | AATT | 56 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0124others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.19944+788_19944+79 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151550947
|
A | AATTATT | 7 | a0002c0002t0001g0050a0009c0017t0001g0121a0033c0024t0001g0096others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.19944+785_19944+79 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151550947
|
A | AATTATTA others(2): Show |
25 | a0004c0018t0001g0134a0004c0018t0001g0135a0008c0004t0001g0009others(22): Show | 25 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.19944+782_19944+79 others(13): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151550947
|
A | AATTATTA others(5): Show |
6 | a0015c0108t0001g0136a0021c0056t0001g0041a0042c0095t0001g0020others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.19944+779_19944+79 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151550947
|
A | AATTATTA others(8): Show |
6 | a0025c0011t0001g0089a0025c0011t0001g0090a0037c0087t0001g0107others(3): Show | 6 | HG00639.hp2 HG01891.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.19944+776_19944+79 others(19): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151550947
|
A | AATTATTA others(11): Show |
3 | a0035c0146t0001g0103a0050c0099t0001g0098a0103c0066t0001g0065 | 3 | HG00639.hp1 HG03654.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19944+773_19944+79 others(22): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151550947 | ||||||
| chr2:151551097
|
AGCTGGGA others(129): Show |
A | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.19944+505_19944+64 others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551097 | ||||||
| chr2:151551148
|
T | C | 1 | a0007c0003t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19944+590A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551148 | ||||||
| chr2:151551306
|
G | C | 1 | a0003c0005t0001g0006 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.19944+432C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551306 | ||||||
| chr2:151551418
|
T | C | 5 | a0017c0015t0001g0164a0017c0015t0001g0165a0043c0084t0001g0018others(2): Show | 5 | HG00544.hp2 HG02683.hp1 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.19944+320A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551418 | ||||||
| chr2:151551520
|
G | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.19944+218C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551520 | ||||||
| chr2:151551628
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.19944+110A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 129/181 | chr2 | 151551628 | ||||||
| chr2:151552119
|
T | C | 2 | a0129c0022t0001g0114a0133c0152t0001g0169 | 2 | HG01192.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.19837-274A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/181 | chr2 | 151552119 | ||||||
| chr2:151552152
|
G | C | 1 | a0014c0113t0001g0120 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19837-307C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/181 | chr2 | 151552152 | ||||||
| chr2:151552275
|
T | C | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.19836+397A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/181 | chr2 | 151552275 | ||||||
| chr2:151552459
|
C | G | 103 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.19836+213G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/181 | chr2 | 151552459 | ||||||
| chr2:151552662
|
G | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19836+10C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 128/181 | chr2 | 151552662 | ||||||
| chr2:151552782
|
G | A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.19732-6C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 127/181 | chr2 | 151552782 | ||||||
| chr2:151552902
|
C | T | 103 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.19732-126G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 127/181 | chr2 | 151552902 | ||||||
| chr2:151553196
|
C | T | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.19731+202G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 127/181 | chr2 | 151553196 | ||||||
| chr2:151553295
|
C | A | 93 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.19731+103G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 127/181 | chr2 | 151553295 | ||||||
| chr2:151553796
|
G | A | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.19626+32C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 126/181 | chr2 | 151553796 | ||||||
| chr2:151554095
|
G | A | 5 | a0035c0146t0001g0103a0049c0096t0001g0184a0065c0119t0001g0145others(2): Show | 5 | HG00639.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.19429-70C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 125/181 | chr2 | 151554095 | ||||||
| chr2:151554181
|
A | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.19429-156T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 125/181 | chr2 | 151554181 | ||||||
| chr2:151554218
|
A | G | 60 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(57): Show | 60 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.19429-193T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 125/181 | chr2 | 151554218 | ||||||
| chr2:151555267
|
T | C | 1 | a0101c0068t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19315-223A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555267 | ||||||
| chr2:151555429
|
G | A | 58 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.19315-385C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555429 | ||||||
| chr2:151555689
|
C | T | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.19315-645G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555689 | ||||||
| chr2:151555786
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.19315-742T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555786 | ||||||
| chr2:151555803
|
C | A | 2 | a0001c0001t0001g0124a0116c0052t0001g0069 | 2 | NA18946.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.19315-759G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555803 | ||||||
| chr2:151555871
|
T | TA | 110 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.19315-828dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555871 | ||||||
| chr2:151555871
|
T | TAA | 5 | a0036c0029t0001g0176a0046c0091t0001g0017a0056c0145t0001g0177others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.19315-829_19315-82 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555871 | ||||||
| chr2:151555923
|
T | A | 22 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(19): Show | 22 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.19315-879A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151555923 | ||||||
| chr2:151556292
|
C | T | 58 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.19315-1248G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556292 | ||||||
| chr2:151556299
|
C | T | 61 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.19315-1255G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556299 | ||||||
| chr2:151556371
|
G | A | 1 | a0062c0106t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19315-1327C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556371 | ||||||
| chr2:151556424
|
G | A | 1 | a0100c0072t0001g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.19315-1380C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556424 | ||||||
| chr2:151556578
|
C | T | 1 | a0129c0022t0001g0114 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.19315-1534G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556578 | ||||||
| chr2:151556744
|
A | C | 61 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.19315-1700T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556744 | ||||||
| chr2:151556779
|
C | CA | 130 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.19315-1736_19315-1 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556779 | ||||||
| chr2:151556801
|
A | G | 35 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.19315-1757T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556801 | ||||||
| chr2:151556922
|
C | G | 15 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(12): Show | 15 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.19315-1878G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556922 | ||||||
| chr2:151556937
|
TA | T | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.19315-1894delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151556937 | ||||||
| chr2:151557073
|
C | T | 1 | a0096c0060t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19315-2029G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557073 | ||||||
| chr2:151557198
|
C | A | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.19315-2154G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557198 | ||||||
| chr2:151557342
|
C | T | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.19315-2298G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557342 | ||||||
| chr2:151557410
|
T | C | 61 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.19315-2366A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557410 | ||||||
| chr2:151557411
|
G | A | 59 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.19315-2367C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557411 | ||||||
| chr2:151557453
|
G | A | 59 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.19315-2409C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557453 | ||||||
| chr2:151557569
|
A | G | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.19315-2525T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557569 | ||||||
| chr2:151557690
|
A | G | 65 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(62): Show | 65 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.19315-2646T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557690 | ||||||
| chr2:151557711
|
A | G | 2 | a0003c0005t0001g0013a0068c0125t0001g0111 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.19315-2667T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557711 | ||||||
| chr2:151557733
|
T | C | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19315-2689A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557733 | ||||||
| chr2:151557958
|
C | T | 1 | a0014c0113t0001g0120 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19314+2634G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151557958 | ||||||
| chr2:151558066
|
A | G | 1 | a0005c0008t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.19314+2526T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151558066 | ||||||
| chr2:151558327
|
C | T | 1 | a0090c0035t0001g0054 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.19314+2265G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151558327 | ||||||
| chr2:151558530
|
C | T | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.19314+2062G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151558530 | ||||||
| chr2:151558847
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19314+1745G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151558847 | ||||||
| chr2:151558881
|
C | T | 64 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.19314+1711G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151558881 | ||||||
| chr2:151559103
|
AAAC | A | 59 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.19314+1486_19314+1 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559103 | ||||||
| chr2:151559105
|
A | G | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.19314+1487T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559105 | ||||||
| chr2:151559346
|
G | C | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.19314+1246C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559346 | ||||||
| chr2:151559472
|
C | T | 15 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(12): Show | 15 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.19314+1120G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559472 | ||||||
| chr2:151559492
|
G | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19314+1100C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559492 | ||||||
| chr2:151559507
|
C | T | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19314+1085G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559507 | ||||||
| chr2:151559734
|
G | A | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19314+858C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559734 | ||||||
| chr2:151559849
|
T | C | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19314+743A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559849 | ||||||
| chr2:151559963
|
G | A | 55 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(52): Show | 55 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.19314+629C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151559963 | ||||||
| chr2:151560022
|
A | G | 35 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.19314+570T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151560022 | ||||||
| chr2:151560322
|
C | T | 2 | a0057c0114t0002g0115a0093c0058t0002g0025 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19314+270G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151560322 | ||||||
| chr2:151560418
|
C | T | 21 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(18): Show | 21 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.19314+174G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151560418 | ||||||
| chr2:151560550
|
G | A | 56 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.19314+42C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 124/181 | chr2 | 151560550 | ||||||
| chr2:151560775
|
T | C | 2 | a0014c0112t0001g0141a0095c0062t0001g0081 | 2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.19207-76A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 123/181 | chr2 | 151560775 | ||||||
| chr2:151560797
|
T | TC | 38 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.19207-99dupG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 123/181 | chr2 | 151560797 | ||||||
| chr2:151560958
|
G | T | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.19206+46C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 123/181 | chr2 | 151560958 | ||||||
| chr2:151561167
|
G | A | 23 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(20): Show | 23 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.19101+41C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 122/181 | chr2 | 151561167 | ||||||
| chr2:151561322
|
A | G | 4 | a0016c0016t0002g0100a0016c0016t0002g0137a0041c0085t0002g0010others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.18997-10T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561322 | ||||||
| chr2:151561457
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18997-145C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561457 | ||||||
| chr2:151561484
|
G | C | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.18997-172C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561484 | ||||||
| chr2:151561485
|
C | T | 134 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.18997-173G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561485 | ||||||
| chr2:151561505
|
G | C | 4 | a0002c0002t0001g0026a0007c0003t0001g0001a0007c0003t0001g0002others(1): Show | 4 | HG01175.hp2 HG01258.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.18997-193C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561505 | ||||||
| chr2:151561508
|
T | C | 134 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.18997-196A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561508 | ||||||
| chr2:151561572
|
C | CT | 26 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.18997-261dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561572 | ||||||
| chr2:151561597
|
A | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18997-285T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561597 | ||||||
| chr2:151561598
|
CT | C | 9 | a0015c0108t0001g0136a0028c0021t0001g0182a0028c0021t0001g0183others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.18997-287delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561598 | ||||||
| chr2:151561608
|
T | A | 11 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(8): Show | 11 | HG00544.hp2 HG00639.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.18997-296A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561608 | ||||||
| chr2:151561609
|
TTA | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18997-299_18997-29 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561609 | ||||||
| chr2:151561719
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.18996+391A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561719 | ||||||
| chr2:151561754
|
C | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18996+356G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561754 | ||||||
| chr2:151561882
|
G | A | 10 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.18996+228C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151561882 | ||||||
| chr2:151562067
|
T | C | 1 | a0120c0023t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.18996+43A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 121/181 | chr2 | 151562067 | ||||||
| chr2:151562279
|
A | C | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.18892-65T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/181 | chr2 | 151562279 | ||||||
| chr2:151562292
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18892-78A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/181 | chr2 | 151562292 | ||||||
| chr2:151562404
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18892-190A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/181 | chr2 | 151562404 | ||||||
| chr2:151562429
|
T | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.18891+182A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/181 | chr2 | 151562429 | ||||||
| chr2:151562524
|
C | T | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.18891+87G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 120/181 | chr2 | 151562524 | ||||||
| chr2:151562878
|
A | T | 5 | a0017c0015t0001g0164a0017c0015t0001g0165a0043c0084t0001g0018others(2): Show | 5 | HG00544.hp2 HG02683.hp1 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.18694-70T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151562878 | ||||||
| chr2:151563011
|
CT | C | 111 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.18694-204delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151563011 | ||||||
| chr2:151563011
|
CTT | C | 18 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(15): Show | 18 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.18694-205_18694-20 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151563011 | ||||||
| chr2:151563011
|
CTTTTTTT others(6): Show |
C | 3 | a0037c0087t0001g0107a0085c0031t0001g0108a0130c0150t0001g0180 | 3 | HG02451.hp2 HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.18694-216_18694-20 others(17): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151563011 | ||||||
| chr2:151563341
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.18693+265C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151563341 | ||||||
| chr2:151563491
|
C | CCTACGTA others(4): Show |
2 | a0003c0005t0001g0013a0068c0125t0001g0111 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.18693+114_18693+11 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 119/181 | chr2 | 151563491 | ||||||
| chr2:151564130
|
TA | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.18472-201delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/181 | chr2 | 151564130 | ||||||
| chr2:151564215
|
C | T | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.18472-285G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/181 | chr2 | 151564215 | ||||||
| chr2:151564810
|
C | G | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18471+234G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/181 | chr2 | 151564810 | ||||||
| chr2:151564843
|
G | A | 171 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.18471+201C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 117/181 | chr2 | 151564843 | ||||||
| chr2:151565301
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18367-153C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 116/181 | chr2 | 151565301 | ||||||
| chr2:151565423
|
A | G | 53 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(50): Show | 53 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.18366+78T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 116/181 | chr2 | 151565423 | ||||||
| chr2:151565465
|
A | T | 1 | a0081c0141t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.18366+36T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 116/181 | chr2 | 151565465 | ||||||
| chr2:151565908
|
T | C | 1 | a0015c0111t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18157-88A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151565908 | ||||||
| chr2:151566145
|
T | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.18157-325A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566145 | ||||||
| chr2:151566600
|
T | C | 1 | a0003c0005t0001g0004 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.18156+568A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566600 | ||||||
| chr2:151566812
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.18156+356A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566812 | ||||||
| chr2:151566945
|
T | A | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.18156+223A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566945 | ||||||
| chr2:151566946
|
A | T | 33 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.18156+222T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566946 | ||||||
| chr2:151566947
|
A | T | 1 | a0005c0008t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.18156+221T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566947 | ||||||
| chr2:151566959
|
T | C | 1 | a0094c0061t0001g0080 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18156+209A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566959 | ||||||
| chr2:151566971
|
A | G | 1 | a0126c0027t0001g0067 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.18156+197T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151566971 | ||||||
| chr2:151567091
|
G | A | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.18156+77C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 114/181 | chr2 | 151567091 | ||||||
| chr2:151567675
|
A | G | 1 | a0113c0042t0001g0035 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.17845-196T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151567675 | ||||||
| chr2:151567740
|
A | G | 1 | a0013c0014t0001g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.17845-261T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151567740 | ||||||
| chr2:151567837
|
T | C | 1 | a0127c0144t0001g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.17844+234A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151567837 | ||||||
| chr2:151567896
|
C | T | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.17844+175G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151567896 | ||||||
| chr2:151567949
|
G | A | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.17844+122C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151567949 | ||||||
| chr2:151568002
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.17844+69A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 113/181 | chr2 | 151568002 | ||||||
| chr2:151568244
|
A | C | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.17737-66T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 112/181 | chr2 | 151568244 | ||||||
| chr2:151568419
|
T | TA | 130 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
splice_region_variant&intron_variant | LOW | c.17635-3dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 111/181 | chr2 | 151568419 | ||||||
| chr2:151568792
|
G | T | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.17536-76C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 110/181 | chr2 | 151568792 | ||||||
| chr2:151568823
|
G | A | 16 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.17536-107C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 110/181 | chr2 | 151568823 | ||||||
| chr2:151568866
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.17536-150G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 110/181 | chr2 | 151568866 | ||||||
| chr2:151569178
|
T | C | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.17535+90A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 110/181 | chr2 | 151569178 | ||||||
| chr2:151569544
|
G | A | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17431-172C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 109/181 | chr2 | 151569544 | ||||||
| chr2:151569835
|
T | C | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.17430+246A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 109/181 | chr2 | 151569835 | ||||||
| chr2:151570024
|
C | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.17430+57G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 109/181 | chr2 | 151570024 | ||||||
| chr2:151570049
|
A | T | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17430+32T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 109/181 | chr2 | 151570049 | ||||||
| chr2:151570735
|
A | G | 132 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.17014-134T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151570735 | ||||||
| chr2:151570980
|
C | T | 1 | a0031c0078t0001g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.17014-379G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151570980 | ||||||
| chr2:151571027
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.17014-426G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571027 | ||||||
| chr2:151571077
|
C | T | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.17014-476G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571077 | ||||||
| chr2:151571194
|
A | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.17014-593T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571194 | ||||||
| chr2:151571258
|
G | A | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.17014-657C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571258 | ||||||
| chr2:151571500
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.17014-899A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571500 | ||||||
| chr2:151571610
|
C | G | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.17014-1009G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571610 | ||||||
| chr2:151571758
|
G | A | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.17014-1157C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571758 | ||||||
| chr2:151571762
|
C | T | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.17014-1161G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571762 | ||||||
| chr2:151571862
|
T | C | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.17014-1261A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151571862 | ||||||
| chr2:151572298
|
G | T | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.17014-1697C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572298 | ||||||
| chr2:151572418
|
T | A | 1 | a0052c0100t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.17014-1817A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572418 | ||||||
| chr2:151572473
|
A | ATATATAT others(10): Show |
5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.17014-1889_17014-1 others(23): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572473 | ||||||
| chr2:151572507
|
T | TTA | 6 | a0004c0126t0001g0118a0021c0057t0001g0037a0022c0054t0001g0030others(3): Show | 6 | HG00280.hp2 HG02735.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.17014-1908_17014-1 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572507 | ||||||
| chr2:151572553
|
C | CT | 5 | a0045c0089t0002g0138a0049c0096t0001g0184a0065c0119t0001g0145others(2): Show | 5 | HG03195.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.17014-1953dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572553 | ||||||
| chr2:151572608
|
C | A | 2 | a0030c0076t0001g0174a0054c0104t0001g0162 | 2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.17014-2007G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572608 | ||||||
| chr2:151572620
|
A | G | 132 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.17014-2019T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572620 | ||||||
| chr2:151572668
|
C | T | 1 | a0023c0043t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.17014-2067G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572668 | ||||||
| chr2:151572677
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.17014-2076G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572677 | ||||||
| chr2:151572763
|
C | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.17014-2162G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572763 | ||||||
| chr2:151572820
|
G | C | 1 | a0012c0090t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.17014-2219C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151572820 | ||||||
| chr2:151573059
|
T | C | 33 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.17014-2458A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573059 | ||||||
| chr2:151573165
|
C | T | 36 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.17013+2530G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573165 | ||||||
| chr2:151573367
|
G | A | 1 | a0104c0059t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.17013+2328C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573367 | ||||||
| chr2:151573706
|
C | T | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17013+1989G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573706 | ||||||
| chr2:151573867
|
T | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.17013+1828A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573867 | ||||||
| chr2:151573874
|
T | C | 17 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.17013+1821A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573874 | ||||||
| chr2:151573902
|
ACTT | A | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.17013+1790_17013+1 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151573902 | ||||||
| chr2:151574196
|
G | C | 52 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.17013+1499C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574196 | ||||||
| chr2:151574398
|
A | G | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17013+1297T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574398 | ||||||
| chr2:151574661
|
T | C | 51 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(48): Show | 51 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.17013+1034A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574661 | ||||||
| chr2:151574722
|
T | TTTTA | 40 | a0003c0005t0001g0004a0009c0017t0001g0121a0009c0017t0001g0159others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.17013+969_17013+97 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
T | TTTTATTT others(1): Show |
6 | a0013c0014t0001g0099a0013c0014t0001g0102a0023c0043t0001g0047others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.17013+965_17013+97 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
T | TTTTATTT others(9): Show |
6 | a0002c0048t0001g0086a0014c0112t0001g0141a0014c0113t0001g0120others(3): Show | 6 | HG02165.hp2 HG02965.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.17013+957_17013+97 others(20): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
T | TTTTATTT others(13): Show |
25 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(22): Show | 25 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.17013+953_17013+97 others(24): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
T | TTTTATTT others(17): Show |
3 | a0007c0003t0001g0001a0095c0062t0001g0081a0096c0060t0001g0022 | 3 | HG03239.hp1 HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.17013+949_17013+97 others(28): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
T | TTTTATTT others(21): Show |
1 | a0094c0061t0001g0080 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.17013+972_17013+97 others(32): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574722
|
TTTTA | T | 51 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(48): Show | 51 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.17013+969_17013+97 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574722 | ||||||
| chr2:151574825
|
G | A | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.17013+870C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151574825 | ||||||
| chr2:151575020
|
A | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.17013+675T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575020 | ||||||
| chr2:151575101
|
C | T | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.17013+594G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575101 | ||||||
| chr2:151575228
|
C | T | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.17013+467G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575228 | ||||||
| chr2:151575257
|
G | T | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.17013+438C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575257 | ||||||
| chr2:151575319
|
T | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17013+376A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575319 | ||||||
| chr2:151575354
|
T | A | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17013+341A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575354 | ||||||
| chr2:151575374
|
C | T | 60 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.17013+321G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575374 | ||||||
| chr2:151575426
|
G | A | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.17013+269C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575426 | ||||||
| chr2:151575561
|
G | A | 1 | a0053c0127t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17013+134C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 107/181 | chr2 | 151575561 | ||||||
| chr2:151575861
|
T | G | 1 | a0031c0078t0001g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.16909-62A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 106/181 | chr2 | 151575861 | ||||||
| chr2:151575967
|
G | A | 37 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.16909-168C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 106/181 | chr2 | 151575967 | ||||||
| chr2:151576372
|
G | A | 48 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.16705-18C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576372 | ||||||
| chr2:151576398
|
G | A | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.16705-44C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576398 | ||||||
| chr2:151576477
|
C | A | 15 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(12): Show | 15 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.16705-123G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576477 | ||||||
| chr2:151576485
|
C | CAT | 4 | a0014c0112t0001g0141a0014c0113t0001g0120a0043c0084t0001g0018others(1): Show | 4 | HG00544.hp2 HG00741.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.16705-133_16705-13 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576485 | ||||||
| chr2:151576485
|
C | CATAT | 4 | a0034c0147t0001g0178a0039c0153t0001g0021a0051c0131t0001g0187others(1): Show | 4 | HG00673.hp2 HG02630.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.16705-135_16705-13 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576485 | ||||||
| chr2:151576485
|
CAT | C | 4 | a0004c0018t0001g0135a0055c0116t0001g0150a0099c0067t0001g0023others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.16705-133_16705-13 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576485 | ||||||
| chr2:151576485
|
CATAT | C | 4 | a0020c0007t0001g0042a0020c0007t0001g0043a0024c0038t0001g0085others(1): Show | 4 | HG00597.hp1 HG02976.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.16705-135_16705-13 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576485 | ||||||
| chr2:151576500
|
ATATATAT others(25): Show |
A | 2 | a0010c0137t0001g0093a0010c0139t0001g0106 | 2 | HG00423.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.16705-178_16705-14 others(36): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576500 | ||||||
| chr2:151576500
|
ATATATAT others(26): Show |
A | 3 | a0016c0016t0002g0137a0032c0077t0001g0175a0079c0130t0002g0105 | 3 | HG03098.hp2 HG06807.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.16705-179_16705-14 others(37): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576500 | ||||||
| chr2:151576502
|
ATATATAT others(18): Show |
A | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.16705-173_16705-14 others(29): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576502 | ||||||
| chr2:151576502
|
ATATATAT others(26): Show |
A | 8 | a0009c0017t0001g0121a0016c0016t0002g0100a0023c0043t0001g0047others(5): Show | 8 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.16705-181_16705-14 others(37): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576502 | ||||||
| chr2:151576504
|
ATATATAT others(6): Show |
A | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.16705-163_16705-15 others(17): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(7): Show |
A | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.16705-164_16705-15 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(9): Show |
A | 1 | a0067c0117t0001g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.16705-166_16705-15 others(20): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(15): Show |
A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16705-172_16705-15 others(26): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0117a0069c0120t0001g0104 | 2 | HG02523.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.16705-175_16705-15 others(29): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(24): Show |
A | 2 | a0010c0138t0001g0091a0050c0099t0001g0098 | 2 | HG02040.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.16705-181_16705-15 others(35): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(25): Show |
A | 3 | a0009c0109t0001g0130a0076c0101t0001g0167a0113c0042t0001g0035 | 3 | HG00609.hp2 HG02735.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.16705-182_16705-15 others(36): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576504
|
ATATATAT others(26): Show |
A | 5 | a0009c0017t0001g0159a0041c0085t0002g0010a0060c0107t0001g0157others(2): Show | 5 | HG00597.hp2 HG02165.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.16705-183_16705-15 others(37): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576504 | ||||||
| chr2:151576506
|
ATATATAT others(4): Show |
A | 1 | a0065c0119t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16705-163_16705-15 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(7): Show |
A | 3 | a0008c0004t0001g0011a0008c0004t0001g0012a0058c0110t0001g0149 | 3 | HG02976.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.16705-166_16705-15 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(8): Show |
A | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16705-167_16705-15 others(19): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(9): Show |
A | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.16705-168_16705-15 others(20): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(17): Show |
A | 1 | a0123c0034t0001g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16705-176_16705-15 others(28): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(18): Show |
A | 13 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0127others(10): Show | 13 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.16705-177_16705-15 others(29): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576506
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.16705-178_16705-15 others(30): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576506 | ||||||
| chr2:151576508
|
ATATATAT others(9): Show |
A | 2 | a0015c0108t0001g0136a0080c0030t0001g0074 | 2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.16705-170_16705-15 others(20): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576508 | ||||||
| chr2:151576508
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.16705-177_16705-15 others(27): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576508 | ||||||
| chr2:151576508
|
ATATATAT others(17): Show |
A | 1 | a0059c0143t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.16705-178_16705-15 others(28): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576508 | ||||||
| chr2:151576508
|
ATATATAT others(18): Show |
A | 10 | a0001c0001t0001g0125a0005c0008t0001g0077a0005c0063t0001g0052others(7): Show | 10 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.16705-179_16705-15 others(29): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576508 | ||||||
| chr2:151576508
|
ATATATAT others(19): Show |
A | 1 | a0116c0052t0001g0069 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.16705-180_16705-15 others(30): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576508 | ||||||
| chr2:151576510
|
ATATATAT others(3): Show |
A | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16705-166_16705-15 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576510 | ||||||
| chr2:151576510
|
ATATATAT others(7): Show |
A | 2 | a0008c0004t0001g0009a0015c0111t0001g0139 | 2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.16705-170_16705-15 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576510 | ||||||
| chr2:151576510
|
ATATATAT others(15): Show |
A | 1 | a0005c0008t0001g0038 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16705-178_16705-15 others(26): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576510 | ||||||
| chr2:151576510
|
ATATATAT others(16): Show |
A | 1 | a0129c0022t0001g0114 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.16705-179_16705-15 others(27): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576510 | ||||||
| chr2:151576512
|
ATATATTT others(7): Show |
A | 3 | a0004c0126t0001g0118a0028c0021t0001g0182a0028c0021t0001g0183 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.16705-172_16705-15 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576512 | ||||||
| chr2:151576513
|
TA | T | 3 | a0007c0003t0001g0002a0109c0046t0001g0048a0118c0073t0001g0051 | 3 | HG04115.hp1 NA18947.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.16705-160delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576513 | ||||||
| chr2:151576514
|
A | AT | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0011c0009t0001g0040others(3): Show | 6 | HG01884.hp2 HG02897.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.16705-161dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576514 | ||||||
| chr2:151576514
|
A | T | 2 | a0004c0018t0001g0135a0096c0060t0001g0022 | 2 | HG03654.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.16705-160T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576514 | ||||||
| chr2:151576514
|
ATATTTTT others(3): Show |
A | 1 | a0053c0127t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.16705-170_16705-16 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576514 | ||||||
| chr2:151576514
|
ATATTTTT others(7): Show |
A | 1 | a0132c0151t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16705-174_16705-16 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576514 | ||||||
| chr2:151576515
|
TA | T | 3 | a0027c0013t0001g0070a0086c0032t0001g0109a0117c0039t0001g0063 | 3 | HG02257.hp2 HG02572.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.16705-162delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576515 | ||||||
| chr2:151576516
|
A | ATATATAT others(5): Show |
1 | a0003c0005t0001g0013 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.16705-163_16705-16 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576516 | ||||||
| chr2:151576516
|
A | ATATATTT others(4): Show |
1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.16705-163_16705-16 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576516 | ||||||
| chr2:151576516
|
A | T | 17 | a0004c0018t0001g0135a0006c0012t0001g0172a0006c0012t0001g0173others(14): Show | 17 | HG01884.hp2 HG02258.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.16705-162T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576516 | ||||||
| chr2:151576516
|
AT | A | 8 | a0002c0002t0001g0060a0021c0057t0001g0037a0031c0078t0001g0171others(5): Show | 8 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.16705-163delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576516 | ||||||
| chr2:151576516
|
ATTTTTTT others(8): Show |
A | 1 | a0017c0015t0001g0165 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.16705-177_16705-16 others(19): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576516 | ||||||
| chr2:151576517
|
T | TA | 7 | a0002c0002t0001g0036a0002c0002t0001g0050a0004c0018t0001g0134others(4): Show | 7 | HG03453.hp2 HG03710.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.16705-164_16705-16 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576517 | ||||||
| chr2:151576517
|
T | TATATATA others(8): Show |
2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16705-164_16705-16 others(19): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576517 | ||||||
| chr2:151576518
|
T | A | 14 | a0002c0002t0001g0046a0002c0048t0001g0086a0003c0094t0001g0014others(11): Show | 14 | HG00741.hp1 HG01074.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.16705-164A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576518 | ||||||
| chr2:151576519
|
T | A | 10 | a0002c0002t0001g0036a0002c0002t0001g0060a0004c0018t0001g0134others(7): Show | 10 | HG00280.hp2 HG00741.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.16705-165A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576519 | ||||||
| chr2:151576520
|
T | A | 5 | a0002c0002t0001g0046a0014c0113t0001g0120a0093c0058t0002g0025others(2): Show | 5 | HG02683.hp1 NA18960.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.16705-166A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576520 | ||||||
| chr2:151576521
|
T | A | 7 | a0004c0018t0001g0134a0026c0006t0001g0027a0042c0095t0001g0020others(4): Show | 7 | HG00280.hp2 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.16705-167A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576521 | ||||||
| chr2:151576522
|
T | A | 1 | a0110c0041t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.16705-168A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576522 | ||||||
| chr2:151576523
|
T | A | 2 | a0026c0006t0001g0027a0121c0074t0001g0058 | 2 | HG01891.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.16705-169A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576523 | ||||||
| chr2:151576524
|
T | A | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.16705-170A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576524 | ||||||
| chr2:151576525
|
T | A | 2 | a0026c0006t0001g0027a0121c0074t0001g0058 | 2 | HG01891.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.16705-171A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576525 | ||||||
| chr2:151576526
|
T | A | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.16705-172A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576526 | ||||||
| chr2:151576751
|
T | A | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.16705-397A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151576751 | ||||||
| chr2:151577503
|
A | G | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.16705-1149T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577503 | ||||||
| chr2:151577648
|
G | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16705-1294C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577648 | ||||||
| chr2:151577682
|
G | A | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16705-1328C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577682 | ||||||
| chr2:151577687
|
T | C | 1 | a0004c0018t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.16705-1333A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577687 | ||||||
| chr2:151577735
|
C | G | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.16705-1381G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577735 | ||||||
| chr2:151577803
|
T | C | 132 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.16705-1449A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577803 | ||||||
| chr2:151577909
|
C | T | 2 | a0005c0063t0001g0052a0005c0064t0001g0083 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.16704+1429G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151577909 | ||||||
| chr2:151578057
|
A | G | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16704+1281T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578057 | ||||||
| chr2:151578099
|
A | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16704+1239T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578099 | ||||||
| chr2:151578178
|
T | G | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.16704+1160A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578178 | ||||||
| chr2:151578276
|
CGTCAAGT others(7): Show |
C | 8 | a0003c0083t0001g0003a0003c0094t0001g0014a0021c0057t0001g0037others(5): Show | 8 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.16704+1048_16704+1 others(20): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578276 | ||||||
| chr2:151578292
|
A | T | 8 | a0003c0083t0001g0003a0003c0094t0001g0014a0021c0057t0001g0037others(5): Show | 8 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.16704+1046T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578292 | ||||||
| chr2:151578307
|
T | C | 10 | a0003c0083t0001g0003a0003c0094t0001g0014a0021c0057t0001g0037others(7): Show | 10 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.16704+1031A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578307 | ||||||
| chr2:151578365
|
A | T | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.16704+973T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578365 | ||||||
| chr2:151578372
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.16704+966T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578372 | ||||||
| chr2:151578468
|
T | C | 1 | a0120c0023t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.16704+870A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578468 | ||||||
| chr2:151578687
|
G | A | 1 | a0103c0066t0001g0065 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.16704+651C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578687 | ||||||
| chr2:151578842
|
A | G | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.16704+496T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578842 | ||||||
| chr2:151578867
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16704+471G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578867 | ||||||
| chr2:151578904
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.16704+434T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151578904 | ||||||
| chr2:151579072
|
C | A | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.16704+266G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579072 | ||||||
| chr2:151579080
|
C | CA | 14 | a0003c0094t0001g0014a0008c0004t0001g0012a0013c0014t0001g0099others(11): Show | 14 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.16704+257dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579080 | ||||||
| chr2:151579080
|
CA | C | 62 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.16704+257delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579080 | ||||||
| chr2:151579109
|
T | A | 7 | a0004c0126t0001g0118a0011c0009t0001g0040a0011c0070t0001g0055others(4): Show | 7 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.16704+229A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579109 | ||||||
| chr2:151579185
|
CT | C | 33 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.16704+152delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579185 | ||||||
| chr2:151579194
|
C | A | 1 | a0069c0120t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.16704+144G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579194 | ||||||
| chr2:151579196
|
T | A | 33 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.16704+142A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579196 | ||||||
| chr2:151579253
|
C | T | 4 | a0009c0017t0001g0121a0023c0044t0001g0068a0032c0077t0001g0175others(1): Show | 4 | HG00673.hp1 NA18953.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.16704+85G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579253 | ||||||
| chr2:151579326
|
C | G | 69 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.16704+12G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 105/181 | chr2 | 151579326 | ||||||
| chr2:151579759
|
CG | C | 22 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.16393-111delC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151579759 | ||||||
| chr2:151579855
|
T | G | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.16393-206A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151579855 | ||||||
| chr2:151579950
|
T | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.16393-301A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151579950 | ||||||
| chr2:151580002
|
C | CT | 5 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123others(2): Show | 5 | HG01891.hp1 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.16393-354dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580002 | ||||||
| chr2:151580002
|
CT | C | 82 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.16393-354delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580002 | ||||||
| chr2:151580002
|
CTT | C | 11 | a0015c0108t0001g0136a0028c0021t0001g0182a0028c0021t0001g0183others(8): Show | 11 | HG00639.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.16393-355_16393-35 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580002 | ||||||
| chr2:151580002
|
CTTTTTTT others(2): Show |
C | 36 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.16393-362_16393-35 others(13): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580002 | ||||||
| chr2:151580007
|
T | TC | 21 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.16393-359_16393-35 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580007 | ||||||
| chr2:151580008
|
T | C | 2 | a0016c0016t0002g0100a0120c0023t0001g0088 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16393-359A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580008 | ||||||
| chr2:151580101
|
G | A | 1 | a0018c0020t0001g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.16393-452C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580101 | ||||||
| chr2:151580154
|
C | T | 1 | a0085c0031t0001g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.16393-505G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580154 | ||||||
| chr2:151580165
|
C | T | 5 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.16393-516G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580165 | ||||||
| chr2:151580238
|
T | C | 17 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.16392+559A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580238 | ||||||
| chr2:151580277
|
A | AT | 174 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.16392+519dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580277 | ||||||
| chr2:151580307
|
G | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16392+490C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580307 | ||||||
| chr2:151580314
|
T | C | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.16392+483A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580314 | ||||||
| chr2:151580356
|
A | G | 6 | a0018c0020t0001g0122a0018c0020t0001g0131a0051c0131t0001g0187others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.16392+441T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580356 | ||||||
| chr2:151580385
|
G | A | 156 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.16392+412C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580385 | ||||||
| chr2:151580468
|
A | C | 23 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16392+329T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580468 | ||||||
| chr2:151580485
|
G | A | 1 | a0002c0048t0001g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.16392+312C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580485 | ||||||
| chr2:151580540
|
G | A | 22 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.16392+257C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580540 | ||||||
| chr2:151580615
|
G | A | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.16392+182C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580615 | ||||||
| chr2:151580621
|
A | G | 22 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.16392+176T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580621 | ||||||
| chr2:151580627
|
G | C | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.16392+170C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 104/181 | chr2 | 151580627 | ||||||
| chr2:151580917
|
A | G | 1 | a0115c0053t0001g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.16285-13T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151580917 | ||||||
| chr2:151581068
|
A | G | 1 | a0127c0144t0001g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.16285-164T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581068 | ||||||
| chr2:151581192
|
C | CA | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.16285-289dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581192 | ||||||
| chr2:151581239
|
G | A | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16284+244C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581239 | ||||||
| chr2:151581301
|
T | C | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16284+182A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581301 | ||||||
| chr2:151581318
|
T | C | 14 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(11): Show | 14 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.16284+165A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581318 | ||||||
| chr2:151581442
|
C | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.16284+41G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581442 | ||||||
| chr2:151581472
|
T | C | 7 | a0002c0002t0001g0026a0007c0003t0001g0001a0007c0003t0001g0002others(4): Show | 7 | HG01175.hp2 HG01258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.16284+11A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 103/181 | chr2 | 151581472 | ||||||
| chr2:151581612
|
A | G | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0121c0074t0001g0058others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16180-25T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581612 | ||||||
| chr2:151581665
|
A | G | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16180-78T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581665 | ||||||
| chr2:151581669
|
C | CAT | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16180-84_16180-83d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581669 | ||||||
| chr2:151581687
|
TG | T | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16180-101delC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581687 | ||||||
| chr2:151581694
|
A | T | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.16180-107T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581694 | ||||||
| chr2:151581723
|
T | A | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16180-136A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581723 | ||||||
| chr2:151581801
|
A | C | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.16180-214T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581801 | ||||||
| chr2:151581827
|
C | T | 5 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.16180-240G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581827 | ||||||
| chr2:151581905
|
G | C | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0022c0054t0001g0030others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.16180-318C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581905 | ||||||
| chr2:151581906
|
T | A | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.16180-319A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581906 | ||||||
| chr2:151581909
|
C | G | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.16180-322G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581909 | ||||||
| chr2:151581911
|
T | G | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.16180-324A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581911 | ||||||
| chr2:151581914
|
A | G | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.16180-327T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581914 | ||||||
| chr2:151581966
|
T | C | 18 | a0002c0002t0001g0049a0006c0079t0001g0170a0017c0015t0001g0164others(15): Show | 18 | HG00544.hp2 HG00621.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.16180-379A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151581966 | ||||||
| chr2:151582217
|
GATCAAAG others(5): Show |
G | 11 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(8): Show | 11 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.16179+235_16179+24 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151582217 | ||||||
| chr2:151582273
|
G | A | 2 | a0110c0041t0001g0075a0124c0075t0001g0057 | 2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.16179+191C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151582273 | ||||||
| chr2:151582286
|
T | C | 3 | a0010c0137t0001g0093a0010c0138t0001g0091a0113c0042t0001g0035 | 3 | HG00609.hp2 HG01993.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.16179+178A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 102/181 | chr2 | 151582286 | ||||||
| chr2:151582901
|
G | A | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15976-234C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151582901 | ||||||
| chr2:151583016
|
C | T | 35 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.15976-349G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583016 | ||||||
| chr2:151583075
|
T | G | 95 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.15975+380A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583075 | ||||||
| chr2:151583083
|
T | C | 108 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.15975+372A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583083 | ||||||
| chr2:151583172
|
A | G | 3 | a0009c0017t0001g0159a0010c0137t0001g0093a0010c0139t0001g0106 | 3 | HG00423.hp2 HG00597.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.15975+283T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583172 | ||||||
| chr2:151583176
|
C | T | 44 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(41): Show | 44 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.15975+279G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583176 | ||||||
| chr2:151583191
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15975+264C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 101/181 | chr2 | 151583191 | ||||||
| chr2:151583841
|
T | C | 52 | a0001c0001t0001g0097a0001c0082t0001g0147a0003c0005t0001g0004others(49): Show | 52 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.15664-75A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151583841 | ||||||
| chr2:151583918
|
A | AAATTAGA others(10545): Show |
1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15664-153_15664-15 others(10556): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151583918 | ||||||
| chr2:151583918
|
A | G | 81 | a0001c0001t0001g0097a0001c0082t0001g0147a0002c0002t0001g0026others(78): Show | 81 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.15664-152T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151583918 | ||||||
| chr2:151583920
|
G | A | 86 | a0001c0001t0001g0097a0001c0082t0001g0147a0002c0002t0001g0026others(83): Show | 86 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.15664-154C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151583920 | ||||||
| chr2:151583938
|
G | A | 90 | a0001c0001t0001g0097a0001c0082t0001g0147a0002c0002t0001g0026others(87): Show | 90 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.15664-172C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151583938 | ||||||
| chr2:151584195
|
T | A | 41 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.15664-429A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584195 | ||||||
| chr2:151584236
|
T | C | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-470A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584236 | ||||||
| chr2:151584295
|
A | C | 1 | a0081c0141t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.15664-529T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584295 | ||||||
| chr2:151584313
|
C | T | 36 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(33): Show | 36 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.15664-547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584313 | ||||||
| chr2:151584314
|
G | A | 2 | a0013c0014t0001g0099a0122c0033t0001g0087 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.15664-548C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584314 | ||||||
| chr2:151584335
|
C | T | 40 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.15664-569G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584335 | ||||||
| chr2:151584371
|
C | T | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-605G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584371 | ||||||
| chr2:151584397
|
C | T | 25 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.15664-631G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584397 | ||||||
| chr2:151584398
|
A | T | 25 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.15664-632T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584398 | ||||||
| chr2:151584400
|
A | G | 25 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.15664-634T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584400 | ||||||
| chr2:151584411
|
A | G | 12 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(9): Show | 12 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.15664-645T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584411 | ||||||
| chr2:151584429
|
T | C | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-663A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584429 | ||||||
| chr2:151584465
|
T | C | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.15664-699A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584465 | ||||||
| chr2:151584476
|
T | C | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-710A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584476 | ||||||
| chr2:151584482
|
T | C | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.15664-716A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584482 | ||||||
| chr2:151584494
|
G | A | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-728C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584494 | ||||||
| chr2:151584631
|
G | A | 38 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.15664-865C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584631 | ||||||
| chr2:151584735
|
G | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15663+772C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584735 | ||||||
| chr2:151584751
|
C | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.15663+756G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584751 | ||||||
| chr2:151584814
|
C | T | 24 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(21): Show | 24 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.15663+693G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584814 | ||||||
| chr2:151584842
|
C | G | 187 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.15663+665G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584842 | ||||||
| chr2:151584843
|
G | GC | 187 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.15663+663_15663+66 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584843 | ||||||
| chr2:151584868
|
TTTTG | T | 13 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.15663+635_15663+63 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584868 | ||||||
| chr2:151584868
|
TTTTGTTT others(1): Show |
T | 24 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(21): Show | 24 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.15663+631_15663+63 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151584868 | ||||||
| chr2:151585090
|
G | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15663+417C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151585090 | ||||||
| chr2:151585264
|
C | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15663+243G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151585264 | ||||||
| chr2:151585391
|
G | C | 41 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.15663+116C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151585391 | ||||||
| chr2:151585461
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15663+46G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 100/181 | chr2 | 151585461 | ||||||
| chr2:151585703
|
T | C | 1 | a0024c0038t0001g0085 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.15556-89A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585703 | ||||||
| chr2:151585707
|
A | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15556-93T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585707 | ||||||
| chr2:151585780
|
C | G | 3 | a0046c0091t0001g0017a0087c0132t0001g0101a0105c0080t0001g0034 | 3 | HG02886.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15556-166G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585780 | ||||||
| chr2:151585826
|
T | C | 10 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.15556-212A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585826 | ||||||
| chr2:151585913
|
G | A | 1 | a0125c0028t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15556-299C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585913 | ||||||
| chr2:151585915
|
A | G | 1 | a0125c0028t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15556-301T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151585915 | ||||||
| chr2:151586036
|
C | T | 8 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(5): Show | 8 | HG00423.hp2 HG00609.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.15555+369G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151586036 | ||||||
| chr2:151586080
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.15555+325A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151586080 | ||||||
| chr2:151586111
|
G | T | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.15555+294C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151586111 | ||||||
| chr2:151586342
|
A | C | 2 | a0033c0024t0001g0096a0037c0087t0001g0107 | 2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.15555+63T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 99/181 | chr2 | 151586342 | ||||||
| chr2:151586541
|
T | C | 3 | a0035c0146t0001g0103a0037c0087t0001g0107a0117c0039t0001g0063 | 3 | HG00639.hp1 HG02965.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.15451-32A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151586541 | ||||||
| chr2:151586799
|
C | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.15451-290G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151586799 | ||||||
| chr2:151587002
|
TACAAACA others(7): Show |
T | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15450+358_15450+37 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587002 | ||||||
| chr2:151587141
|
G | A | 78 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(75): Show | 78 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.15450+233C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587141 | ||||||
| chr2:151587152
|
C | G | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.15450+222G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587152 | ||||||
| chr2:151587163
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.15450+211T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587163 | ||||||
| chr2:151587195
|
G | C | 6 | a0017c0015t0001g0164a0017c0015t0001g0165a0043c0084t0001g0018others(3): Show | 6 | HG00544.hp2 HG02683.hp1 NA19080.hp1 others(3): Show |
intron_variant | MODIFIER | c.15450+179C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587195 | ||||||
| chr2:151587197
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15450+177C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587197 | ||||||
| chr2:151587300
|
A | C | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.15450+74T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587300 | ||||||
| chr2:151587340
|
G | C | 4 | a0016c0016t0002g0100a0016c0016t0002g0137a0041c0085t0002g0010others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15450+34C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587340 | ||||||
| chr2:151587342
|
A | T | 4 | a0016c0016t0002g0100a0016c0016t0002g0137a0041c0085t0002g0010others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15450+32T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 98/181 | chr2 | 151587342 | ||||||
| chr2:151587605
|
C | T | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15247-28G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587605 | ||||||
| chr2:151587729
|
G | A | 1 | a0002c0002t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.15247-152C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587729 | ||||||
| chr2:151587734
|
G | T | 2 | a0110c0041t0001g0075a0124c0075t0001g0057 | 2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.15247-157C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587734 | ||||||
| chr2:151587775
|
G | T | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.15247-198C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587775 | ||||||
| chr2:151587806
|
C | CA | 37 | a0004c0018t0001g0134a0005c0008t0001g0038a0008c0004t0001g0011others(34): Show | 37 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.15247-230dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587806 | ||||||
| chr2:151587806
|
C | CAA | 11 | a0006c0012t0001g0173a0008c0004t0001g0009a0010c0137t0001g0093others(8): Show | 11 | HG00423.hp2 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.15247-231_15247-23 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587806 | ||||||
| chr2:151587806
|
C | CAAA | 6 | a0013c0014t0001g0099a0050c0099t0001g0098a0065c0119t0001g0145others(3): Show | 6 | HG00609.hp2 HG02647.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.15247-232_15247-23 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587806 | ||||||
| chr2:151587806
|
CAAAAAAA others(4): Show |
C | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.15247-240_15247-23 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587806 | ||||||
| chr2:151587832
|
G | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15247-255C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587832 | ||||||
| chr2:151587918
|
G | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15247-341C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587918 | ||||||
| chr2:151587945
|
A | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15247-368T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587945 | ||||||
| chr2:151587975
|
T | A | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.15247-398A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587975 | ||||||
| chr2:151587985
|
A | G | 5 | a0036c0029t0001g0176a0037c0087t0001g0107a0046c0091t0001g0017others(2): Show | 5 | HG01884.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.15247-408T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587985 | ||||||
| chr2:151587992
|
G | A | 115 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.15247-415C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587992 | ||||||
| chr2:151587998
|
G | A | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.15247-421C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151587998 | ||||||
| chr2:151588021
|
T | A | 20 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(17): Show | 20 | HG00639.hp2 HG01192.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.15247-444A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588021 | ||||||
| chr2:151588091
|
CAAAAAAA others(4): Show |
C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.15247-525_15247-51 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588091 | ||||||
| chr2:151588100
|
A | G | 1 | a0006c0012t0001g0173 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.15247-523T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588100 | ||||||
| chr2:151588101
|
G | A | 1 | a0006c0012t0001g0173 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.15247-524C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588101 | ||||||
| chr2:151588160
|
A | G | 1 | a0010c0137t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.15247-583T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588160 | ||||||
| chr2:151588236
|
C | G | 9 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.15247-659G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588236 | ||||||
| chr2:151588310
|
G | A | 1 | a0013c0014t0001g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15247-733C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588310 | ||||||
| chr2:151588338
|
A | G | 49 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.15247-761T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588338 | ||||||
| chr2:151588457
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15247-880A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588457 | ||||||
| chr2:151588563
|
C | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15247-986G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588563 | ||||||
| chr2:151588577
|
A | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.15247-1000T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588577 | ||||||
| chr2:151588618
|
C | G | 7 | a0017c0015t0001g0164a0017c0015t0001g0165a0043c0084t0001g0018others(4): Show | 7 | HG00544.hp2 HG02683.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.15247-1041G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588618 | ||||||
| chr2:151588637
|
C | T | 2 | a0060c0107t0001g0157a0104c0059t0001g0019 | 2 | HG02165.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.15247-1060G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588637 | ||||||
| chr2:151588698
|
G | A | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.15247-1121C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588698 | ||||||
| chr2:151588740
|
T | C | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.15246+1149A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588740 | ||||||
| chr2:151588969
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15246+920T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588969 | ||||||
| chr2:151588986
|
G | A | 1 | a0061c0115t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15246+903C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151588986 | ||||||
| chr2:151589074
|
T | C | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.15246+815A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589074 | ||||||
| chr2:151589254
|
G | A | 1 | a0021c0057t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.15246+635C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589254 | ||||||
| chr2:151589264
|
G | A | 2 | a0002c0002t0001g0036a0112c0051t0001g0072 | 2 | HG00099.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.15246+625C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589264 | ||||||
| chr2:151589300
|
T | A | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.15246+589A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589300 | ||||||
| chr2:151589306
|
G | A | 31 | a0002c0002t0001g0026a0002c0002t0001g0039a0002c0002t0001g0046others(28): Show | 31 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.15246+583C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589306 | ||||||
| chr2:151589317
|
C | T | 1 | a0016c0016t0002g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.15246+572G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589317 | ||||||
| chr2:151589351
|
G | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.15246+538C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589351 | ||||||
| chr2:151589356
|
G | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.15246+533C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589356 | ||||||
| chr2:151589365
|
G | A | 14 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.15246+524C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589365 | ||||||
| chr2:151589465
|
C | T | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.15246+424G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589465 | ||||||
| chr2:151589568
|
G | A | 13 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.15246+321C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589568 | ||||||
| chr2:151589589
|
T | C | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.15246+300A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589589 | ||||||
| chr2:151589617
|
C | T | 9 | a0017c0015t0001g0164a0017c0015t0001g0165a0043c0084t0001g0018others(6): Show | 9 | HG00544.hp2 HG02683.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.15246+272G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589617 | ||||||
| chr2:151589637
|
C | CA | 47 | a0001c0001t0001g0126a0001c0082t0001g0147a0002c0002t0001g0036others(44): Show | 47 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.15246+251dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589637 | ||||||
| chr2:151589637
|
C | CAA | 47 | a0002c0002t0001g0026a0002c0002t0001g0039a0002c0002t0001g0046others(44): Show | 47 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.15246+250_15246+25 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589637 | ||||||
| chr2:151589637
|
C | CAAA | 5 | a0010c0137t0001g0093a0010c0139t0001g0106a0014c0113t0001g0120others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.15246+249_15246+25 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589637 | ||||||
| chr2:151589655
|
A | AG | 2 | a0017c0015t0001g0164a0035c0146t0001g0103 | 2 | HG00639.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.15246+233_15246+23 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589655 | ||||||
| chr2:151589689
|
C | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15246+200G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589689 | ||||||
| chr2:151589783
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.15246+106T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589783 | ||||||
| chr2:151589817
|
G | A | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.15246+72C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589817 | ||||||
| chr2:151589877
|
G | C | 4 | a0027c0013t0001g0070a0027c0013t0001g0071a0065c0119t0001g0145others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.15246+12C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 97/181 | chr2 | 151589877 | ||||||
| chr2:151590301
|
T | TG | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.14935-102dupC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590301 | ||||||
| chr2:151590404
|
C | G | 17 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.14935-204G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590404 | ||||||
| chr2:151590406
|
T | G | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.14935-206A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590406 | ||||||
| chr2:151590553
|
C | CT | 26 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0125others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.14935-354dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590553 | ||||||
| chr2:151590553
|
CT | C | 63 | a0001c0001t0001g0112a0002c0002t0001g0026a0002c0002t0001g0036others(60): Show | 63 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.14935-354delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590553 | ||||||
| chr2:151590558
|
T | C | 20 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(17): Show | 20 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.14935-358A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590558 | ||||||
| chr2:151590559
|
T | C | 47 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.14935-359A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590559 | ||||||
| chr2:151590560
|
T | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.14935-360A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590560 | ||||||
| chr2:151590671
|
C | T | 1 | a0004c0126t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.14935-471G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590671 | ||||||
| chr2:151590828
|
A | AT | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.14934+519dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590828 | ||||||
| chr2:151590914
|
T | A | 33 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.14934+434A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590914 | ||||||
| chr2:151590944
|
A | G | 1 | a0076c0101t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.14934+404T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590944 | ||||||
| chr2:151590971
|
A | G | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.14934+377T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151590971 | ||||||
| chr2:151591013
|
T | G | 2 | a0003c0005t0001g0013a0068c0125t0001g0111 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.14934+335A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591013 | ||||||
| chr2:151591019
|
A | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.14934+329T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591019 | ||||||
| chr2:151591136
|
CA | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.14934+211delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591136 | ||||||
| chr2:151591179
|
A | G | 33 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.14934+169T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591179 | ||||||
| chr2:151591240
|
A | G | 11 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(8): Show | 11 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.14934+108T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591240 | ||||||
| chr2:151591331
|
G | GC | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.14934+16_14934+17i others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 96/181 | chr2 | 151591331 | ||||||
| chr2:151591632
|
T | A | 1 | a0027c0013t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14827-177A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/181 | chr2 | 151591632 | ||||||
| chr2:151591719
|
T | C | 8 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(5): Show | 8 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.14827-264A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/181 | chr2 | 151591719 | ||||||
| chr2:151591852
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.14826+182G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/181 | chr2 | 151591852 | ||||||
| chr2:151591869
|
C | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.14826+165G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 95/181 | chr2 | 151591869 | ||||||
| chr2:151592265
|
T | G | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.14722-127A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592265 | ||||||
| chr2:151592277
|
AAACT | A | 6 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(3): Show | 6 | HG01891.hp2 HG02683.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.14722-143_14722-14 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592277 | ||||||
| chr2:151592457
|
G | C | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.14722-319C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592457 | ||||||
| chr2:151592466
|
A | G | 1 | a0101c0068t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.14722-328T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592466 | ||||||
| chr2:151592518
|
C | T | 18 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(15): Show | 18 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.14722-380G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592518 | ||||||
| chr2:151592615
|
G | A | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.14721+401C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592615 | ||||||
| chr2:151592762
|
C | G | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0110c0041t0001g0075 | 3 | HG01891.hp2 HG02683.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.14721+254G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592762 | ||||||
| chr2:151592769
|
GATCAAAG others(5): Show |
G | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.14721+235_14721+24 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 94/181 | chr2 | 151592769 | ||||||
| chr2:151593568
|
T | C | 117 | a0001c0001t0001g0124a0002c0002t0001g0026a0002c0002t0001g0036others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.14518-349A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/181 | chr2 | 151593568 | ||||||
| chr2:151593627
|
T | G | 66 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.14517+380A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/181 | chr2 | 151593627 | ||||||
| chr2:151593635
|
T | C | 74 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.14517+372A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/181 | chr2 | 151593635 | ||||||
| chr2:151593728
|
T | C | 34 | a0009c0017t0001g0121a0009c0017t0001g0159a0010c0137t0001g0093others(31): Show | 34 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.14517+279A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/181 | chr2 | 151593728 | ||||||
| chr2:151593743
|
G | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.14517+264C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 93/181 | chr2 | 151593743 | ||||||
| chr2:151594393
|
C | T | 56 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(53): Show | 56 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.14206-75G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594393 | ||||||
| chr2:151594470
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.14206-152C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594470 | ||||||
| chr2:151594472
|
A | G | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0093c0058t0002g0025 | 3 | NA19080.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14206-154T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594472 | ||||||
| chr2:151594490
|
A | G | 5 | a0017c0015t0001g0164a0017c0015t0001g0165a0056c0145t0001g0177others(2): Show | 5 | HG02280.hp2 NA19060.hp1 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.14206-172T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594490 | ||||||
| chr2:151594747
|
T | A | 42 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.14206-429A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594747 | ||||||
| chr2:151594749
|
G | A | 9 | a0025c0011t0001g0089a0025c0011t0001g0090a0042c0095t0001g0020others(6): Show | 9 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.14206-431C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594749 | ||||||
| chr2:151594788
|
T | C | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0039c0153t0001g0021others(7): Show | 10 | HG00558.hp2 HG00673.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.14206-470A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594788 | ||||||
| chr2:151594802
|
G | T | 2 | a0050c0099t0001g0098a0131c0149t0001g0181 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.14206-484C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594802 | ||||||
| chr2:151594831
|
G | T | 11 | a0025c0011t0001g0089a0025c0011t0001g0090a0035c0146t0001g0103others(8): Show | 11 | HG00544.hp2 HG00639.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.14206-513C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594831 | ||||||
| chr2:151594840
|
G | C | 1 | a0085c0031t0001g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14206-522C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594840 | ||||||
| chr2:151594843
|
C | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.14206-525G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594843 | ||||||
| chr2:151594847
|
A | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.14206-529T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594847 | ||||||
| chr2:151594863
|
T | C | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.14206-545A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594863 | ||||||
| chr2:151594865
|
C | T | 4 | a0017c0015t0001g0164a0017c0015t0001g0165a0056c0145t0001g0177others(1): Show | 4 | HG02280.hp2 NA19080.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.14206-547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594865 | ||||||
| chr2:151594887
|
C | T | 6 | a0017c0015t0001g0164a0017c0015t0001g0165a0039c0153t0001g0021others(3): Show | 6 | HG00558.hp2 HG00673.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.14206-569G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594887 | ||||||
| chr2:151594923
|
C | T | 6 | a0017c0015t0001g0164a0017c0015t0001g0165a0039c0153t0001g0021others(3): Show | 6 | HG00558.hp2 HG00673.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.14206-605G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594923 | ||||||
| chr2:151594949
|
C | T | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0093c0058t0002g0025 | 3 | NA19080.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14206-631G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594949 | ||||||
| chr2:151594950
|
A | T | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0093c0058t0002g0025 | 3 | NA19080.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14206-632T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594950 | ||||||
| chr2:151594952
|
A | G | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0093c0058t0002g0025 | 3 | NA19080.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14206-634T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594952 | ||||||
| chr2:151594963
|
A | G | 11 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(8): Show | 11 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.14206-645T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594963 | ||||||
| chr2:151594981
|
T | C | 4 | a0017c0015t0001g0164a0017c0015t0001g0165a0056c0145t0001g0177others(1): Show | 4 | HG02280.hp2 NA19080.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.14206-663A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151594981 | ||||||
| chr2:151595028
|
T | C | 4 | a0017c0015t0001g0164a0017c0015t0001g0165a0056c0145t0001g0177others(1): Show | 4 | HG02280.hp2 NA19080.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.14206-710A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595028 | ||||||
| chr2:151595034
|
T | C | 82 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(79): Show | 82 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.14206-716A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595034 | ||||||
| chr2:151595046
|
G | A | 4 | a0017c0015t0001g0164a0017c0015t0001g0165a0056c0145t0001g0177others(1): Show | 4 | HG02280.hp2 NA19080.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.14206-728C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595046 | ||||||
| chr2:151595173
|
G | A | 2 | a0039c0153t0001g0021a0082c0140t0001g0094 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.14206-855C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595173 | ||||||
| chr2:151595183
|
G | A | 15 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(12): Show | 15 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.14206-865C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595183 | ||||||
| chr2:151595272
|
C | T | 3 | a0036c0029t0001g0176a0087c0132t0001g0101a0105c0080t0001g0034 | 3 | HG01884.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.14205+788G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595272 | ||||||
| chr2:151595366
|
C | T | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0093c0058t0002g0025 | 3 | NA19080.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14205+694G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595366 | ||||||
| chr2:151595408
|
C | T | 2 | a0002c0002t0001g0046a0002c0002t0001g0060 | 2 | HG01993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.14205+652G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595408 | ||||||
| chr2:151595421
|
T | TTTTG | 7 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.14205+635_14205+63 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595421 | ||||||
| chr2:151595421
|
TTTTG | T | 24 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(21): Show | 24 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.14205+635_14205+63 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595421 | ||||||
| chr2:151595421
|
TTTTGTTT others(1): Show |
T | 12 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(9): Show | 12 | HG00544.hp2 HG01891.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.14205+631_14205+63 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595421 | ||||||
| chr2:151595736
|
T | G | 1 | a0115c0053t0001g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.14205+324A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595736 | ||||||
| chr2:151595766
|
TA | T | 42 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.14205+293delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595766 | ||||||
| chr2:151595944
|
G | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.14205+116C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595944 | ||||||
| chr2:151595955
|
GC | G | 2 | a0082c0140t0001g0094a0121c0074t0001g0058 | 2 | HG00558.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.14205+104delG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595955 | ||||||
| chr2:151595979
|
A | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.14205+81T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 92/181 | chr2 | 151595979 | ||||||
| chr2:151596283
|
G | A | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.14098-116C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596283 | ||||||
| chr2:151596306
|
G | A | 2 | a0024c0040t0001g0062a0117c0039t0001g0063 | 2 | HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.14098-139C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596306 | ||||||
| chr2:151596333
|
C | G | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.14098-166G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596333 | ||||||
| chr2:151596338
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.14098-171A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596338 | ||||||
| chr2:151596365
|
A | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.14098-198T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596365 | ||||||
| chr2:151596379
|
T | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.14098-212A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596379 | ||||||
| chr2:151596462
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.14098-295A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596462 | ||||||
| chr2:151596563
|
G | A | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+395C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596563 | ||||||
| chr2:151596585
|
A | C | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+373T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596585 | ||||||
| chr2:151596597
|
T | C | 2 | a0082c0140t0001g0094a0084c0133t0001g0154 | 2 | HG00558.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.14097+361A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596597 | ||||||
| chr2:151596602
|
T | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.14097+356A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596602 | ||||||
| chr2:151596607
|
T | A | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+351A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596607 | ||||||
| chr2:151596610
|
A | G | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+348T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596610 | ||||||
| chr2:151596619
|
C | T | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+339G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596619 | ||||||
| chr2:151596633
|
T | C | 4 | a0002c0002t0001g0036a0013c0014t0001g0099a0013c0014t0001g0102others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.14097+325A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596633 | ||||||
| chr2:151596671
|
A | T | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+287T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596671 | ||||||
| chr2:151596673
|
G | A | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+285C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596673 | ||||||
| chr2:151596742
|
A | T | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+216T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596742 | ||||||
| chr2:151596781
|
A | T | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+177T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596781 | ||||||
| chr2:151596886
|
G | A | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.14097+72C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596886 | ||||||
| chr2:151596895
|
A | C | 7 | a0033c0024t0001g0096a0036c0029t0001g0176a0037c0087t0001g0107others(4): Show | 7 | HG00558.hp2 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14097+63T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596895 | ||||||
| chr2:151596947
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.14097+11C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 91/181 | chr2 | 151596947 | ||||||
| chr2:151597094
|
T | C | 40 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.13993-32A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597094 | ||||||
| chr2:151597222
|
G | A | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13993-160C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597222 | ||||||
| chr2:151597293
|
T | C | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.13993-231A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597293 | ||||||
| chr2:151597352
|
C | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.13993-290G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597352 | ||||||
| chr2:151597374
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13993-312G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597374 | ||||||
| chr2:151597589
|
C | G | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.13992+338G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597589 | ||||||
| chr2:151597694
|
G | A | 78 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(75): Show | 78 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.13992+233C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597694 | ||||||
| chr2:151597716
|
A | G | 1 | a0010c0137t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.13992+211T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597716 | ||||||
| chr2:151597893
|
G | C | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13992+34C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597893 | ||||||
| chr2:151597895
|
A | T | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13992+32T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 90/181 | chr2 | 151597895 | ||||||
| chr2:151598185
|
C | A | 4 | a0070c0123t0001g0116a0071c0124t0001g0128a0089c0036t0001g0053others(1): Show | 4 | NA18966.hp2 NA18984.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.13789-55G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598185 | ||||||
| chr2:151598214
|
G | A | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13789-84C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598214 | ||||||
| chr2:151598229
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.13789-99A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598229 | ||||||
| chr2:151598252
|
G | A | 4 | a0070c0123t0001g0116a0071c0124t0001g0128a0089c0036t0001g0053others(1): Show | 4 | NA18966.hp2 NA18984.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.13789-122C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598252 | ||||||
| chr2:151598328
|
G | T | 1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13789-198C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598328 | ||||||
| chr2:151598348
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13789-218G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598348 | ||||||
| chr2:151598359
|
C | CA | 40 | a0001c0001t0001g0126a0006c0012t0001g0173a0008c0004t0001g0009others(37): Show | 40 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.13789-230dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598359 | ||||||
| chr2:151598359
|
C | CAAA | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0050c0099t0001g0098others(3): Show | 6 | HG01993.hp1 HG02040.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.13789-232_13789-23 others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598359 | ||||||
| chr2:151598359
|
C | CAAAA | 5 | a0010c0139t0001g0106a0049c0096t0001g0184a0091c0142t0001g0119others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.13789-233_13789-23 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598359 | ||||||
| chr2:151598359
|
CAAAAAAA others(4): Show |
C | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.13789-240_13789-23 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598359 | ||||||
| chr2:151598385
|
G | T | 2 | a0042c0095t0001g0020a0120c0023t0001g0088 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.13789-255C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598385 | ||||||
| chr2:151598538
|
A | G | 6 | a0033c0024t0001g0096a0035c0146t0001g0103a0036c0029t0001g0176others(3): Show | 6 | HG00639.hp1 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.13789-408T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598538 | ||||||
| chr2:151598545
|
G | A | 127 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.13789-415C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598545 | ||||||
| chr2:151598574
|
T | A | 19 | a0003c0005t0001g0006a0008c0004t0001g0009a0008c0004t0001g0011others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.13789-444A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598574 | ||||||
| chr2:151598644
|
CAAAAAAA others(4): Show |
C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.13789-525_13789-51 others(15): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598644 | ||||||
| chr2:151598699
|
T | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13789-569A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598699 | ||||||
| chr2:151598779
|
T | G | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13789-649A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598779 | ||||||
| chr2:151598789
|
C | G | 8 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(5): Show | 8 | HG00423.hp2 HG00609.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.13789-659G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598789 | ||||||
| chr2:151598891
|
A | G | 46 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(43): Show | 46 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.13789-761T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151598891 | ||||||
| chr2:151599010
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.13789-880A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599010 | ||||||
| chr2:151599028
|
A | G | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13789-898T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599028 | ||||||
| chr2:151599130
|
A | T | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.13789-1000T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599130 | ||||||
| chr2:151599293
|
T | C | 11 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(8): Show | 11 | HG00544.hp2 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.13788+1149A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599293 | ||||||
| chr2:151599405
|
T | C | 1 | a0005c0008t0001g0038 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.13788+1037A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599405 | ||||||
| chr2:151599522
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.13788+920T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599522 | ||||||
| chr2:151599627
|
T | C | 15 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(12): Show | 15 | HG00280.hp1 HG00621.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.13788+815A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599627 | ||||||
| chr2:151599817
|
G | A | 32 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.13788+625C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599817 | ||||||
| chr2:151599899
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.13788+543C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599899 | ||||||
| chr2:151599916
|
G | A | 1 | a0037c0087t0001g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.13788+526C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599916 | ||||||
| chr2:151599918
|
G | A | 2 | a0059c0143t0001g0161a0106c0050t0001g0045 | 2 | HG00544.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.13788+524C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599918 | ||||||
| chr2:151599980
|
AGGAGTTC others(20): Show |
A | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.13788+435_13788+46 others(31): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151599980 | ||||||
| chr2:151600018
|
C | T | 77 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(74): Show | 77 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.13788+424G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600018 | ||||||
| chr2:151600121
|
G | A | 12 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(9): Show | 12 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.13788+321C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600121 | ||||||
| chr2:151600133
|
G | A | 1 | a0022c0026t0001g0032 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.13788+309C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600133 | ||||||
| chr2:151600190
|
C | CA | 18 | a0002c0002t0001g0039a0003c0005t0001g0004a0003c0094t0001g0014others(15): Show | 18 | HG00639.hp2 HG00673.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.13788+251dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600190 | ||||||
| chr2:151600190
|
C | CAA | 54 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0046others(51): Show | 54 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.13788+250_13788+25 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600190 | ||||||
| chr2:151600190
|
CA | C | 19 | a0005c0063t0001g0052a0009c0017t0001g0121a0009c0017t0001g0159others(16): Show | 19 | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.13788+251delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600190 | ||||||
| chr2:151600208
|
A | AG | 4 | a0028c0021t0001g0182a0028c0021t0001g0183a0119c0136t0001g0132others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.13788+233_13788+23 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600208 | ||||||
| chr2:151600208
|
A | G | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.13788+234T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600208 | ||||||
| chr2:151600242
|
C | T | 11 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(8): Show | 11 | HG00544.hp2 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.13788+200G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600242 | ||||||
| chr2:151600276
|
C | A | 2 | a0003c0005t0001g0013a0068c0125t0001g0111 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.13788+166G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600276 | ||||||
| chr2:151600370
|
G | A | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.13788+72C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600370 | ||||||
| chr2:151600430
|
G | C | 9 | a0027c0013t0001g0070a0027c0013t0001g0071a0049c0096t0001g0184others(6): Show | 9 | HG02257.hp2 HG02976.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.13788+12C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 89/181 | chr2 | 151600430 | ||||||
| chr2:151600853
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.13477-100A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151600853 | ||||||
| chr2:151600957
|
C | G | 15 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(12): Show | 15 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.13477-204G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151600957 | ||||||
| chr2:151601037
|
G | A | 38 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.13477-284C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601037 | ||||||
| chr2:151601038
|
T | C | 38 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.13477-285A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601038 | ||||||
| chr2:151601083
|
T | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-330A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601083 | ||||||
| chr2:151601087
|
TTTATTTT others(2): Show |
T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-343_13477-33 others(13): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601087 | ||||||
| chr2:151601101
|
C | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-348G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601101 | ||||||
| chr2:151601105
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-352A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601105 | ||||||
| chr2:151601106
|
C | CT | 64 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(61): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.13477-354dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601106 | ||||||
| chr2:151601106
|
C | CTT | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0012c0090t0001g0005others(4): Show | 7 | HG00099.hp1 HG03669.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.13477-355_13477-35 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601106 | ||||||
| chr2:151601106
|
C | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-353G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601106 | ||||||
| chr2:151601110
|
T | TC | 16 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(13): Show | 16 | HG00639.hp2 HG01192.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.13477-358_13477-35 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601110 | ||||||
| chr2:151601111
|
T | C | 21 | a0013c0014t0001g0099a0013c0014t0001g0102a0017c0015t0001g0164others(18): Show | 21 | HG00544.hp2 HG00639.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.13477-358A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601111 | ||||||
| chr2:151601113
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13477-360A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601113 | ||||||
| chr2:151601113
|
T | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-360A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601113 | ||||||
| chr2:151601117
|
T | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-364A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601117 | ||||||
| chr2:151601119
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-366A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601119 | ||||||
| chr2:151601121
|
T | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-368A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601121 | ||||||
| chr2:151601126
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-373C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601126 | ||||||
| chr2:151601139
|
G | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-386C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601139 | ||||||
| chr2:151601143
|
T | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-390A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601143 | ||||||
| chr2:151601145
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-392G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601145 | ||||||
| chr2:151601156
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-403T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601156 | ||||||
| chr2:151601166
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-413T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601166 | ||||||
| chr2:151601169
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-416T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601169 | ||||||
| chr2:151601170
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-417G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601170 | ||||||
| chr2:151601177
|
G | A | 5 | a0009c0017t0001g0159a0060c0107t0001g0157a0063c0105t0001g0160others(2): Show | 5 | HG00597.hp2 HG02165.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.13477-424C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601177 | ||||||
| chr2:151601186
|
G | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-433C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601186 | ||||||
| chr2:151601201
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-448A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601201 | ||||||
| chr2:151601202
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-449C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601202 | ||||||
| chr2:151601211
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-458A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601211 | ||||||
| chr2:151601212
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-459C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601212 | ||||||
| chr2:151601226
|
T | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-473A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601226 | ||||||
| chr2:151601243
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-490C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601243 | ||||||
| chr2:151601246
|
T | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-493A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601246 | ||||||
| chr2:151601265
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-512A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601265 | ||||||
| chr2:151601266
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-513C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601266 | ||||||
| chr2:151601267
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-514G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601267 | ||||||
| chr2:151601269
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-516G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601269 | ||||||
| chr2:151601270
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13477-517T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601270 | ||||||
| chr2:151601328
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+573G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601328 | ||||||
| chr2:151601350
|
C | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+551G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601350 | ||||||
| chr2:151601355
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+546G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601355 | ||||||
| chr2:151601372
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+529T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601372 | ||||||
| chr2:151601380
|
AT | A | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13476+520delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601380 | ||||||
| chr2:151601400
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+501T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601400 | ||||||
| chr2:151601406
|
T | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+495A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601406 | ||||||
| chr2:151601460
|
G | A | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13476+441C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601460 | ||||||
| chr2:151601463
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+438T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601463 | ||||||
| chr2:151601466
|
C | T | 1 | a0102c0069t0001g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.13476+435G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601466 | ||||||
| chr2:151601473
|
C | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+428G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601473 | ||||||
| chr2:151601474
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+427C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601474 | ||||||
| chr2:151601476
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+425C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601476 | ||||||
| chr2:151601483
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+418T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601483 | ||||||
| chr2:151601485
|
C | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+416G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601485 | ||||||
| chr2:151601487
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+414C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601487 | ||||||
| chr2:151601489
|
A | G | 138 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.13476+412T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601489 | ||||||
| chr2:151601491
|
A | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+410T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601491 | ||||||
| chr2:151601497
|
A | AGCACACA others(10542): Show |
1 | a0059c0143t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.13476+403_13476+40 others(10553): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601497 | ||||||
| chr2:151601497
|
A | G | 19 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(16): Show | 19 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.13476+404T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601497 | ||||||
| chr2:151601499
|
C | G | 35 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.13476+402G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601499 | ||||||
| chr2:151601572
|
A | C | 36 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0046others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.13476+329T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601572 | ||||||
| chr2:151601580
|
A | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+321T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601580 | ||||||
| chr2:151601588
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+313G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601588 | ||||||
| chr2:151601617
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+284G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601617 | ||||||
| chr2:151601619
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+282C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601619 | ||||||
| chr2:151601624
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+277T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601624 | ||||||
| chr2:151601663
|
C | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+238G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601663 | ||||||
| chr2:151601665
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+236A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601665 | ||||||
| chr2:151601683
|
GA | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+217delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601683 | ||||||
| chr2:151601699
|
G | T | 1 | a0002c0002t0001g0039 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.13476+202C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601699 | ||||||
| chr2:151601725
|
A | G | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+176T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601725 | ||||||
| chr2:151601735
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13476+166G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601735 | ||||||
| chr2:151601749
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+152C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601749 | ||||||
| chr2:151601758
|
A | T | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+143T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601758 | ||||||
| chr2:151601759
|
G | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+142C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601759 | ||||||
| chr2:151601760
|
T | C | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+141A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601760 | ||||||
| chr2:151601762
|
G | A | 39 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.13476+139C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601762 | ||||||
| chr2:151601768
|
G | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.13476+133C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601768 | ||||||
| chr2:151601793
|
A | G | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0084c0133t0001g0154 | 3 | HG01891.hp2 HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.13476+108T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601793 | ||||||
| chr2:151601884
|
G | GC | 38 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.13476+16_13476+17i others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 88/181 | chr2 | 151601884 | ||||||
| chr2:151602314
|
C | T | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13368+273G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/181 | chr2 | 151602314 | ||||||
| chr2:151602405
|
T | C | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13368+182A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/181 | chr2 | 151602405 | ||||||
| chr2:151602422
|
T | C | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13368+165A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/181 | chr2 | 151602422 | ||||||
| chr2:151602576
|
T | C | 177 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.13368+11A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 87/181 | chr2 | 151602576 | ||||||
| chr2:151602830
|
AAACT | A | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.13264-143_13264-14 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151602830 | ||||||
| chr2:151602862
|
A | G | 2 | a0109c0046t0001g0048a0118c0073t0001g0051 | 2 | NA18947.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.13264-171T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151602862 | ||||||
| chr2:151603010
|
G | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13264-319C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151603010 | ||||||
| chr2:151603071
|
C | T | 16 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(13): Show | 16 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.13264-380G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151603071 | ||||||
| chr2:151603315
|
C | G | 10 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.13263+254G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151603315 | ||||||
| chr2:151603477
|
C | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.13263+92G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151603477 | ||||||
| chr2:151603503
|
C | T | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13263+66G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 86/181 | chr2 | 151603503 | ||||||
| chr2:151604080
|
T | G | 1 | a0128c0148t0001g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.13060-308A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/181 | chr2 | 151604080 | ||||||
| chr2:151604121
|
C | T | 42 | a0001c0082t0001g0147a0003c0083t0001g0003a0003c0094t0001g0014others(39): Show | 42 | HG00621.hp1 HG00673.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.13060-349G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/181 | chr2 | 151604121 | ||||||
| chr2:151604180
|
G | T | 89 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(86): Show | 89 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.13059+380C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/181 | chr2 | 151604180 | ||||||
| chr2:151604188
|
C | T | 79 | a0002c0002t0001g0046a0002c0002t0001g0049a0003c0005t0001g0004others(76): Show | 79 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.13059+372G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/181 | chr2 | 151604188 | ||||||
| chr2:151604281
|
T | C | 34 | a0009c0017t0001g0121a0009c0017t0001g0159a0010c0137t0001g0093others(31): Show | 34 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.13059+279A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 85/181 | chr2 | 151604281 | ||||||
| chr2:151604946
|
T | C | 54 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.12748-75A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151604946 | ||||||
| chr2:151605023
|
A | G | 48 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.12748-152T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605023 | ||||||
| chr2:151605025
|
A | G | 1 | a0061c0115t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.12748-154T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605025 | ||||||
| chr2:151605043
|
A | G | 3 | a0017c0015t0001g0164a0017c0015t0001g0165a0061c0115t0001g0158 | 3 | NA18943.hp2 NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.12748-172T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605043 | ||||||
| chr2:151605300
|
A | T | 50 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.12748-429T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605300 | ||||||
| chr2:151605341
|
C | T | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.12748-470G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605341 | ||||||
| chr2:151605373
|
A | C | 2 | a0006c0012t0001g0172a0006c0012t0001g0173 | 2 | NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.12748-502T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605373 | ||||||
| chr2:151605400
|
A | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(1): Show | 4 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.12748-529T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605400 | ||||||
| chr2:151605418
|
C | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.12748-547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605418 | ||||||
| chr2:151605440
|
T | C | 87 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.12748-569A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605440 | ||||||
| chr2:151605476
|
T | C | 86 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.12748-605A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605476 | ||||||
| chr2:151605516
|
A | G | 11 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(8): Show | 11 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.12748-645T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605516 | ||||||
| chr2:151605587
|
C | T | 26 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.12748-716G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605587 | ||||||
| chr2:151605640
|
C | T | 1 | a0094c0061t0001g0080 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.12748-769G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605640 | ||||||
| chr2:151605695
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.12748-824T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605695 | ||||||
| chr2:151605726
|
A | G | 83 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.12748-855T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605726 | ||||||
| chr2:151605734
|
A | AG | 71 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.12748-864dupC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605734 | ||||||
| chr2:151605735
|
G | GA | 11 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(8): Show | 11 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.12748-865_12748-86 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605735 | ||||||
| chr2:151605810
|
A | AT | 82 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.12747+795dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605810 | ||||||
| chr2:151605972
|
T | TTTTG | 73 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.12747+630_12747+63 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605972 | ||||||
| chr2:151605999
|
T | C | 1 | a0099c0067t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.12747+607A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151605999 | ||||||
| chr2:151606091
|
A | T | 6 | a0013c0014t0001g0099a0013c0014t0001g0102a0035c0146t0001g0103others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.12747+515T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606091 | ||||||
| chr2:151606120
|
G | A | 6 | a0004c0018t0001g0134a0004c0018t0001g0135a0021c0056t0001g0041others(3): Show | 6 | HG00741.hp1 HG02040.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.12747+486C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606120 | ||||||
| chr2:151606256
|
T | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12747+350A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606256 | ||||||
| chr2:151606259
|
G | A | 1 | a0011c0070t0001g0055 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.12747+347C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606259 | ||||||
| chr2:151606313
|
TA | T | 5 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(2): Show | 5 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.12747+292delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606313 | ||||||
| chr2:151606491
|
C | G | 35 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.12747+115G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606491 | ||||||
| chr2:151606502
|
G | GC | 70 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.12747+103_12747+10 others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 84/181 | chr2 | 151606502 | ||||||
| chr2:151606829
|
G | A | 10 | a0002c0048t0001g0086a0010c0137t0001g0093a0010c0138t0001g0091others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.12640-116C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151606829 | ||||||
| chr2:151606925
|
T | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12640-212A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151606925 | ||||||
| chr2:151606944
|
T | C | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.12640-231A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151606944 | ||||||
| chr2:151607109
|
A | G | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+395T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607109 | ||||||
| chr2:151607131
|
C | A | 66 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.12639+373G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607131 | ||||||
| chr2:151607135
|
C | T | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.12639+369G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607135 | ||||||
| chr2:151607143
|
C | T | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+361G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607143 | ||||||
| chr2:151607153
|
A | T | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+351T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607153 | ||||||
| chr2:151607156
|
G | A | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+348C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607156 | ||||||
| chr2:151607165
|
T | C | 66 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.12639+339A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607165 | ||||||
| chr2:151607179
|
T | C | 3 | a0026c0006t0001g0027a0026c0006t0001g0079a0125c0028t0001g0031 | 3 | NA18960.hp1 NA19010.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.12639+325A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607179 | ||||||
| chr2:151607217
|
T | A | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+287A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607217 | ||||||
| chr2:151607219
|
A | G | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+285T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607219 | ||||||
| chr2:151607235
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.12639+269A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607235 | ||||||
| chr2:151607288
|
T | A | 65 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.12639+216A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607288 | ||||||
| chr2:151607313
|
A | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12639+191T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607313 | ||||||
| chr2:151607327
|
T | A | 71 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.12639+177A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607327 | ||||||
| chr2:151607432
|
A | G | 72 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.12639+72T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607432 | ||||||
| chr2:151607441
|
C | A | 70 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.12639+63G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 83/181 | chr2 | 151607441 | ||||||
| chr2:151607640
|
T | C | 75 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(72): Show | 75 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.12535-32A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151607640 | ||||||
| chr2:151607657
|
T | C | 1 | a0004c0126t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.12535-49A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151607657 | ||||||
| chr2:151607768
|
G | A | 26 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.12535-160C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151607768 | ||||||
| chr2:151607839
|
T | C | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.12535-231A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151607839 | ||||||
| chr2:151607920
|
C | A | 1 | a0011c0070t0001g0055 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.12535-312G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151607920 | ||||||
| chr2:151608119
|
A | AAC | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.12534+352_12534+35 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608119 | ||||||
| chr2:151608119
|
AAC | A | 39 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.12534+352_12534+35 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608119 | ||||||
| chr2:151608135
|
C | G | 33 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.12534+338G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608135 | ||||||
| chr2:151608240
|
G | A | 84 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(81): Show | 84 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.12534+233C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608240 | ||||||
| chr2:151608267
|
G | C | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.12534+206C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608267 | ||||||
| chr2:151608279
|
C | T | 36 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(33): Show | 36 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.12534+194G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608279 | ||||||
| chr2:151608388
|
G | A | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12534+85C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608388 | ||||||
| chr2:151608422
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.12534+51G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608422 | ||||||
| chr2:151608423
|
G | A | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.12534+50C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608423 | ||||||
| chr2:151608439
|
G | C | 20 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(17): Show | 20 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.12534+34C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608439 | ||||||
| chr2:151608441
|
A | T | 20 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(17): Show | 20 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.12534+32T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 82/181 | chr2 | 151608441 | ||||||
| chr2:151608704
|
C | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.12331-28G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608704 | ||||||
| chr2:151608731
|
C | A | 29 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.12331-55G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608731 | ||||||
| chr2:151608798
|
G | A | 95 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.12331-122C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608798 | ||||||
| chr2:151608818
|
G | A | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.12331-142C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608818 | ||||||
| chr2:151608874
|
G | T | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.12331-198C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608874 | ||||||
| chr2:151608905
|
C | CA | 17 | a0003c0005t0001g0013a0004c0019t0001g0148a0011c0009t0001g0040others(14): Show | 17 | HG00673.hp1 HG01358.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.12331-230dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608905 | ||||||
| chr2:151608905
|
C | CAA | 21 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(18): Show | 21 | HG01192.hp1 HG01884.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.12331-231_12331-23 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608905 | ||||||
| chr2:151608905
|
C | CAAAAA | 5 | a0010c0137t0001g0093a0015c0108t0001g0136a0081c0141t0001g0092others(2): Show | 5 | HG00609.hp2 HG01993.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.12331-234_12331-23 others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608905 | ||||||
| chr2:151608905
|
CAAAAAAA others(1): Show |
C | 24 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.12331-237_12331-23 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608905 | ||||||
| chr2:151608905
|
CAAAAAAA others(8): Show |
C | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.12331-244_12331-23 others(19): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608905 | ||||||
| chr2:151608929
|
A | T | 1 | a0090c0035t0001g0054 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.12331-253T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608929 | ||||||
| chr2:151608935
|
T | G | 45 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(42): Show | 45 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.12331-259A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608935 | ||||||
| chr2:151608955
|
A | G | 2 | a0129c0022t0001g0114a0133c0152t0001g0169 | 2 | HG01192.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.12331-279T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608955 | ||||||
| chr2:151608959
|
A | C | 2 | a0051c0131t0001g0187a0083c0134t0001g0153 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.12331-283T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608959 | ||||||
| chr2:151608962
|
T | A | 41 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.12331-286A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608962 | ||||||
| chr2:151608981
|
A | G | 34 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.12331-305T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608981 | ||||||
| chr2:151608995
|
C | T | 35 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.12331-319G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151608995 | ||||||
| chr2:151609010
|
T | C | 1 | a0133c0152t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.12331-334A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609010 | ||||||
| chr2:151609025
|
C | A | 12 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(9): Show | 12 | HG00639.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.12331-349G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609025 | ||||||
| chr2:151609095
|
G | A | 184 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.12331-419C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609095 | ||||||
| chr2:151609124
|
T | A | 1 | a0007c0003t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12331-448A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609124 | ||||||
| chr2:151609154
|
T | C | 1 | a0106c0050t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.12331-478A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609154 | ||||||
| chr2:151609174
|
C | T | 1 | a0106c0050t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.12331-498G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609174 | ||||||
| chr2:151609202
|
A | AG | 31 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.12331-527dupC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609202 | ||||||
| chr2:151609203
|
G | GA | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.12331-528dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609203 | ||||||
| chr2:151609291
|
C | G | 114 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.12330+518G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609291 | ||||||
| chr2:151609313
|
C | T | 31 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0124others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.12330+496G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609313 | ||||||
| chr2:151609337
|
G | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.12330+472C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609337 | ||||||
| chr2:151609504
|
A | G | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12330+305T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609504 | ||||||
| chr2:151609512
|
T | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12330+297A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609512 | ||||||
| chr2:151609525
|
G | A | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12330+284C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609525 | ||||||
| chr2:151609526
|
C | T | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12330+283G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609526 | ||||||
| chr2:151609570
|
A | G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.12330+239T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609570 | ||||||
| chr2:151609678
|
A | G | 1 | a0010c0137t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.12330+131T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609678 | ||||||
| chr2:151609700
|
C | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.12330+109G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 81/181 | chr2 | 151609700 | ||||||
| chr2:151610214
|
T | C | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.12019-94A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 80/181 | chr2 | 151610214 | ||||||
| chr2:151610300
|
T | C | 1 | a0015c0111t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.12019-180A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 80/181 | chr2 | 151610300 | ||||||
| chr2:151610487
|
C | T | 49 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(46): Show | 49 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.12018+29G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 80/181 | chr2 | 151610487 | ||||||
| chr2:151610679
|
C | T | 1 | a0039c0153t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.11911-56G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 79/181 | chr2 | 151610679 | ||||||
| chr2:151610703
|
C | T | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.11910+59G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 79/181 | chr2 | 151610703 | ||||||
| chr2:151610974
|
C | T | 9 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.11806-108G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151610974 | ||||||
| chr2:151611083
|
A | G | 1 | a0083c0134t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.11806-217T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611083 | ||||||
| chr2:151611175
|
G | C | 1 | a0089c0036t0001g0053 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.11806-309C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611175 | ||||||
| chr2:151611272
|
A | G | 2 | a0075c0102t0001g0166a0076c0101t0001g0167 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.11806-406T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611272 | ||||||
| chr2:151611277
|
T | G | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11806-411A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611277 | ||||||
| chr2:151611353
|
T | G | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11806-487A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611353 | ||||||
| chr2:151611413
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.11806-547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611413 | ||||||
| chr2:151611434
|
A | G | 8 | a0036c0029t0001g0176a0046c0091t0001g0017a0049c0096t0001g0184others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.11806-568T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611434 | ||||||
| chr2:151611478
|
G | A | 4 | a0036c0029t0001g0176a0046c0091t0001g0017a0087c0132t0001g0101others(1): Show | 4 | HG01884.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.11806-612C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611478 | ||||||
| chr2:151611628
|
T | C | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11805+558A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 78/181 | chr2 | 151611628 | ||||||
| chr2:151612499
|
A | C | 2 | a0005c0008t0001g0038a0005c0008t0001g0077 | 2 | HG01074.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.11602-110T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151612499 | ||||||
| chr2:151612702
|
C | T | 6 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(3): Show | 6 | HG00544.hp2 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.11602-313G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151612702 | ||||||
| chr2:151612850
|
T | C | 1 | a0067c0117t0001g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.11602-461A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151612850 | ||||||
| chr2:151613030
|
A | T | 2 | a0004c0019t0001g0148a0004c0019t0001g0151 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.11602-641T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613030 | ||||||
| chr2:151613344
|
T | A | 40 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(37): Show | 40 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.11601+932A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613344 | ||||||
| chr2:151613432
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.11601+844A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613432 | ||||||
| chr2:151613526
|
C | T | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11601+750G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613526 | ||||||
| chr2:151613542
|
C | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.11601+734G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613542 | ||||||
| chr2:151613600
|
T | C | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11601+676A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613600 | ||||||
| chr2:151613704
|
T | C | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.11601+572A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613704 | ||||||
| chr2:151613734
|
A | G | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11601+542T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613734 | ||||||
| chr2:151613827
|
T | C | 2 | a0110c0041t0001g0075a0124c0075t0001g0057 | 2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.11601+449A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613827 | ||||||
| chr2:151613884
|
T | A | 4 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.11601+392A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151613884 | ||||||
| chr2:151614116
|
G | A | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.11601+160C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 77/181 | chr2 | 151614116 | ||||||
| chr2:151614678
|
C | T | 4 | a0056c0145t0001g0177a0084c0133t0001g0154a0085c0031t0001g0108others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.11290-91G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151614678 | ||||||
| chr2:151615409
|
G | C | 40 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(37): Show | 40 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.11289+593C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151615409 | ||||||
| chr2:151615442
|
C | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.11289+560G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151615442 | ||||||
| chr2:151615492
|
G | A | 4 | a0056c0145t0001g0177a0084c0133t0001g0154a0085c0031t0001g0108others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.11289+510C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151615492 | ||||||
| chr2:151615704
|
A | T | 30 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(27): Show | 30 | HG00597.hp2 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.11289+298T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151615704 | ||||||
| chr2:151615903
|
C | T | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.11289+99G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 76/181 | chr2 | 151615903 | ||||||
| chr2:151616311
|
T | C | 1 | a0003c0005t0001g0004 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.11182-202A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616311 | ||||||
| chr2:151616354
|
T | C | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11182-245A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616354 | ||||||
| chr2:151616475
|
G | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.11182-366C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616475 | ||||||
| chr2:151616647
|
T | C | 1 | a0072c0121t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.11182-538A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616647 | ||||||
| chr2:151616883
|
A | G | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11181+481T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616883 | ||||||
| chr2:151616892
|
A | C | 80 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.11181+472T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616892 | ||||||
| chr2:151616976
|
G | A | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11181+388C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151616976 | ||||||
| chr2:151617204
|
C | T | 3 | a0056c0145t0001g0177a0085c0031t0001g0108a0130c0150t0001g0180 | 3 | HG02280.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.11181+160G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 75/181 | chr2 | 151617204 | ||||||
| chr2:151617472
|
C | CA | 8 | a0011c0009t0001g0040a0015c0108t0001g0136a0019c0010t0003g0188others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.11077-5dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617472 | ||||||
| chr2:151617487
|
A | G | 29 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.11077-19T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617487 | ||||||
| chr2:151617487
|
AAG | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.11077-21_11077-20d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617487 | ||||||
| chr2:151617491
|
G | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.11077-23C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617491 | ||||||
| chr2:151617724
|
A | C | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.11077-256T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617724 | ||||||
| chr2:151617727
|
A | AT | 10 | a0003c0005t0001g0013a0035c0146t0001g0103a0036c0029t0001g0176others(7): Show | 10 | HG00639.hp1 HG01884.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.11077-260dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617727 | ||||||
| chr2:151617849
|
C | G | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11077-381G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617849 | ||||||
| chr2:151617928
|
C | T | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.11076+347G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617928 | ||||||
| chr2:151617946
|
G | C | 3 | a0036c0029t0001g0176a0046c0091t0001g0017a0105c0080t0001g0034 | 3 | HG01884.hp1 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.11076+329C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617946 | ||||||
| chr2:151617987
|
G | A | 3 | a0020c0007t0001g0042a0020c0007t0001g0043a0024c0038t0001g0085 | 3 | HG00597.hp1 NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.11076+288C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151617987 | ||||||
| chr2:151618096
|
T | G | 1 | a0002c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.11076+179A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151618096 | ||||||
| chr2:151618125
|
T | G | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.11076+150A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 74/181 | chr2 | 151618125 | ||||||
| chr2:151618619
|
T | C | 1 | a0114c0055t0001g0044 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.10873-141A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151618619 | ||||||
| chr2:151619014
|
C | T | 1 | a0024c0038t0001g0085 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.10872+437G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619014 | ||||||
| chr2:151619040
|
A | G | 1 | a0133c0152t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.10872+411T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619040 | ||||||
| chr2:151619096
|
C | G | 1 | a0125c0028t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.10872+355G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619096 | ||||||
| chr2:151619217
|
G | C | 1 | a0101c0068t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.10872+234C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619217 | ||||||
| chr2:151619309
|
C | T | 1 | a0118c0073t0001g0051 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.10872+142G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619309 | ||||||
| chr2:151619319
|
C | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.10872+132G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619319 | ||||||
| chr2:151619396
|
C | T | 35 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(32): Show | 35 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.10872+55G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619396 | ||||||
| chr2:151619424
|
T | G | 44 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(41): Show | 44 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.10872+27A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 73/181 | chr2 | 151619424 | ||||||
| chr2:151619808
|
T | C | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10561-46A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151619808 | ||||||
| chr2:151619886
|
G | A | 1 | a0039c0153t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.10561-124C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151619886 | ||||||
| chr2:151620107
|
A | G | 2 | a0072c0121t0001g0143a0121c0074t0001g0058 | 2 | HG01891.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.10561-345T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620107 | ||||||
| chr2:151620109
|
G | C | 5 | a0017c0015t0001g0164a0017c0015t0001g0165a0025c0011t0001g0089others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.10561-347C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620109 | ||||||
| chr2:151620339
|
ATG | A | 11 | a0002c0002t0001g0049a0010c0137t0001g0093a0015c0108t0001g0136others(8): Show | 11 | HG00609.hp2 HG00621.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.10560+578_10561-57 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620339 | ||||||
| chr2:151620339
|
ATGTG | A | 9 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(6): Show | 9 | HG01192.hp1 HG02040.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.10560+576_10561-57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620339 | ||||||
| chr2:151620343
|
G | GTA | 2 | a0060c0107t0001g0157a0084c0133t0001g0154 | 2 | HG02165.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.10560+575_10560+57 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
G | GTATA | 2 | a0009c0109t0001g0130a0067c0117t0001g0144 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.10560+575_10560+57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
G | GTATATA | 4 | a0015c0111t0001g0139a0023c0043t0001g0047a0041c0085t0002g0010others(1): Show | 4 | HG02523.hp2 HG03486.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.10560+575_10560+57 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
G | GTATATAT others(3): Show |
3 | a0010c0139t0001g0106a0033c0024t0001g0096a0126c0027t0001g0067 | 3 | HG00423.hp2 HG02630.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.10560+575_10560+57 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTA | G | 2 | a0023c0044t0001g0068a0025c0011t0001g0090 | 2 | HG00673.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10560+570_10560+57 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(1): Show |
G | 3 | a0025c0011t0001g0089a0036c0029t0001g0176a0043c0084t0001g0018 | 3 | HG00544.hp2 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.10560+568_10560+57 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(5): Show |
G | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.10560+564_10560+57 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(7): Show |
G | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.10560+562_10560+57 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(11): Show |
G | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.10560+558_10560+57 others(22): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(15): Show |
G | 2 | a0050c0099t0001g0098a0056c0145t0001g0177 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.10560+554_10560+57 others(26): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(21): Show |
G | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0087c0132t0001g0101others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.10560+548_10560+57 others(32): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620343
|
GTGTGTAT others(29): Show |
G | 3 | a0062c0106t0001g0140a0075c0102t0001g0166a0076c0101t0001g0167 | 3 | HG03688.hp1 NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.10560+540_10560+57 others(40): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620343 | ||||||
| chr2:151620345
|
G | A | 24 | a0009c0017t0001g0121a0009c0017t0001g0159a0009c0109t0001g0130others(21): Show | 24 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.10560+574C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTA | 5 | a0002c0048t0001g0086a0007c0003t0001g0029a0107c0045t0001g0028others(2): Show | 5 | HG00741.hp2 HG01258.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.10560+573_10560+57 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATA | 4 | a0014c0112t0001g0141a0026c0006t0001g0027a0037c0087t0001g0107others(1): Show | 4 | HG02965.hp2 HG03239.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.10560+573_10560+57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATATA | 4 | a0007c0003t0001g0001a0007c0003t0001g0002a0024c0038t0001g0085others(1): Show | 4 | HG04115.hp1 NA18947.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.10560+573_10560+57 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATATAT others(1): Show |
2 | a0002c0002t0001g0026a0125c0028t0001g0031 | 2 | HG01175.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.10560+573_10560+57 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATATAT others(3): Show |
3 | a0094c0061t0001g0080a0106c0050t0001g0045a0112c0051t0001g0072 | 3 | HG00099.hp2 HG00544.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.10560+573_10560+57 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATATAT others(5): Show |
2 | a0002c0002t0001g0039a0024c0040t0001g0062 | 2 | HG02523.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.10560+573_10560+57 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
G | GTATATAT others(7): Show |
3 | a0020c0007t0001g0042a0020c0007t0001g0043a0127c0144t0001g0129 | 3 | HG00597.hp1 HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.10560+573_10560+57 others(18): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
GTGTA | G | 6 | a0002c0002t0001g0036a0002c0002t0001g0060a0014c0113t0001g0120others(3): Show | 6 | HG01515.hp1 HG01993.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.10560+570_10560+57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
GTGTATAT others(25): Show |
G | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.10560+542_10560+57 others(36): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620345
|
GTGTATAT others(27): Show |
G | 29 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.10560+540_10560+57 others(38): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620345 | ||||||
| chr2:151620347
|
G | A | 58 | a0002c0002t0001g0026a0002c0002t0001g0039a0002c0002t0001g0050others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.10560+572C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
G | GTA | 12 | a0003c0005t0001g0013a0004c0019t0001g0148a0004c0126t0001g0118others(9): Show | 12 | HG00673.hp2 HG02040.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.10560+570_10560+57 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
G | GTATA | 8 | a0003c0005t0001g0004a0011c0009t0001g0078a0027c0013t0001g0071others(5): Show | 8 | HG01175.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.10560+568_10560+57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
G | GTATATA | 5 | a0021c0056t0001g0041a0057c0114t0002g0115a0078c0128t0001g0163others(2): Show | 5 | HG00280.hp2 HG03225.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.10560+566_10560+57 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
G | GTATATAT others(1): Show |
3 | a0018c0020t0001g0131a0021c0057t0001g0037a0099c0067t0001g0023 | 3 | HG02258.hp2 HG02735.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.10560+564_10560+57 others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
G | GTATATAT others(3): Show |
1 | a0044c0092t0001g0008 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.10560+562_10560+57 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTA | G | 11 | a0006c0012t0001g0173a0011c0070t0001g0055a0019c0010t0001g0059others(8): Show | 11 | HG00558.hp2 HG00741.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.10560+570_10560+57 others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATA | G | 6 | a0003c0094t0001g0014a0004c0019t0001g0151a0011c0009t0001g0040others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.10560+568_10560+57 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATA | G | 2 | a0034c0147t0001g0178a0068c0125t0001g0111 | 2 | HG06807.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.10560+566_10560+57 others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATAT others(3): Show |
G | 1 | a0103c0066t0001g0065 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.10560+562_10560+57 others(14): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATAT others(5): Show |
G | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.10560+560_10560+57 others(16): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATAT others(13): Show |
G | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.10560+552_10560+57 others(24): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATAT others(23): Show |
G | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.10560+542_10560+57 others(34): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620347
|
GTATATAT others(25): Show |
G | 1 | a0022c0026t0001g0032 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.10560+540_10560+57 others(36): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620347 | ||||||
| chr2:151620581
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.10560+338A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620581 | ||||||
| chr2:151620708
|
C | A | 2 | a0089c0036t0001g0053a0090c0035t0001g0054 | 2 | NA19062.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.10560+211G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 72/181 | chr2 | 151620708 | ||||||
| chr2:151621071
|
C | G | 1 | a0062c0106t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.10453-45G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151621071 | ||||||
| chr2:151621279
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.10453-253G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151621279 | ||||||
| chr2:151621283
|
T | C | 1 | a0072c0121t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10453-257A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151621283 | ||||||
| chr2:151621291
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10453-265A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151621291 | ||||||
| chr2:151621530
|
T | C | 9 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.10453-504A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151621530 | ||||||
| chr2:151622106
|
T | G | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.10453-1080A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622106 | ||||||
| chr2:151622305
|
G | A | 1 | a0078c0128t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10453-1279C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622305 | ||||||
| chr2:151622394
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0087c0132t0001g0101others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.10453-1368A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622394 | ||||||
| chr2:151622456
|
C | A | 28 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.10453-1430G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622456 | ||||||
| chr2:151622502
|
A | T | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.10453-1476T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622502 | ||||||
| chr2:151622628
|
G | C | 7 | a0005c0008t0001g0038a0005c0008t0001g0077a0017c0015t0001g0164others(4): Show | 7 | HG00544.hp2 HG01074.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.10453-1602C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622628 | ||||||
| chr2:151622885
|
C | G | 1 | a0115c0053t0001g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.10453-1859G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151622885 | ||||||
| chr2:151623220
|
C | T | 1 | a0015c0111t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10453-2194G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623220 | ||||||
| chr2:151623393
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.10452+2141G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623393 | ||||||
| chr2:151623472
|
C | T | 40 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(37): Show | 40 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.10452+2062G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623472 | ||||||
| chr2:151623622
|
T | A | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.10452+1912A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623622 | ||||||
| chr2:151623626
|
A | C | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.10452+1908T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623626 | ||||||
| chr2:151623632
|
T | C | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.10452+1902A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623632 | ||||||
| chr2:151623733
|
A | C | 9 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.10452+1801T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623733 | ||||||
| chr2:151623828
|
G | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.10452+1706C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151623828 | ||||||
| chr2:151624577
|
G | A | 1 | a0072c0121t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10452+957C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151624577 | ||||||
| chr2:151624614
|
A | T | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.10452+920T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151624614 | ||||||
| chr2:151624651
|
A | C | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.10452+883T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151624651 | ||||||
| chr2:151625198
|
C | T | 42 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(39): Show | 42 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.10452+336G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625198 | ||||||
| chr2:151625199
|
G | A | 3 | a0056c0145t0001g0177a0085c0031t0001g0108a0130c0150t0001g0180 | 3 | HG02280.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.10452+335C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625199 | ||||||
| chr2:151625322
|
GTGTC | G | 3 | a0036c0029t0001g0176a0046c0091t0001g0017a0105c0080t0001g0034 | 3 | HG01884.hp1 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.10452+208_10452+21 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625322 | ||||||
| chr2:151625332
|
G | A | 125 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.10452+202C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625332 | ||||||
| chr2:151625332
|
GTCTA | G | 3 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.10452+198_10452+20 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625332 | ||||||
| chr2:151625340
|
G | A | 3 | a0036c0029t0001g0176a0046c0091t0001g0017a0105c0080t0001g0034 | 3 | HG01884.hp1 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.10452+194C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625340 | ||||||
| chr2:151625463
|
A | G | 76 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.10452+71T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625463 | ||||||
| chr2:151625525
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.10452+9A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 71/181 | chr2 | 151625525 | ||||||
| chr2:151625900
|
G | A | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0122c0033t0001g0087 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.10348-262C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151625900 | ||||||
| chr2:151625947
|
T | C | 128 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.10348-309A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151625947 | ||||||
| chr2:151626037
|
T | C | 1 | a0091c0142t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10348-399A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626037 | ||||||
| chr2:151626114
|
C | CT | 8 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(5): Show | 8 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.10348-477dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626114 | ||||||
| chr2:151626114
|
CT | C | 9 | a0049c0096t0001g0184a0050c0099t0001g0098a0056c0145t0001g0177others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.10348-477delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626114 | ||||||
| chr2:151626250
|
G | A | 1 | a0112c0051t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.10348-612C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626250 | ||||||
| chr2:151626598
|
G | A | 1 | a0061c0115t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.10347+404C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626598 | ||||||
| chr2:151626644
|
C | A | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10347+358G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626644 | ||||||
| chr2:151626720
|
T | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.10347+282A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626720 | ||||||
| chr2:151626903
|
C | T | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.10347+99G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626903 | ||||||
| chr2:151626996
|
G | A | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.10347+6C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 70/181 | chr2 | 151626996 | ||||||
| chr2:151627418
|
GA | G | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.10143+104delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 69/181 | chr2 | 151627418 | ||||||
| chr2:151628027
|
C | T | 7 | a0036c0029t0001g0176a0046c0091t0001g0017a0049c0096t0001g0184others(4): Show | 7 | HG01884.hp1 HG02886.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.9832-193G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628027 | ||||||
| chr2:151628049
|
C | A | 1 | a0126c0027t0001g0067 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.9832-215G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628049 | ||||||
| chr2:151628155
|
G | A | 1 | a0120c0023t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.9832-321C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628155 | ||||||
| chr2:151628268
|
C | T | 1 | a0047c0097t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.9832-434G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628268 | ||||||
| chr2:151628347
|
C | T | 2 | a0011c0070t0001g0055a0101c0068t0001g0024 | 2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.9832-513G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628347 | ||||||
| chr2:151628568
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9832-734A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628568 | ||||||
| chr2:151628656
|
C | T | 1 | a0114c0055t0001g0044 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.9832-822G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628656 | ||||||
| chr2:151628787
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9831+752C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628787 | ||||||
| chr2:151628903
|
A | AAAG | 4 | a0049c0096t0001g0184a0066c0118t0001g0146a0067c0117t0001g0144others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.9831+633_9831+635d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628903 | ||||||
| chr2:151628903
|
AAAG | A | 75 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.9831+633_9831+635d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151628903 | ||||||
| chr2:151629073
|
C | CA | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.9831+465dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629073 | ||||||
| chr2:151629079
|
A | C | 1 | a0004c0126t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.9831+460T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629079 | ||||||
| chr2:151629087
|
T | C | 1 | a0100c0072t0001g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.9831+452A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629087 | ||||||
| chr2:151629240
|
A | G | 40 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(37): Show | 40 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.9831+299T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629240 | ||||||
| chr2:151629244
|
A | G | 2 | a0001c0001t0001g0117a0115c0053t0001g0084 | 2 | NA18952.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.9831+295T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629244 | ||||||
| chr2:151629310
|
A | G | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9831+229T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629310 | ||||||
| chr2:151629370
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0070c0123t0001g0116others(1): Show | 4 | NA18966.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.9831+169G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629370 | ||||||
| chr2:151629445
|
A | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9831+94T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 68/181 | chr2 | 151629445 | ||||||
| chr2:151629752
|
G | A | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.9724-106C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151629752 | ||||||
| chr2:151629755
|
A | C | 2 | a0091c0142t0001g0119a0131c0149t0001g0181 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9724-109T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151629755 | ||||||
| chr2:151629779
|
A | C | 4 | a0056c0145t0001g0177a0084c0133t0001g0154a0085c0031t0001g0108others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.9724-133T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151629779 | ||||||
| chr2:151629819
|
G | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.9724-173C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151629819 | ||||||
| chr2:151629922
|
G | A | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.9724-276C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151629922 | ||||||
| chr2:151630026
|
A | G | 2 | a0037c0087t0001g0107a0057c0114t0002g0115 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.9724-380T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151630026 | ||||||
| chr2:151630122
|
G | T | 5 | a0049c0096t0001g0184a0050c0099t0001g0098a0065c0119t0001g0145others(2): Show | 5 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.9724-476C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151630122 | ||||||
| chr2:151630268
|
C | A | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.9723+447G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151630268 | ||||||
| chr2:151630423
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9723+292A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151630423 | ||||||
| chr2:151630605
|
T | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9723+110A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 67/181 | chr2 | 151630605 | ||||||
| chr2:151630860
|
A | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.9619-41T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/181 | chr2 | 151630860 | ||||||
| chr2:151631018
|
A | C | 1 | a0012c0090t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.9618+125T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/181 | chr2 | 151631018 | ||||||
| chr2:151631052
|
C | T | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.9618+91G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/181 | chr2 | 151631052 | ||||||
| chr2:151631060
|
T | C | 31 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.9618+83A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 66/181 | chr2 | 151631060 | ||||||
| chr2:151631481
|
A | G | 3 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.9415-135T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151631481 | ||||||
| chr2:151631711
|
C | T | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.9415-365G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151631711 | ||||||
| chr2:151631893
|
C | T | 2 | a0001c0001t0001g0124a0116c0052t0001g0069 | 2 | NA18946.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.9415-547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151631893 | ||||||
| chr2:151631935
|
C | G | 20 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(17): Show | 20 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.9415-589G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151631935 | ||||||
| chr2:151631982
|
G | T | 1 | a0003c0094t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.9415-636C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151631982 | ||||||
| chr2:151632137
|
C | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9415-791G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632137 | ||||||
| chr2:151632163
|
A | T | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.9415-817T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632163 | ||||||
| chr2:151632164
|
T | A | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9415-818A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632164 | ||||||
| chr2:151632179
|
G | T | 35 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(32): Show | 35 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.9415-833C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632179 | ||||||
| chr2:151632315
|
C | CA | 33 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(30): Show | 33 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.9415-970dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632315 | ||||||
| chr2:151632367
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.9415-1021G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632367 | ||||||
| chr2:151632468
|
G | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0087c0132t0001g0101others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.9415-1122C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632468 | ||||||
| chr2:151632631
|
G | A | 3 | a0008c0004t0001g0011a0008c0004t0001g0012a0058c0110t0001g0149 | 3 | HG02976.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.9414+1023C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632631 | ||||||
| chr2:151632677
|
G | GA | 10 | a0009c0017t0001g0121a0010c0137t0001g0093a0010c0138t0001g0091others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.9414+976dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632677 | ||||||
| chr2:151632810
|
A | G | 4 | a0016c0016t0002g0100a0016c0016t0002g0137a0041c0085t0002g0010others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.9414+844T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632810 | ||||||
| chr2:151632916
|
G | GAATTGCA | 4 | a0049c0096t0001g0184a0065c0119t0001g0145a0066c0118t0001g0146others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.9414+731_9414+737d others(9): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632916 | ||||||
| chr2:151632919
|
T | C | 30 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.9414+735A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151632919 | ||||||
| chr2:151633040
|
T | C | 129 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.9414+614A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151633040 | ||||||
| chr2:151633182
|
T | C | 2 | a0001c0001t0001g0124a0116c0052t0001g0069 | 2 | NA18946.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.9414+472A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151633182 | ||||||
| chr2:151633377
|
T | TA | 31 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.9414+276dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151633377 | ||||||
| chr2:151633506
|
T | C | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.9414+148A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 65/181 | chr2 | 151633506 | ||||||
| chr2:151634159
|
A | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9103-194T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634159 | ||||||
| chr2:151634178
|
C | T | 36 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(33): Show | 36 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.9103-213G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634178 | ||||||
| chr2:151634499
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9103-534C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634499 | ||||||
| chr2:151634514
|
C | T | 1 | a0002c0048t0001g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9103-549G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634514 | ||||||
| chr2:151634616
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0070c0123t0001g0116others(1): Show | 4 | NA18966.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.9103-651A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634616 | ||||||
| chr2:151634716
|
C | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9103-751G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634716 | ||||||
| chr2:151634731
|
A | C | 9 | a0033c0024t0001g0096a0036c0029t0001g0176a0046c0091t0001g0017others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.9103-766T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634731 | ||||||
| chr2:151634755
|
T | C | 34 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.9103-790A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634755 | ||||||
| chr2:151634804
|
A | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9103-839T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634804 | ||||||
| chr2:151634886
|
T | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9103-921A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634886 | ||||||
| chr2:151634948
|
A | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9103-983T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151634948 | ||||||
| chr2:151635339
|
C | A | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9102+888G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635339 | ||||||
| chr2:151635398
|
G | C | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9102+829C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635398 | ||||||
| chr2:151635707
|
C | CA | 78 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.9102+519dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635707 | ||||||
| chr2:151635707
|
C | CAAAAA | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.9102+515_9102+519d others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635707 | ||||||
| chr2:151635790
|
A | T | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9102+437T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635790 | ||||||
| chr2:151635807
|
A | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9102+420T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635807 | ||||||
| chr2:151635810
|
G | A | 123 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.9102+417C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151635810 | ||||||
| chr2:151636027
|
C | T | 1 | a0110c0041t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.9102+200G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 64/181 | chr2 | 151636027 | ||||||
| chr2:151636348
|
A | G | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.8995-14T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151636348 | ||||||
| chr2:151636712
|
C | T | 1 | a0114c0055t0001g0044 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.8995-378G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151636712 | ||||||
| chr2:151636799
|
A | C | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8995-465T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151636799 | ||||||
| chr2:151636995
|
G | A | 2 | a0085c0031t0001g0108a0130c0150t0001g0180 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8995-661C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151636995 | ||||||
| chr2:151637298
|
G | GT | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0087c0132t0001g0101others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.8995-965dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637298 | ||||||
| chr2:151637340
|
C | A | 1 | a0002c0002t0001g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.8995-1006G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637340 | ||||||
| chr2:151637439
|
C | T | 7 | a0003c0005t0001g0013a0010c0137t0001g0093a0010c0138t0001g0091others(4): Show | 7 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.8995-1105G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637439 | ||||||
| chr2:151637473
|
A | T | 12 | a0009c0017t0001g0159a0012c0088t0001g0016a0039c0153t0001g0021others(9): Show | 12 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.8995-1139T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637473 | ||||||
| chr2:151637526
|
C | T | 3 | a0049c0096t0001g0184a0056c0145t0001g0177a0067c0117t0001g0144 | 3 | HG02280.hp2 HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.8995-1192G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637526 | ||||||
| chr2:151637538
|
C | T | 2 | a0107c0045t0001g0028a0111c0049t0001g0073 | 2 | HG00741.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.8995-1204G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637538 | ||||||
| chr2:151637704
|
A | G | 37 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(34): Show | 37 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.8995-1370T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637704 | ||||||
| chr2:151637743
|
G | C | 2 | a0004c0019t0001g0148a0004c0019t0001g0151 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.8995-1409C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151637743 | ||||||
| chr2:151638425
|
C | T | 1 | a0083c0134t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.8994+855G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638425 | ||||||
| chr2:151638438
|
T | G | 2 | a0001c0001t0001g0156a0068c0125t0001g0111 | 2 | NA19062.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.8994+842A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638438 | ||||||
| chr2:151638733
|
C | T | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8994+547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638733 | ||||||
| chr2:151638797
|
TTC | T | 3 | a0024c0040t0001g0062a0117c0039t0001g0063a0127c0144t0001g0129 | 3 | HG00609.hp1 HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.8994+481_8994+482d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638797 | ||||||
| chr2:151638807
|
CTG | C | 69 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.8994+471_8994+472d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638807 | ||||||
| chr2:151638807
|
CTGTG | C | 81 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(78): Show | 81 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.8994+469_8994+472d others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638807 | ||||||
| chr2:151638807
|
CTGTGTG | C | 25 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(22): Show | 25 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.8994+467_8994+472d others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638807 | ||||||
| chr2:151638807
|
CTGTGTGT others(1): Show |
C | 3 | a0035c0146t0001g0103a0050c0099t0001g0098a0080c0030t0001g0074 | 3 | HG00639.hp1 HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.8994+465_8994+472d others(10): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638807 | ||||||
| chr2:151638809
|
G | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8994+471C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638809 | ||||||
| chr2:151638813
|
G | C | 1 | a0052c0100t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8994+467C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638813 | ||||||
| chr2:151638825
|
G | A | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.8994+455C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638825 | ||||||
| chr2:151638838
|
T | G | 1 | a0038c0086t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.8994+442A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151638838 | ||||||
| chr2:151639039
|
G | T | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8994+241C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151639039 | ||||||
| chr2:151639248
|
C | T | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8994+32G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 63/181 | chr2 | 151639248 | ||||||
| chr2:151639524
|
G | A | 111 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.8890-140C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 62/181 | chr2 | 151639524 | ||||||
| chr2:151639682
|
C | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8889+175G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 62/181 | chr2 | 151639682 | ||||||
| chr2:151640239
|
CA | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.8685+115delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 61/181 | chr2 | 151640239 | ||||||
| chr2:151640873
|
T | C | 24 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(21): Show | 24 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.8374-207A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151640873 | ||||||
| chr2:151640896
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8374-230A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151640896 | ||||||
| chr2:151641030
|
T | C | 46 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.8374-364A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641030 | ||||||
| chr2:151641086
|
A | G | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.8374-420T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641086 | ||||||
| chr2:151641095
|
G | A | 4 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(1): Show | 4 | NA18943.hp1 NA18980.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.8374-429C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641095 | ||||||
| chr2:151641117
|
T | C | 112 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.8374-451A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641117 | ||||||
| chr2:151641134
|
C | G | 62 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.8374-468G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641134 | ||||||
| chr2:151641578
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.8374-912C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641578 | ||||||
| chr2:151641952
|
A | G | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.8373+622T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641952 | ||||||
| chr2:151641959
|
C | T | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.8373+615G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151641959 | ||||||
| chr2:151642111
|
A | C | 6 | a0002c0002t0001g0046a0020c0007t0001g0042a0020c0007t0001g0043others(3): Show | 6 | HG00597.hp1 HG00609.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.8373+463T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642111 | ||||||
| chr2:151642185
|
G | C | 26 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(23): Show | 26 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.8373+389C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642185 | ||||||
| chr2:151642230
|
T | G | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8373+344A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642230 | ||||||
| chr2:151642451
|
C | T | 1 | a0053c0127t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8373+123G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642451 | ||||||
| chr2:151642474
|
A | G | 1 | a0089c0036t0001g0053 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.8373+100T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642474 | ||||||
| chr2:151642561
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8373+13G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 60/181 | chr2 | 151642561 | ||||||
| chr2:151642987
|
T | A | 55 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(52): Show | 55 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.8161-118A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 58/181 | chr2 | 151642987 | ||||||
| chr2:151643066
|
C | T | 108 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.8160+84G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 58/181 | chr2 | 151643066 | ||||||
| chr2:151643459
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7957-106G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/181 | chr2 | 151643459 | ||||||
| chr2:151643505
|
G | A | 53 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(50): Show | 53 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.7957-152C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/181 | chr2 | 151643505 | ||||||
| chr2:151643611
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7956+207T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/181 | chr2 | 151643611 | ||||||
| chr2:151643703
|
G | A | 14 | a0028c0021t0001g0182a0028c0021t0001g0183a0047c0097t0001g0185others(11): Show | 14 | HG02040.hp1 HG02258.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.7956+115C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/181 | chr2 | 151643703 | ||||||
| chr2:151643707
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7956+111C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 57/181 | chr2 | 151643707 | ||||||
| chr2:151644327
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7644+141G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 56/181 | chr2 | 151644327 | ||||||
| chr2:151644443
|
A | G | 2 | a0021c0056t0001g0041a0108c0047t0001g0064 | 2 | HG03491.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.7644+25T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 56/181 | chr2 | 151644443 | ||||||
| chr2:151644901
|
G | C | 4 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(1): Show | 4 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.7537-326C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151644901 | ||||||
| chr2:151645001
|
G | A | 1 | a0005c0008t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.7537-426C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645001 | ||||||
| chr2:151645079
|
C | T | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7537-504G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645079 | ||||||
| chr2:151645203
|
G | T | 15 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(12): Show | 15 | HG02040.hp1 HG02258.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.7537-628C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645203 | ||||||
| chr2:151645210
|
T | G | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7537-635A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645210 | ||||||
| chr2:151645287
|
G | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.7537-712C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645287 | ||||||
| chr2:151645416
|
T | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7536+714A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645416 | ||||||
| chr2:151645619
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7536+511A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645619 | ||||||
| chr2:151645866
|
G | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7536+264C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645866 | ||||||
| chr2:151645907
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7536+223G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 55/181 | chr2 | 151645907 | ||||||
| chr2:151646321
|
T | G | 1 | a0022c0054t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7432-87A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646321 | ||||||
| chr2:151646503
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.7432-269T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646503 | ||||||
| chr2:151646728
|
C | T | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7432-494G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646728 | ||||||
| chr2:151646758
|
T | C | 9 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(6): Show | 9 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.7432-524A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646758 | ||||||
| chr2:151646846
|
C | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7432-612G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646846 | ||||||
| chr2:151646886
|
C | G | 2 | a0006c0079t0001g0170a0031c0078t0001g0171 | 2 | HG02080.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.7432-652G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646886 | ||||||
| chr2:151646960
|
C | T | 1 | a0102c0069t0001g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7432-726G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151646960 | ||||||
| chr2:151647060
|
CA | C | 20 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(17): Show | 20 | HG02040.hp1 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.7432-827delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647060 | ||||||
| chr2:151647115
|
AT | A | 5 | a0025c0011t0001g0089a0025c0011t0001g0090a0033c0024t0001g0096others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.7432-882delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647115 | ||||||
| chr2:151647163
|
T | C | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7432-929A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647163 | ||||||
| chr2:151647268
|
C | T | 1 | a0023c0043t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7432-1034G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647268 | ||||||
| chr2:151647361
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7432-1127G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647361 | ||||||
| chr2:151647362
|
G | A | 1 | a0014c0112t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.7432-1128C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647362 | ||||||
| chr2:151647406
|
G | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7432-1172C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647406 | ||||||
| chr2:151647515
|
C | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.7432-1281G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647515 | ||||||
| chr2:151647855
|
T | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.7432-1621A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647855 | ||||||
| chr2:151647856
|
A | G | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7432-1622T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647856 | ||||||
| chr2:151647857
|
A | G | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.7432-1623T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647857 | ||||||
| chr2:151647876
|
T | C | 86 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.7432-1642A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647876 | ||||||
| chr2:151647901
|
A | G | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7432-1667T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647901 | ||||||
| chr2:151647918
|
C | T | 22 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(19): Show | 22 | HG00639.hp1 HG02040.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.7432-1684G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647918 | ||||||
| chr2:151647980
|
C | T | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.7432-1746G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647980 | ||||||
| chr2:151647981
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7432-1747C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151647981 | ||||||
| chr2:151648166
|
T | G | 6 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(3): Show | 6 | HG02040.hp1 HG02683.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.7432-1932A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151648166 | ||||||
| chr2:151648188
|
T | C | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7432-1954A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151648188 | ||||||
| chr2:151648633
|
G | A | 1 | a0010c0138t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.7431+1543C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151648633 | ||||||
| chr2:151648673
|
C | T | 53 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(50): Show | 53 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.7431+1503G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151648673 | ||||||
| chr2:151649089
|
T | G | 13 | a0028c0021t0001g0182a0028c0021t0001g0183a0047c0097t0001g0185others(10): Show | 13 | HG02040.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.7431+1087A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649089 | ||||||
| chr2:151649274
|
A | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7431+902T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649274 | ||||||
| chr2:151649328
|
C | G | 1 | a0021c0056t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.7431+848G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649328 | ||||||
| chr2:151649470
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7431+706G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649470 | ||||||
| chr2:151649611
|
C | T | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7431+565G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649611 | ||||||
| chr2:151649872
|
C | T | 1 | a0018c0020t0001g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7431+304G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649872 | ||||||
| chr2:151649947
|
T | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.7431+229A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151649947 | ||||||
| chr2:151650004
|
A | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7431+172T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151650004 | ||||||
| chr2:151650147
|
A | G | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7431+29T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 54/181 | chr2 | 151650147 | ||||||
| chr2:151651050
|
G | A | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.6916-165C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651050 | ||||||
| chr2:151651061
|
C | T | 2 | a0007c0003t0001g0001a0007c0003t0001g0029 | 2 | HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6916-176G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651061 | ||||||
| chr2:151651537
|
A | G | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6916-652T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651537 | ||||||
| chr2:151651577
|
G | A | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.6916-692C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651577 | ||||||
| chr2:151651583
|
C | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6916-698G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651583 | ||||||
| chr2:151651590
|
C | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6916-705G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651590 | ||||||
| chr2:151651797
|
A | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6916-912T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651797 | ||||||
| chr2:151651835
|
A | C | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6916-950T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651835 | ||||||
| chr2:151651915
|
G | A | 93 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.6916-1030C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151651915 | ||||||
| chr2:151652302
|
T | A | 1 | a0012c0090t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6916-1417A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652302 | ||||||
| chr2:151652319
|
A | G | 28 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(25): Show | 28 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.6916-1434T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652319 | ||||||
| chr2:151652480
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.6915+1512G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652480 | ||||||
| chr2:151652627
|
C | T | 1 | a0081c0141t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6915+1365G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652627 | ||||||
| chr2:151652704
|
G | C | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6915+1288C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652704 | ||||||
| chr2:151652770
|
G | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6915+1222C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151652770 | ||||||
| chr2:151653055
|
A | G | 8 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(5): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.6915+937T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151653055 | ||||||
| chr2:151653289
|
C | T | 1 | a0128c0148t0001g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.6915+703G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151653289 | ||||||
| chr2:151653675
|
G | C | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6915+317C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151653675 | ||||||
| chr2:151653792
|
C | G | 1 | a0094c0061t0001g0080 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6915+200G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151653792 | ||||||
| chr2:151653955
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6915+37T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 52/181 | chr2 | 151653955 | ||||||
| chr2:151654335
|
A | G | 1 | a0006c0012t0001g0172 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6808-236T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654335 | ||||||
| chr2:151654440
|
A | G | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6808-341T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654440 | ||||||
| chr2:151654477
|
A | T | 1 | a0084c0133t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6808-378T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654477 | ||||||
| chr2:151654486
|
A | T | 21 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(18): Show | 21 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.6808-387T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654486 | ||||||
| chr2:151654654
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6808-555A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654654 | ||||||
| chr2:151654720
|
C | T | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6807+550G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654720 | ||||||
| chr2:151654802
|
T | TA | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.6807+467_6807+468i others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654802 | ||||||
| chr2:151654832
|
T | C | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6807+438A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654832 | ||||||
| chr2:151654838
|
C | T | 8 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(5): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.6807+432G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654838 | ||||||
| chr2:151654936
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6807+334G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151654936 | ||||||
| chr2:151655001
|
T | A | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.6807+269A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151655001 | ||||||
| chr2:151655203
|
G | A | 1 | a0063c0105t0001g0160 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.6807+67C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151655203 | ||||||
| chr2:151655249
|
T | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6807+21A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151655249 | ||||||
| chr2:151655264
|
A | C | 112 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(109): Show |
splice_region_variant&intron_variant | LOW | c.6807+6T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 51/181 | chr2 | 151655264 | ||||||
| chr2:151655537
|
TA | T | 7 | a0005c0008t0001g0038a0005c0008t0001g0077a0005c0063t0001g0052others(4): Show | 7 | HG01074.hp2 HG01099.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.6703-164delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 50/181 | chr2 | 151655537 | ||||||
| chr2:151655545
|
A | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6703-171T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 50/181 | chr2 | 151655545 | ||||||
| chr2:151655667
|
G | A | 7 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(4): Show | 7 | HG01192.hp1 HG01891.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.6702+150C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 50/181 | chr2 | 151655667 | ||||||
| chr2:151656478
|
A | T | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.6184-14T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656478 | ||||||
| chr2:151656527
|
C | A | 1 | a0008c0004t0001g0009 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6184-63G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656527 | ||||||
| chr2:151656537
|
T | C | 1 | a0078c0128t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6184-73A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656537 | ||||||
| chr2:151656598
|
TCA | T | 84 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.6184-136_6184-135d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656598 | ||||||
| chr2:151656691
|
T | C | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.6184-227A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656691 | ||||||
| chr2:151656760
|
T | C | 1 | a0075c0102t0001g0166 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.6184-296A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656760 | ||||||
| chr2:151656761
|
T | C | 1 | a0002c0002t0001g0046 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6184-297A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656761 | ||||||
| chr2:151656817
|
C | G | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6184-353G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656817 | ||||||
| chr2:151656847
|
G | GA | 100 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.6184-384dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656847 | ||||||
| chr2:151656847
|
G | GAA | 12 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.6184-385_6184-384d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656847 | ||||||
| chr2:151656867
|
AC | A | 2 | a0096c0060t0001g0022a0103c0066t0001g0065 | 2 | HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.6184-404delG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656867 | ||||||
| chr2:151656924
|
G | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.6184-460C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656924 | ||||||
| chr2:151656985
|
C | T | 26 | a0004c0019t0001g0148a0004c0019t0001g0151a0009c0017t0001g0121others(23): Show | 26 | HG00597.hp2 HG02074.hp2 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.6184-521G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151656985 | ||||||
| chr2:151657001
|
A | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6184-537T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657001 | ||||||
| chr2:151657068
|
G | A | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.6184-604C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657068 | ||||||
| chr2:151657072
|
A | T | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.6184-608T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657072 | ||||||
| chr2:151657110
|
C | A | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6184-646G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657110 | ||||||
| chr2:151657251
|
T | C | 119 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.6183+732A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657251 | ||||||
| chr2:151657508
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6183+475C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657508 | ||||||
| chr2:151657936
|
G | A | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6183+47C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 48/181 | chr2 | 151657936 | ||||||
| chr2:151658176
|
CTT | C | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.6076-88_6076-87del others(2): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658176 | ||||||
| chr2:151658206
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6076-116C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658206 | ||||||
| chr2:151658239
|
T | C | 88 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.6076-149A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658239 | ||||||
| chr2:151658494
|
T | TA | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6076-405dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658494 | ||||||
| chr2:151658591
|
G | GA | 5 | a0056c0145t0001g0177a0085c0031t0001g0108a0086c0032t0001g0109others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.6075+473dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658591 | ||||||
| chr2:151658804
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6075+261G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 47/181 | chr2 | 151658804 | ||||||
| chr2:151659273
|
T | C | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.5971-104A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659273 | ||||||
| chr2:151659293
|
A | T | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5971-124T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659293 | ||||||
| chr2:151659297
|
T | A | 3 | a0062c0106t0001g0140a0064c0025t0001g0095a0089c0036t0001g0053 | 3 | HG03453.hp2 HG03688.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.5971-128A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659297 | ||||||
| chr2:151659327
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5971-158A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659327 | ||||||
| chr2:151659335
|
C | T | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5971-166G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659335 | ||||||
| chr2:151659486
|
A | G | 1 | a0074c0103t0001g0168 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.5971-317T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659486 | ||||||
| chr2:151659516
|
G | C | 1 | a0023c0043t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5971-347C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659516 | ||||||
| chr2:151659601
|
C | CA | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5971-433dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659601 | ||||||
| chr2:151659674
|
GT | G | 7 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(4): Show | 7 | HG01192.hp1 HG01891.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.5971-506delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151659674 | ||||||
| chr2:151660037
|
C | G | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.5971-868G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660037 | ||||||
| chr2:151660139
|
T | C | 1 | a0014c0112t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5971-970A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660139 | ||||||
| chr2:151660163
|
G | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5971-994C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660163 | ||||||
| chr2:151660247
|
C | A | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5971-1078G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660247 | ||||||
| chr2:151660317
|
G | A | 88 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.5971-1148C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660317 | ||||||
| chr2:151660416
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5971-1247T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660416 | ||||||
| chr2:151660442
|
G | C | 1 | a0016c0016t0002g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5971-1273C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660442 | ||||||
| chr2:151660623
|
T | C | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5971-1454A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660623 | ||||||
| chr2:151660812
|
G | A | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.5970+1323C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151660812 | ||||||
| chr2:151661378
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5970+757C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661378 | ||||||
| chr2:151661465
|
T | C | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.5970+670A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661465 | ||||||
| chr2:151661697
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5970+438C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661697 | ||||||
| chr2:151661876
|
T | C | 3 | a0002c0002t0001g0036a0113c0042t0001g0035a0115c0053t0001g0084 | 3 | HG00609.hp2 NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.5970+259A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661876 | ||||||
| chr2:151661904
|
C | T | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5970+231G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661904 | ||||||
| chr2:151661996
|
C | T | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5970+139G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151661996 | ||||||
| chr2:151662013
|
T | C | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5970+122A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 46/181 | chr2 | 151662013 | ||||||
| chr2:151662505
|
A | G | 1 | a0007c0003t0001g0029 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.5764-164T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151662505 | ||||||
| chr2:151662668
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-327A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151662668 | ||||||
| chr2:151662713
|
A | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.5764-372T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151662713 | ||||||
| chr2:151662983
|
G | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5763+565C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151662983 | ||||||
| chr2:151663066
|
T | C | 8 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(5): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.5763+482A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151663066 | ||||||
| chr2:151663159
|
G | A | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.5763+389C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151663159 | ||||||
| chr2:151663267
|
C | T | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.5763+281G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151663267 | ||||||
| chr2:151663513
|
A | G | 107 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5763+35T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151663513 | ||||||
| chr2:151663544
|
G | A | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | splice_region_variant&intron_variant | LOW | c.5763+4C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 45/181 | chr2 | 151663544 | ||||||
| chr2:151663989
|
G | A | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.5452-130C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151663989 | ||||||
| chr2:151664021
|
AT | A | 174 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.5452-163delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664021 | ||||||
| chr2:151664036
|
G | C | 76 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.5452-177C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664036 | ||||||
| chr2:151664092
|
A | C | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5452-233T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664092 | ||||||
| chr2:151664226
|
C | T | 3 | a0010c0137t0001g0093a0010c0139t0001g0106a0081c0141t0001g0092 | 3 | HG00423.hp2 HG01993.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.5451+275G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664226 | ||||||
| chr2:151664245
|
T | C | 1 | a0023c0043t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5451+256A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664245 | ||||||
| chr2:151664338
|
A | G | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5451+163T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664338 | ||||||
| chr2:151664340
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5451+161A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 44/181 | chr2 | 151664340 | ||||||
| chr2:151664939
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5239-76T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/181 | chr2 | 151664939 | ||||||
| chr2:151664999
|
T | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5239-136A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/181 | chr2 | 151664999 | ||||||
| chr2:151665025
|
A | G | 91 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.5239-162T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/181 | chr2 | 151665025 | ||||||
| chr2:151665199
|
T | C | 7 | a0011c0070t0001g0055a0096c0060t0001g0022a0098c0071t0001g0056others(4): Show | 7 | HG01358.hp1 HG03239.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.5238+134A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/181 | chr2 | 151665199 | ||||||
| chr2:151665220
|
G | A | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5238+113C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 42/181 | chr2 | 151665220 | ||||||
| chr2:151665554
|
A | G | 1 | a0064c0025t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5032-15T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151665554 | ||||||
| chr2:151665635
|
G | A | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5032-96C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151665635 | ||||||
| chr2:151665745
|
C | G | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.5032-206G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151665745 | ||||||
| chr2:151665882
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5031+208T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151665882 | ||||||
| chr2:151665950
|
G | A | 1 | a0053c0127t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5031+140C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151665950 | ||||||
| chr2:151666015
|
G | A | 1 | a0022c0026t0001g0032 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5031+75C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151666015 | ||||||
| chr2:151666042
|
T | C | 79 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(76): Show | 79 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.5031+48A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 41/181 | chr2 | 151666042 | ||||||
| chr2:151666453
|
T | A | 1 | a0110c0041t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4720-52A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151666453 | ||||||
| chr2:151666515
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4720-114C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151666515 | ||||||
| chr2:151666953
|
T | C | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.4720-552A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151666953 | ||||||
| chr2:151667115
|
G | A | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4719+689C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151667115 | ||||||
| chr2:151667173
|
T | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.4719+631A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151667173 | ||||||
| chr2:151667388
|
A | G | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4719+416T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151667388 | ||||||
| chr2:151667597
|
A | C | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4719+207T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151667597 | ||||||
| chr2:151667648
|
C | T | 1 | a0102c0069t0001g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4719+156G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 40/181 | chr2 | 151667648 | ||||||
| chr2:151667972
|
T | A | 1 | a0026c0006t0001g0027 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4612-61A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151667972 | ||||||
| chr2:151667999
|
C | T | 1 | a0039c0153t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4612-88G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151667999 | ||||||
| chr2:151668267
|
G | A | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4612-356C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668267 | ||||||
| chr2:151668488
|
C | A | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0050c0099t0001g0098 | 3 | HG02647.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4611+539G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668488 | ||||||
| chr2:151668606
|
C | T | 70 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(67): Show | 70 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.4611+421G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668606 | ||||||
| chr2:151668735
|
T | C | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4611+292A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668735 | ||||||
| chr2:151668939
|
G | A | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4611+88C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668939 | ||||||
| chr2:151668957
|
A | G | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.4611+70T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 39/181 | chr2 | 151668957 | ||||||
| chr2:151669236
|
T | A | 11 | a0003c0083t0001g0003a0003c0094t0001g0014a0008c0004t0001g0009others(8): Show | 11 | HG00099.hp1 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.4507-105A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669236 | ||||||
| chr2:151669240
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG00280.hp1 HG00609.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.4507-109G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669240 | ||||||
| chr2:151669253
|
T | C | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4507-122A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669253 | ||||||
| chr2:151669270
|
G | C | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4507-139C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669270 | ||||||
| chr2:151669535
|
A | G | 86 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(83): Show | 86 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4507-404T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669535 | ||||||
| chr2:151669568
|
A | G | 86 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(83): Show | 86 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4507-437T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669568 | ||||||
| chr2:151669816
|
C | A | 1 | a0022c0026t0001g0032 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4507-685G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669816 | ||||||
| chr2:151669820
|
C | A | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4507-689G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669820 | ||||||
| chr2:151669863
|
T | C | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4507-732A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151669863 | ||||||
| chr2:151670161
|
C | A | 53 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(50): Show | 53 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.4506+862G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670161 | ||||||
| chr2:151670197
|
A | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4506+826T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670197 | ||||||
| chr2:151670359
|
C | A | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4506+664G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670359 | ||||||
| chr2:151670367
|
A | G | 7 | a0028c0021t0001g0182a0028c0021t0001g0183a0083c0134t0001g0153others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4506+656T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670367 | ||||||
| chr2:151670425
|
C | CCATACAG others(18): Show |
23 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.4506+573_4506+597d others(27): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670425 | ||||||
| chr2:151670425
|
CCATACAG others(18): Show |
C | 66 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(63): Show | 66 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.4506+573_4506+597d others(27): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 38/181 | chr2 | 151670425 | ||||||
| chr2:151671325
|
A | G | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4300-96T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671325 | ||||||
| chr2:151671416
|
A | G | 1 | a0057c0114t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4300-187T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671416 | ||||||
| chr2:151671511
|
G | C | 9 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(6): Show | 9 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.4300-282C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671511 | ||||||
| chr2:151671542
|
T | A | 1 | a0080c0030t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4300-313A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671542 | ||||||
| chr2:151671594
|
T | A | 7 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.4300-365A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671594 | ||||||
| chr2:151671759
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4300-530T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671759 | ||||||
| chr2:151671899
|
T | C | 3 | a0002c0002t0001g0036a0113c0042t0001g0035a0115c0053t0001g0084 | 3 | HG00609.hp2 NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.4299+470A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671899 | ||||||
| chr2:151671986
|
G | GA | 64 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.4299+382dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151671986 | ||||||
| chr2:151672061
|
A | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4299+308T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151672061 | ||||||
| chr2:151672152
|
C | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.4299+217G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151672152 | ||||||
| chr2:151672183
|
T | C | 4 | a0003c0083t0001g0003a0003c0094t0001g0014a0012c0090t0001g0005others(1): Show | 4 | HG00099.hp1 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.4299+186A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151672183 | ||||||
| chr2:151672304
|
T | C | 1 | a0069c0120t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4299+65A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 37/181 | chr2 | 151672304 | ||||||
| chr2:151673018
|
T | C | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3988-338A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673018 | ||||||
| chr2:151673060
|
A | G | 3 | a0016c0016t0002g0100a0016c0016t0002g0137a0057c0114t0002g0115 | 3 | HG02965.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3988-380T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673060 | ||||||
| chr2:151673105
|
A | G | 1 | a0076c0101t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3988-425T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673105 | ||||||
| chr2:151673228
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3988-548G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673228 | ||||||
| chr2:151673436
|
T | TA | 16 | a0028c0021t0001g0182a0028c0021t0001g0183a0034c0147t0001g0178others(13): Show | 16 | HG00639.hp1 HG02040.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3988-757dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673436 | ||||||
| chr2:151673443
|
A | G | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3988-763T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673443 | ||||||
| chr2:151673667
|
C | G | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3987+810G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673667 | ||||||
| chr2:151673732
|
CT | C | 96 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3987+744delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673732 | ||||||
| chr2:151673862
|
C | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3987+615G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151673862 | ||||||
| chr2:151674070
|
C | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3987+407G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151674070 | ||||||
| chr2:151674273
|
T | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3987+204A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151674273 | ||||||
| chr2:151674344
|
T | C | 1 | a0041c0085t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3987+133A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151674344 | ||||||
| chr2:151674466
|
T | A | 5 | a0002c0002t0001g0039a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG00621.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.3987+11A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 36/181 | chr2 | 151674466 | ||||||
| chr2:151674950
|
G | C | 8 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(5): Show | 8 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.3879+337C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/181 | chr2 | 151674950 | ||||||
| chr2:151675107
|
A | G | 2 | a0013c0014t0001g0099a0013c0014t0001g0102 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3879+180T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/181 | chr2 | 151675107 | ||||||
| chr2:151675137
|
G | C | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3879+150C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/181 | chr2 | 151675137 | ||||||
| chr2:151675267
|
C | A | 71 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(68): Show | 71 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.3879+20G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 35/181 | chr2 | 151675267 | ||||||
| chr2:151675397
|
A | G | 2 | a0064c0025t0001g0095a0080c0030t0001g0074 | 2 | HG00639.hp2 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.3775-6T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675397 | ||||||
| chr2:151675507
|
G | A | 1 | a0107c0045t0001g0028 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3775-116C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675507 | ||||||
| chr2:151675508
|
C | A | 1 | a0128c0148t0001g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3775-117G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675508 | ||||||
| chr2:151675770
|
A | ATTATCC | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.3775-380_3775-379i others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675770 | ||||||
| chr2:151675771
|
G | C | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.3775-380C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675771 | ||||||
| chr2:151675775
|
T | A | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.3775-384A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675775 | ||||||
| chr2:151675776
|
T | G | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.3775-385A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675776 | ||||||
| chr2:151675863
|
G | A | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3775-472C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151675863 | ||||||
| chr2:151676267
|
T | C | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3775-876A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151676267 | ||||||
| chr2:151676710
|
C | A | 13 | a0005c0008t0001g0038a0005c0008t0001g0077a0005c0063t0001g0052others(10): Show | 13 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3774+855G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151676710 | ||||||
| chr2:151676874
|
T | G | 1 | a0121c0074t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3774+691A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151676874 | ||||||
| chr2:151676908
|
C | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3774+657G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151676908 | ||||||
| chr2:151676911
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3774+654T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151676911 | ||||||
| chr2:151677122
|
A | G | 19 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(16): Show | 19 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.3774+443T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151677122 | ||||||
| chr2:151677228
|
T | A | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3774+337A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151677228 | ||||||
| chr2:151677429
|
T | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3774+136A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 34/181 | chr2 | 151677429 | ||||||
| chr2:151678410
|
C | T | 1 | a0076c0101t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3256-223G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678410 | ||||||
| chr2:151678518
|
A | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3256-331T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678518 | ||||||
| chr2:151678621
|
C | T | 90 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3256-434G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678621 | ||||||
| chr2:151678790
|
C | T | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(3): Show | 6 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.3256-603G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678790 | ||||||
| chr2:151678900
|
A | C | 1 | a0052c0100t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3256-713T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678900 | ||||||
| chr2:151678901
|
A | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3256-714T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678901 | ||||||
| chr2:151678967
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3255+754C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151678967 | ||||||
| chr2:151679115
|
C | A | 2 | a0129c0022t0001g0114a0133c0152t0001g0169 | 2 | HG01192.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3255+606G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151679115 | ||||||
| chr2:151679263
|
A | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | NA18948.hp2 NA18966.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3255+458T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151679263 | ||||||
| chr2:151679446
|
T | A | 2 | a0004c0018t0001g0134a0004c0018t0001g0135 | 2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3255+275A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151679446 | ||||||
| chr2:151679543
|
A | G | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0010c0139t0001g0106others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.3255+178T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 32/181 | chr2 | 151679543 | ||||||
| chr2:151679857
|
C | G | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3148-29G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 31/181 | chr2 | 151679857 | ||||||
| chr2:151679913
|
C | T | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
splice_region_variant&intron_variant | LOW | c.3147+5G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 31/181 | chr2 | 151679913 | ||||||
| chr2:151680164
|
C | A | 1 | a0060c0107t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3043-142G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680164 | ||||||
| chr2:151680272
|
G | GC | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.3043-251dupG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680272 | ||||||
| chr2:151680320
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3043-298A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680320 | ||||||
| chr2:151680366
|
T | C | 1 | a0005c0008t0001g0038 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3043-344A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680366 | ||||||
| chr2:151680372
|
AT | A | 181 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.3043-351delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680372 | ||||||
| chr2:151680531
|
A | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3042+199T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 30/181 | chr2 | 151680531 | ||||||
| chr2:151680837
|
C | T | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.2944-9G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151680837 | ||||||
| chr2:151680943
|
A | T | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2944-115T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151680943 | ||||||
| chr2:151681322
|
G | T | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2944-494C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681322 | ||||||
| chr2:151681517
|
T | C | 12 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(9): Show | 12 | HG00558.hp2 HG01884.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.2944-689A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681517 | ||||||
| chr2:151681619
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2944-791G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681619 | ||||||
| chr2:151681699
|
G | A | 1 | a0066c0118t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2944-871C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681699 | ||||||
| chr2:151681816
|
T | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2943+846A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681816 | ||||||
| chr2:151681871
|
C | T | 4 | a0034c0147t0001g0178a0035c0146t0001g0103a0080c0030t0001g0074others(1): Show | 4 | HG00639.hp1 HG00639.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.2943+791G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681871 | ||||||
| chr2:151681938
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2943+724G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681938 | ||||||
| chr2:151681972
|
T | C | 1 | a0057c0114t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2943+690A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151681972 | ||||||
| chr2:151682220
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2943+442C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151682220 | ||||||
| chr2:151682268
|
T | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2943+394A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151682268 | ||||||
| chr2:151682305
|
T | C | 11 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(8): Show | 11 | HG00558.hp2 HG01884.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.2943+357A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 29/181 | chr2 | 151682305 | ||||||
| chr2:151682804
|
T | C | 1 | a0010c0139t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2836-35A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151682804 | ||||||
| chr2:151682960
|
T | A | 1 | a0090c0035t0001g0054 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2836-191A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151682960 | ||||||
| chr2:151682963
|
C | T | 75 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(72): Show | 75 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.2836-194G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151682963 | ||||||
| chr2:151682993
|
CT | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.2836-225delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151682993 | ||||||
| chr2:151683036
|
T | C | 127 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2836-267A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683036 | ||||||
| chr2:151683313
|
C | T | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2836-544G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683313 | ||||||
| chr2:151683334
|
G | A | 1 | a0024c0038t0001g0085 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2836-565C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683334 | ||||||
| chr2:151683399
|
G | A | 88 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2836-630C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683399 | ||||||
| chr2:151683458
|
G | A | 1 | a0117c0039t0001g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2836-689C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683458 | ||||||
| chr2:151683658
|
G | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2836-889C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683658 | ||||||
| chr2:151683691
|
T | C | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2836-922A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683691 | ||||||
| chr2:151683976
|
T | G | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2835+802A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151683976 | ||||||
| chr2:151684165
|
C | T | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2835+613G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684165 | ||||||
| chr2:151684177
|
G | A | 1 | a0112c0051t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2835+601C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684177 | ||||||
| chr2:151684322
|
C | A | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.2835+456G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684322 | ||||||
| chr2:151684368
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2835+410A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684368 | ||||||
| chr2:151684389
|
A | T | 1 | a0009c0109t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2835+389T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684389 | ||||||
| chr2:151684401
|
G | A | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2835+377C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684401 | ||||||
| chr2:151684506
|
A | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2835+272T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684506 | ||||||
| chr2:151684563
|
C | T | 97 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2835+215G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684563 | ||||||
| chr2:151684620
|
T | C | 75 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(72): Show | 75 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.2835+158A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684620 | ||||||
| chr2:151684666
|
A | T | 1 | a0119c0136t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2835+112T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684666 | ||||||
| chr2:151684690
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2835+88T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 28/181 | chr2 | 151684690 | ||||||
| chr2:151685044
|
T | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2638-69A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685044 | ||||||
| chr2:151685125
|
T | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2638-150A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685125 | ||||||
| chr2:151685136
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2638-161A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685136 | ||||||
| chr2:151685152
|
G | A | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2638-177C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685152 | ||||||
| chr2:151685409
|
G | C | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2638-434C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685409 | ||||||
| chr2:151685633
|
G | A | 1 | a0093c0058t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2638-658C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685633 | ||||||
| chr2:151685660
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2638-685C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685660 | ||||||
| chr2:151685719
|
A | G | 2 | a0006c0012t0001g0172a0006c0012t0001g0173 | 2 | NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.2638-744T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685719 | ||||||
| chr2:151685730
|
A | G | 1 | a0015c0108t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2638-755T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685730 | ||||||
| chr2:151685767
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2638-792C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685767 | ||||||
| chr2:151685778
|
G | T | 95 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2638-803C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685778 | ||||||
| chr2:151685971
|
A | G | 19 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(16): Show | 19 | HG00558.hp2 HG00639.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2638-996T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685971 | ||||||
| chr2:151685994
|
T | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2638-1019A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151685994 | ||||||
| chr2:151686090
|
G | A | 2 | a0022c0026t0001g0032a0124c0075t0001g0057 | 2 | NA18942.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2638-1115C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686090 | ||||||
| chr2:151686209
|
T | C | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2637+1210A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686209 | ||||||
| chr2:151686225
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2637+1194T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686225 | ||||||
| chr2:151686302
|
T | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2637+1117A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686302 | ||||||
| chr2:151686370
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2637+1049T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686370 | ||||||
| chr2:151686406
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2637+1013A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686406 | ||||||
| chr2:151686892
|
A | G | 3 | a0019c0010t0001g0059a0019c0010t0003g0188a0104c0059t0001g0019 | 3 | NA18950.hp1 NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2637+527T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686892 | ||||||
| chr2:151686906
|
T | C | 3 | a0011c0070t0001g0055a0098c0071t0001g0056a0100c0072t0001g0076 | 3 | HG01358.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2637+513A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151686906 | ||||||
| chr2:151687001
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2637+418T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687001 | ||||||
| chr2:151687012
|
T | A | 1 | a0039c0153t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2637+407A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687012 | ||||||
| chr2:151687098
|
G | A | 183 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2637+321C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687098 | ||||||
| chr2:151687192
|
C | T | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2637+227G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687192 | ||||||
| chr2:151687292
|
A | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2637+127T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687292 | ||||||
| chr2:151687314
|
T | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2637+105A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687314 | ||||||
| chr2:151687402
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2637+17A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 27/181 | chr2 | 151687402 | ||||||
| chr2:151687547
|
C | A | 2 | a0006c0079t0001g0170a0031c0078t0001g0171 | 2 | HG02080.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2524-15G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 26/181 | chr2 | 151687547 | ||||||
| chr2:151687915
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.2416-182T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151687915 | ||||||
| chr2:151687979
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2416-246G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151687979 | ||||||
| chr2:151688048
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2415+244C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151688048 | ||||||
| chr2:151688146
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2415+146T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151688146 | ||||||
| chr2:151688211
|
CCTTGT | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415+76_2415+80del others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151688211 | ||||||
| chr2:151688235
|
A | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2415+57T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151688235 | ||||||
| chr2:151688255
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2415+37A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 25/181 | chr2 | 151688255 | ||||||
| chr2:151688478
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2311-82A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688478 | ||||||
| chr2:151688654
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2311-258G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688654 | ||||||
| chr2:151688700
|
T | G | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2311-304A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688700 | ||||||
| chr2:151688726
|
TAAC | T | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2311-333_2311-331d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688726 | ||||||
| chr2:151688764
|
A | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-368T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688764 | ||||||
| chr2:151688933
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2311-537G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151688933 | ||||||
| chr2:151689108
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-712A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689108 | ||||||
| chr2:151689197
|
C | CT | 56 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(53): Show | 56 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2311-802dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689197 | ||||||
| chr2:151689197
|
CT | C | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2311-802delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689197 | ||||||
| chr2:151689197
|
CTT | C | 6 | a0016c0016t0002g0100a0022c0026t0001g0032a0048c0098t0001g0186others(3): Show | 6 | HG02683.hp2 HG02965.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2311-803_2311-802d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689197 | ||||||
| chr2:151689197
|
CTTT | C | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-804_2311-802d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689197 | ||||||
| chr2:151689260
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2311-864T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689260 | ||||||
| chr2:151689353
|
T | C | 1 | a0045c0089t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2311-957A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689353 | ||||||
| chr2:151689361
|
T | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2311-965A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689361 | ||||||
| chr2:151689532
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2311-1136G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689532 | ||||||
| chr2:151689595
|
G | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+1132C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689595 | ||||||
| chr2:151689629
|
A | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+1098T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689629 | ||||||
| chr2:151689631
|
T | C | 58 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.2310+1096A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689631 | ||||||
| chr2:151689683
|
C | G | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2310+1044G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689683 | ||||||
| chr2:151689684
|
T | C | 68 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2310+1043A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689684 | ||||||
| chr2:151689695
|
A | G | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2310+1032T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689695 | ||||||
| chr2:151689738
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+989C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689738 | ||||||
| chr2:151689791
|
C | T | 2 | a0018c0020t0001g0131a0078c0128t0001g0163 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2310+936G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689791 | ||||||
| chr2:151689798
|
T | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+929A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689798 | ||||||
| chr2:151689847
|
G | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+880C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689847 | ||||||
| chr2:151689911
|
T | C | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2310+816A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689911 | ||||||
| chr2:151689973
|
G | GT | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+753_2310+754i others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689973 | ||||||
| chr2:151689975
|
T | A | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+752A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689975 | ||||||
| chr2:151689977
|
T | TG | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+749_2310+750i others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151689977 | ||||||
| chr2:151690172
|
T | C | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2310+555A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151690172 | ||||||
| chr2:151690341
|
T | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+386A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 24/181 | chr2 | 151690341 | ||||||
| chr2:151690862
|
T | C | 1 | a0124c0075t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2212-37A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151690862 | ||||||
| chr2:151690971
|
GTC | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2212-148_2212-147d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151690971 | ||||||
| chr2:151690977
|
C | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2212-152G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151690977 | ||||||
| chr2:151691265
|
G | A | 1 | a0026c0006t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2212-440C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691265 | ||||||
| chr2:151691280
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-455A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691280 | ||||||
| chr2:151691347
|
C | T | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+517G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691347 | ||||||
| chr2:151691356
|
A | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2211+508T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691356 | ||||||
| chr2:151691363
|
G | C | 30 | a0001c0001t0001g0156a0004c0018t0001g0134a0004c0018t0001g0135others(27): Show | 30 | HG00423.hp2 HG00597.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.2211+501C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691363 | ||||||
| chr2:151691420
|
T | C | 9 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.2211+444A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691420 | ||||||
| chr2:151691465
|
T | C | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2211+399A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691465 | ||||||
| chr2:151691573
|
T | C | 1 | a0122c0033t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2211+291A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691573 | ||||||
| chr2:151691720
|
C | T | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2211+144G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 23/181 | chr2 | 151691720 | ||||||
| chr2:151692034
|
CATGAACC others(15): Show |
C | 1 | a0004c0018t0001g0135 | 1 | NA18962.hp2 | splice_region_variant&intron_variant | LOW | c.2106+3_2106+24delA others(21): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 22/181 | chr2 | 151692034 | ||||||
| chr2:151692187
|
A | C | 1 | a0126c0027t0001g0067 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1999-21T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 21/181 | chr2 | 151692187 | ||||||
| chr2:151692826
|
C | T | 75 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(72): Show | 75 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1897-464G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151692826 | ||||||
| chr2:151693050
|
T | C | 1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1897-688A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693050 | ||||||
| chr2:151693189
|
G | A | 127 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1897-827C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693189 | ||||||
| chr2:151693205
|
G | T | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1897-843C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693205 | ||||||
| chr2:151693245
|
T | G | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1897-883A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693245 | ||||||
| chr2:151693313
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1897-951A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693313 | ||||||
| chr2:151693425
|
C | A | 1 | a0060c0107t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1896+898G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693425 | ||||||
| chr2:151693477
|
T | C | 1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1896+846A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693477 | ||||||
| chr2:151693492
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1896+831G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693492 | ||||||
| chr2:151693655
|
A | C | 95 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1896+668T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693655 | ||||||
| chr2:151693864
|
C | T | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1896+459G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693864 | ||||||
| chr2:151693913
|
C | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1896+410G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151693913 | ||||||
| chr2:151694213
|
T | C | 23 | a0001c0001t0001g0156a0009c0017t0001g0121a0009c0017t0001g0159others(20): Show | 23 | HG00423.hp2 HG00597.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1896+110A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151694213 | ||||||
| chr2:151694288
|
G | A | 1 | a0002c0002t0001g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1896+35C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 20/181 | chr2 | 151694288 | ||||||
| chr2:151694638
|
A | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675-9T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151694638 | ||||||
| chr2:151694680
|
C | T | 8 | a0010c0137t0001g0093a0010c0138t0001g0091a0013c0014t0001g0099others(5): Show | 8 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675-51G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151694680 | ||||||
| chr2:151694696
|
G | A | 108 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1675-67C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151694696 | ||||||
| chr2:151695038
|
G | A | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675-409C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695038 | ||||||
| chr2:151695049
|
T | C | 1 | a0112c0051t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1675-420A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695049 | ||||||
| chr2:151695051
|
G | A | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675-422C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695051 | ||||||
| chr2:151695121
|
G | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1674+457C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695121 | ||||||
| chr2:151695319
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1674+259A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695319 | ||||||
| chr2:151695398
|
C | T | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1674+180G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695398 | ||||||
| chr2:151695515
|
C | T | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1674+63G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695515 | ||||||
| chr2:151695548
|
A | C | 60 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1674+30T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 18/181 | chr2 | 151695548 | ||||||
| chr2:151695824
|
C | T | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1570-142G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151695824 | ||||||
| chr2:151695828
|
T | A | 112 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1570-146A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151695828 | ||||||
| chr2:151695965
|
G | A | 3 | a0002c0002t0001g0036a0113c0042t0001g0035a0115c0053t0001g0084 | 3 | HG00609.hp2 NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1570-283C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151695965 | ||||||
| chr2:151695996
|
C | T | 1 | a0011c0009t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1570-314G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151695996 | ||||||
| chr2:151695997
|
G | A | 3 | a0019c0010t0001g0059a0019c0010t0003g0188a0104c0059t0001g0019 | 3 | NA18950.hp1 NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1570-315C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151695997 | ||||||
| chr2:151696093
|
T | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1570-411A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696093 | ||||||
| chr2:151696231
|
C | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1569+406G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696231 | ||||||
| chr2:151696353
|
C | G | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1569+284G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696353 | ||||||
| chr2:151696385
|
G | A | 1 | a0038c0086t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1569+252C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696385 | ||||||
| chr2:151696509
|
T | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1569+128A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696509 | ||||||
| chr2:151696599
|
C | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1569+38G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696599 | ||||||
| chr2:151696622
|
G | C | 1 | a0002c0002t0001g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1569+15C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 17/181 | chr2 | 151696622 | ||||||
| chr2:151696789
|
T | G | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1471-54A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 16/181 | chr2 | 151696789 | ||||||
| chr2:151696795
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-60T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 16/181 | chr2 | 151696795 | ||||||
| chr2:151696857
|
T | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1471-122A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 16/181 | chr2 | 151696857 | ||||||
| chr2:151697531
|
T | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1257+13A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 14/181 | chr2 | 151697531 | ||||||
| chr2:151697702
|
T | C | 1 | a0102c0069t0001g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1153-54A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151697702 | ||||||
| chr2:151697848
|
C | G | 18 | a0001c0001t0001g0156a0009c0017t0001g0121a0009c0017t0001g0159others(15): Show | 18 | HG00423.hp2 HG00597.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1153-200G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151697848 | ||||||
| chr2:151697944
|
T | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1153-296A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151697944 | ||||||
| chr2:151697991
|
G | T | 2 | a0002c0048t0001g0086a0024c0038t0001g0085 | 2 | NA18962.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1153-343C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151697991 | ||||||
| chr2:151698050
|
T | C | 74 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1153-402A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698050 | ||||||
| chr2:151698064
|
T | TCAAAA | 80 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1153-421_1153-417d others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698064 | ||||||
| chr2:151698064
|
T | TCAAAACA others(3): Show |
4 | a0001c0001t0001g0097a0001c0001t0001g0112a0069c0120t0001g0104others(1): Show | 4 | HG00423.hp1 HG02523.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-426_1153-417d others(12): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698064 | ||||||
| chr2:151698064
|
TCAAAA | T | 93 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1153-421_1153-417d others(7): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698064 | ||||||
| chr2:151698088
|
A | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-440T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698088 | ||||||
| chr2:151698151
|
C | T | 2 | a0003c0094t0001g0014a0012c0090t0001g0005 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1153-503G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698151 | ||||||
| chr2:151698458
|
A | G | 3 | a0007c0003t0001g0001a0007c0003t0001g0002a0007c0003t0001g0029 | 3 | HG01258.hp2 HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1153-810T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698458 | ||||||
| chr2:151698486
|
T | G | 2 | a0034c0147t0001g0178a0035c0146t0001g0103 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1153-838A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698486 | ||||||
| chr2:151698624
|
G | A | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1153-976C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698624 | ||||||
| chr2:151698635
|
A | AT | 5 | a0002c0002t0001g0026a0002c0002t0001g0039a0024c0038t0001g0085others(2): Show | 5 | HG01175.hp2 HG03688.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-988dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698635 | ||||||
| chr2:151698635
|
AT | A | 26 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(23): Show | 26 | HG00639.hp1 HG01192.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1153-988delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698635 | ||||||
| chr2:151698669
|
C | G | 125 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1153-1021G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698669 | ||||||
| chr2:151698765
|
G | A | 3 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1153-1117C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698765 | ||||||
| chr2:151698816
|
T | A | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1153-1168A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698816 | ||||||
| chr2:151698865
|
CT | C | 5 | a0004c0126t0001g0118a0015c0111t0001g0139a0028c0021t0001g0183others(2): Show | 5 | HG00609.hp2 HG02451.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-1218delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698865 | ||||||
| chr2:151698868
|
T | C | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1153-1220A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698868 | ||||||
| chr2:151698870
|
T | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1153-1222A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698870 | ||||||
| chr2:151698880
|
T | A | 185 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1153-1232A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698880 | ||||||
| chr2:151698915
|
T | A | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1153-1267A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698915 | ||||||
| chr2:151698976
|
G | A | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1153-1328C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151698976 | ||||||
| chr2:151699009
|
T | C | 99 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1153-1361A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699009 | ||||||
| chr2:151699018
|
C | G | 1 | a0053c0127t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1153-1370G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699018 | ||||||
| chr2:151699131
|
C | T | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1483G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699131 | ||||||
| chr2:151699133
|
A | T | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1485T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699133 | ||||||
| chr2:151699140
|
A | G | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1492T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699140 | ||||||
| chr2:151699298
|
T | C | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1153-1650A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699298 | ||||||
| chr2:151699325
|
G | A | 1 | a0094c0061t0001g0080 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1153-1677C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699325 | ||||||
| chr2:151699486
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-1838T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699486 | ||||||
| chr2:151699548
|
T | C | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1153-1900A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699548 | ||||||
| chr2:151699704
|
G | A | 4 | a0009c0017t0001g0159a0059c0143t0001g0161a0061c0115t0001g0158others(1): Show | 4 | HG00597.hp2 HG02074.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-2056C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699704 | ||||||
| chr2:151699736
|
T | G | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1153-2088A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699736 | ||||||
| chr2:151699787
|
C | T | 10 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1153-2139G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699787 | ||||||
| chr2:151699788
|
G | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1153-2140C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699788 | ||||||
| chr2:151699804
|
T | G | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1153-2156A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699804 | ||||||
| chr2:151699807
|
G | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1153-2159C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699807 | ||||||
| chr2:151699876
|
G | C | 2 | a0009c0017t0001g0121a0054c0104t0001g0162 | 2 | NA18946.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1153-2228C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699876 | ||||||
| chr2:151699983
|
T | G | 1 | a0009c0109t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1153-2335A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151699983 | ||||||
| chr2:151700003
|
C | T | 6 | a0010c0139t0001g0106a0017c0015t0001g0164a0017c0015t0001g0165others(3): Show | 6 | HG00423.hp2 NA18945.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153-2355G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700003 | ||||||
| chr2:151700087
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-2439C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700087 | ||||||
| chr2:151700185
|
G | A | 1 | a0002c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1153-2537C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700185 | ||||||
| chr2:151700339
|
C | T | 6 | a0028c0021t0001g0182a0028c0021t0001g0183a0087c0132t0001g0101others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-2691G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700339 | ||||||
| chr2:151700405
|
T | G | 1 | a0122c0033t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1153-2757A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700405 | ||||||
| chr2:151700488
|
A | G | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1153-2840T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700488 | ||||||
| chr2:151700523
|
A | G | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-2875T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700523 | ||||||
| chr2:151700581
|
T | A | 18 | a0001c0001t0001g0156a0009c0017t0001g0121a0009c0017t0001g0159others(15): Show | 18 | HG00423.hp2 HG00597.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1153-2933A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700581 | ||||||
| chr2:151700622
|
A | G | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1153-2974T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700622 | ||||||
| chr2:151700705
|
C | T | 1 | a0025c0011t0001g0090 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1153-3057G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700705 | ||||||
| chr2:151700773
|
C | A | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1153-3125G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700773 | ||||||
| chr2:151700802
|
G | A | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1153-3154C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700802 | ||||||
| chr2:151700924
|
A | G | 102 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1153-3276T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151700924 | ||||||
| chr2:151701178
|
T | C | 117 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1153-3530A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701178 | ||||||
| chr2:151701242
|
T | G | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-3594A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701242 | ||||||
| chr2:151701261
|
T | G | 3 | a0008c0004t0001g0011a0008c0004t0001g0012a0041c0085t0002g0010 | 3 | HG03225.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1153-3613A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701261 | ||||||
| chr2:151701412
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-3764T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701412 | ||||||
| chr2:151701447
|
T | C | 1 | a0004c0019t0001g0151 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1153-3799A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701447 | ||||||
| chr2:151701590
|
T | C | 1 | a0088c0037t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1153-3942A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701590 | ||||||
| chr2:151701605
|
T | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-3957A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701605 | ||||||
| chr2:151701660
|
T | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1153-4012A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701660 | ||||||
| chr2:151701673
|
T | C | 2 | a0042c0095t0001g0020a0046c0091t0001g0017 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1153-4025A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701673 | ||||||
| chr2:151701715
|
C | G | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1153-4067G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701715 | ||||||
| chr2:151701719
|
T | C | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1153-4071A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701719 | ||||||
| chr2:151701780
|
C | T | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153-4132G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701780 | ||||||
| chr2:151701781
|
A | G | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153-4133T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701781 | ||||||
| chr2:151701813
|
C | T | 1 | a0005c0008t0001g0038 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1153-4165G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701813 | ||||||
| chr2:151701918
|
T | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-4270A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701918 | ||||||
| chr2:151701989
|
T | A | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1153-4341A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701989 | ||||||
| chr2:151701991
|
T | C | 4 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(1): Show | 4 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-4343A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151701991 | ||||||
| chr2:151702040
|
C | T | 1 | a0083c0134t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1153-4392G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702040 | ||||||
| chr2:151702110
|
C | T | 1 | a0046c0091t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1153-4462G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702110 | ||||||
| chr2:151702115
|
C | T | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1153-4467G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702115 | ||||||
| chr2:151702171
|
C | T | 73 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1153-4523G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702171 | ||||||
| chr2:151702174
|
T | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1153-4526A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702174 | ||||||
| chr2:151702195
|
C | T | 1 | a0033c0024t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153-4547G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702195 | ||||||
| chr2:151702203
|
T | C | 63 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1153-4555A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702203 | ||||||
| chr2:151702227
|
A | T | 5 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-4579T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702227 | ||||||
| chr2:151702251
|
TC | T | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1153-4604delG | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702251 | ||||||
| chr2:151702253
|
T | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1153-4605A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702253 | ||||||
| chr2:151702263
|
G | T | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1153-4615C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702263 | ||||||
| chr2:151702324
|
G | GA | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+4556dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702324 | ||||||
| chr2:151702384
|
G | A | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+4497C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702384 | ||||||
| chr2:151702592
|
G | C | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1152+4289C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702592 | ||||||
| chr2:151702594
|
G | T | 124 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1152+4287C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702594 | ||||||
| chr2:151702663
|
G | A | 1 | a0012c0088t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1152+4218C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702663 | ||||||
| chr2:151702694
|
C | T | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1152+4187G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702694 | ||||||
| chr2:151702695
|
C | CT | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+4185dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702695 | ||||||
| chr2:151702695
|
C | T | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1152+4186G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702695 | ||||||
| chr2:151702701
|
T | G | 1 | a0111c0049t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1152+4180A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702701 | ||||||
| chr2:151702732
|
C | G | 69 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1152+4149G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702732 | ||||||
| chr2:151702951
|
G | T | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+3930C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702951 | ||||||
| chr2:151702955
|
C | T | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1152+3926G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151702955 | ||||||
| chr2:151703228
|
T | C | 183 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1152+3653A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703228 | ||||||
| chr2:151703356
|
A | G | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1152+3525T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703356 | ||||||
| chr2:151703373
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+3508C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703373 | ||||||
| chr2:151703408
|
CCTTG | C | 21 | a0003c0005t0001g0006a0003c0005t0001g0013a0003c0083t0001g0003others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1152+3469_1152+347 others(8): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703408 | ||||||
| chr2:151703501
|
C | G | 115 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1152+3380G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703501 | ||||||
| chr2:151703564
|
T | C | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1152+3317A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703564 | ||||||
| chr2:151703592
|
T | C | 115 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1152+3289A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703592 | ||||||
| chr2:151703611
|
C | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3270G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703611 | ||||||
| chr2:151703618
|
C | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3263G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703618 | ||||||
| chr2:151703621
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3260A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703621 | ||||||
| chr2:151703622
|
G | A | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3259C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703622 | ||||||
| chr2:151703630
|
C | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+3251G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703630 | ||||||
| chr2:151703679
|
C | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1152+3202G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703679 | ||||||
| chr2:151703689
|
G | A | 2 | a0024c0040t0001g0062a0117c0039t0001g0063 | 2 | HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1152+3192C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703689 | ||||||
| chr2:151703835
|
C | T | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1152+3046G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151703835 | ||||||
| chr2:151704000
|
C | T | 1 | a0032c0077t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1152+2881G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704000 | ||||||
| chr2:151704037
|
T | C | 2 | a0032c0077t0001g0175a0094c0061t0001g0080 | 2 | HG02074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1152+2844A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704037 | ||||||
| chr2:151704042
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+2839A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704042 | ||||||
| chr2:151704043
|
G | A | 3 | a0027c0013t0001g0070a0027c0013t0001g0071a0032c0077t0001g0175 | 3 | HG02257.hp2 HG02976.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1152+2838C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704043 | ||||||
| chr2:151704054
|
C | A | 1 | a0110c0041t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1152+2827G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704054 | ||||||
| chr2:151704057
|
T | G | 3 | a0027c0013t0001g0070a0027c0013t0001g0071a0032c0077t0001g0175 | 3 | HG02257.hp2 HG02976.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1152+2824A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704057 | ||||||
| chr2:151704059
|
T | C | 6 | a0028c0021t0001g0182a0028c0021t0001g0183a0087c0132t0001g0101others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+2822A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704059 | ||||||
| chr2:151704109
|
A | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0082t0001g0147others(2): Show | 5 | HG00423.hp1 HG00621.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+2772T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704109 | ||||||
| chr2:151704115
|
T | G | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1152+2766A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704115 | ||||||
| chr2:151704134
|
G | C | 1 | a0001c0082t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1152+2747C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704134 | ||||||
| chr2:151704159
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2722T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704159 | ||||||
| chr2:151704172
|
G | A | 2 | a0024c0040t0001g0062a0117c0039t0001g0063 | 2 | HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1152+2709C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704172 | ||||||
| chr2:151704204
|
G | A | 2 | a0024c0040t0001g0062a0117c0039t0001g0063 | 2 | HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1152+2677C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704204 | ||||||
| chr2:151704213
|
C | T | 2 | a0021c0057t0001g0037a0022c0054t0001g0030 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1152+2668G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704213 | ||||||
| chr2:151704214
|
C | G | 2 | a0021c0057t0001g0037a0022c0054t0001g0030 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1152+2667G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704214 | ||||||
| chr2:151704295
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1152+2586C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704295 | ||||||
| chr2:151704326
|
C | G | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1152+2555G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704326 | ||||||
| chr2:151704403
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+2478G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704403 | ||||||
| chr2:151704423
|
T | G | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1152+2458A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704423 | ||||||
| chr2:151704432
|
G | C | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1152+2449C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704432 | ||||||
| chr2:151704441
|
G | A | 1 | a0108c0047t0001g0064 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1152+2440C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704441 | ||||||
| chr2:151704535
|
G | A | 2 | a0008c0004t0001g0011a0008c0004t0001g0012 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1152+2346C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704535 | ||||||
| chr2:151704559
|
G | A | 22 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(19): Show | 22 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1152+2322C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704559 | ||||||
| chr2:151704604
|
G | A | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2277C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704604 | ||||||
| chr2:151704620
|
T | A | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1152+2261A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704620 | ||||||
| chr2:151704705
|
G | A | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1152+2176C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704705 | ||||||
| chr2:151704766
|
G | C | 183 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1152+2115C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704766 | ||||||
| chr2:151704783
|
C | T | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1152+2098G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704783 | ||||||
| chr2:151704794
|
A | G | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1152+2087T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151704794 | ||||||
| chr2:151705086
|
G | C | 69 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1152+1795C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705086 | ||||||
| chr2:151705107
|
G | A | 5 | a0004c0019t0001g0148a0004c0019t0001g0151a0029c0081t0001g0123others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152+1774C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705107 | ||||||
| chr2:151705201
|
A | T | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1152+1680T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705201 | ||||||
| chr2:151705218
|
C | T | 1 | a0068c0125t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1152+1663G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705218 | ||||||
| chr2:151705347
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+1534T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705347 | ||||||
| chr2:151705506
|
A | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1152+1375T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705506 | ||||||
| chr2:151705545
|
A | T | 1 | a0110c0041t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1152+1336T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705545 | ||||||
| chr2:151705884
|
G | A | 1 | a0131c0149t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1152+997C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151705884 | ||||||
| chr2:151706170
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+711G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706170 | ||||||
| chr2:151706388
|
T | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1152+493A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706388 | ||||||
| chr2:151706416
|
C | T | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1152+465G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706416 | ||||||
| chr2:151706425
|
C | A | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+456G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706425 | ||||||
| chr2:151706441
|
A | G | 22 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1152+440T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706441 | ||||||
| chr2:151706444
|
C | T | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1152+437G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706444 | ||||||
| chr2:151706547
|
G | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1152+334C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706547 | ||||||
| chr2:151706695
|
A | C | 1 | a0009c0109t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1152+186T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706695 | ||||||
| chr2:151706698
|
C | G | 6 | a0028c0021t0001g0182a0028c0021t0001g0183a0087c0132t0001g0101others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+183G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706698 | ||||||
| chr2:151706728
|
A | G | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1152+153T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706728 | ||||||
| chr2:151706775
|
C | T | 3 | a0002c0002t0001g0036a0113c0042t0001g0035a0115c0053t0001g0084 | 3 | HG00609.hp2 NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1152+106G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706775 | ||||||
| chr2:151706832
|
T | C | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1152+49A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 13/181 | chr2 | 151706832 | ||||||
| chr2:151707074
|
C | T | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1036-77G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707074 | ||||||
| chr2:151707234
|
A | G | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1036-237T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707234 | ||||||
| chr2:151707387
|
C | T | 2 | a0003c0094t0001g0014a0012c0090t0001g0005 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1036-390G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707387 | ||||||
| chr2:151707514
|
TAGG | T | 65 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1036-520_1036-518d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707514 | ||||||
| chr2:151707674
|
C | T | 8 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG00280.hp1 HG00609.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036-677G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707674 | ||||||
| chr2:151707807
|
C | G | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1036-810G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707807 | ||||||
| chr2:151707836
|
T | C | 76 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1036-839A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707836 | ||||||
| chr2:151707935
|
G | A | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1036-938C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151707935 | ||||||
| chr2:151708001
|
C | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1036-1004G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708001 | ||||||
| chr2:151708008
|
G | A | 2 | a0006c0012t0001g0172a0006c0012t0001g0173 | 2 | NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1036-1011C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708008 | ||||||
| chr2:151708062
|
G | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-1065C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708062 | ||||||
| chr2:151708179
|
G | T | 1 | a0057c0114t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1036-1182C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708179 | ||||||
| chr2:151708183
|
CT | C | 11 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(8): Show | 11 | HG00544.hp2 HG00673.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036-1187delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708183 | ||||||
| chr2:151708187
|
C | G | 11 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(8): Show | 11 | HG00544.hp2 HG00673.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036-1190G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708187 | ||||||
| chr2:151708188
|
C | G | 11 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(8): Show | 11 | HG00544.hp2 HG00673.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036-1191G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708188 | ||||||
| chr2:151708473
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035+1183C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708473 | ||||||
| chr2:151708541
|
C | T | 124 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1035+1115G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708541 | ||||||
| chr2:151708683
|
C | T | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1035+973G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708683 | ||||||
| chr2:151708706
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1035+950C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708706 | ||||||
| chr2:151708720
|
G | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1035+936C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708720 | ||||||
| chr2:151708767
|
C | T | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1035+889G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708767 | ||||||
| chr2:151708795
|
C | A | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1035+861G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708795 | ||||||
| chr2:151708886
|
T | C | 1 | a0082c0140t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1035+770A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708886 | ||||||
| chr2:151708940
|
C | G | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1035+716G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708940 | ||||||
| chr2:151708963
|
T | C | 23 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(20): Show | 23 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1035+693A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151708963 | ||||||
| chr2:151709005
|
A | C | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035+651T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709005 | ||||||
| chr2:151709303
|
G | T | 1 | a0005c0008t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1035+353C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709303 | ||||||
| chr2:151709398
|
G | A | 1 | a0103c0066t0001g0065 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1035+258C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709398 | ||||||
| chr2:151709566
|
C | T | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1035+90G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709566 | ||||||
| chr2:151709573
|
T | A | 1 | a0097c0065t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1035+83A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709573 | ||||||
| chr2:151709640
|
G | T | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1035+16C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 12/181 | chr2 | 151709640 | ||||||
| chr2:151709919
|
A | G | 83 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.928-156T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/181 | chr2 | 151709919 | ||||||
| chr2:151710004
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-241T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/181 | chr2 | 151710004 | ||||||
| chr2:151710099
|
A | G | 83 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.927+335T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/181 | chr2 | 151710099 | ||||||
| chr2:151710124
|
G | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+310C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/181 | chr2 | 151710124 | ||||||
| chr2:151710174
|
C | A | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.927+260G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 11/181 | chr2 | 151710174 | ||||||
| chr2:151710629
|
A | T | 2 | a0017c0015t0001g0164a0017c0015t0001g0165 | 2 | NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.823-91T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151710629 | ||||||
| chr2:151710646
|
T | C | 2 | a0004c0126t0001g0118a0053c0127t0001g0152 | 2 | HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.823-108A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151710646 | ||||||
| chr2:151710757
|
G | A | 1 | a0086c0032t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-219C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151710757 | ||||||
| chr2:151710784
|
C | G | 2 | a0091c0142t0001g0119a0105c0080t0001g0034 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823-246G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151710784 | ||||||
| chr2:151711003
|
C | T | 1 | a0113c0042t0001g0035 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.823-465G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151711003 | ||||||
| chr2:151711164
|
C | T | 1 | a0050c0099t0001g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.823-626G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151711164 | ||||||
| chr2:151711394
|
A | G | 72 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.823-856T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151711394 | ||||||
| chr2:151711738
|
G | A | 3 | a0033c0024t0001g0096a0050c0099t0001g0098a0064c0025t0001g0095 | 3 | HG02630.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-1200C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151711738 | ||||||
| chr2:151711985
|
T | A | 5 | a0002c0048t0001g0086a0023c0044t0001g0068a0024c0038t0001g0085others(2): Show | 5 | HG00673.hp1 NA18946.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-1447A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151711985 | ||||||
| chr2:151712052
|
T | C | 2 | a0083c0134t0001g0153a0084c0133t0001g0154 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.823-1514A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151712052 | ||||||
| chr2:151712130
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-1592A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151712130 | ||||||
| chr2:151712583
|
G | A | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.823-2045C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151712583 | ||||||
| chr2:151712698
|
A | G | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-2160T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151712698 | ||||||
| chr2:151713229
|
C | G | 6 | a0028c0021t0001g0182a0028c0021t0001g0183a0087c0132t0001g0101others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-2691G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713229 | ||||||
| chr2:151713343
|
T | C | 1 | a0101c0068t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.823-2805A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713343 | ||||||
| chr2:151713441
|
T | C | 185 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.823-2903A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713441 | ||||||
| chr2:151713465
|
T | C | 66 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.823-2927A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713465 | ||||||
| chr2:151713759
|
A | G | 6 | a0028c0021t0001g0182a0028c0021t0001g0183a0087c0132t0001g0101others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-3221T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713759 | ||||||
| chr2:151713828
|
G | A | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3290C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713828 | ||||||
| chr2:151713934
|
C | T | 1 | a0105c0080t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.823-3396G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151713934 | ||||||
| chr2:151714219
|
C | T | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.822+3197G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714219 | ||||||
| chr2:151714222
|
C | T | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+3194G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714222 | ||||||
| chr2:151714518
|
C | G | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+2898G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714518 | ||||||
| chr2:151714751
|
T | C | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+2665A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714751 | ||||||
| chr2:151714758
|
T | C | 1 | a0047c0097t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+2658A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714758 | ||||||
| chr2:151714810
|
T | C | 2 | a0027c0013t0001g0070a0027c0013t0001g0071 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+2606A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714810 | ||||||
| chr2:151714956
|
T | C | 185 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.822+2460A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151714956 | ||||||
| chr2:151715235
|
G | T | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+2181C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151715235 | ||||||
| chr2:151715250
|
A | G | 5 | a0008c0004t0001g0009a0008c0004t0001g0011a0008c0004t0001g0012others(2): Show | 5 | HG01192.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+2166T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151715250 | ||||||
| chr2:151715481
|
G | A | 1 | a0043c0084t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.822+1935C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151715481 | ||||||
| chr2:151715713
|
G | A | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1703C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151715713 | ||||||
| chr2:151716142
|
CT | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+1273delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151716142 | ||||||
| chr2:151716153
|
T | C | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.822+1263A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151716153 | ||||||
| chr2:151716428
|
C | T | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+988G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151716428 | ||||||
| chr2:151716614
|
C | T | 1 | a0128c0148t0001g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.822+802G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151716614 | ||||||
| chr2:151716942
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+474G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151716942 | ||||||
| chr2:151717214
|
A | G | 1 | a0102c0069t0001g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.822+202T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151717214 | ||||||
| chr2:151717248
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+168G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151717248 | ||||||
| chr2:151717294
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+122A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151717294 | ||||||
| chr2:151717388
|
A | AGGC | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.822+25_822+27dupGC others(1): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 10/181 | chr2 | 151717388 | ||||||
| chr2:151717558
|
A | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.718-38T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717558 | ||||||
| chr2:151717632
|
C | T | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.718-112G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717632 | ||||||
| chr2:151717770
|
G | A | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.718-250C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717770 | ||||||
| chr2:151717850
|
T | C | 123 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.718-330A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717850 | ||||||
| chr2:151717855
|
C | CTT | 70 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.718-337_718-336dup others(2): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717855 | ||||||
| chr2:151717885
|
A | G | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.718-365T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717885 | ||||||
| chr2:151717903
|
G | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.718-383C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717903 | ||||||
| chr2:151717946
|
T | C | 78 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.718-426A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151717946 | ||||||
| chr2:151718002
|
C | T | 2 | a0003c0094t0001g0014a0012c0090t0001g0005 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.718-482G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718002 | ||||||
| chr2:151718043
|
C | T | 2 | a0025c0011t0001g0089a0025c0011t0001g0090 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.718-523G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718043 | ||||||
| chr2:151718130
|
G | A | 6 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(3): Show | 6 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-610C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718130 | ||||||
| chr2:151718132
|
C | T | 3 | a0107c0045t0001g0028a0111c0049t0001g0073a0112c0051t0001g0072 | 3 | HG00099.hp2 HG00741.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.718-612G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718132 | ||||||
| chr2:151718291
|
C | T | 3 | a0003c0083t0001g0003a0003c0094t0001g0014a0012c0090t0001g0005 | 3 | HG00099.hp1 HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.718-771G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718291 | ||||||
| chr2:151718314
|
C | T | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-794G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718314 | ||||||
| chr2:151718467
|
C | A | 1 | a0091c0142t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718-947G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718467 | ||||||
| chr2:151718562
|
A | G | 26 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(23): Show | 26 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.718-1042T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718562 | ||||||
| chr2:151718605
|
C | T | 1 | a0099c0067t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.718-1085G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718605 | ||||||
| chr2:151718619
|
A | G | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-1099T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718619 | ||||||
| chr2:151718903
|
A | G | 110 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.718-1383T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151718903 | ||||||
| chr2:151719448
|
A | T | 5 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(2): Show | 5 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1928T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719448 | ||||||
| chr2:151719465
|
T | C | 2 | a0122c0033t0001g0087a0123c0034t0001g0082 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.718-1945A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719465 | ||||||
| chr2:151719488
|
C | T | 72 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.718-1968G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719488 | ||||||
| chr2:151719493
|
A | C | 80 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.718-1973T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719493 | ||||||
| chr2:151719623
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.718-2103C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719623 | ||||||
| chr2:151719633
|
C | G | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.718-2113G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719633 | ||||||
| chr2:151719690
|
G | T | 18 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(15): Show | 18 | HG00558.hp2 HG01884.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.718-2170C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719690 | ||||||
| chr2:151719697
|
G | A | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2177C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719697 | ||||||
| chr2:151719886
|
C | CAA | 8 | a0010c0137t0001g0093a0010c0138t0001g0091a0022c0054t0001g0030others(5): Show | 8 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-2368_718-2367d others(4): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719886 | ||||||
| chr2:151719886
|
C | CAAA | 74 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(71): Show | 74 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.718-2369_718-2367d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719886 | ||||||
| chr2:151719886
|
C | CAAAA | 8 | a0028c0021t0001g0182a0028c0021t0001g0183a0107c0045t0001g0028others(5): Show | 8 | HG00099.hp2 HG00741.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2370_718-2367d others(6): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719886 | ||||||
| chr2:151719922
|
C | T | 91 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.718-2402G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719922 | ||||||
| chr2:151719935
|
GGAC | G | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.718-2418_718-2416d others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719935 | ||||||
| chr2:151719947
|
T | A | 73 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.718-2427A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151719947 | ||||||
| chr2:151720138
|
T | TA | 17 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(14): Show | 17 | HG00558.hp2 HG01884.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.718-2619dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151720138 | ||||||
| chr2:151720323
|
A | C | 187 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0117others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.718-2803T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151720323 | ||||||
| chr2:151720509
|
C | A | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.717+2873G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151720509 | ||||||
| chr2:151720737
|
T | A | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.717+2645A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151720737 | ||||||
| chr2:151720973
|
A | G | 1 | a0010c0138t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.717+2409T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151720973 | ||||||
| chr2:151721241
|
C | A | 1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.717+2141G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721241 | ||||||
| chr2:151721500
|
T | C | 123 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.717+1882A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721500 | ||||||
| chr2:151721534
|
A | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.717+1848T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721534 | ||||||
| chr2:151721636
|
A | C | 7 | a0034c0147t0001g0178a0047c0097t0001g0185a0048c0098t0001g0186others(4): Show | 7 | HG02040.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1746T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721636 | ||||||
| chr2:151721842
|
T | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.717+1540A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721842 | ||||||
| chr2:151721920
|
T | C | 7 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(4): Show | 7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+1462A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151721920 | ||||||
| chr2:151722009
|
G | A | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.717+1373C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722009 | ||||||
| chr2:151722048
|
T | C | 28 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.717+1334A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722048 | ||||||
| chr2:151722126
|
G | A | 9 | a0001c0001t0001g0156a0009c0017t0001g0121a0009c0017t0001g0159others(6): Show | 9 | HG00597.hp2 HG02074.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+1256C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722126 | ||||||
| chr2:151722165
|
T | C | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1217A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722165 | ||||||
| chr2:151722198
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.717+1184C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722198 | ||||||
| chr2:151722392
|
C | T | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.717+990G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722392 | ||||||
| chr2:151722397
|
A | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.717+985T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722397 | ||||||
| chr2:151722405
|
A | G | 1 | a0049c0096t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.717+977T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722405 | ||||||
| chr2:151722430
|
A | C | 4 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(1): Show | 4 | HG02080.hp2 HG02165.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+952T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722430 | ||||||
| chr2:151722470
|
GA | G | 28 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.717+911delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722470 | ||||||
| chr2:151722471
|
A | T | 19 | a0010c0137t0001g0093a0010c0138t0001g0091a0028c0021t0001g0182others(16): Show | 19 | HG00558.hp2 HG01993.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.717+911T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722471 | ||||||
| chr2:151722472
|
T | A | 19 | a0010c0137t0001g0093a0010c0138t0001g0091a0028c0021t0001g0182others(16): Show | 19 | HG00558.hp2 HG01993.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.717+910A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722472 | ||||||
| chr2:151722473
|
A | G | 19 | a0010c0137t0001g0093a0010c0138t0001g0091a0028c0021t0001g0182others(16): Show | 19 | HG00558.hp2 HG01993.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.717+909T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722473 | ||||||
| chr2:151722485
|
T | C | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.717+897A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722485 | ||||||
| chr2:151722499
|
T | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.717+883A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722499 | ||||||
| chr2:151722534
|
G | C | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.717+848C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722534 | ||||||
| chr2:151722694
|
C | T | 1 | a0044c0092t0001g0008 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.717+688G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151722694 | ||||||
| chr2:151723150
|
G | T | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.717+232C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151723150 | ||||||
| chr2:151723168
|
G | T | 1 | a0044c0092t0001g0008 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.717+214C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 9/181 | chr2 | 151723168 | ||||||
| chr2:151723547
|
A | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.613-61T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723547 | ||||||
| chr2:151723746
|
CTTTGT | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-265_613-261del others(5): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723746 | ||||||
| chr2:151723747
|
TTTG | T | 13 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0083t0001g0003others(10): Show | 13 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-264_613-262del others(3): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723747 | ||||||
| chr2:151723748
|
TTG | T | 7 | a0003c0005t0001g0013a0008c0004t0001g0009a0008c0004t0001g0011others(4): Show | 7 | HG01192.hp1 HG02965.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-264_613-263del others(2): Show |
NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723748 | ||||||
| chr2:151723750
|
G | GT | 14 | a0001c0001t0001g0117a0002c0002t0001g0026a0004c0126t0001g0118others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.613-265dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723750 | ||||||
| chr2:151723750
|
GT | G | 20 | a0005c0008t0001g0077a0011c0009t0001g0078a0025c0011t0001g0090others(17): Show | 20 | HG00639.hp2 HG01074.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.613-265delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723750 | ||||||
| chr2:151723751
|
T | G | 6 | a0010c0137t0001g0093a0010c0138t0001g0091a0033c0024t0001g0096others(3): Show | 6 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-265A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723751 | ||||||
| chr2:151723752
|
T | G | 12 | a0028c0021t0001g0182a0028c0021t0001g0183a0034c0147t0001g0178others(9): Show | 12 | HG02040.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.613-266A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723752 | ||||||
| chr2:151723758
|
T | G | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.613-272A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151723758 | ||||||
| chr2:151724245
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.612+15C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151724245 | ||||||
| chr2:151724252
|
A | G | 7 | a0034c0147t0001g0178a0047c0097t0001g0185a0048c0098t0001g0186others(4): Show | 7 | HG02040.hp1 HG02280.hp2 HG02630.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.612+8T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 8/181 | chr2 | 151724252 | ||||||
| chr2:151724462
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.508-98C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 7/181 | chr2 | 151724462 | ||||||
| chr2:151724630
|
G | A | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.507+227C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 7/181 | chr2 | 151724630 | ||||||
| chr2:151725104
|
A | C | 2 | a0085c0031t0001g0108a0086c0032t0001g0109 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.403-143T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 6/181 | chr2 | 151725104 | ||||||
| chr2:151725352
|
T | C | 99 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.402+101A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 6/181 | chr2 | 151725352 | ||||||
| chr2:151725634
|
T | TA | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-75dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151725634 | ||||||
| chr2:151725635
|
A | T | 1 | a0036c0029t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.295-75T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151725635 | ||||||
| chr2:151725764
|
G | A | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-204C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151725764 | ||||||
| chr2:151726009
|
A | G | 123 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.295-449T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726009 | ||||||
| chr2:151726023
|
C | T | 1 | a0101c0068t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295-463G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726023 | ||||||
| chr2:151726280
|
T | C | 1 | a0011c0009t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.295-720A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726280 | ||||||
| chr2:151726410
|
T | C | 18 | a0010c0137t0001g0093a0010c0138t0001g0091a0028c0021t0001g0182others(15): Show | 18 | HG00558.hp2 HG01993.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-850A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726410 | ||||||
| chr2:151726736
|
T | G | 1 | a0048c0098t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.294+955A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726736 | ||||||
| chr2:151726826
|
G | T | 1 | a0099c0067t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.294+865C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726826 | ||||||
| chr2:151726882
|
C | T | 69 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.294+809G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726882 | ||||||
| chr2:151726888
|
AT | A | 28 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.294+802delA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151726888 | ||||||
| chr2:151727035
|
G | A | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.294+656C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727035 | ||||||
| chr2:151727053
|
T | TA | 13 | a0003c0005t0001g0004a0017c0015t0001g0164a0017c0015t0001g0165others(10): Show | 13 | HG01884.hp1 HG02040.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.294+637dupT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727053 | ||||||
| chr2:151727053
|
TA | T | 8 | a0003c0005t0001g0006a0012c0090t0001g0005a0013c0014t0001g0099others(5): Show | 8 | HG00099.hp1 HG01515.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+637delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727053 | ||||||
| chr2:151727163
|
C | T | 6 | a0001c0001t0001g0097a0001c0001t0001g0112a0068c0125t0001g0111others(3): Show | 6 | HG00423.hp1 HG02523.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+528G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727163 | ||||||
| chr2:151727282
|
T | A | 3 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100 | 3 | HG02647.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.294+409A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727282 | ||||||
| chr2:151727299
|
G | A | 28 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.294+392C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727299 | ||||||
| chr2:151727639
|
A | C | 123 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.294+52T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 5/181 | chr2 | 151727639 | ||||||
| chr2:151728064
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-158G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151728064 | ||||||
| chr2:151728140
|
T | G | 1 | a0087c0132t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-234A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151728140 | ||||||
| chr2:151728233
|
T | A | 1 | a0095c0062t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.79-327A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151728233 | ||||||
| chr2:151728506
|
C | T | 28 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.79-600G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151728506 | ||||||
| chr2:151729045
|
G | T | 1 | a0010c0139t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.78+570C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151729045 | ||||||
| chr2:151729068
|
GA | G | 66 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.78+546delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151729068 | ||||||
| chr2:151729163
|
C | T | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.78+452G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151729163 | ||||||
| chr2:151729169
|
C | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+446G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 4/181 | chr2 | 151729169 | ||||||
| chr2:151729679
|
T | C | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-23A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151729679 | ||||||
| chr2:151729903
|
G | T | 1 | a0079c0130t0002g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.37-247C>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151729903 | ||||||
| chr2:151729926
|
T | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-270A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151729926 | ||||||
| chr2:151730120
|
A | G | 4 | a0013c0014t0001g0099a0013c0014t0001g0102a0016c0016t0002g0100others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-464T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730120 | ||||||
| chr2:151730123
|
A | G | 1 | a0096c0060t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.37-467T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730123 | ||||||
| chr2:151730144
|
G | A | 120 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.37-488C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730144 | ||||||
| chr2:151730301
|
G | A | 1 | a0005c0064t0001g0083 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.37-645C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730301 | ||||||
| chr2:151730325
|
T | C | 1 | a0056c0145t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.37-669A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730325 | ||||||
| chr2:151730615
|
T | TA | 6 | a0002c0048t0001g0086a0019c0010t0003g0188a0024c0038t0001g0085others(3): Show | 6 | HG01884.hp1 HG02809.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-960_37-959insT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730615 | ||||||
| chr2:151730615
|
TGA | T | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.37-961_37-960delTC | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730615 | ||||||
| chr2:151730616
|
G | A | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.37-960C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730616 | ||||||
| chr2:151730616
|
GA | G | 14 | a0010c0137t0001g0093a0010c0138t0001g0091a0033c0024t0001g0096others(11): Show | 14 | HG00558.hp2 HG01993.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-961delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730616 | ||||||
| chr2:151730722
|
C | T | 1 | a0003c0005t0001g0004 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.37-1066G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730722 | ||||||
| chr2:151730794
|
C | T | 1 | a0035c0146t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.37-1138G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730794 | ||||||
| chr2:151730830
|
G | A | 100 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.37-1174C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151730830 | ||||||
| chr2:151731030
|
T | C | 7 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(4): Show | 7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-1374A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731030 | ||||||
| chr2:151731091
|
T | C | 1 | a0013c0014t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.37-1435A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731091 | ||||||
| chr2:151731300
|
T | C | 79 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.37-1644A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731300 | ||||||
| chr2:151731510
|
A | T | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.36+1611T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731510 | ||||||
| chr2:151731578
|
C | G | 1 | a0003c0083t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.36+1543G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731578 | ||||||
| chr2:151731606
|
A | C | 120 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.36+1515T>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731606 | ||||||
| chr2:151731636
|
G | C | 7 | a0006c0012t0001g0172a0006c0012t0001g0173a0006c0079t0001g0170others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+1485C>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731636 | ||||||
| chr2:151731787
|
T | G | 3 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184 | 3 | HG02040.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.36+1334A>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731787 | ||||||
| chr2:151731864
|
T | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+1257A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731864 | ||||||
| chr2:151731971
|
T | C | 1 | a0034c0147t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.36+1150A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151731971 | ||||||
| chr2:151732233
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.36+888G>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732233 | ||||||
| chr2:151732267
|
T | C | 2 | a0034c0147t0001g0178a0056c0145t0001g0177 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.36+854A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732267 | ||||||
| chr2:151732338
|
G | A | 1 | a0042c0095t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.36+783C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732338 | ||||||
| chr2:151732418
|
C | A | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.36+703G>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732418 | ||||||
| chr2:151732419
|
T | A | 3 | a0025c0011t0001g0089a0025c0011t0001g0090a0120c0023t0001g0088 | 3 | HG01891.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.36+702A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732419 | ||||||
| chr2:151732698
|
A | T | 2 | a0007c0003t0001g0001a0007c0003t0001g0002 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.36+423T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732698 | ||||||
| chr2:151732794
|
G | A | 94 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.36+327C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151732794 | ||||||
| chr2:151733008
|
C | G | 2 | a0033c0024t0001g0096a0064c0025t0001g0095 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.36+113G>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151733008 | ||||||
| chr2:151733101
|
G | GT | 7 | a0028c0021t0001g0182a0028c0021t0001g0183a0033c0024t0001g0096others(4): Show | 7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+19dupA | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 3/181 | chr2 | 151733101 | ||||||
| chr2:151733422
|
A | T | 4 | a0010c0137t0001g0093a0010c0138t0001g0091a0081c0141t0001g0092others(1): Show | 4 | HG00558.hp2 HG01993.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-237T>A | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 2/181 | chr2 | 151733422 | ||||||
| chr2:151733507
|
A | G | 70 | a0002c0002t0001g0026a0002c0002t0001g0036a0002c0002t0001g0039others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.-30+205T>C | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 2/181 | chr2 | 151733507 | ||||||
| chr2:151733606
|
TA | T | 21 | a0003c0005t0001g0004a0003c0005t0001g0006a0003c0005t0001g0013others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30+105delT | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 2/181 | chr2 | 151733606 | ||||||
| chr2:151733838
|
T | C | 5 | a0028c0021t0001g0182a0028c0021t0001g0183a0130c0150t0001g0180others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113-43A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 1/181 | chr2 | 151733838 | ||||||
| chr2:151734099
|
G | A | 1 | a0051c0131t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-114+299C>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 1/181 | chr2 | 151734099 | ||||||
| chr2:151734111
|
T | C | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-114+287A>G | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 1/181 | chr2 | 151734111 | ||||||
| chr2:151734272
|
T | A | 4 | a0047c0097t0001g0185a0048c0098t0001g0186a0049c0096t0001g0184others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-114+126A>T | NEB | ENSG00000183091.21 | transcript | ENST00000397345.8 | protein_coding | 1/181 | chr2 | 151734272 |