| geneid | 341640 |
|---|---|
| ensemblid | ENSG00000150893.11 |
| hgncid | 25396 |
| symbol | FREM2 |
| name | FRAS1 related extracellular matrix 2 |
| refseq_nuc | NM_207361.6 |
| refseq_prot | NP_997244.4 |
| ensembl_nuc | ENST00000280481.9 |
| ensembl_prot | ENSP00000280481.7 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 38687077 |
| end | 38887131 |
| strand | + |
| ver | v1.2 |
| region | chr13:38687077-38887131 |
| region5000 | chr13:38682077-38892131 |
| regionname0 | FREM2_chr13_38687077_38887131 |
| regionname5000 | FREM2_chr13_38682077_38892131 |
| 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 | 3169 | 70 | 20 | 9 | 33 | 3 | 5 | 21 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002 | 0/0 | 3169 | 37 | 2 | 12 | 13 | 1 | 9 | 10 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003 | 0/0 | 3169 | 25 | 2 | 0 | 20 | 1 | 2 | 15 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004 | 0/0 | 3169 | 22 | 3 | 3 | 16 | 0 | 0 | 12 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005 | 1/0 | 3169 | 15 | 0 | 9 | 1 | 1 | 3 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006 | 0/0 | 3169 | 10 | 5 | 1 | 1 | 0 | 3 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007 | 0/1 | 3169 | 8 | 0 | 7 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008 | 0/0 | 3169 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009 | 0/0 | 3169 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010 | 0/0 | 3169 | 5 | 1 | 4 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0011 | 0/0 | 3169 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0012 | 0/0 | 3169 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0013 | 0/0 | 3169 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0014 | 0/0 | 3169 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0015 | 0/0 | 3169 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0016 | 0/0 | 3169 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0017 | 0/0 | 3169 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0018 | 0/0 | 3169 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0019 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0020 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0021 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0022 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0023 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0024 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0025 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0026 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0027 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0028 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0029 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0030 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0031 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0032 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0033 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0034 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0035 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0036 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0037 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0038 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0039 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0040 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0041 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0042 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0043 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0044 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0045 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0046 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0047 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0048 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0049 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0050 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0051 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0052 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0053 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0054 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0055 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0056 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0057 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0058 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| 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 | 9510 | 27 | 1 | 6 | 17 | 2 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0002 | 0/0 | 9510 | 19 | 2 | 3 | 11 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0003 | 0/0 | 9510 | 14 | 0 | 0 | 14 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0004 | 0/0 | 9510 | 12 | 1 | 1 | 10 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0005 | 0/0 | 9510 | 10 | 2 | 0 | 5 | 1 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0006 | 0/0 | 9510 | 9 | 1 | 3 | 2 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0007 | 0/0 | 9510 | 8 | 1 | 1 | 6 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0008 | 0/0 | 9510 | 8 | 0 | 1 | 4 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0009 | 0/0 | 9510 | 6 | 6 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0010 | 0/0 | 9510 | 6 | 0 | 2 | 3 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0011 | 0/0 | 9510 | 6 | 0 | 0 | 4 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0012 | 0/0 | 9510 | 4 | 4 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0013 | 0/0 | 9510 | 4 | 1 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0014 | 0/0 | 9510 | 4 | 0 | 1 | 1 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0015 | 0/0 | 9510 | 4 | 0 | 3 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0016 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0017 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0018 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0019 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0020 | 0/0 | 9510 | 3 | 2 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0021 | 0/0 | 9510 | 3 | 1 | 0 | 0 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0022 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0023 | 0/0 | 9510 | 3 | 1 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0024 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0025 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0026 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0027 | 0/0 | 9510 | 3 | 0 | 2 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0028 | 0/0 | 9510 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0029 | 0/0 | 9510 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0030 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0031 | 0/0 | 9510 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0032 | 0/0 | 9510 | 2 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0033 | 0/0 | 9510 | 2 | 0 | 0 | 0 | 1 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0034 | 0/0 | 9510 | 2 | 0 | 0 | 0 | 2 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0035 | 0/0 | 9510 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0036 | 0/0 | 9510 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0037 | 0/1 | 9510 | 2 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0038 | 0/0 | 9510 | 2 | 0 | 0 | 2 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0039 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0040 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0041 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0042 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0043 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0044 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0045 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0046 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0047 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0048 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0049 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0050 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0051 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0052 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0053 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0054 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0055 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0056 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0057 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0058 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0059 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0060 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0061 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0062 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0063 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0064 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0065 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0066 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0067 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0068 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0069 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0070 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0071 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0072 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0073 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0074 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0075 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0076 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0077 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0078 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0079 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0080 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0081 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0082 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0083 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0084 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0085 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0086 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0087 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0088 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0089 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0090 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0091 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0092 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0093 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0094 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0095 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0096 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0097 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| c0098 | 1/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| 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 | 0/0 | 6612 | 56 | 0 | 12 | 36 | 3 | 5 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0002 | 1/0 | 6613 | 35 | 6 | 8 | 9 | 1 | 10 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0003 | 0/0 | 6612 | 33 | 26 | 4 | 1 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0004 | 0/0 | 6614 | 27 | 2 | 2 | 20 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0005 | 0/0 | 6609 | 13 | 0 | 0 | 13 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0006 | 0/1 | 6612 | 12 | 0 | 10 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0007 | 0/0 | 6612 | 11 | 1 | 4 | 4 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0008 | 0/0 | 6612 | 6 | 6 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0009 | 0/0 | 6612 | 5 | 5 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0010 | 0/0 | 6612 | 5 | 0 | 1 | 0 | 3 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0011 | 0/0 | 6612 | 3 | 2 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0012 | 0/0 | 6612 | 3 | 2 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0013 | 0/0 | 6612 | 2 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0014 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0015 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0016 | 0/0 | 6613 | 2 | 1 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0017 | 0/0 | 6613 | 2 | 1 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0018 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0019 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0020 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0021 | 0/0 | 6613 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0022 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0023 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0024 | 0/0 | 6612 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0025 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0026 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0027 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0028 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0029 | 0/0 | 6613 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0030 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0031 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0032 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0033 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0034 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0035 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0036 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0037 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0038 | 0/0 | 6613 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0039 | 0/0 | 6613 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0040 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0041 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0042 | 0/0 | 6613 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0043 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0044 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0045 | 0/0 | 6614 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0046 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0047 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0048 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0049 | 0/0 | 6613 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0050 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0051 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0052 | 0/0 | 6613 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0053 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0054 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0055 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| t0056 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| 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 | 9510 | 27 | 1 | 6 | 17 | 2 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002 | 0/0 | 9510 | 19 | 2 | 3 | 11 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0009 | 0/0 | 9510 | 6 | 6 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0012 | 0/0 | 9510 | 4 | 4 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0017 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0029 | 0/0 | 9510 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0030 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0033 | 0/0 | 9510 | 2 | 0 | 0 | 0 | 1 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0067 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0068 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0070 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0006 | 0/0 | 9510 | 9 | 1 | 3 | 2 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0008 | 0/0 | 9510 | 8 | 0 | 1 | 4 | 0 | 3 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0010 | 0/0 | 9510 | 6 | 0 | 2 | 3 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0011 | 0/0 | 9510 | 6 | 0 | 0 | 4 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0027 | 0/0 | 9510 | 3 | 0 | 2 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0036 | 0/0 | 9510 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0077 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0091 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0092 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003 | 0/0 | 9510 | 14 | 0 | 0 | 14 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0005 | 0/0 | 9510 | 10 | 2 | 0 | 5 | 1 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0078 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004 | 0/0 | 9510 | 12 | 1 | 1 | 10 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0007 | 0/0 | 9510 | 8 | 1 | 1 | 6 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0089 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0093 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0014 | 0/0 | 9510 | 4 | 0 | 1 | 1 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0015 | 0/0 | 9510 | 4 | 0 | 3 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0026 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0035 | 0/0 | 9510 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0090 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0098 | 1/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0016 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0021 | 0/0 | 9510 | 3 | 1 | 0 | 0 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0032 | 0/0 | 9510 | 2 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0095 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0096 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0024 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0025 | 0/0 | 9510 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0037 | 0/1 | 9510 | 2 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0019 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0050 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0051 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009c0028 | 0/0 | 9510 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009c0038 | 0/0 | 9510 | 2 | 0 | 0 | 2 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010c0013 | 0/0 | 9510 | 4 | 1 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010c0094 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0011c0018 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0012c0020 | 0/0 | 9510 | 3 | 2 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0013c0023 | 0/0 | 9510 | 3 | 1 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0014c0022 | 0/0 | 9510 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0015c0031 | 0/0 | 9510 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0016c0059 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0016c0060 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0017c0034 | 0/0 | 9510 | 2 | 0 | 0 | 0 | 2 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0018c0072 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0018c0073 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0019c0039 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0020c0040 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0021c0044 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0022c0043 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0023c0042 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0024c0041 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0025c0048 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0026c0052 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0027c0053 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0028c0054 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0029c0049 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0030c0055 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0031c0056 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0032c0058 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0033c0057 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0034c0088 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0035c0062 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0036c0061 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0037c0063 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0038c0064 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0039c0086 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0040c0081 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0041c0079 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0042c0080 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0043c0082 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0044c0084 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0045c0085 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0046c0083 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0047c0087 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0048c0065 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0049c0097 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0050c0075 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0051c0046 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0052c0045 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0053c0069 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0054c0066 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0055c0071 | 0/0 | 9510 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0056c0074 | 0/0 | 9510 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0057c0076 | 0/0 | 9510 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0058c0047 | 0/0 | 9510 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 16121 | 18 | 0 | 3 | 13 | 2 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0002 | 0/0 | 16122 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0007 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0013 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0018 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0023 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0027 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0001t0028 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0001 | 0/0 | 16121 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0003 | 0/0 | 16121 | 2 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0004 | 0/0 | 16123 | 7 | 1 | 1 | 4 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0005 | 0/0 | 16118 | 4 | 0 | 0 | 4 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0006 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0007 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0002t0032 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0009t0008 | 0/0 | 16121 | 4 | 4 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0009t0020 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0012t0019 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0012t0050 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0012t0053 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0017t0008 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0017t0055 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0029t0001 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0029t0002 | 0/0 | 16122 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0029t0025 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0030t0003 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0030t0047 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0033t0010 | 0/0 | 16121 | 2 | 0 | 0 | 0 | 1 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0067t0001 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0068t0005 | 0/0 | 16118 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0001c0070t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0006t0001 | 0/0 | 16121 | 5 | 0 | 1 | 2 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0006t0002 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0006t0007 | 0/0 | 16121 | 2 | 1 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0006t0013 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0008t0001 | 0/0 | 16121 | 6 | 0 | 1 | 3 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0008t0002 | 0/0 | 16122 | 2 | 0 | 0 | 1 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0010t0001 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0010t0004 | 0/0 | 16123 | 4 | 0 | 1 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0010t0045 | 0/0 | 16123 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0011t0004 | 0/0 | 16123 | 5 | 0 | 0 | 3 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0011t0035 | 0/0 | 16123 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0027t0001 | 0/0 | 16121 | 3 | 0 | 2 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0036t0007 | 0/0 | 16121 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0077t0009 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0091t0007 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0002c0092t0046 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0002 | 0/0 | 16122 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0003 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0004 | 0/0 | 16123 | 6 | 0 | 0 | 6 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0005 | 0/0 | 16118 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0007 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0034 | 0/0 | 16122 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0003t0036 | 0/0 | 16123 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0005t0001 | 0/0 | 16121 | 4 | 0 | 0 | 3 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0005t0002 | 0/0 | 16122 | 4 | 1 | 0 | 2 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0005t0024 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0005t0026 | 0/0 | 16106 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0003c0078t0001 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0004 | 0/0 | 16123 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0005 | 0/0 | 16118 | 4 | 0 | 0 | 4 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0007 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0011 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0012 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0004t0044 | 0/0 | 16123 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0007t0001 | 0/0 | 16121 | 7 | 0 | 1 | 6 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0007t0018 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0089t0001 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0004c0093t0004 | 0/0 | 16123 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0014t0001 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0014t0002 | 0/0 | 16122 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0014t0003 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0014t0040 | 0/0 | 16122 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0015t0002 | 0/0 | 16122 | 3 | 0 | 2 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0015t0042 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0026t0002 | 0/0 | 16122 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0035t0002 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0035t0038 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0090t0002 | 0/0 | 16122 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0005c0098t0002 | 1/0 | 16122 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0016t0021 | 0/0 | 16122 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0016t0052 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0021t0002 | 0/0 | 16122 | 2 | 0 | 0 | 0 | 0 | 2 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0021t0016 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0032t0002 | 0/0 | 16122 | 2 | 0 | 1 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0095t0037 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0006c0096t0015 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0024t0006 | 0/0 | 16121 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0025t0003 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0025t0006 | 0/0 | 16121 | 2 | 0 | 2 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0037t0006 | 0/1 | 16121 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0007c0037t0030 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0019t0003 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0019t0012 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0050t0001 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0008c0051t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009c0028t0001 | 0/0 | 16121 | 3 | 0 | 0 | 3 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009c0038t0005 | 0/0 | 16118 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0009c0038t0007 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010c0013t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010c0013t0006 | 0/0 | 16121 | 3 | 0 | 3 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0010c0094t0006 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0011c0018t0003 | 0/0 | 16121 | 3 | 3 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0012c0020t0002 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0012c0020t0017 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0012c0020t0049 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0013c0023t0002 | 0/0 | 16122 | 2 | 1 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0013c0023t0016 | 0/0 | 16122 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0014c0022t0003 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0014c0022t0014 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0015c0031t0003 | 0/0 | 16121 | 2 | 2 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0016c0059t0043 | 0/0 | 16139 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0016c0060t0029 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0017c0034t0010 | 0/0 | 16121 | 2 | 0 | 0 | 0 | 2 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0018c0072t0002 | 0/0 | 16122 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0018c0073t0002 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0019c0039t0011 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0020c0040t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0021c0044t0056 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0022c0043t0012 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0023c0042t0048 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0024c0041t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0025c0048t0003 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0026c0052t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0027c0053t0041 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0028c0054t0009 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0029c0049t0002 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0030c0055t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0031c0056t0015 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0032c0058t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0033c0057t0022 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0034c0088t0011 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0035c0062t0009 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0036c0061t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0037c0063t0014 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0038c0064t0033 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0039c0086t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0040c0081t0006 | 0/0 | 16121 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0041c0079t0039 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0042c0080t0004 | 0/0 | 16123 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0043c0082t0017 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0044c0084t0009 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0045c0085t0009 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0046c0083t0002 | 0/0 | 16122 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0047c0087t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0048c0065t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0049c0097t0007 | 0/0 | 16121 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0050c0075t0003 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0051c0046t0051 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0052c0045t0054 | 0/0 | 16139 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0053c0069t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0054c0066t0003 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0055c0071t0031 | 0/0 | 16121 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0056c0074t0010 | 0/0 | 16121 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0057c0076t0002 | 0/0 | 16122 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| a0058c0047t0002 | 0/0 | 16122 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | copy fasta | chr13 | 38682077 | 38892131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0027g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0001t0028g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0002t0032g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0020g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0009t0020g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0012t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0012t0019g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0012t0050g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0012t0053g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0017t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0017t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0017t0055g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0029t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0029t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0029t0025g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0030t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0030t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0030t0047g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0033t0010g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0033t0010g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0067t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0068t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0001c0070t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0006t0013g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0010t0045g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0011t0035g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0027t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0027t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0027t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0036t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0036t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0077t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0091t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0002c0092t0046g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0034g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0003t0036g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0024g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0005t0026g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0003c0078t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0012g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0004t0044g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0007t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0089t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0004c0093t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0014t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0014t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0014t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0014t0040g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0015t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0015t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0015t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0015t0042g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0026t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0026t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0026t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0035t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0035t0038g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0090t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0005c0098t0002g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0016t0021g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0016t0021g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0016t0052g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0021t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0021t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0021t0016g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0032t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0032t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0095t0037g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0006c0096t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0024t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0024t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0024t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0025t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0025t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0025t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0037t0006g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0007c0037t0030g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0008c0019t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0008c0019t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0008c0019t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0008c0050t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0008c0051t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0009c0028t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0009c0028t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0009c0028t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0009c0038t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0009c0038t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0010c0013t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0010c0013t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0010c0013t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0010c0013t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0010c0094t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0011c0018t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0011c0018t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0011c0018t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0012c0020t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0012c0020t0017g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0012c0020t0049g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0013c0023t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0013c0023t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0013c0023t0016g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0014c0022t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0014c0022t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0014c0022t0014g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0015c0031t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0015c0031t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0016c0059t0043g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0016c0060t0029g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0017c0034t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0017c0034t0010g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0018c0072t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0018c0073t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0019c0039t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0020c0040t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0021c0044t0056g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0022c0043t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0023c0042t0048g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0024c0041t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0025c0048t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0026c0052t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0027c0053t0041g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0028c0054t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0029c0049t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0030c0055t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0031c0056t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0032c0058t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0033c0057t0022g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0034c0088t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0035c0062t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0036c0061t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0037c0063t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0038c0064t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0039c0086t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0040c0081t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0041c0079t0039g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0042c0080t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0043c0082t0017g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0044c0084t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0045c0085t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0046c0083t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0047c0087t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0048c0065t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0049c0097t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0050c0075t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0051c0046t0051g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0052c0045t0054g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0053c0069t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0054c0066t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0055c0071t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0056c0074t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0057c0076t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| a0058c0047t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0003 | c0003 | t0004 | g0083 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00423 | hp2 | a0003 | c0005 | t0002 | g0060 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00438 | hp2 | a0002 | c0011 | t0004 | g0206 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00558 | hp2 | a0002 | c0011 | t0035 | g0227 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00621 | hp1 | a0005 | c0014 | t0040 | g0098 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00639 | hp1 | a0002 | c0006 | t0002 | g0022 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00639 | hp2 | a0013 | c0023 | t0016 | g0077 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00642 | hp1 | a0010 | c0013 | t0006 | g0055 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00642 | hp2 | a0002 | c0008 | t0001 | g0230 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0231 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00735 | hp1 | a0002 | c0006 | t0001 | g0079 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00735 | hp2 | a0007 | c0025 | t0006 | g0216 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00738 | hp1 | a0056 | c0074 | t0010 | g0157 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00738 | hp2 | a0002 | c0006 | t0007 | g0020 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00741 | hp1 | a0005 | c0026 | t0002 | g0242 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG00741 | hp2 | a0002 | c0091 | t0007 | g0040 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01070 | hp1 | a0002 | c0027 | t0001 | g0021 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01070 | hp2 | a0006 | c0032 | t0002 | g0173 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01109 | hp1 | a0007 | c0024 | t0006 | g0045 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01109 | hp2 | a0050 | c0075 | t0003 | g0194 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01167 | hp1 | a0010 | c0013 | t0006 | g0205 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01167 | hp2 | a0002 | c0036 | t0007 | g0024 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01169 | hp1 | a0004 | c0089 | t0001 | g0239 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01169 | hp2 | a0002 | c0036 | t0007 | g0017 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01175 | hp1 | a0008 | c0050 | t0001 | g0123 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01175 | hp2 | a0005 | c0035 | t0038 | g0037 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01192 | hp1 | a0007 | c0025 | t0003 | g0229 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01192 | hp2 | a0001 | c0001 | t0027 | g0110 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01243 | hp1 | a0012 | c0020 | t0017 | g0130 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01243 | hp2 | a0025 | c0048 | t0003 | g0225 | AMR | PUR | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01255 | hp1 | a0005 | c0035 | t0002 | g0018 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0202 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01257 | hp2 | a0005 | c0015 | t0042 | g0137 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0180 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01261 | hp2 | a0005 | c0014 | t0001 | g0025 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01346 | hp1 | a0005 | c0026 | t0002 | g0240 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01346 | hp2 | a0010 | c0094 | t0006 | g0189 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01358 | hp1 | a0001 | c0002 | t0006 | g0188 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01358 | hp2 | a0005 | c0026 | t0002 | g0241 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01361 | hp1 | a0002 | c0092 | t0046 | g0036 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01433 | hp2 | a0002 | c0010 | t0004 | g0068 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01496 | hp1 | a0004 | c0004 | t0012 | g0196 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01496 | hp2 | a0007 | c0024 | t0006 | g0044 | AMR | CLM | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01515 | hp2 | a0005 | c0090 | t0002 | g0099 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01516 | hp1 | a0017 | c0034 | t0010 | g0222 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01516 | hp2 | a0003 | c0005 | t0024 | g0062 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01517 | hp2 | a0017 | c0034 | t0010 | g0223 | EUR | IBS | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01884 | hp1 | a0033 | c0057 | t0022 | g0127 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01884 | hp2 | a0001 | c0009 | t0008 | g0247 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0057 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01891 | hp2 | a0004 | c0004 | t0003 | g0198 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01934 | hp1 | a0005 | c0015 | t0002 | g0207 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01934 | hp2 | a0004 | c0007 | t0001 | g0010 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01943 | hp1 | a0005 | c0015 | t0002 | g0213 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01943 | hp2 | a0001 | c0001 | t0028 | g0056 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01952 | hp1 | a0001 | c0002 | t0004 | g0054 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01952 | hp2 | a0010 | c0013 | t0006 | g0187 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01981 | hp1 | a0023 | c0042 | t0048 | g0236 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01981 | hp2 | a0007 | c0037 | t0030 | g0041 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01993 | hp1 | a0002 | c0010 | t0001 | g0026 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG01993 | hp2 | a0007 | c0024 | t0006 | g0059 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02004 | hp1 | a0002 | c0027 | t0001 | g0027 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02004 | hp2 | a0007 | c0025 | t0006 | g0221 | AMR | PEL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02027 | hp1 | a0006 | c0095 | t0037 | g0152 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02055 | hp1 | a0045 | c0085 | t0009 | g0200 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0184 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02071 | hp2 | a0003 | c0003 | t0004 | g0069 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02083 | hp1 | a0004 | c0004 | t0005 | g0065 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02083 | hp2 | a0004 | c0004 | t0011 | g0061 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02129 | hp1 | a0003 | c0005 | t0001 | g0080 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0169 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02135 | hp1 | a0003 | c0005 | t0001 | g0071 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02135 | hp2 | a0004 | c0004 | t0005 | g0009 | EAS | KHV | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02145 | hp1 | a0026 | c0052 | t0003 | g0122 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02145 | hp2 | a0001 | c0070 | t0003 | g0095 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02155 | hp1 | a0001 | c0029 | t0001 | g0149 | EAS | CDX | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02155 | hp2 | a0004 | c0007 | t0001 | g0043 | EAS | CDX | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02257 | hp1 | a0001 | c0030 | t0047 | g0151 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02257 | hp2 | a0016 | c0059 | t0043 | g0101 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02280 | hp1 | a0032 | c0058 | t0003 | g0195 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02280 | hp2 | a0001 | c0012 | t0019 | g0259 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02572 | hp1 | a0018 | c0073 | t0002 | g0132 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02572 | hp2 | a0001 | c0017 | t0055 | g0256 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02602 | hp1 | a0006 | c0032 | t0002 | g0142 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02602 | hp2 | a0006 | c0021 | t0002 | g0186 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02615 | hp1 | a0051 | c0046 | t0051 | g0245 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02615 | hp2 | a0003 | c0005 | t0026 | g0091 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02622 | hp1 | a0008 | c0019 | t0003 | g0118 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02622 | hp2 | a0001 | c0009 | t0008 | g0260 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02630 | hp1 | a0001 | c0012 | t0053 | g0251 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02630 | hp2 | a0054 | c0066 | t0003 | g0051 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02717 | hp1 | a0006 | c0016 | t0052 | g0244 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02717 | hp2 | a0006 | c0021 | t0016 | g0111 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02723 | hp1 | a0008 | c0019 | t0012 | g0115 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02723 | hp2 | a0020 | c0040 | t0003 | g0005 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02735 | hp1 | a0006 | c0021 | t0002 | g0191 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02735 | hp2 | a0002 | c0010 | t0045 | g0023 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02738 | hp1 | a0005 | c0014 | t0002 | g0031 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02738 | hp2 | a0002 | c0011 | t0004 | g0218 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02809 | hp1 | a0031 | c0056 | t0015 | g0125 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02809 | hp2 | a0006 | c0016 | t0021 | g0246 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02818 | hp1 | a0001 | c0002 | t0032 | g0238 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02818 | hp2 | a0028 | c0054 | t0009 | g0117 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02886 | hp1 | a0001 | c0009 | t0008 | g0253 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02886 | hp2 | a0044 | c0084 | t0009 | g0197 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02895 | hp1 | a0011 | c0018 | t0003 | g0112 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02895 | hp2 | a0046 | c0083 | t0002 | g0201 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02896 | hp1 | a0001 | c0009 | t0020 | g0250 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02896 | hp2 | a0006 | c0096 | t0015 | g0153 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02897 | hp1 | a0011 | c0018 | t0003 | g0113 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02897 | hp2 | a0001 | c0009 | t0020 | g0248 | AFR | GWD | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02922 | hp1 | a0004 | c0007 | t0018 | g0039 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02922 | hp2 | a0006 | c0016 | t0021 | g0255 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02965 | hp1 | a0001 | c0017 | t0008 | g0249 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02965 | hp2 | a0012 | c0020 | t0002 | g0126 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02970 | hp1 | a0013 | c0023 | t0002 | g0049 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02970 | hp2 | a0019 | c0039 | t0011 | g0004 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02976 | hp1 | a0030 | c0055 | t0003 | g0131 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02976 | hp2 | a0043 | c0082 | t0017 | g0048 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03017 | hp1 | a0001 | c0002 | t0007 | g0179 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03017 | hp2 | a0058 | c0047 | t0002 | g0210 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03098 | hp1 | a0052 | c0045 | t0054 | g0257 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03098 | hp2 | a0039 | c0086 | t0003 | g0050 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03130 | hp1 | a0010 | c0013 | t0003 | g0107 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03130 | hp2 | a0008 | c0051 | t0003 | g0120 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03139 | hp1 | a0001 | c0009 | t0008 | g0262 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03139 | hp2 | a0022 | c0043 | t0012 | g0234 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03195 | hp1 | a0038 | c0064 | t0033 | g0103 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03195 | hp2 | a0001 | c0012 | t0019 | g0252 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03225 | hp1 | a0047 | c0087 | t0003 | g0199 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03225 | hp2 | a0011 | c0018 | t0003 | g0114 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03453 | hp1 | a0015 | c0031 | t0003 | g0128 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03453 | hp2 | a0034 | c0088 | t0011 | g0226 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03486 | hp1 | a0008 | c0019 | t0003 | g0121 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03486 | hp2 | a0002 | c0077 | t0009 | g0139 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0174 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03492 | hp2 | a0002 | c0011 | t0004 | g0211 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03516 | hp1 | a0014 | c0022 | t0003 | g0002 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03516 | hp2 | a0036 | c0061 | t0003 | g0102 | AFR | ESN | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03579 | hp1 | a0001 | c0030 | t0003 | g0145 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03579 | hp2 | a0055 | c0071 | t0031 | g0109 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03704 | hp1 | a0002 | c0006 | t0001 | g0030 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03704 | hp2 | a0002 | c0008 | t0002 | g0209 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03710 | hp1 | a0002 | c0008 | t0001 | g0220 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | PJL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03831 | hp1 | a0003 | c0005 | t0001 | g0087 | SAS | BEB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03831 | hp2 | a0005 | c0014 | t0003 | g0203 | SAS | BEB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03834 | hp1 | a0002 | c0008 | t0001 | g0208 | SAS | BEB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03834 | hp2 | a0003 | c0005 | t0002 | g0085 | SAS | BEB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04115 | hp1 | a0005 | c0015 | t0002 | g0233 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04115 | hp2 | a0001 | c0033 | t0010 | g0204 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04199 | hp1 | a0040 | c0081 | t0006 | g0066 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0232 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04204 | hp1 | a0018 | c0072 | t0002 | g0134 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG04204 | hp2 | a0002 | c0006 | t0001 | g0038 | SAS | STU | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18747 | hp1 | a0001 | c0002 | t0005 | g0170 | EAS | CHB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18747 | hp2 | a0002 | c0010 | t0004 | g0035 | EAS | CHB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18906 | hp1 | a0024 | c0041 | t0003 | g0235 | AFR | YRI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18906 | hp2 | a0027 | c0053 | t0041 | g0116 | AFR | YRI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18940 | hp1 | a0002 | c0008 | t0002 | g0215 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18940 | hp2 | a0003 | c0003 | t0007 | g0076 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18944 | hp2 | a0002 | c0008 | t0001 | g0219 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18946 | hp2 | a0003 | c0003 | t0005 | g0089 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18947 | hp1 | a0004 | c0004 | t0005 | g0011 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18947 | hp2 | a0003 | c0003 | t0004 | g0094 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18951 | hp2 | a0003 | c0003 | t0036 | g0073 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18960 | hp1 | a0001 | c0029 | t0025 | g0003 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18960 | hp2 | a0002 | c0011 | t0004 | g0228 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18962 | hp1 | a0001 | c0002 | t0005 | g0140 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18963 | hp1 | a0004 | c0004 | t0007 | g0015 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18963 | hp2 | a0002 | c0010 | t0004 | g0034 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18969 | hp1 | a0003 | c0003 | t0004 | g0090 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18970 | hp2 | a0004 | c0007 | t0001 | g0013 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18977 | hp2 | a0004 | c0004 | t0004 | g0008 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18992 | hp1 | a0009 | c0038 | t0005 | g0133 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18993 | hp1 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18993 | hp2 | a0003 | c0003 | t0005 | g0070 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18994 | hp1 | a0009 | c0038 | t0007 | g0147 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18994 | hp2 | a0002 | c0011 | t0004 | g0217 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0154 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18995 | hp2 | a0004 | c0004 | t0005 | g0064 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19002 | hp1 | a0003 | c0078 | t0001 | g0019 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19002 | hp2 | a0001 | c0002 | t0005 | g0176 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19003 | hp1 | a0002 | c0010 | t0004 | g0097 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19003 | hp2 | a0009 | c0028 | t0001 | g0146 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19004 | hp1 | a0001 | c0001 | t0023 | g0167 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19004 | hp2 | a0003 | c0003 | t0004 | g0084 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19009 | hp1 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19009 | hp2 | a0001 | c0029 | t0002 | g0150 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19010 | hp1 | a0004 | c0007 | t0001 | g0047 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19010 | hp2 | a0049 | c0097 | t0007 | g0006 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19030 | hp1 | a0053 | c0069 | t0003 | g0108 | AFR | LWK | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19030 | hp2 | a0001 | c0030 | t0003 | g0144 | AFR | LWK | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19043 | hp1 | a0035 | c0062 | t0009 | g0105 | AFR | LWK | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19043 | hp2 | a0037 | c0063 | t0014 | g0104 | AFR | LWK | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19056 | hp1 | a0002 | c0006 | t0001 | g0033 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19056 | hp2 | a0001 | c0002 | t0005 | g0163 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19057 | hp1 | a0002 | c0006 | t0001 | g0096 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19057 | hp2 | a0001 | c0068 | t0005 | g0160 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19060 | hp1 | a0004 | c0007 | t0001 | g0046 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19065 | hp1 | a0057 | c0076 | t0002 | g0224 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19065 | hp2 | a0004 | c0004 | t0004 | g0007 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19067 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19067 | hp2 | a0004 | c0007 | t0001 | g0012 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19070 | hp1 | a0002 | c0008 | t0001 | g0214 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19070 | hp2 | a0003 | c0003 | t0034 | g0081 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19079 | hp1 | a0003 | c0003 | t0004 | g0078 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19081 | hp1 | a0009 | c0028 | t0001 | g0148 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19081 | hp2 | a0004 | c0004 | t0004 | g0063 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19082 | hp1 | a0003 | c0005 | t0002 | g0075 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19082 | hp2 | a0001 | c0067 | t0001 | g0182 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19084 | hp1 | a0009 | c0028 | t0001 | g0143 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19084 | hp2 | a0004 | c0004 | t0044 | g0016 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19087 | hp1 | a0004 | c0007 | t0001 | g0014 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19087 | hp2 | a0042 | c0080 | t0004 | g0088 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19240 | hp1 | a0015 | c0031 | t0003 | g0129 | AFR | YRI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA19240 | hp2 | a0016 | c0060 | t0029 | g0106 | AFR | YRI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20805 | hp1 | a0002 | c0027 | t0001 | g0029 | EUR | TSI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20805 | hp2 | a0001 | c0033 | t0010 | g0136 | EUR | TSI | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20905 | hp1 | a0002 | c0006 | t0013 | g0032 | SAS | GIH | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20905 | hp2 | a0013 | c0023 | t0002 | g0074 | SAS | GIH | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02109 | hp1 | a0014 | c0022 | t0014 | g0193 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02109 | hp2 | a0048 | c0065 | t0003 | g0100 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02486 | hp1 | a0029 | c0049 | t0002 | g0119 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02486 | hp2 | a0021 | c0044 | t0056 | g0254 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02559 | hp1 | a0001 | c0012 | t0050 | g0258 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG02559 | hp2 | a0041 | c0079 | t0039 | g0093 | AFR | ACB | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03471 | hp1 | a0003 | c0005 | t0002 | g0092 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG03471 | hp2 | a0001 | c0017 | t0008 | g0261 | AFR | MSL | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG06807 | hp1 | a0012 | c0020 | t0049 | g0124 | AFR | USA | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| HG06807 | hp2 | a0004 | c0093 | t0004 | g0042 | AFR | USA | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18955 | hp1 | a0003 | c0003 | t0005 | g0082 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA18955 | hp2 | a0002 | c0008 | t0001 | g0212 | EAS | JPT | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20300 | hp1 | a0014 | c0022 | t0003 | g0001 | AFR | USA | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| NA20300 | hp2 | a0002 | c0006 | t0007 | g0237 | AFR | USA | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0037 | t0006 | g0028 | REF | REF | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| homoSapiens_grch38 | hp1 | a0005 | c0098 | t0002 | g0243 | REF | REF | FREM2_chr13_38682077_38892131 | FREM2 | chr13 | 38682077 | 38892131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:38687520
|
G | A | 2 | a0019a0020 | 2 | HG02723.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.176G>A | p.Gly59Asp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 444/16122 | 176/9510 | 59/3169 | chr13 | 38687520 | ||
| chr13:38687649
|
G | C | 1 | a0021 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.305G>C | p.Gly102Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 573/16122 | 305/9510 | 102/3169 | chr13 | 38687649 | ||
| chr13:38688594
|
T | C | 1 | a0058 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1250T>C | p.Leu417Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 1518/16122 | 1250/9510 | 417/3169 | chr13 | 38688594 | ||
| chr13:38688924
|
C | T | 3 | a0022a0023a0024 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1580C>T | p.Ser527Leu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 1848/16122 | 1580/9510 | 527/3169 | chr13 | 38688924 | ||
| chr13:38689477
|
G | A | 1 | a0025 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2133G>A | p.Met711Ile | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2401/16122 | 2133/9510 | 711/3169 | chr13 | 38689477 | ||
| chr13:38689509
|
G | A | 13 | a0008a0011a0012others(10): Show | 22 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
missense_variant | MODERATE | c.2165G>A | p.Arg722Lys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2433/16122 | 2165/9510 | 722/3169 | chr13 | 38689509 | ||
| chr13:38689652
|
G | A | 6 | a0008a0011a0026others(3): Show | 12 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.2308G>A | p.Val770Met | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2576/16122 | 2308/9510 | 770/3169 | chr13 | 38689652 | ||
| chr13:38689944
|
C | T | 1 | a0034 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2600C>T | p.Thr867Ile | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2868/16122 | 2600/9510 | 867/3169 | chr13 | 38689944 | ||
| chr13:38689946
|
C | G | 13 | a0008a0011a0012others(10): Show | 22 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
missense_variant | MODERATE | c.2602C>G | p.Leu868Val | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2870/16122 | 2602/9510 | 868/3169 | chr13 | 38689946 | ||
| chr13:38690322
|
A | G | 4 | a0015a0025a0032others(1): Show | 5 | HG01243.hp2 HG01884.hp1 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.2978A>G | p.Glu993Gly | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3246/16122 | 2978/9510 | 993/3169 | chr13 | 38690322 | ||
| chr13:38690460
|
T | A | 5 | a0016a0035a0036others(2): Show | 6 | HG02257.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
missense_variant | MODERATE | c.3116T>A | p.Met1039Lys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3384/16122 | 3116/9510 | 1039/3169 | chr13 | 38690460 | ||
| chr13:38690553
|
T | C | 41 | a0001a0006a0008others(38): Show | 140 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(137): Show |
missense_variant | MODERATE | c.3209T>C | p.Phe1070Ser | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3477/16122 | 3209/9510 | 1070/3169 | chr13 | 38690553 | ||
| chr13:38690610
|
A | T | 1 | a0047 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.3266A>T | p.His1089Leu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3534/16122 | 3266/9510 | 1089/3169 | chr13 | 38690610 | ||
| chr13:38691323
|
T | A | 1 | a0048 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3979T>A | p.Leu1327Ile | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4247/16122 | 3979/9510 | 1327/3169 | chr13 | 38691323 | ||
| chr13:38691374
|
C | T | 1 | a0049 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.4030C>T | p.Arg1344Cys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4298/16122 | 4030/9510 | 1344/3169 | chr13 | 38691374 | ||
| chr13:38691599
|
A | G | 1 | a0057 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.4255A>G | p.Ile1419Val | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4523/16122 | 4255/9510 | 1419/3169 | chr13 | 38691599 | ||
| chr13:38692070
|
C | G | 2 | a0019a0020 | 2 | HG02723.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.4726C>G | p.Pro1576Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4994/16122 | 4726/9510 | 1576/3169 | chr13 | 38692070 | ||
| chr13:38692074
|
T | C | 2 | a0019a0020 | 2 | HG02723.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.4730T>C | p.Ile1577Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4998/16122 | 4730/9510 | 1577/3169 | chr13 | 38692074 | ||
| chr13:38692230
|
A | G | 1 | a0039 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.4886A>G | p.Tyr1629Cys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 5154/16122 | 4886/9510 | 1629/3169 | chr13 | 38692230 | ||
| chr13:38692245
|
C | T | 3 | a0014a0032a0050 | 5 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.4901C>T | p.Thr1634Met | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 5169/16122 | 4901/9510 | 1634/3169 | chr13 | 38692245 | ||
| chr13:38692260
|
G | A | 1 | a0009 | 5 | NA18992.hp1 NA18994.hp1 NA19003.hp2 others(2): Show |
missense_variant | MODERATE | c.4916G>A | p.Arg1639Lys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 5184/16122 | 4916/9510 | 1639/3169 | chr13 | 38692260 | ||
| chr13:38692347
|
G | A | 7 | a0003a0013a0039others(4): Show | 33 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(30): Show |
missense_variant | MODERATE | c.5003G>A | p.Arg1668His | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 5271/16122 | 5003/9510 | 1668/3169 | chr13 | 38692347 | ||
| chr13:38769685
|
C | T | 18 | a0004a0012a0015others(15): Show | 43 | HG00738.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
missense_variant | MODERATE | c.5518C>T | p.Arg1840Trp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/24 | 5786/16122 | 5518/9510 | 1840/3169 | chr13 | 38769685 | ||
| chr13:38848487
|
C | T | 14 | a0007a0010a0022others(11): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
missense_variant | MODERATE | c.6196C>T | p.Arg2066Cys | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/24 | 6464/16122 | 6196/9510 | 2066/3169 | chr13 | 38848487 | ||
| chr13:38848526
|
G | A | 1 | a0035 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.6235G>A | p.Val2079Ile | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/24 | 6503/16122 | 6235/9510 | 2079/3169 | chr13 | 38848526 | ||
| chr13:38850116
|
C | G | 10 | a0007a0010a0022others(7): Show | 21 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(18): Show |
missense_variant | MODERATE | c.6458C>G | p.Thr2153Ser | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/24 | 6726/16122 | 6458/9510 | 2153/3169 | chr13 | 38850116 | ||
| chr13:38851734
|
A | G | 1 | a0055 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.6791A>G | p.Lys2264Arg | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/24 | 7059/16122 | 6791/9510 | 2264/3169 | chr13 | 38851734 | ||
| chr13:38856177
|
C | T | 43 | a0001a0002a0003others(40): Show | 217 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(214): Show |
missense_variant | MODERATE | c.6977C>T | p.Thr2326Ile | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/24 | 7245/16122 | 6977/9510 | 2326/3169 | chr13 | 38856177 | ||
| chr13:38856189
|
T | C | 3 | a0016a0041a0052 | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.6989T>C | p.Val2330Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/24 | 7257/16122 | 6989/9510 | 2330/3169 | chr13 | 38856189 | ||
| chr13:38864589
|
A | T | 1 | a0017 | 2 | HG01516.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.7966A>T | p.Ile2656Phe | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/24 | 8234/16122 | 7966/9510 | 2656/3169 | chr13 | 38864589 | ||
| chr13:38878250
|
T | C | 1 | a0042 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.8788T>C | p.Tyr2930His | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/24 | 9056/16122 | 8788/9510 | 2930/3169 | chr13 | 38878250 | ||
| chr13:38878856
|
C | T | 9 | a0011a0020a0024others(6): Show | 11 | HG02630.hp2 HG02723.hp2 HG02895.hp1 others(8): Show |
missense_variant | MODERATE | c.8885C>T | p.Ala2962Val | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/24 | 9153/16122 | 8885/9510 | 2962/3169 | chr13 | 38878856 | ||
| chr13:38880461
|
G | T | 1 | a0058 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.9184G>T | p.Ala3062Ser | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 9452/16122 | 9184/9510 | 3062/3169 | chr13 | 38880461 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:38687521
|
T | C | 3 | a0022c0043a0023c0042a0024c0041 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.177T>C | p.Gly59Gly | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 445/16122 | 177/9510 | 59/3169 | chr13 | 38687521 | ||
| chr13:38687647
|
C | A | 7 | a0001c0009a0001c0012a0001c0017others(4): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
synonymous_variant | LOW | c.303C>A | p.Pro101Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 571/16122 | 303/9510 | 101/3169 | chr13 | 38687647 | ||
| chr13:38687920
|
G | A | 97 | a0001c0001a0001c0002a0001c0009others(94): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
synonymous_variant | LOW | c.576G>A | p.Glu192Glu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 844/16122 | 576/9510 | 192/3169 | chr13 | 38687920 | ||
| chr13:38688298
|
C | G | 7 | a0001c0029a0001c0030a0006c0095others(4): Show | 14 | HG02027.hp1 HG02155.hp1 HG02257.hp1 others(11): Show |
synonymous_variant | LOW | c.954C>G | p.Pro318Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 1222/16122 | 954/9510 | 318/3169 | chr13 | 38688298 | ||
| chr13:38688553
|
C | T | 1 | a0010c0094 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1209C>T | p.Asp403Asp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 1477/16122 | 1209/9510 | 403/3169 | chr13 | 38688553 | ||
| chr13:38688886
|
C | T | 8 | a0002c0027a0002c0036a0002c0091others(5): Show | 13 | HG00741.hp2 HG01070.hp1 HG01167.hp2 others(10): Show |
synonymous_variant | LOW | c.1542C>T | p.Ala514Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 1810/16122 | 1542/9510 | 514/3169 | chr13 | 38688886 | ||
| chr13:38689285
|
C | T | 2 | a0004c0089a0005c0026 | 4 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
synonymous_variant | LOW | c.1941C>T | p.Asp647Asp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2209/16122 | 1941/9510 | 647/3169 | chr13 | 38689285 | ||
| chr13:38689594
|
C | T | 6 | a0002c0008a0002c0011a0005c0015others(3): Show | 24 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
synonymous_variant | LOW | c.2250C>T | p.Asp750Asp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2518/16122 | 2250/9510 | 750/3169 | chr13 | 38689594 | ||
| chr13:38689711
|
G | A | 3 | a0022c0043a0023c0042a0024c0041 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.2367G>A | p.Pro789Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 2635/16122 | 2367/9510 | 789/3169 | chr13 | 38689711 | ||
| chr13:38690167
|
C | T | 3 | a0022c0043a0023c0042a0024c0041 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.2823C>T | p.Pro941Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3091/16122 | 2823/9510 | 941/3169 | chr13 | 38690167 | ||
| chr13:38690998
|
T | C | 1 | a0002c0077 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.3654T>C | p.Ala1218Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 3922/16122 | 3654/9510 | 1218/3169 | chr13 | 38690998 | ||
| chr13:38691421
|
T | A | 2 | a0004c0089a0005c0026 | 4 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
synonymous_variant | LOW | c.4077T>A | p.Gly1359Gly | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 4345/16122 | 4077/9510 | 1359/3169 | chr13 | 38691421 | ||
| chr13:38784579
|
G | A | 1 | a0003c0078 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.5790G>A | p.Pro1930Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/24 | 6058/16122 | 5790/9510 | 1930/3169 | chr13 | 38784579 | ||
| chr13:38846589
|
C | T | 3 | a0028c0054a0035c0062a0045c0085 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.6036C>T | p.Phe2012Phe | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/24 | 6304/16122 | 6036/9510 | 2012/3169 | chr13 | 38846589 | ||
| chr13:38848621
|
T | G | 2 | a0016c0059a0052c0045 | 2 | HG02257.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.6330T>G | p.Leu2110Leu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/24 | 6598/16122 | 6330/9510 | 2110/3169 | chr13 | 38848621 | ||
| chr13:38848630
|
C | T | 2 | a0006c0096a0031c0056 | 2 | HG02809.hp1 HG02896.hp2 |
synonymous_variant | LOW | c.6339C>T | p.Pro2113Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/24 | 6607/16122 | 6339/9510 | 2113/3169 | chr13 | 38848630 | ||
| chr13:38850054
|
C | T | 1 | a0051c0046 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.6396C>T | p.Phe2132Phe | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/24 | 6664/16122 | 6396/9510 | 2132/3169 | chr13 | 38850054 | ||
| chr13:38850117
|
T | C | 13 | a0007c0024a0007c0025a0007c0037others(10): Show | 21 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(18): Show |
synonymous_variant | LOW | c.6459T>C | p.Thr2153Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/24 | 6727/16122 | 6459/9510 | 2153/3169 | chr13 | 38850117 | ||
| chr13:38850972
|
G | A | 4 | a0028c0054a0035c0062a0045c0085others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.6606G>A | p.Glu2202Glu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 10/24 | 6874/16122 | 6606/9510 | 2202/3169 | chr13 | 38850972 | ||
| chr13:38857970
|
C | T | 1 | a0044c0084 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.7152C>T | p.Asp2384Asp | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/24 | 7420/16122 | 7152/9510 | 2384/3169 | chr13 | 38857970 | ||
| chr13:38859364
|
G | A | 1 | a0044c0084 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.7293G>A | p.Thr2431Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/24 | 7561/16122 | 7293/9510 | 2431/3169 | chr13 | 38859364 | ||
| chr13:38859469
|
A | G | 59 | a0001c0002a0001c0009a0001c0017others(56): Show | 138 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
synonymous_variant | LOW | c.7398A>G | p.Thr2466Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/24 | 7666/16122 | 7398/9510 | 2466/3169 | chr13 | 38859469 | ||
| chr13:38861501
|
C | T | 1 | a0002c0091 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.7590C>T | p.Gly2530Gly | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/24 | 7858/16122 | 7590/9510 | 2530/3169 | chr13 | 38861501 | ||
| chr13:38864285
|
C | T | 1 | a0044c0084 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.7662C>T | p.Pro2554Pro | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/24 | 7930/16122 | 7662/9510 | 2554/3169 | chr13 | 38864285 | ||
| chr13:38864423
|
C | T | 1 | a0001c0067 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.7800C>T | p.Thr2600Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/24 | 8068/16122 | 7800/9510 | 2600/3169 | chr13 | 38864423 | ||
| chr13:38874531
|
C | T | 7 | a0001c0017a0001c0070a0008c0051others(4): Show | 9 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
synonymous_variant | LOW | c.8226C>T | p.Ala2742Ala | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/24 | 8494/16122 | 8226/9510 | 2742/3169 | chr13 | 38874531 | ||
| chr13:38876077
|
C | T | 1 | a0002c0036 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.8337C>T | p.Ser2779Ser | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 19/24 | 8605/16122 | 8337/9510 | 2779/3169 | chr13 | 38876077 | ||
| chr13:38878878
|
A | G | 1 | a0001c0068 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.8907A>G | p.Leu2969Leu | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/24 | 9175/16122 | 8907/9510 | 2969/3169 | chr13 | 38878878 | ||
| chr13:38880634
|
G | C | 2 | a0005c0090a0006c0032 | 3 | HG01070.hp2 HG01515.hp2 HG02602.hp1 |
synonymous_variant | LOW | c.9357G>C | p.Thr3119Thr | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 9625/16122 | 9357/9510 | 3119/3169 | chr13 | 38880634 | ||
| chr13:38880706
|
G | A | 4 | a0001c0033a0002c0092a0017c0034others(1): Show | 6 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(3): Show |
synonymous_variant | LOW | c.9429G>A | p.Gly3143Gly | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 9697/16122 | 9429/9510 | 3143/3169 | chr13 | 38880706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:38687085
|
A | G | 12 | a0001c0009t0008a0001c0009t0020a0001c0012t0019others(9): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-260A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | 260 | chr13 | 38687085 | |||||
| chr13:38687301
|
C | T | 1 | a0012c0020t0049 | 1 | HG06807.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/24 | chr13 | 38687301 | ||||||
| chr13:38880996
|
A | G | 7 | a0001c0017t0055a0001c0030t0047a0004c0004t0012others(4): Show | 7 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*209A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 209 | chr13 | 38880996 | |||||
| chr13:38881010
|
C | T | 2 | a0001c0001t0018a0004c0007t0018 | 2 | HG01891.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*223C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 223 | chr13 | 38881010 | |||||
| chr13:38881129
|
G | A | 45 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(42): Show | 90 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*342G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 342 | chr13 | 38881129 | |||||
| chr13:38881191
|
A | C | 7 | a0001c0017t0055a0001c0030t0047a0004c0004t0012others(4): Show | 7 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*404A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 404 | chr13 | 38881191 | |||||
| chr13:38881264
|
T | C | 1 | a0016c0060t0029 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 477 | chr13 | 38881264 | |||||
| chr13:38881277
|
A | T | 4 | a0004c0004t0012a0008c0019t0012a0022c0043t0012others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*490A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 490 | chr13 | 38881277 | |||||
| chr13:38881314
|
C | T | 1 | a0002c0092t0046 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 527 | chr13 | 38881314 | |||||
| chr13:38881361
|
A | T | 1 | a0002c0010t0045 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 574 | chr13 | 38881361 | |||||
| chr13:38881447
|
A | G | 1 | a0004c0004t0044 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 660 | chr13 | 38881447 | |||||
| chr13:38881779
|
T | C | 12 | a0001c0002t0006a0001c0033t0010a0002c0092t0046others(9): Show | 19 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*992T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 992 | chr13 | 38881779 | |||||
| chr13:38881828
|
C | T | 8 | a0001c0002t0006a0007c0024t0006a0007c0025t0006others(5): Show | 13 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1041C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1041 | chr13 | 38881828 | |||||
| chr13:38882104
|
C | A | 1 | a0023c0042t0048 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1317 | chr13 | 38882104 | |||||
| chr13:38882108
|
G | A | 2 | a0001c0001t0013a0002c0006t0013 | 2 | HG01255.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1321G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1321 | chr13 | 38882108 | |||||
| chr13:38882166
|
T | C | 2 | a0014c0022t0014a0037c0063t0014 | 2 | HG02109.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1379T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1379 | chr13 | 38882166 | |||||
| chr13:38882215
|
A | G | 64 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(61): Show | 124 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1428A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1428 | chr13 | 38882215 | |||||
| chr13:38882254
|
G | A | 8 | a0001c0002t0006a0007c0024t0006a0007c0025t0006others(5): Show | 13 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1467G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1467 | chr13 | 38882254 | |||||
| chr13:38882411
|
G | A | 4 | a0001c0033t0010a0002c0092t0046a0017c0034t0010others(1): Show | 6 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1624G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1624 | chr13 | 38882411 | |||||
| chr13:38882438
|
A | T | 1 | a0001c0001t0028 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1651A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1651 | chr13 | 38882438 | |||||
| chr13:38882480
|
A | G | 6 | a0001c0030t0047a0004c0004t0012a0008c0019t0012others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1693A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1693 | chr13 | 38882480 | |||||
| chr13:38882481
|
A | G | 1 | a0005c0015t0042 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1694A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1694 | chr13 | 38882481 | |||||
| chr13:38882532
|
A | T | 6 | a0001c0030t0047a0004c0004t0012a0008c0019t0012others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1745A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1745 | chr13 | 38882532 | |||||
| chr13:38882598
|
C | T | 6 | a0001c0030t0047a0004c0004t0012a0008c0019t0012others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1811C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 1811 | chr13 | 38882598 | |||||
| chr13:38882927
|
C | G | 64 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(61): Show | 124 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2140C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2140 | chr13 | 38882927 | |||||
| chr13:38882928
|
G | A | 6 | a0001c0030t0047a0004c0004t0012a0008c0019t0012others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2141G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2141 | chr13 | 38882928 | |||||
| chr13:38882946
|
G | A | 1 | a0055c0071t0031 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2159 | chr13 | 38882946 | |||||
| chr13:38883162
|
C | G | 1 | a0001c0012t0053 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2375 | chr13 | 38883162 | |||||
| chr13:38883176
|
CAGA | C | 5 | a0001c0002t0005a0001c0068t0005a0003c0003t0005others(2): Show | 13 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2390_*2392delAGA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2390 | chr13 | 38883176 | |||||
| chr13:38883671
|
G | T | 3 | a0012c0020t0017a0012c0020t0049a0043c0082t0017 | 3 | HG01243.hp1 HG02976.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2884G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2884 | chr13 | 38883671 | |||||
| chr13:38883682
|
G | T | 1 | a0027c0053t0041 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2895G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2895 | chr13 | 38883682 | |||||
| chr13:38883713
|
G | A | 50 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(47): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2926G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 2926 | chr13 | 38883713 | |||||
| chr13:38883979
|
T | C | 51 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(48): Show | 82 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3192T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 3192 | chr13 | 38883979 | |||||
| chr13:38884268
|
G | A | 51 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(48): Show | 82 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3481G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 3481 | chr13 | 38884268 | |||||
| chr13:38884716
|
G | T | 4 | a0001c0001t0018a0001c0001t0027a0001c0012t0050others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3929G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 3929 | chr13 | 38884716 | |||||
| chr13:38884938
|
T | C | 1 | a0001c0012t0053 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4151T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4151 | chr13 | 38884938 | |||||
| chr13:38885012
|
A | G | 1 | a0005c0014t0040 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4225A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4225 | chr13 | 38885012 | |||||
| chr13:38885036
|
A | C | 1 | a0003c0005t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4249A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4249 | chr13 | 38885036 | |||||
| chr13:38885224
|
A | G | 1 | a0016c0060t0029 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4437A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4437 | chr13 | 38885224 | |||||
| chr13:38885252
|
C | T | 122 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(119): Show | 213 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*4465C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4465 | chr13 | 38885252 | |||||
| chr13:38885347
|
G | A | 50 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(47): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4560G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4560 | chr13 | 38885347 | |||||
| chr13:38885404
|
A | G | 1 | a0001c0029t0025 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4617A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4617 | chr13 | 38885404 | |||||
| chr13:38885557
|
C | T | 56 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(53): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*4770C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4770 | chr13 | 38885557 | |||||
| chr13:38885694
|
C | T | 1 | a0003c0005t0024 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4907C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 4907 | chr13 | 38885694 | |||||
| chr13:38885806
|
A | T | 2 | a0006c0096t0015a0031c0056t0015 | 2 | HG02809.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5019A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5019 | chr13 | 38885806 | |||||
| chr13:38885887
|
C | T | 1 | a0041c0079t0039 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5100C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5100 | chr13 | 38885887 | |||||
| chr13:38886005
|
C | T | 1 | a0007c0037t0030 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5218C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5218 | chr13 | 38886005 | |||||
| chr13:38886122
|
A | G | 12 | a0001c0002t0006a0001c0033t0010a0002c0092t0046others(9): Show | 19 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5335A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5335 | chr13 | 38886122 | |||||
| chr13:38886131
|
T | G | 1 | a0001c0002t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5344T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5344 | chr13 | 38886131 | |||||
| chr13:38886278
|
G | A | 123 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(120): Show | 214 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*5491G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5491 | chr13 | 38886278 | |||||
| chr13:38886329
|
T | A | 57 | a0001c0002t0003a0001c0002t0004a0001c0002t0032others(54): Show | 88 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*5542T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5542 | chr13 | 38886329 | |||||
| chr13:38886333
|
T | TATATACA others(11): Show |
2 | a0016c0059t0043a0052c0045t0054 | 2 | HG02257.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5561_*5562insGACA others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5562 | INFO_REALIGN_3_PRIME | chr13 | 38886333 | ||||
| chr13:38886349
|
C | G | 65 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(62): Show | 125 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*5562C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5562 | chr13 | 38886349 | |||||
| chr13:38886383
|
T | G | 7 | a0001c0030t0047a0004c0004t0012a0008c0019t0012others(4): Show | 7 | HG01496.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5596T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5596 | chr13 | 38886383 | |||||
| chr13:38886385
|
T | G | 75 | a0001c0001t0001a0001c0001t0013a0001c0001t0023others(72): Show | 128 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*5598T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5598 | chr13 | 38886385 | |||||
| chr13:38886385
|
T | TAG | 11 | a0001c0002t0004a0002c0010t0004a0002c0010t0045others(8): Show | 31 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5610_*5611dupGA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5612 | INFO_REALIGN_3_PRIME | chr13 | 38886385 | ||||
| chr13:38886387
|
G | T | 5 | a0006c0016t0021a0006c0021t0016a0013c0023t0016others(2): Show | 6 | HG00639.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5600G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5600 | chr13 | 38886387 | |||||
| chr13:38886399
|
T | G | 6 | a0001c0033t0010a0002c0092t0046a0003c0003t0034others(3): Show | 8 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5612T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5612 | chr13 | 38886399 | |||||
| chr13:38886402
|
AT | A | 122 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(119): Show | 213 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*5627delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5627 | INFO_REALIGN_3_PRIME | chr13 | 38886402 | ||||
| chr13:38886403
|
T | A | 1 | a0003c0003t0034 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5616T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5616 | chr13 | 38886403 | |||||
| chr13:38886520
|
C | T | 65 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(62): Show | 125 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*5733C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5733 | chr13 | 38886520 | |||||
| chr13:38886686
|
C | T | 31 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(28): Show | 74 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*5899C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 5899 | chr13 | 38886686 | |||||
| chr13:38886849
|
TAATGGAA others(8): Show |
T | 1 | a0003c0005t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6064_*6078delATGG others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 6064 | INFO_REALIGN_3_PRIME | chr13 | 38886849 | ||||
| chr13:38886890
|
C | T | 1 | a0005c0035t0038 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6103C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 6103 | chr13 | 38886890 | |||||
| chr13:38887043
|
C | T | 1 | a0003c0003t0036 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6256C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 6256 | chr13 | 38887043 | |||||
| chr13:38887052
|
G | A | 1 | a0001c0001t0023 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6265G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 6265 | chr13 | 38887052 | |||||
| chr13:38887109
|
A | C | 1 | a0002c0011t0035 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6322A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 24/24 | 6322 | chr13 | 38887109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:38692592
|
A | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5173+75A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38692592 | ||||||
| chr13:38692725
|
T | C | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.5173+208T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38692725 | ||||||
| chr13:38692958
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5173+441G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38692958 | ||||||
| chr13:38693137
|
C | T | 4 | a0004c0089t0001g0239a0005c0026t0002g0240a0005c0026t0002g0241others(1): Show | 4 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.5173+620C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693137 | ||||||
| chr13:38693178
|
C | T | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5173+661C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693178 | ||||||
| chr13:38693378
|
C | T | 1 | a0002c0006t0007g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5173+861C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693378 | ||||||
| chr13:38693539
|
T | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5173+1022T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693539 | ||||||
| chr13:38693909
|
T | A | 1 | a0001c0029t0025g0003 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5173+1392T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693909 | ||||||
| chr13:38693948
|
G | A | 2 | a0019c0039t0011g0004a0020c0040t0003g0005 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5173+1431G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38693948 | ||||||
| chr13:38694232
|
C | G | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5173+1715C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694232 | ||||||
| chr13:38694416
|
G | A | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5173+1899G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694416 | ||||||
| chr13:38694449
|
T | G | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5173+1932T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694449 | ||||||
| chr13:38694708
|
T | C | 98 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(95): Show | 98 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.5173+2191T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694708 | ||||||
| chr13:38694777
|
T | G | 13 | a0010c0013t0003g0107a0016c0059t0043g0101a0016c0060t0029g0106others(10): Show | 13 | HG01981.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.5173+2260T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694777 | ||||||
| chr13:38694915
|
A | G | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5173+2398A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38694915 | ||||||
| chr13:38695348
|
A | G | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5174-2350A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38695348 | ||||||
| chr13:38695414
|
T | G | 14 | a0004c0004t0004g0007a0004c0004t0004g0008a0004c0004t0005g0009others(11): Show | 14 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.5174-2284T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38695414 | ||||||
| chr13:38695458
|
T | C | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5174-2240T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38695458 | ||||||
| chr13:38695543
|
T | C | 21 | a0008c0019t0003g0118a0008c0019t0003g0121a0008c0019t0012g0115others(18): Show | 21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.5174-2155T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38695543 | ||||||
| chr13:38695820
|
A | C | 3 | a0012c0020t0017g0130a0018c0073t0002g0132a0030c0055t0003g0131 | 3 | HG01243.hp1 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5174-1878A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38695820 | ||||||
| chr13:38696122
|
A | C | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.5174-1576A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696122 | ||||||
| chr13:38696176
|
G | A | 12 | a0008c0019t0003g0118a0008c0019t0003g0121a0008c0019t0012g0115others(9): Show | 12 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.5174-1522G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696176 | ||||||
| chr13:38696276
|
C | T | 1 | a0008c0050t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5174-1422C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696276 | ||||||
| chr13:38696462
|
G | A | 1 | a0009c0038t0005g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5174-1236G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696462 | ||||||
| chr13:38696648
|
G | A | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5174-1050G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696648 | ||||||
| chr13:38696810
|
C | CT | 48 | a0001c0002t0004g0231a0001c0002t0004g0232a0001c0070t0003g0095others(45): Show | 48 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.5174-873dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr13 | 38696810 | |||||
| chr13:38696810
|
CT | C | 5 | a0001c0002t0001g0135a0001c0033t0010g0136a0002c0036t0007g0017others(2): Show | 5 | HG01169.hp2 HG01257.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.5174-873delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr13 | 38696810 | |||||
| chr13:38696834
|
G | A | 1 | a0001c0002t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5174-864G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696834 | ||||||
| chr13:38696843
|
T | C | 6 | a0016c0059t0043g0101a0016c0060t0029g0106a0035c0062t0009g0105others(3): Show | 6 | HG02257.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.5174-855T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696843 | ||||||
| chr13:38696850
|
C | T | 2 | a0002c0008t0001g0230a0007c0025t0003g0229 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.5174-848C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696850 | ||||||
| chr13:38696993
|
T | C | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5174-705T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38696993 | ||||||
| chr13:38697212
|
G | A | 1 | a0005c0035t0002g0018 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5174-486G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38697212 | ||||||
| chr13:38697233
|
A | G | 2 | a0002c0011t0004g0228a0002c0011t0035g0227 | 2 | HG00558.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.5174-465A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38697233 | ||||||
| chr13:38697490
|
A | G | 3 | a0004c0004t0004g0063a0004c0004t0005g0064a0004c0004t0005g0065 | 3 | HG02083.hp1 NA18995.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.5174-208A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38697490 | ||||||
| chr13:38697566
|
C | T | 1 | a0003c0005t0024g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5174-132C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 1/23 | chr13 | 38697566 | ||||||
| chr13:38697941
|
C | G | 13 | a0012c0020t0002g0126a0012c0020t0017g0130a0012c0020t0049g0124others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.5263+154C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38697941 | ||||||
| chr13:38698027
|
G | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+240G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698027 | ||||||
| chr13:38698243
|
C | G | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5263+456C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698243 | ||||||
| chr13:38698321
|
G | A | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5263+534G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698321 | ||||||
| chr13:38698379
|
A | G | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5263+592A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698379 | ||||||
| chr13:38698510
|
A | G | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5263+723A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698510 | ||||||
| chr13:38698528
|
G | T | 3 | a0010c0013t0003g0107a0053c0069t0003g0108a0055c0071t0031g0109 | 3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5263+741G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698528 | ||||||
| chr13:38698642
|
G | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+855G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38698642 | ||||||
| chr13:38699003
|
C | T | 1 | a0057c0076t0002g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5263+1216C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699003 | ||||||
| chr13:38699016
|
A | C | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+1229A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699016 | ||||||
| chr13:38699026
|
C | T | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+1239C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699026 | ||||||
| chr13:38699033
|
A | T | 1 | a0004c0004t0011g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5263+1246A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699033 | ||||||
| chr13:38699038
|
A | G | 1 | a0018c0073t0002g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5263+1251A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699038 | ||||||
| chr13:38699260
|
A | G | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+1473A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699260 | ||||||
| chr13:38699321
|
AAC | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+1544_5263+154 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38699321 | |||||
| chr13:38699331
|
C | T | 1 | a0010c0013t0006g0205 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5263+1544C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699331 | ||||||
| chr13:38699543
|
C | G | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5263+1756C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699543 | ||||||
| chr13:38699562
|
T | G | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5263+1775T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699562 | ||||||
| chr13:38699620
|
T | C | 1 | a0022c0043t0012g0234 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5263+1833T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699620 | ||||||
| chr13:38699631
|
T | C | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+1844T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699631 | ||||||
| chr13:38699790
|
T | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5263+2003T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699790 | ||||||
| chr13:38699815
|
T | A | 66 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(63): Show | 66 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.5263+2028T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699815 | ||||||
| chr13:38699856
|
G | T | 1 | a0034c0088t0011g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5263+2069G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699856 | ||||||
| chr13:38699897
|
C | T | 3 | a0001c0001t0013g0202a0001c0033t0010g0204a0005c0014t0003g0203 | 3 | HG01255.hp2 HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5263+2110C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699897 | ||||||
| chr13:38699941
|
C | T | 6 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.5263+2154C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38699941 | ||||||
| chr13:38700081
|
A | G | 3 | a0019c0039t0011g0004a0020c0040t0003g0005a0025c0048t0003g0225 | 3 | HG01243.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+2294A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700081 | ||||||
| chr13:38700292
|
G | C | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5263+2505G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700292 | ||||||
| chr13:38700463
|
C | T | 1 | a0003c0003t0004g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5263+2676C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700463 | ||||||
| chr13:38700608
|
CA | C | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+2829delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38700608 | |||||
| chr13:38700620
|
A | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+2833A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700620 | ||||||
| chr13:38700674
|
T | C | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+2887T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700674 | ||||||
| chr13:38700763
|
T | C | 4 | a0010c0013t0003g0107a0048c0065t0003g0100a0053c0069t0003g0108others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+2976T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700763 | ||||||
| chr13:38700820
|
T | C | 2 | a0016c0059t0043g0101a0036c0061t0003g0102 | 2 | HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5263+3033T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700820 | ||||||
| chr13:38700842
|
G | C | 2 | a0001c0002t0004g0141a0001c0002t0005g0140 | 2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.5263+3055G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38700842 | ||||||
| chr13:38701160
|
A | G | 3 | a0003c0005t0002g0092a0003c0005t0026g0091a0041c0079t0039g0093 | 3 | HG02559.hp2 HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5263+3373A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701160 | ||||||
| chr13:38701314
|
G | A | 75 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(72): Show | 75 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5263+3527G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701314 | ||||||
| chr13:38701359
|
G | T | 1 | a0001c0009t0008g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5263+3572G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701359 | ||||||
| chr13:38701443
|
C | T | 1 | a0007c0024t0006g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5263+3656C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701443 | ||||||
| chr13:38701546
|
G | A | 1 | a0001c0070t0003g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5263+3759G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701546 | ||||||
| chr13:38701632
|
G | A | 3 | a0012c0020t0002g0126a0012c0020t0049g0124a0031c0056t0015g0125 | 3 | HG02809.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5263+3845G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701632 | ||||||
| chr13:38701670
|
T | C | 3 | a0012c0020t0002g0126a0012c0020t0049g0124a0031c0056t0015g0125 | 3 | HG02809.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5263+3883T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701670 | ||||||
| chr13:38701703
|
A | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+3916A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701703 | ||||||
| chr13:38701780
|
A | G | 1 | a0003c0003t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5263+3993A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701780 | ||||||
| chr13:38701952
|
G | A | 2 | a0011c0018t0003g0112a0011c0018t0003g0113 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5263+4165G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38701952 | ||||||
| chr13:38702125
|
A | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+4338A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702125 | ||||||
| chr13:38702463
|
C | A | 1 | a0006c0032t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5263+4676C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702463 | ||||||
| chr13:38702466
|
G | A | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5263+4679G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702466 | ||||||
| chr13:38702601
|
GAGAAAAA others(51): Show |
G | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+4834_5263+489 others(62): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38702601 | |||||
| chr13:38702612
|
A | G | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+4825A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702612 | ||||||
| chr13:38702688
|
G | A | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5263+4901G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702688 | ||||||
| chr13:38702688
|
G | C | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+4901G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702688 | ||||||
| chr13:38702833
|
G | A | 15 | a0001c0029t0001g0149a0001c0029t0002g0150a0001c0029t0025g0003others(12): Show | 15 | HG00423.hp2 HG02027.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.5263+5046G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702833 | ||||||
| chr13:38702932
|
T | C | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+5145T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38702932 | ||||||
| chr13:38703364
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5263+5577A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38703364 | ||||||
| chr13:38703520
|
C | T | 3 | a0010c0013t0003g0107a0053c0069t0003g0108a0055c0071t0031g0109 | 3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5263+5733C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38703520 | ||||||
| chr13:38703747
|
A | G | 1 | a0004c0004t0044g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5263+5960A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38703747 | ||||||
| chr13:38703819
|
G | C | 28 | a0002c0006t0001g0030a0002c0006t0001g0033a0002c0006t0001g0038others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+6032G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38703819 | ||||||
| chr13:38704147
|
A | G | 6 | a0016c0059t0043g0101a0016c0060t0029g0106a0035c0062t0009g0105others(3): Show | 6 | HG02257.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.5263+6360A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704147 | ||||||
| chr13:38704209
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+6422A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704209 | ||||||
| chr13:38704524
|
T | A | 1 | a0001c0002t0001g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5263+6737T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704524 | ||||||
| chr13:38704586
|
T | G | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5263+6799T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704586 | ||||||
| chr13:38704612
|
T | C | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5263+6825T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704612 | ||||||
| chr13:38704755
|
T | A | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+6968T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704755 | ||||||
| chr13:38704926
|
T | G | 3 | a0001c0001t0001g0155a0001c0002t0001g0135a0001c0002t0004g0154 | 3 | NA18992.hp2 NA18995.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.5263+7139T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704926 | ||||||
| chr13:38704941
|
G | A | 13 | a0012c0020t0002g0126a0012c0020t0017g0130a0012c0020t0049g0124others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.5263+7154G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38704941 | ||||||
| chr13:38705204
|
G | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+7417G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38705204 | ||||||
| chr13:38705268
|
T | C | 66 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.5263+7481T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38705268 | ||||||
| chr13:38705322
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0013g0202others(7): Show | 10 | HG00621.hp2 HG01167.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.5263+7535A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38705322 | ||||||
| chr13:38705910
|
G | T | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5263+8123G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38705910 | ||||||
| chr13:38705972
|
T | A | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+8185T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38705972 | ||||||
| chr13:38706006
|
C | T | 3 | a0012c0020t0002g0126a0012c0020t0049g0124a0031c0056t0015g0125 | 3 | HG02809.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5263+8219C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706006 | ||||||
| chr13:38706225
|
G | A | 4 | a0004c0004t0004g0007a0004c0004t0004g0008a0004c0004t0005g0009others(1): Show | 4 | HG01934.hp2 HG02135.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+8438G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706225 | ||||||
| chr13:38706237
|
A | G | 3 | a0005c0015t0042g0137a0017c0034t0010g0222a0017c0034t0010g0223 | 3 | HG01257.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.5263+8450A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706237 | ||||||
| chr13:38706295
|
T | G | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+8508T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706295 | ||||||
| chr13:38706368
|
G | T | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5263+8581G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706368 | ||||||
| chr13:38706480
|
T | C | 72 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(69): Show | 72 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5263+8693T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706480 | ||||||
| chr13:38706497
|
A | G | 3 | a0001c0009t0008g0260a0001c0012t0019g0259a0001c0017t0008g0261 | 3 | HG02280.hp2 HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5263+8710A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706497 | ||||||
| chr13:38706552
|
T | TC | 51 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(48): Show | 51 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.5263+8765_5263+876 others(5): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706552 | ||||||
| chr13:38706782
|
T | C | 70 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(67): Show | 70 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.5263+8995T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706782 | ||||||
| chr13:38706958
|
C | T | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5263+9171C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706958 | ||||||
| chr13:38706977
|
T | A | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5263+9190T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706977 | ||||||
| chr13:38706993
|
C | T | 1 | a0026c0052t0003g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5263+9206C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38706993 | ||||||
| chr13:38707249
|
A | T | 6 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.5263+9462A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707249 | ||||||
| chr13:38707288
|
T | A | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+9501T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707288 | ||||||
| chr13:38707439
|
G | C | 1 | a0034c0088t0011g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5263+9652G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707439 | ||||||
| chr13:38707642
|
G | A | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+9855G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707642 | ||||||
| chr13:38707846
|
A | G | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5263+10059A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707846 | ||||||
| chr13:38707898
|
A | C | 100 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.5263+10111A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707898 | ||||||
| chr13:38707946
|
G | A | 1 | a0054c0066t0003g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5263+10159G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38707946 | ||||||
| chr13:38708155
|
A | G | 3 | a0019c0039t0011g0004a0020c0040t0003g0005a0025c0048t0003g0225 | 3 | HG01243.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+10368A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708155 | ||||||
| chr13:38708204
|
T | C | 3 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197 | 3 | HG01496.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5263+10417T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708204 | ||||||
| chr13:38708235
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+10448C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708235 | ||||||
| chr13:38708452
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+10665G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708452 | ||||||
| chr13:38708534
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+10747A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708534 | ||||||
| chr13:38708536
|
C | T | 1 | a0006c0096t0015g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5263+10749C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708536 | ||||||
| chr13:38708590
|
G | A | 1 | a0009c0028t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.5263+10803G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708590 | ||||||
| chr13:38708663
|
A | G | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+10876A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708663 | ||||||
| chr13:38708710
|
T | A | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+10923T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708710 | ||||||
| chr13:38708831
|
C | G | 9 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0013g0202others(6): Show | 9 | HG00621.hp2 HG01167.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.5263+11044C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708831 | ||||||
| chr13:38708869
|
C | T | 1 | a0002c0091t0007g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5263+11082C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38708869 | ||||||
| chr13:38709317
|
A | G | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.5263+11530A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709317 | ||||||
| chr13:38709367
|
A | T | 1 | a0034c0088t0011g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5263+11580A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709367 | ||||||
| chr13:38709372
|
A | G | 2 | a0001c0002t0004g0141a0001c0002t0005g0140 | 2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.5263+11585A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709372 | ||||||
| chr13:38709457
|
A | G | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+11670A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709457 | ||||||
| chr13:38709464
|
T | C | 221 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(218): Show | 221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.5263+11677T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709464 | ||||||
| chr13:38709523
|
A | G | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5263+11736A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709523 | ||||||
| chr13:38709789
|
TTACCCTT others(1): Show |
T | 115 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(112): Show | 115 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.5263+12003_5263+12 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709789 | ||||||
| chr13:38709866
|
G | A | 1 | a0002c0027t0001g0021 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5263+12079G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709866 | ||||||
| chr13:38709869
|
C | T | 2 | a0015c0031t0003g0128a0015c0031t0003g0129 | 2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5263+12082C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709869 | ||||||
| chr13:38709892
|
C | T | 1 | a0001c0012t0050g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5263+12105C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38709892 | ||||||
| chr13:38709986
|
T | TAC | 4 | a0002c0077t0009g0139a0004c0004t0005g0065a0007c0025t0006g0221others(1): Show | 4 | HG02004.hp2 HG02083.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+12249_5263+12 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TAC | T | 16 | a0001c0001t0001g0155a0001c0001t0002g0183a0001c0002t0004g0154others(13): Show | 16 | HG01109.hp1 HG01175.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.5263+12249_5263+12 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACAC | T | 86 | a0001c0001t0001g0058a0001c0001t0001g0161a0001c0001t0001g0164others(83): Show | 86 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.5263+12247_5263+12 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACAC | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0158others(27): Show | 30 | HG00558.hp1 HG00642.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.5263+12245_5263+12 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(1): Show |
T | 18 | a0001c0002t0001g0156a0001c0002t0032g0238a0001c0029t0001g0149others(15): Show | 18 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.5263+12243_5263+12 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(3): Show |
T | 17 | a0001c0001t0027g0110a0001c0002t0004g0141a0001c0002t0005g0140others(14): Show | 17 | HG01175.hp1 HG01192.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.5263+12241_5263+12 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(5): Show |
T | 42 | a0001c0001t0013g0202a0001c0002t0004g0231a0002c0006t0001g0079others(39): Show | 42 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5263+12239_5263+12 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(7): Show |
T | 18 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(15): Show | 18 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.5263+12237_5263+12 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(9): Show |
T | 5 | a0006c0016t0052g0244a0019c0039t0011g0004a0020c0040t0003g0005others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5263+12235_5263+12 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38709986
|
TACACACA others(13): Show |
T | 1 | a0002c0091t0007g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5263+12231_5263+12 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38709986 | |||||
| chr13:38710026
|
CACACACA others(4): Show |
C | 1 | a0003c0003t0004g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5263+12241_5263+12 others(17): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38710026 | |||||
| chr13:38710032
|
CACACA | C | 3 | a0002c0011t0004g0218a0006c0095t0037g0152a0031c0056t0015g0125 | 3 | HG02027.hp1 HG02738.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.5263+12247_5263+12 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38710032 | |||||
| chr13:38710049
|
C | T | 6 | a0016c0059t0043g0101a0016c0060t0029g0106a0035c0062t0009g0105others(3): Show | 6 | HG02257.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.5263+12262C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38710049 | ||||||
| chr13:38710137
|
T | C | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+12350T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38710137 | ||||||
| chr13:38710558
|
G | T | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5263+12771G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38710558 | ||||||
| chr13:38710567
|
T | G | 1 | a0005c0035t0038g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5263+12780T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38710567 | ||||||
| chr13:38710663
|
C | T | 3 | a0019c0039t0011g0004a0020c0040t0003g0005a0025c0048t0003g0225 | 3 | HG01243.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+12876C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38710663 | ||||||
| chr13:38711071
|
C | T | 2 | a0001c0029t0002g0150a0001c0029t0025g0003 | 2 | NA18960.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.5263+13284C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711071 | ||||||
| chr13:38711172
|
A | G | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5263+13385A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711172 | ||||||
| chr13:38711215
|
C | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+13428C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711215 | ||||||
| chr13:38711352
|
G | C | 1 | a0004c0004t0012g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5263+13565G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711352 | ||||||
| chr13:38711445
|
C | T | 2 | a0004c0004t0003g0198a0004c0004t0012g0196 | 2 | HG01496.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.5263+13658C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711445 | ||||||
| chr13:38711525
|
A | G | 4 | a0012c0020t0017g0130a0018c0073t0002g0132a0030c0055t0003g0131others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5263+13738A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711525 | ||||||
| chr13:38711557
|
A | G | 1 | a0002c0092t0046g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5263+13770A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711557 | ||||||
| chr13:38711594
|
T | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+13807T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711594 | ||||||
| chr13:38711650
|
A | G | 61 | a0001c0002t0004g0232a0002c0006t0001g0030a0002c0006t0001g0033others(58): Show | 61 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.5263+13863A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711650 | ||||||
| chr13:38711815
|
G | T | 254 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(251): Show | 254 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.5263+14028G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711815 | ||||||
| chr13:38711913
|
C | CT | 18 | a0001c0002t0004g0231a0001c0070t0003g0095a0002c0011t0004g0217others(15): Show | 18 | HG00673.hp1 HG00741.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.5263+14151dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38711913 | |||||
| chr13:38711913
|
CT | C | 13 | a0001c0001t0027g0110a0001c0002t0032g0238a0003c0003t0005g0089others(10): Show | 13 | HG01109.hp2 HG01192.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5263+14151delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38711913 | |||||
| chr13:38711920
|
T | TC | 4 | a0001c0001t0001g0181a0001c0030t0047g0151a0002c0006t0002g0022others(1): Show | 4 | HG00639.hp1 HG01175.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+14133_5263+14 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711920 | ||||||
| chr13:38711921
|
T | C | 95 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.5263+14134T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711921 | ||||||
| chr13:38711922
|
T | C | 1 | a0009c0028t0001g0146 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.5263+14135T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711922 | ||||||
| chr13:38711966
|
C | A | 143 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(140): Show | 143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.5263+14179C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38711966 | ||||||
| chr13:38712043
|
C | T | 28 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(25): Show | 28 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+14256C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712043 | ||||||
| chr13:38712073
|
C | A | 34 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(31): Show | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.5263+14286C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712073 | ||||||
| chr13:38712159
|
G | A | 1 | a0001c0002t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5263+14372G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712159 | ||||||
| chr13:38712183
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+14396C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712183 | ||||||
| chr13:38712520
|
A | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+14733A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712520 | ||||||
| chr13:38712553
|
C | T | 2 | a0008c0019t0003g0121a0008c0051t0003g0120 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5263+14766C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712553 | ||||||
| chr13:38712650
|
TCA | T | 75 | a0001c0002t0003g0180a0001c0002t0004g0231a0001c0002t0004g0232others(72): Show | 75 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.5263+14888_5263+14 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38712650 | |||||
| chr13:38712650
|
TCACA | T | 146 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(143): Show | 146 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.5263+14886_5263+14 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38712650 | |||||
| chr13:38712650
|
TCACACA | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+14884_5263+14 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38712650 | |||||
| chr13:38712650
|
TCACACAC others(7): Show |
T | 1 | a0004c0089t0001g0239 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5263+14876_5263+14 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38712650 | |||||
| chr13:38712652
|
A | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+14865A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712652 | ||||||
| chr13:38712654
|
A | T | 72 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(69): Show | 72 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.5263+14867A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712654 | ||||||
| chr13:38712656
|
A | T | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+14869A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712656 | ||||||
| chr13:38712677
|
A | AAC | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+14904_5263+14 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38712677 | |||||
| chr13:38712759
|
T | C | 2 | a0004c0004t0011g0061a0004c0007t0001g0043 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5263+14972T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712759 | ||||||
| chr13:38712767
|
T | C | 13 | a0012c0020t0002g0126a0012c0020t0017g0130a0012c0020t0049g0124others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.5263+14980T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712767 | ||||||
| chr13:38712783
|
G | C | 1 | a0001c0001t0002g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5263+14996G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712783 | ||||||
| chr13:38712991
|
C | T | 1 | a0004c0093t0004g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5263+15204C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38712991 | ||||||
| chr13:38713004
|
C | T | 1 | a0005c0035t0038g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5263+15217C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713004 | ||||||
| chr13:38713013
|
A | T | 6 | a0016c0059t0043g0101a0016c0060t0029g0106a0035c0062t0009g0105others(3): Show | 6 | HG02257.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.5263+15226A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713013 | ||||||
| chr13:38713046
|
A | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+15259A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713046 | ||||||
| chr13:38713188
|
T | C | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+15401T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713188 | ||||||
| chr13:38713191
|
A | T | 3 | a0001c0029t0001g0149a0003c0005t0002g0060a0006c0095t0037g0152 | 3 | HG00423.hp2 HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.5263+15404A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713191 | ||||||
| chr13:38713192
|
G | T | 3 | a0001c0029t0001g0149a0003c0005t0002g0060a0006c0095t0037g0152 | 3 | HG00423.hp2 HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.5263+15405G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713192 | ||||||
| chr13:38713197
|
T | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(39): Show | 42 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.5263+15410T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713197 | ||||||
| chr13:38713214
|
G | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+15427G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713214 | ||||||
| chr13:38713239
|
G | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+15452G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713239 | ||||||
| chr13:38713344
|
C | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+15557C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713344 | ||||||
| chr13:38713352
|
A | G | 29 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5263+15565A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713352 | ||||||
| chr13:38713660
|
A | T | 160 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.5263+15873A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713660 | ||||||
| chr13:38713715
|
C | T | 1 | a0001c0002t0007g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5263+15928C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713715 | ||||||
| chr13:38713775
|
A | G | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+15988A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713775 | ||||||
| chr13:38713784
|
T | C | 221 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(218): Show | 221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.5263+15997T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713784 | ||||||
| chr13:38713872
|
C | A | 3 | a0001c0030t0003g0144a0001c0030t0003g0145a0006c0096t0015g0153 | 3 | HG02896.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5263+16085C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38713872 | ||||||
| chr13:38714077
|
G | A | 5 | a0012c0020t0002g0126a0015c0031t0003g0128a0015c0031t0003g0129others(2): Show | 5 | HG01884.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.5263+16290G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714077 | ||||||
| chr13:38714184
|
A | C | 100 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.5263+16397A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714184 | ||||||
| chr13:38714246
|
A | T | 29 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5263+16459A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714246 | ||||||
| chr13:38714371
|
TATAATTT others(8): Show |
T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+16586_5263+16 others(21): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38714371 | |||||
| chr13:38714388
|
A | C | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+16601A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714388 | ||||||
| chr13:38714389
|
A | C | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+16602A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714389 | ||||||
| chr13:38714390
|
A | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+16603A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714390 | ||||||
| chr13:38714491
|
A | T | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+16704A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714491 | ||||||
| chr13:38714685
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+16898C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714685 | ||||||
| chr13:38714815
|
T | A | 3 | a0010c0013t0003g0107a0053c0069t0003g0108a0055c0071t0031g0109 | 3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5263+17028T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714815 | ||||||
| chr13:38714883
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+17096C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714883 | ||||||
| chr13:38714930
|
CA | C | 189 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(186): Show | 189 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.5263+17155delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38714930 | |||||
| chr13:38714960
|
C | T | 18 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(15): Show | 18 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.5263+17173C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38714960 | ||||||
| chr13:38715002
|
A | G | 221 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(218): Show | 221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.5263+17215A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715002 | ||||||
| chr13:38715007
|
G | A | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+17220G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715007 | ||||||
| chr13:38715280
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+17493G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715280 | ||||||
| chr13:38715400
|
C | G | 25 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(22): Show | 25 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5263+17613C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715400 | ||||||
| chr13:38715554
|
C | T | 3 | a0003c0003t0003g0086a0003c0003t0004g0084a0003c0005t0002g0085 | 3 | HG03834.hp2 NA19004.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.5263+17767C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715554 | ||||||
| chr13:38715603
|
G | T | 3 | a0001c0001t0001g0178a0001c0068t0005g0160a0048c0065t0003g0100 | 3 | HG01257.hp1 HG02109.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5263+17816G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715603 | ||||||
| chr13:38715862
|
ATTAAT | A | 2 | a0002c0011t0004g0211a0002c0011t0004g0217 | 2 | HG03492.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.5263+18080_5263+18 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38715862 | |||||
| chr13:38715927
|
A | G | 2 | a0019c0039t0011g0004a0020c0040t0003g0005 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+18140A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38715927 | ||||||
| chr13:38716138
|
TA | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+18357delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38716138 | |||||
| chr13:38716144
|
A | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+18357A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716144 | ||||||
| chr13:38716432
|
C | T | 100 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.5263+18645C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716432 | ||||||
| chr13:38716443
|
A | G | 2 | a0019c0039t0011g0004a0020c0040t0003g0005 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+18656A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716443 | ||||||
| chr13:38716694
|
G | A | 29 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5263+18907G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716694 | ||||||
| chr13:38716767
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+18980C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716767 | ||||||
| chr13:38716797
|
C | T | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5263+19010C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716797 | ||||||
| chr13:38716933
|
G | A | 28 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(25): Show | 28 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+19146G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38716933 | ||||||
| chr13:38717022
|
T | C | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+19235T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717022 | ||||||
| chr13:38717160
|
ATTTAT | A | 10 | a0004c0004t0004g0063a0004c0004t0005g0064a0004c0004t0005g0065others(7): Show | 10 | HG01109.hp1 HG01981.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.5263+19377_5263+19 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717160 | |||||
| chr13:38717291
|
A | G | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5263+19504A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717291 | ||||||
| chr13:38717390
|
C | T | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+19603C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717390 | ||||||
| chr13:38717412
|
C | CT | 8 | a0001c0002t0004g0232a0004c0004t0005g0009a0004c0089t0001g0239others(5): Show | 8 | HG01109.hp2 HG01169.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.5263+19647dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717412 | |||||
| chr13:38717412
|
C | CTT | 5 | a0015c0031t0003g0128a0015c0031t0003g0129a0018c0073t0002g0132others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+19646_5263+19 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717412 | |||||
| chr13:38717412
|
C | CTTT | 86 | a0001c0001t0001g0161a0001c0002t0001g0135a0001c0002t0001g0156others(83): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.5263+19645_5263+19 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717412 | |||||
| chr13:38717412
|
C | CTTTT | 88 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0164others(85): Show | 88 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.5263+19644_5263+19 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717412 | |||||
| chr13:38717412
|
C | CTTTTT | 6 | a0001c0002t0004g0184a0001c0030t0047g0151a0002c0006t0002g0022others(3): Show | 6 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.5263+19643_5263+19 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717412 | |||||
| chr13:38717439
|
C | T | 4 | a0009c0028t0001g0143a0009c0028t0001g0146a0009c0028t0001g0148others(1): Show | 4 | NA18992.hp1 NA19003.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.5263+19652C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717439 | ||||||
| chr13:38717579
|
G | GCTAATTT others(304): Show |
2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+19809_5263+19 others(317): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38717579 | |||||
| chr13:38717710
|
C | T | 6 | a0003c0003t0002g0067a0003c0003t0004g0083a0003c0003t0005g0082others(3): Show | 6 | HG00423.hp1 HG02129.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5263+19923C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717710 | ||||||
| chr13:38717756
|
G | A | 3 | a0018c0073t0002g0132a0030c0055t0003g0131a0034c0088t0011g0226 | 3 | HG02572.hp1 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5263+19969G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717756 | ||||||
| chr13:38717788
|
G | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+20001G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717788 | ||||||
| chr13:38717950
|
T | C | 1 | a0046c0083t0002g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5263+20163T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38717950 | ||||||
| chr13:38718012
|
C | A | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5263+20225C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718012 | ||||||
| chr13:38718017
|
A | G | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+20230A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718017 | ||||||
| chr13:38718121
|
G | C | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+20334G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718121 | ||||||
| chr13:38718154
|
G | T | 1 | a0003c0003t0004g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5263+20367G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718154 | ||||||
| chr13:38718312
|
A | T | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5263+20525A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718312 | ||||||
| chr13:38718384
|
A | G | 3 | a0012c0020t0002g0126a0012c0020t0049g0124a0031c0056t0015g0125 | 3 | HG02809.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5263+20597A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718384 | ||||||
| chr13:38718394
|
T | C | 13 | a0012c0020t0002g0126a0012c0020t0017g0130a0012c0020t0049g0124others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.5263+20607T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718394 | ||||||
| chr13:38718435
|
A | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+20648A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718435 | ||||||
| chr13:38718540
|
C | T | 2 | a0019c0039t0011g0004a0020c0040t0003g0005 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5263+20753C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718540 | ||||||
| chr13:38718549
|
C | A | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5263+20762C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718549 | ||||||
| chr13:38718661
|
C | CA | 29 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5263+20880dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38718661 | |||||
| chr13:38718680
|
T | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+20893T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718680 | ||||||
| chr13:38718683
|
AAG | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+20900_5263+20 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38718683 | |||||
| chr13:38718805
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5263+21018G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718805 | ||||||
| chr13:38718859
|
C | G | 1 | a0004c0004t0004g0008 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5263+21072C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718859 | ||||||
| chr13:38718897
|
G | A | 1 | a0002c0027t0001g0029 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5263+21110G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38718897 | ||||||
| chr13:38719107
|
A | G | 189 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(186): Show | 189 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.5263+21320A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38719107 | ||||||
| chr13:38719214
|
G | A | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+21427G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38719214 | ||||||
| chr13:38719302
|
C | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+21515C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38719302 | ||||||
| chr13:38719388
|
T | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+21601T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38719388 | ||||||
| chr13:38719453
|
T | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+21666T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38719453 | ||||||
| chr13:38720219
|
T | C | 1 | a0034c0088t0011g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5263+22432T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720219 | ||||||
| chr13:38720228
|
T | C | 28 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(25): Show | 28 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+22441T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720228 | ||||||
| chr13:38720292
|
C | G | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+22505C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720292 | ||||||
| chr13:38720593
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(24): Show | 27 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.5263+22806G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720593 | ||||||
| chr13:38720656
|
C | T | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5263+22869C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720656 | ||||||
| chr13:38720661
|
T | C | 189 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(186): Show | 189 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.5263+22874T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720661 | ||||||
| chr13:38720696
|
AG | A | 100 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.5263+22912delG | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38720696 | |||||
| chr13:38720729
|
C | T | 1 | a0002c0008t0001g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5263+22942C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720729 | ||||||
| chr13:38720862
|
G | A | 221 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(218): Show | 221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.5263+23075G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720862 | ||||||
| chr13:38720960
|
C | G | 1 | a0021c0044t0056g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5263+23173C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38720960 | ||||||
| chr13:38721072
|
T | C | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+23285T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721072 | ||||||
| chr13:38721119
|
A | G | 1 | a0003c0005t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5263+23332A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721119 | ||||||
| chr13:38721209
|
GT | G | 33 | a0001c0002t0004g0232a0004c0004t0004g0007a0004c0004t0004g0008others(30): Show | 33 | HG00741.hp1 HG01109.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.5263+23425delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38721209 | |||||
| chr13:38721319
|
G | A | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+23532G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721319 | ||||||
| chr13:38721363
|
A | G | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5263+23576A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721363 | ||||||
| chr13:38721433
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+23646G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721433 | ||||||
| chr13:38721456
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+23669G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721456 | ||||||
| chr13:38721467
|
C | A | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+23680C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721467 | ||||||
| chr13:38721486
|
A | G | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.5263+23699A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721486 | ||||||
| chr13:38721667
|
A | C | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5263+23880A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721667 | ||||||
| chr13:38721667
|
A | G | 42 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(39): Show | 42 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.5263+23880A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721667 | ||||||
| chr13:38721895
|
T | C | 1 | a0001c0002t0006g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5263+24108T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721895 | ||||||
| chr13:38721973
|
C | T | 1 | a0001c0002t0004g0231 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5263+24186C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38721973 | ||||||
| chr13:38722012
|
A | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+24225A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722012 | ||||||
| chr13:38722128
|
TC | T | 3 | a0018c0073t0002g0132a0030c0055t0003g0131a0034c0088t0011g0226 | 3 | HG02572.hp1 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5263+24343delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722128 | |||||
| chr13:38722160
|
G | A | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5263+24373G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722160 | ||||||
| chr13:38722167
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+24380G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722167 | ||||||
| chr13:38722300
|
G | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+24513G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722300 | ||||||
| chr13:38722311
|
C | T | 2 | a0004c0004t0003g0198a0004c0004t0012g0196 | 2 | HG01496.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.5263+24524C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722311 | ||||||
| chr13:38722361
|
A | AAT | 23 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(20): Show | 23 | HG00438.hp2 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.5263+24589_5263+24 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722361 | |||||
| chr13:38722361
|
A | AATAT | 29 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(26): Show | 29 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.5263+24587_5263+24 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722361 | |||||
| chr13:38722361
|
A | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+24574A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722361 | ||||||
| chr13:38722526
|
G | T | 10 | a0004c0004t0004g0063a0004c0004t0005g0064a0004c0004t0005g0065others(7): Show | 10 | HG01109.hp1 HG01981.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.5263+24739G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722526 | ||||||
| chr13:38722744
|
C | T | 4 | a0001c0002t0032g0238a0015c0031t0003g0128a0015c0031t0003g0129others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.5263+24957C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722744 | ||||||
| chr13:38722745
|
G | GT | 78 | a0001c0001t0001g0177a0001c0001t0001g0192a0001c0002t0004g0231others(75): Show | 78 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.5263+24973dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722745 | |||||
| chr13:38722745
|
G | GTT | 42 | a0001c0033t0010g0136a0002c0006t0001g0079a0002c0008t0001g0208others(39): Show | 42 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.5263+24972_5263+24 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722745 | |||||
| chr13:38722745
|
G | GTTT | 9 | a0004c0004t0005g0009a0004c0007t0001g0014a0007c0037t0030g0041others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.5263+24971_5263+24 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38722745 | |||||
| chr13:38722748
|
T | A | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+24961T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722748 | ||||||
| chr13:38722779
|
C | T | 14 | a0012c0020t0017g0130a0012c0020t0049g0124a0014c0022t0014g0193others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.5263+24992C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722779 | ||||||
| chr13:38722801
|
A | G | 1 | a0004c0004t0003g0198 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5263+25014A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722801 | ||||||
| chr13:38722903
|
A | C | 1 | a0012c0020t0049g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5263+25116A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722903 | ||||||
| chr13:38722966
|
C | T | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5263+25179C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38722966 | ||||||
| chr13:38723078
|
T | TA | 11 | a0012c0020t0017g0130a0012c0020t0049g0124a0015c0031t0003g0128others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.5263+25292dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38723078 | |||||
| chr13:38723143
|
G | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+25356G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723143 | ||||||
| chr13:38723266
|
T | A | 254 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(251): Show | 254 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.5263+25479T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723266 | ||||||
| chr13:38723552
|
G | C | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5263+25765G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723552 | ||||||
| chr13:38723670
|
C | G | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5263+25883C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723670 | ||||||
| chr13:38723690
|
A | G | 1 | a0002c0011t0004g0217 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5263+25903A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723690 | ||||||
| chr13:38723714
|
T | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5263+25927T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723714 | ||||||
| chr13:38723722
|
C | T | 2 | a0002c0027t0001g0027a0002c0091t0007g0040 | 2 | HG00741.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.5263+25935C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723722 | ||||||
| chr13:38723942
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+26155G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723942 | ||||||
| chr13:38723956
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+26169G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38723956 | ||||||
| chr13:38724151
|
C | T | 32 | a0002c0006t0001g0030a0002c0006t0001g0033a0002c0006t0001g0038others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.5263+26364C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724151 | ||||||
| chr13:38724432
|
T | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+26645T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724432 | ||||||
| chr13:38724485
|
A | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+26698A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724485 | ||||||
| chr13:38724649
|
C | T | 1 | a0033c0057t0022g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5263+26862C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724649 | ||||||
| chr13:38724708
|
G | C | 7 | a0012c0020t0002g0126a0016c0059t0043g0101a0016c0060t0029g0106others(4): Show | 7 | HG02257.hp2 HG02965.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.5263+26921G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724708 | ||||||
| chr13:38724725
|
A | T | 1 | a0039c0086t0003g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5263+26938A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724725 | ||||||
| chr13:38724893
|
G | A | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+27106G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724893 | ||||||
| chr13:38724969
|
C | A | 1 | a0005c0015t0002g0207 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5263+27182C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38724969 | ||||||
| chr13:38725134
|
A | C | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5263+27347A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725134 | ||||||
| chr13:38725355
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+27568G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725355 | ||||||
| chr13:38725371
|
C | CAT | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+27585_5263+27 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38725371 | |||||
| chr13:38725492
|
G | A | 11 | a0012c0020t0017g0130a0012c0020t0049g0124a0015c0031t0003g0128others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.5263+27705G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725492 | ||||||
| chr13:38725585
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+27798G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725585 | ||||||
| chr13:38725653
|
G | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+27866G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725653 | ||||||
| chr13:38725723
|
G | A | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+27936G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725723 | ||||||
| chr13:38725933
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+28146A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38725933 | ||||||
| chr13:38726030
|
T | C | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5263+28243T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726030 | ||||||
| chr13:38726099
|
G | A | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+28312G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726099 | ||||||
| chr13:38726230
|
G | A | 1 | a0002c0006t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5263+28443G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726230 | ||||||
| chr13:38726336
|
T | C | 197 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(194): Show | 197 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.5263+28549T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726336 | ||||||
| chr13:38726551
|
A | G | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+28764A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726551 | ||||||
| chr13:38726749
|
A | G | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5263+28962A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726749 | ||||||
| chr13:38726798
|
C | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+29011C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726798 | ||||||
| chr13:38726849
|
G | T | 1 | a0019c0039t0011g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5263+29062G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726849 | ||||||
| chr13:38726973
|
A | G | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5263+29186A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38726973 | ||||||
| chr13:38727000
|
C | G | 22 | a0001c0001t0018g0057a0001c0009t0008g0247a0001c0009t0008g0253others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.5263+29213C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727000 | ||||||
| chr13:38727017
|
T | C | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+29230T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727017 | ||||||
| chr13:38727202
|
T | C | 197 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(194): Show | 197 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.5263+29415T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727202 | ||||||
| chr13:38727299
|
A | C | 24 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.5263+29512A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727299 | ||||||
| chr13:38727309
|
C | T | 1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5263+29522C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727309 | ||||||
| chr13:38727316
|
C | T | 107 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(104): Show | 107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.5263+29529C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727316 | ||||||
| chr13:38727434
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+29647A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727434 | ||||||
| chr13:38727546
|
A | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+29759A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727546 | ||||||
| chr13:38727698
|
G | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5263+29911G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727698 | ||||||
| chr13:38727705
|
G | T | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5263+29918G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727705 | ||||||
| chr13:38727805
|
A | AATG | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5263+30020_5263+30 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38727805 | |||||
| chr13:38727865
|
A | G | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5263+30078A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38727865 | ||||||
| chr13:38728148
|
C | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+30361C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728148 | ||||||
| chr13:38728274
|
A | G | 4 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+30487A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728274 | ||||||
| chr13:38728355
|
A | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5263+30568A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728355 | ||||||
| chr13:38728545
|
A | G | 1 | a0001c0068t0005g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5263+30758A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728545 | ||||||
| chr13:38728639
|
T | A | 2 | a0004c0004t0011g0061a0004c0007t0001g0043 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5263+30852T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728639 | ||||||
| chr13:38728699
|
AC | A | 254 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(251): Show | 254 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.5263+30915delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38728699 | |||||
| chr13:38728898
|
C | T | 2 | a0012c0020t0049g0124a0031c0056t0015g0125 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5263+31111C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38728898 | ||||||
| chr13:38729077
|
C | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5263+31290C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729077 | ||||||
| chr13:38729185
|
AT | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+31408delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38729185 | |||||
| chr13:38729206
|
C | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5263+31419C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729206 | ||||||
| chr13:38729358
|
T | C | 4 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5263+31571T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729358 | ||||||
| chr13:38729384
|
T | C | 2 | a0020c0040t0003g0005a0025c0048t0003g0225 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5263+31597T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729384 | ||||||
| chr13:38729467
|
T | C | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5263+31680T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729467 | ||||||
| chr13:38729510
|
T | A | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5263+31723T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729510 | ||||||
| chr13:38729574
|
ACT | A | 10 | a0001c0002t0004g0231a0003c0003t0004g0069a0003c0003t0004g0078others(7): Show | 10 | HG00673.hp1 HG02071.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.5263+31791_5263+31 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38729574 | |||||
| chr13:38729659
|
G | C | 36 | a0001c0001t0018g0057a0001c0002t0004g0232a0001c0070t0003g0095others(33): Show | 36 | HG00741.hp1 HG01109.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.5263+31872G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729659 | ||||||
| chr13:38729835
|
G | A | 1 | a0001c0001t0027g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5263+32048G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729835 | ||||||
| chr13:38729864
|
G | A | 2 | a0020c0040t0003g0005a0025c0048t0003g0225 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5263+32077G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729864 | ||||||
| chr13:38729938
|
T | C | 1 | a0003c0003t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5263+32151T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38729938 | ||||||
| chr13:38730142
|
A | G | 105 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(102): Show | 105 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.5263+32355A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730142 | ||||||
| chr13:38730310
|
T | C | 1 | a0029c0049t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5263+32523T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730310 | ||||||
| chr13:38730319
|
G | A | 10 | a0012c0020t0049g0124a0015c0031t0003g0128a0015c0031t0003g0129others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.5263+32532G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730319 | ||||||
| chr13:38730386
|
G | A | 1 | a0041c0079t0039g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5263+32599G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730386 | ||||||
| chr13:38730414
|
C | T | 10 | a0012c0020t0049g0124a0015c0031t0003g0128a0015c0031t0003g0129others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.5263+32627C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730414 | ||||||
| chr13:38730533
|
A | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5263+32746A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730533 | ||||||
| chr13:38730677
|
G | A | 115 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(112): Show | 115 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.5263+32890G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730677 | ||||||
| chr13:38730770
|
A | G | 6 | a0008c0019t0003g0118a0008c0019t0003g0121a0008c0051t0003g0120others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5263+32983A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730770 | ||||||
| chr13:38730930
|
G | GT | 171 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(168): Show | 171 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.5263+33155dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38730930 | |||||
| chr13:38730983
|
T | C | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5263+33196T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38730983 | ||||||
| chr13:38731037
|
C | T | 5 | a0012c0020t0002g0126a0016c0059t0043g0101a0036c0061t0003g0102others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+33250C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731037 | ||||||
| chr13:38731038
|
T | A | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5263+33251T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731038 | ||||||
| chr13:38731246
|
A | G | 113 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.5264-33058A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731246 | ||||||
| chr13:38731276
|
T | C | 110 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(107): Show | 110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.5264-33028T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731276 | ||||||
| chr13:38731281
|
A | T | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5264-33023A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731281 | ||||||
| chr13:38731409
|
A | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5264-32895A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731409 | ||||||
| chr13:38731455
|
A | AT | 4 | a0012c0020t0017g0130a0018c0073t0002g0132a0030c0055t0003g0131others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-32847dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38731455 | |||||
| chr13:38731538
|
C | T | 19 | a0004c0004t0004g0007a0004c0004t0004g0008a0004c0004t0005g0009others(16): Show | 19 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.5264-32766C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731538 | ||||||
| chr13:38731605
|
G | A | 2 | a0012c0020t0049g0124a0031c0056t0015g0125 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5264-32699G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731605 | ||||||
| chr13:38731659
|
G | A | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5264-32645G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731659 | ||||||
| chr13:38731666
|
G | A | 2 | a0020c0040t0003g0005a0025c0048t0003g0225 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5264-32638G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731666 | ||||||
| chr13:38731757
|
G | A | 2 | a0020c0040t0003g0005a0025c0048t0003g0225 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5264-32547G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38731757 | ||||||
| chr13:38732003
|
T | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-32301T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732003 | ||||||
| chr13:38732272
|
G | C | 43 | a0001c0002t0004g0231a0002c0006t0001g0079a0002c0010t0004g0068others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5264-32032G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732272 | ||||||
| chr13:38732280
|
C | T | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5264-32024C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732280 | ||||||
| chr13:38732327
|
A | G | 197 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(194): Show | 197 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.5264-31977A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732327 | ||||||
| chr13:38732466
|
A | T | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5264-31838A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732466 | ||||||
| chr13:38732553
|
G | A | 47 | a0001c0029t0001g0149a0001c0029t0002g0150a0001c0029t0025g0003others(44): Show | 47 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.5264-31751G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732553 | ||||||
| chr13:38732586
|
G | A | 4 | a0008c0019t0012g0115a0011c0018t0003g0114a0027c0053t0041g0116others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-31718G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732586 | ||||||
| chr13:38732888
|
T | G | 107 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(104): Show | 107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.5264-31416T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732888 | ||||||
| chr13:38732987
|
A | G | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-31317A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38732987 | ||||||
| chr13:38733207
|
G | A | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5264-31097G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733207 | ||||||
| chr13:38733211
|
C | G | 1 | a0012c0020t0049g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5264-31093C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733211 | ||||||
| chr13:38733296
|
T | C | 1 | a0004c0004t0005g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5264-31008T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733296 | ||||||
| chr13:38733303
|
C | T | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5264-31001C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733303 | ||||||
| chr13:38733314
|
GT | G | 212 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(209): Show | 212 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.5264-30977delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38733314 | |||||
| chr13:38733564
|
A | G | 1 | a0013c0023t0016g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5264-30740A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733564 | ||||||
| chr13:38733579
|
G | A | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5264-30725G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733579 | ||||||
| chr13:38733599
|
G | T | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5264-30705G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733599 | ||||||
| chr13:38733614
|
TTA | T | 9 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0013g0202others(6): Show | 9 | HG00621.hp2 HG01167.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.5264-30682_5264-30 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38733614 | |||||
| chr13:38733637
|
A | T | 212 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(209): Show | 212 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.5264-30667A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733637 | ||||||
| chr13:38733746
|
A | G | 2 | a0001c0001t0018g0057a0001c0070t0003g0095 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.5264-30558A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733746 | ||||||
| chr13:38733747
|
A | G | 99 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(96): Show | 99 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.5264-30557A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733747 | ||||||
| chr13:38733778
|
G | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-30526G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733778 | ||||||
| chr13:38733871
|
A | G | 3 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197 | 3 | HG01496.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5264-30433A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733871 | ||||||
| chr13:38733876
|
A | C | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5264-30428A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733876 | ||||||
| chr13:38733963
|
A | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5264-30341A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38733963 | ||||||
| chr13:38734147
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0185others(3): Show | 6 | HG00673.hp2 NA18970.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.5264-30157G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734147 | ||||||
| chr13:38734164
|
C | CA | 4 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-30139dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38734164 | |||||
| chr13:38734166
|
C | A | 4 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-30138C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734166 | ||||||
| chr13:38734371
|
C | T | 1 | a0027c0053t0041g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5264-29933C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734371 | ||||||
| chr13:38734372
|
G | T | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5264-29932G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734372 | ||||||
| chr13:38734476
|
T | C | 3 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197 | 3 | HG01496.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5264-29828T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734476 | ||||||
| chr13:38734648
|
C | A | 5 | a0009c0028t0001g0143a0009c0028t0001g0146a0009c0028t0001g0148others(2): Show | 5 | NA18992.hp1 NA18994.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-29656C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734648 | ||||||
| chr13:38734651
|
T | A | 195 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(192): Show | 195 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.5264-29653T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734651 | ||||||
| chr13:38734700
|
TA | T | 22 | a0001c0001t0018g0057a0001c0009t0008g0247a0001c0009t0008g0253others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.5264-29601delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38734700 | |||||
| chr13:38734738
|
C | CT | 143 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(140): Show | 143 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.5264-29542dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38734738 | |||||
| chr13:38734738
|
C | CTT | 9 | a0001c0001t0028g0056a0001c0002t0004g0054a0001c0002t0004g0184others(6): Show | 9 | HG00642.hp1 HG01943.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.5264-29543_5264-29 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38734738 | |||||
| chr13:38734738
|
CT | C | 14 | a0003c0003t0036g0073a0004c0004t0004g0063a0007c0025t0006g0221others(11): Show | 14 | HG01884.hp1 HG02004.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5264-29542delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38734738 | |||||
| chr13:38734810
|
G | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-29494G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734810 | ||||||
| chr13:38734937
|
G | A | 1 | a0012c0020t0049g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5264-29367G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734937 | ||||||
| chr13:38734955
|
C | G | 2 | a0012c0020t0049g0124a0031c0056t0015g0125 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5264-29349C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38734955 | ||||||
| chr13:38735084
|
T | A | 2 | a0003c0003t0034g0081a0003c0005t0001g0080 | 2 | HG02129.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.5264-29220T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38735084 | ||||||
| chr13:38735323
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5264-28981T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38735323 | ||||||
| chr13:38735325
|
A | G | 2 | a0003c0003t0007g0076a0003c0003t0036g0073 | 2 | NA18940.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.5264-28979A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38735325 | ||||||
| chr13:38735383
|
G | A | 199 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(196): Show | 199 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.5264-28921G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38735383 | ||||||
| chr13:38735592
|
TA | T | 4 | a0012c0020t0017g0130a0018c0073t0002g0132a0030c0055t0003g0131others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-28704delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38735592 | |||||
| chr13:38735849
|
G | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-28455G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38735849 | ||||||
| chr13:38736033
|
G | A | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5264-28271G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38736033 | ||||||
| chr13:38736058
|
T | C | 102 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(99): Show | 102 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.5264-28246T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38736058 | ||||||
| chr13:38736609
|
A | G | 47 | a0001c0002t0004g0231a0001c0029t0002g0150a0002c0006t0001g0079others(44): Show | 47 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.5264-27695A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38736609 | ||||||
| chr13:38736867
|
GT | G | 182 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(179): Show | 182 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.5264-27427delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38736867 | |||||
| chr13:38736868
|
T | A | 2 | a0012c0020t0049g0124a0031c0056t0015g0125 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5264-27436T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38736868 | ||||||
| chr13:38737511
|
T | G | 4 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-26793T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38737511 | ||||||
| chr13:38738077
|
G | A | 1 | a0001c0033t0010g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5264-26227G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38738077 | ||||||
| chr13:38738191
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5264-26113A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38738191 | ||||||
| chr13:38738565
|
C | CA | 7 | a0002c0010t0004g0068a0012c0020t0049g0124a0015c0031t0003g0128others(4): Show | 7 | HG01433.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-25713dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738565 | |||||
| chr13:38738565
|
CA | C | 94 | a0001c0001t0018g0057a0001c0002t0004g0231a0001c0002t0004g0232others(91): Show | 94 | HG00438.hp2 HG00558.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.5264-25713delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738565 | |||||
| chr13:38738565
|
CAA | C | 27 | a0004c0004t0004g0007a0004c0004t0004g0063a0004c0004t0005g0009others(24): Show | 27 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.5264-25714_5264-25 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738565 | |||||
| chr13:38738565
|
CAAAAAAA others(6): Show |
C | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-25725_5264-25 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738565 | |||||
| chr13:38738565
|
CAAAAAAA others(9): Show |
C | 1 | a0004c0004t0005g0011 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.5264-25728_5264-25 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738565 | |||||
| chr13:38738567
|
A | AAT | 19 | a0001c0001t0001g0158a0001c0001t0001g0166a0001c0001t0001g0168others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.5264-25736_5264-25 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38738567 | |||||
| chr13:38738568
|
A | AT | 80 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.5264-25736_5264-25 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38738568 | ||||||
| chr13:38738569
|
A | T | 9 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0005g0140others(6): Show | 9 | HG01167.hp1 HG01167.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.5264-25735A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38738569 | ||||||
| chr13:38738590
|
A | G | 9 | a0001c0002t0004g0141a0001c0002t0005g0140a0006c0021t0002g0186others(6): Show | 9 | HG00738.hp1 HG02257.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.5264-25714A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38738590 | ||||||
| chr13:38739028
|
A | G | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5264-25276A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739028 | ||||||
| chr13:38739063
|
A | G | 3 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111 | 3 | HG01192.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5264-25241A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739063 | ||||||
| chr13:38739169
|
C | A | 2 | a0012c0020t0049g0124a0031c0056t0015g0125 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5264-25135C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739169 | ||||||
| chr13:38739224
|
T | C | 3 | a0010c0013t0003g0107a0053c0069t0003g0108a0055c0071t0031g0109 | 3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5264-25080T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739224 | ||||||
| chr13:38739364
|
C | T | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-24940C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739364 | ||||||
| chr13:38739398
|
T | C | 3 | a0001c0009t0008g0247a0006c0016t0021g0246a0052c0045t0054g0257 | 3 | HG01884.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5264-24906T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739398 | ||||||
| chr13:38739522
|
G | A | 47 | a0001c0002t0004g0231a0001c0029t0002g0150a0002c0006t0001g0079others(44): Show | 47 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.5264-24782G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739522 | ||||||
| chr13:38739589
|
A | G | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-24715A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739589 | ||||||
| chr13:38739597
|
A | G | 1 | a0002c0011t0004g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5264-24707A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739597 | ||||||
| chr13:38739609
|
A | G | 1 | a0013c0023t0002g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5264-24695A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739609 | ||||||
| chr13:38739658
|
C | T | 2 | a0002c0006t0001g0096a0005c0014t0040g0098 | 2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.5264-24646C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739658 | ||||||
| chr13:38739679
|
C | T | 3 | a0002c0006t0001g0033a0002c0010t0004g0034a0002c0010t0004g0035 | 3 | NA18747.hp2 NA18963.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.5264-24625C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739679 | ||||||
| chr13:38739727
|
A | C | 1 | a0005c0026t0002g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5264-24577A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739727 | ||||||
| chr13:38739752
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5264-24552G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739752 | ||||||
| chr13:38739830
|
T | C | 193 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(190): Show | 193 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.5264-24474T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38739830 | ||||||
| chr13:38740094
|
A | AT | 255 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.5264-24209dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38740094 | |||||
| chr13:38740569
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0058 | 2 | HG02074.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.5264-23735C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38740569 | ||||||
| chr13:38740668
|
G | T | 3 | a0018c0073t0002g0132a0030c0055t0003g0131a0034c0088t0011g0226 | 3 | HG02572.hp1 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5264-23636G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38740668 | ||||||
| chr13:38740677
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5264-23627G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38740677 | ||||||
| chr13:38740718
|
A | G | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-23586A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38740718 | ||||||
| chr13:38741588
|
A | G | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5264-22716A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38741588 | ||||||
| chr13:38741667
|
C | T | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-22637C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38741667 | ||||||
| chr13:38741669
|
A | G | 1 | a0030c0055t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5264-22635A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38741669 | ||||||
| chr13:38741726
|
T | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5264-22578T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38741726 | ||||||
| chr13:38742021
|
T | C | 1 | a0001c0002t0004g0169 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5264-22283T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742021 | ||||||
| chr13:38742510
|
T | C | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5264-21794T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742510 | ||||||
| chr13:38742531
|
A | G | 255 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.5264-21773A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742531 | ||||||
| chr13:38742535
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.5264-21769C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742535 | ||||||
| chr13:38742536
|
G | A | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-21768G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742536 | ||||||
| chr13:38742654
|
G | A | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5264-21650G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742654 | ||||||
| chr13:38742676
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5264-21628G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742676 | ||||||
| chr13:38742813
|
G | T | 94 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(91): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.5264-21491G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742813 | ||||||
| chr13:38742916
|
G | A | 184 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(181): Show | 184 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.5264-21388G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38742916 | ||||||
| chr13:38743192
|
A | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-21112A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743192 | ||||||
| chr13:38743198
|
C | T | 3 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197 | 3 | HG01496.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5264-21106C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743198 | ||||||
| chr13:38743463
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5264-20841T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743463 | ||||||
| chr13:38743504
|
A | G | 2 | a0001c0009t0008g0262a0001c0017t0055g0256 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5264-20800A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743504 | ||||||
| chr13:38743831
|
G | A | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.5264-20473G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743831 | ||||||
| chr13:38743868
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5264-20436T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743868 | ||||||
| chr13:38743936
|
G | A | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-20368G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38743936 | ||||||
| chr13:38744203
|
C | CT | 17 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0214others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.5264-20076dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38744203 | |||||
| chr13:38744203
|
CT | C | 55 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(52): Show | 55 | HG00558.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.5264-20076delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38744203 | |||||
| chr13:38744203
|
CTT | C | 165 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(162): Show | 165 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.5264-20077_5264-20 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38744203 | |||||
| chr13:38744203
|
CTTT | C | 9 | a0001c0002t0032g0238a0001c0029t0001g0149a0003c0003t0002g0067others(6): Show | 9 | HG01884.hp1 HG02155.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.5264-20078_5264-20 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38744203 | |||||
| chr13:38744252
|
C | A | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-20052C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744252 | ||||||
| chr13:38744308
|
T | A | 1 | a0001c0002t0001g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5264-19996T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744308 | ||||||
| chr13:38744409
|
G | C | 1 | a0003c0005t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5264-19895G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744409 | ||||||
| chr13:38744534
|
C | G | 1 | a0018c0073t0002g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5264-19770C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744534 | ||||||
| chr13:38744544
|
C | T | 185 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(182): Show | 185 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.5264-19760C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744544 | ||||||
| chr13:38744576
|
C | T | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5264-19728C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744576 | ||||||
| chr13:38744579
|
C | T | 44 | a0001c0002t0004g0231a0001c0029t0002g0150a0002c0006t0001g0079others(41): Show | 44 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.5264-19725C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744579 | ||||||
| chr13:38744585
|
G | A | 47 | a0001c0002t0004g0231a0001c0029t0002g0150a0002c0006t0001g0079others(44): Show | 47 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.5264-19719G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744585 | ||||||
| chr13:38744638
|
C | T | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5264-19666C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744638 | ||||||
| chr13:38744649
|
G | A | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5264-19655G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744649 | ||||||
| chr13:38744909
|
C | T | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5264-19395C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744909 | ||||||
| chr13:38744998
|
T | C | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5264-19306T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38744998 | ||||||
| chr13:38745116
|
A | T | 1 | a0002c0010t0004g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5264-19188A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38745116 | ||||||
| chr13:38745322
|
C | T | 1 | a0007c0025t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5264-18982C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38745322 | ||||||
| chr13:38745385
|
C | CTATCCCA others(52): Show |
1 | a0058c0047t0002g0210 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5264-18907_5264-18 others(65): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38745385 | |||||
| chr13:38745506
|
A | G | 1 | a0006c0016t0021g0246 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5264-18798A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38745506 | ||||||
| chr13:38745517
|
G | T | 180 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(177): Show | 180 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.5264-18787G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38745517 | ||||||
| chr13:38745595
|
AGTCTAGG others(3): Show |
A | 1 | a0002c0010t0004g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5264-18707_5264-18 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38745595 | |||||
| chr13:38745763
|
C | A | 1 | a0002c0091t0007g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5264-18541C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38745763 | ||||||
| chr13:38746021
|
G | A | 31 | a0001c0001t0018g0057a0001c0070t0003g0095a0004c0004t0004g0007others(28): Show | 31 | HG00738.hp1 HG00741.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.5264-18283G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746021 | ||||||
| chr13:38746157
|
C | A | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-18147C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746157 | ||||||
| chr13:38746225
|
A | G | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5264-18079A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746225 | ||||||
| chr13:38746254
|
G | C | 1 | a0026c0052t0003g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5264-18050G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746254 | ||||||
| chr13:38746279
|
A | G | 1 | a0006c0016t0021g0246 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5264-18025A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746279 | ||||||
| chr13:38746398
|
A | G | 1 | a0007c0037t0030g0041 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5264-17906A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746398 | ||||||
| chr13:38746514
|
G | T | 3 | a0002c0077t0009g0139a0014c0022t0003g0001a0014c0022t0003g0002 | 3 | HG03486.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-17790G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746514 | ||||||
| chr13:38746566
|
C | G | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-17738C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746566 | ||||||
| chr13:38746624
|
A | G | 109 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(106): Show | 109 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.5264-17680A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746624 | ||||||
| chr13:38746640
|
G | A | 1 | a0001c0029t0002g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.5264-17664G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746640 | ||||||
| chr13:38746685
|
A | G | 3 | a0004c0004t0004g0063a0004c0004t0005g0064a0004c0004t0005g0065 | 3 | HG02083.hp1 NA18995.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.5264-17619A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746685 | ||||||
| chr13:38746705
|
A | G | 3 | a0002c0077t0009g0139a0014c0022t0003g0001a0014c0022t0003g0002 | 3 | HG03486.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-17599A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38746705 | ||||||
| chr13:38746892
|
TG | T | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-17410delG | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38746892 | |||||
| chr13:38747162
|
A | G | 7 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(4): Show | 7 | HG01192.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-17142A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747162 | ||||||
| chr13:38747228
|
T | C | 102 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(99): Show | 102 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.5264-17076T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747228 | ||||||
| chr13:38747305
|
A | G | 107 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(104): Show | 107 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.5264-16999A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747305 | ||||||
| chr13:38747395
|
A | ATG | 21 | a0001c0002t0004g0169a0001c0009t0008g0247a0001c0009t0008g0253others(18): Show | 21 | HG01884.hp2 HG02129.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-16877_5264-16 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTG | 100 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(97): Show | 100 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.5264-16879_5264-16 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTGTG | 89 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0175others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.5264-16881_5264-16 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0027g0110a0001c0029t0001g0149a0001c0029t0002g0150others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.5264-16883_5264-16 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0159a0006c0021t0016g0111a0053c0069t0003g0108 | 3 | HG02717.hp2 NA18946.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5264-16885_5264-16 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTGTGT others(11): Show |
2 | a0012c0020t0002g0126a0037c0063t0014g0104 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5264-16893_5264-16 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
A | ATGTGTGT others(15): Show |
1 | a0038c0064t0033g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5264-16897_5264-16 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
ATG | A | 24 | a0001c0002t0004g0232a0001c0033t0010g0136a0002c0008t0001g0208others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.5264-16877_5264-16 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
ATGTGTGT others(3): Show |
A | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5264-16885_5264-16 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747395
|
ATGTGTGT others(5): Show |
A | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5264-16887_5264-16 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747395 | |||||
| chr13:38747429
|
A | G | 1 | a0008c0051t0003g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5264-16875A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747429 | ||||||
| chr13:38747431
|
T | G | 1 | a0008c0051t0003g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5264-16873T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747431 | ||||||
| chr13:38747432
|
C | T | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5264-16872C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747432 | ||||||
| chr13:38747471
|
G | GTATA | 5 | a0004c0004t0003g0198a0004c0004t0012g0196a0012c0020t0049g0124others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-16831_5264-16 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747471 | |||||
| chr13:38747486
|
A | G | 1 | a0030c0055t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5264-16818A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747486 | ||||||
| chr13:38747497
|
T | TAC | 7 | a0001c0001t0018g0057a0001c0002t0004g0232a0001c0070t0003g0095others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-16783_5264-16 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747497 | |||||
| chr13:38747497
|
TAC | T | 54 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(51): Show | 54 | HG00423.hp2 HG00621.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.5264-16783_5264-16 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747497 | |||||
| chr13:38747497
|
TACAC | T | 46 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0262others(43): Show | 46 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.5264-16785_5264-16 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747497 | |||||
| chr13:38747688
|
T | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5264-16616T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747688 | ||||||
| chr13:38747711
|
G | A | 1 | a0006c0016t0021g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5264-16593G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747711 | ||||||
| chr13:38747739
|
A | T | 1 | a0004c0004t0004g0007 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5264-16565A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747739 | ||||||
| chr13:38747841
|
A | G | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5264-16463A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747841 | ||||||
| chr13:38747850
|
C | T | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-16454C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747850 | ||||||
| chr13:38747892
|
T | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5264-16412T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747892 | ||||||
| chr13:38747927
|
T | C | 1 | a0004c0007t0001g0013 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5264-16377T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747927 | ||||||
| chr13:38747955
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5264-16349G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38747955 | ||||||
| chr13:38747989
|
G | GA | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-16314dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38747989 | |||||
| chr13:38748017
|
C | T | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-16287C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748017 | ||||||
| chr13:38748018
|
G | A | 15 | a0001c0029t0001g0149a0001c0029t0025g0003a0003c0005t0002g0060others(12): Show | 15 | HG00423.hp2 HG01109.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.5264-16286G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748018 | ||||||
| chr13:38748137
|
G | A | 1 | a0001c0002t0005g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5264-16167G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748137 | ||||||
| chr13:38748204
|
G | A | 214 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(211): Show | 214 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.5264-16100G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748204 | ||||||
| chr13:38748334
|
G | C | 7 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(4): Show | 7 | HG01192.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-15970G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748334 | ||||||
| chr13:38748467
|
C | T | 48 | a0001c0002t0004g0231a0001c0012t0019g0252a0001c0029t0002g0150others(45): Show | 48 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.5264-15837C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748467 | ||||||
| chr13:38748582
|
T | C | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.5264-15722T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748582 | ||||||
| chr13:38748739
|
T | A | 6 | a0012c0020t0017g0130a0012c0020t0049g0124a0016c0060t0029g0106others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.5264-15565T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748739 | ||||||
| chr13:38748740
|
A | T | 1 | a0002c0008t0001g0214 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5264-15564A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748740 | ||||||
| chr13:38748837
|
G | T | 3 | a0001c0030t0003g0144a0001c0030t0003g0145a0006c0096t0015g0153 | 3 | HG02896.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5264-15467G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748837 | ||||||
| chr13:38748846
|
A | T | 258 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(255): Show | 258 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.5264-15458A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748846 | ||||||
| chr13:38748880
|
T | G | 49 | a0001c0002t0004g0231a0001c0012t0019g0252a0001c0029t0002g0150others(46): Show | 49 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.5264-15424T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748880 | ||||||
| chr13:38748923
|
A | G | 1 | a0004c0007t0001g0013 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5264-15381A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748923 | ||||||
| chr13:38748971
|
T | C | 4 | a0012c0020t0017g0130a0012c0020t0049g0124a0018c0073t0002g0132others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-15333T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38748971 | ||||||
| chr13:38749041
|
A | G | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-15263A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749041 | ||||||
| chr13:38749056
|
A | G | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5264-15248A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749056 | ||||||
| chr13:38749269
|
C | G | 101 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(98): Show | 101 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.5264-15035C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749269 | ||||||
| chr13:38749346
|
A | G | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-14958A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749346 | ||||||
| chr13:38749398
|
A | G | 15 | a0001c0029t0001g0149a0001c0029t0025g0003a0003c0005t0002g0060others(12): Show | 15 | HG00423.hp2 HG01109.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.5264-14906A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749398 | ||||||
| chr13:38749761
|
C | T | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5264-14543C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749761 | ||||||
| chr13:38749779
|
G | A | 7 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(4): Show | 7 | HG01192.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-14525G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749779 | ||||||
| chr13:38749956
|
T | C | 38 | a0001c0030t0003g0144a0001c0030t0003g0145a0001c0030t0047g0151others(35): Show | 38 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.5264-14348T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38749956 | ||||||
| chr13:38750123
|
G | A | 19 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0009t0008g0260others(16): Show | 19 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.5264-14181G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750123 | ||||||
| chr13:38750277
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-14027G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750277 | ||||||
| chr13:38750462
|
T | TC | 236 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(233): Show | 236 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.5264-13842_5264-13 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750462 | ||||||
| chr13:38750533
|
A | T | 5 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(2): Show | 5 | HG01192.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-13771A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750533 | ||||||
| chr13:38750678
|
T | G | 17 | a0001c0029t0001g0149a0001c0029t0025g0003a0003c0005t0002g0060others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.5264-13626T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750678 | ||||||
| chr13:38750699
|
C | CT | 7 | a0001c0029t0002g0150a0003c0005t0001g0072a0008c0050t0001g0123others(4): Show | 7 | HG01175.hp1 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.5264-13593dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38750699 | |||||
| chr13:38750779
|
T | C | 255 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.5264-13525T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750779 | ||||||
| chr13:38750891
|
G | A | 34 | a0001c0001t0027g0110a0001c0002t0032g0238a0004c0004t0004g0007others(31): Show | 34 | HG01192.hp2 HG01243.hp2 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.5264-13413G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38750891 | ||||||
| chr13:38751006
|
C | T | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0172others(5): Show | 8 | HG00673.hp2 HG02071.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.5264-13298C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751006 | ||||||
| chr13:38751025
|
T | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5264-13279T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751025 | ||||||
| chr13:38751192
|
C | CT | 93 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(90): Show | 93 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.5264-13096dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751192 | |||||
| chr13:38751192
|
C | CTT | 7 | a0003c0005t0002g0092a0013c0023t0016g0077a0014c0022t0014g0193others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.5264-13097_5264-13 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751192 | |||||
| chr13:38751192
|
CT | C | 91 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(88): Show | 91 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.5264-13096delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751192 | |||||
| chr13:38751326
|
T | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-12978T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751326 | ||||||
| chr13:38751437
|
G | C | 1 | a0002c0011t0004g0228 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5264-12867G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751437 | ||||||
| chr13:38751518
|
G | A | 27 | a0004c0004t0004g0007a0004c0004t0004g0008a0004c0004t0004g0063others(24): Show | 27 | HG01934.hp2 HG01981.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.5264-12786G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751518 | ||||||
| chr13:38751534
|
A | T | 1 | a0003c0005t0002g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5264-12770A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751534 | ||||||
| chr13:38751651
|
G | A | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-12653G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751651 | ||||||
| chr13:38751705
|
G | A | 1 | a0004c0004t0012g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5264-12599G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751705 | ||||||
| chr13:38751716
|
A | C | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-12588A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751716 | ||||||
| chr13:38751758
|
T | G | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-12546T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751758 | ||||||
| chr13:38751821
|
G | A | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5264-12483G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751821 | ||||||
| chr13:38751855
|
G | A | 6 | a0003c0003t0002g0067a0003c0003t0004g0083a0003c0003t0005g0082others(3): Show | 6 | HG00423.hp1 HG02129.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5264-12449G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751855 | ||||||
| chr13:38751864
|
C | CTG | 7 | a0001c0017t0008g0249a0002c0008t0001g0230a0006c0016t0021g0255others(4): Show | 7 | HG00642.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.5264-12408_5264-12 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751864 | |||||
| chr13:38751864
|
CTG | C | 67 | a0001c0001t0027g0110a0001c0002t0004g0231a0001c0002t0032g0238others(64): Show | 67 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.5264-12408_5264-12 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751864 | |||||
| chr13:38751864
|
CTGTG | C | 20 | a0001c0002t0004g0232a0004c0004t0003g0198a0004c0004t0012g0196others(17): Show | 20 | HG01109.hp2 HG01496.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.5264-12410_5264-12 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751864 | |||||
| chr13:38751864
|
CTGTGTG | C | 95 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(92): Show | 95 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.5264-12412_5264-12 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751864 | |||||
| chr13:38751864
|
CTGTGTGT others(13): Show |
C | 1 | a0002c0011t0004g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5264-12426_5264-12 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751864 | |||||
| chr13:38751896
|
G | GTT | 21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0214others(18): Show | 21 | HG00558.hp2 HG00735.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.5264-12405_5264-12 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38751896 | |||||
| chr13:38751896
|
G | T | 69 | a0001c0001t0027g0110a0001c0002t0004g0231a0001c0002t0032g0238others(66): Show | 69 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.5264-12408G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38751896 | ||||||
| chr13:38752023
|
A | G | 1 | a0002c0011t0004g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5264-12281A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752023 | ||||||
| chr13:38752065
|
G | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5264-12239G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752065 | ||||||
| chr13:38752069
|
G | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-12235G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752069 | ||||||
| chr13:38752118
|
G | A | 46 | a0001c0009t0008g0262a0001c0029t0001g0149a0001c0029t0025g0003others(43): Show | 46 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.5264-12186G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752118 | ||||||
| chr13:38752323
|
T | G | 1 | a0015c0031t0003g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5264-11981T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752323 | ||||||
| chr13:38752605
|
A | T | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5264-11699A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752605 | ||||||
| chr13:38752808
|
A | C | 3 | a0005c0015t0002g0213a0007c0025t0006g0216a0007c0025t0006g0221 | 3 | HG00735.hp2 HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.5264-11496A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752808 | ||||||
| chr13:38752870
|
C | A | 4 | a0001c0030t0003g0144a0001c0030t0003g0145a0001c0030t0047g0151others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-11434C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752870 | ||||||
| chr13:38752899
|
T | C | 2 | a0001c0001t0001g0178a0005c0035t0038g0037 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.5264-11405T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752899 | ||||||
| chr13:38752906
|
G | C | 1 | a0003c0003t0004g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5264-11398G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752906 | ||||||
| chr13:38752907
|
C | G | 231 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(228): Show | 231 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.5264-11397C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38752907 | ||||||
| chr13:38753017
|
C | T | 5 | a0001c0001t0027g0110a0001c0002t0032g0238a0006c0021t0016g0111others(2): Show | 5 | HG01192.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-11287C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753017 | ||||||
| chr13:38753162
|
A | G | 1 | a0001c0002t0004g0169 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5264-11142A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753162 | ||||||
| chr13:38753167
|
A | G | 3 | a0002c0008t0001g0220a0005c0015t0002g0233a0058c0047t0002g0210 | 3 | HG03017.hp2 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5264-11137A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753167 | ||||||
| chr13:38753280
|
A | T | 230 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(227): Show | 230 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.5264-11024A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753280 | ||||||
| chr13:38753423
|
C | A | 233 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(230): Show | 233 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.5264-10881C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753423 | ||||||
| chr13:38753479
|
T | C | 1 | a0014c0022t0014g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5264-10825T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753479 | ||||||
| chr13:38753518
|
C | T | 1 | a0002c0006t0002g0022 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5264-10786C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753518 | ||||||
| chr13:38753611
|
T | C | 242 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(239): Show | 242 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.5264-10693T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753611 | ||||||
| chr13:38753937
|
G | C | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5264-10367G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38753937 | ||||||
| chr13:38753956
|
T | TTTTTA | 48 | a0001c0002t0004g0231a0001c0029t0002g0150a0002c0006t0013g0032others(45): Show | 48 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.5264-10333_5264-10 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753956 | |||||
| chr13:38753973
|
T | TTTTTA | 3 | a0007c0024t0006g0045a0007c0025t0003g0229a0007c0037t0030g0041 | 3 | HG01109.hp1 HG01192.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.5264-10311_5264-10 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753973 | |||||
| chr13:38753973
|
T | TTTTTATT others(3): Show |
18 | a0001c0009t0008g0262a0001c0029t0001g0149a0001c0029t0025g0003others(15): Show | 18 | HG00423.hp2 HG02027.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.5264-10316_5264-10 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753973 | |||||
| chr13:38753973
|
T | TTTTTATT others(13): Show |
21 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0212others(18): Show | 21 | HG00558.hp2 HG00642.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.5264-10326_5264-10 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753973 | |||||
| chr13:38753973
|
T | TTTTTATT others(18): Show |
1 | a0002c0011t0004g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5264-10307_5264-10 others(31): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753973 | |||||
| chr13:38753973
|
T | TTTTTATT others(23): Show |
2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5264-10307_5264-10 others(36): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38753973 | |||||
| chr13:38754054
|
C | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5264-10250C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754054 | ||||||
| chr13:38754223
|
C | A | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-10081C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754223 | ||||||
| chr13:38754404
|
A | G | 45 | a0001c0001t0027g0110a0001c0009t0008g0262a0001c0029t0001g0149others(42): Show | 45 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.5264-9900A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754404 | ||||||
| chr13:38754602
|
G | T | 3 | a0001c0002t0032g0238a0016c0059t0043g0101a0036c0061t0003g0102 | 3 | HG02257.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5264-9702G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754602 | ||||||
| chr13:38754603
|
G | A | 3 | a0001c0002t0032g0238a0016c0059t0043g0101a0036c0061t0003g0102 | 3 | HG02257.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5264-9701G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754603 | ||||||
| chr13:38754858
|
A | AGAT | 18 | a0001c0009t0008g0262a0001c0009t0020g0248a0001c0009t0020g0250others(15): Show | 18 | HG00423.hp1 HG00735.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.5264-9403_5264-940 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGAT | A | 15 | a0001c0002t0004g0231a0002c0010t0004g0068a0002c0011t0004g0211others(12): Show | 15 | HG00673.hp1 HG01433.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.5264-9403_5264-940 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGATGAT | A | 4 | a0003c0003t0004g0069a0003c0003t0004g0078a0003c0003t0004g0090others(1): Show | 4 | HG02071.hp2 HG02723.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-9406_5264-940 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGATGATG others(2): Show |
A | 4 | a0002c0010t0004g0034a0014c0022t0014g0193a0032c0058t0003g0195others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-9409_5264-940 others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGATGATG others(5): Show |
A | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5264-9412_5264-940 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGATGATG others(8): Show |
A | 1 | a0003c0003t0036g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5264-9415_5264-940 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754858
|
AGATGATG others(11): Show |
A | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-9418_5264-940 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754858 | |||||
| chr13:38754889
|
G | T | 2 | a0001c0001t0001g0178a0001c0001t0027g0110 | 2 | HG01192.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.5264-9415G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754889 | ||||||
| chr13:38754892
|
G | GATTATT | 15 | a0001c0001t0001g0190a0001c0001t0028g0056a0001c0030t0047g0151others(12): Show | 15 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.5264-9410_5264-940 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754892 | |||||
| chr13:38754892
|
G | GATTATTA others(2): Show |
3 | a0001c0002t0007g0179a0002c0092t0046g0036a0025c0048t0003g0225 | 3 | HG01243.hp2 HG01361.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.5264-9410_5264-940 others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754892 | |||||
| chr13:38754892
|
G | T | 7 | a0001c0001t0001g0178a0001c0001t0027g0110a0001c0002t0004g0232others(4): Show | 7 | HG00738.hp1 HG01192.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5264-9412G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754892 | ||||||
| chr13:38754895
|
G | GATTATT | 33 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0161others(30): Show | 33 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.5264-9407_5264-940 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754895 | |||||
| chr13:38754895
|
G | GATTATTA others(2): Show |
17 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0002g0185others(14): Show | 17 | HG00621.hp1 HG00673.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.5264-9407_5264-940 others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754895 | |||||
| chr13:38754895
|
G | GATTATTA others(5): Show |
4 | a0002c0006t0001g0033a0002c0010t0004g0035a0002c0010t0045g0023others(1): Show | 4 | HG02735.hp2 NA18747.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-9407_5264-940 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754895 | |||||
| chr13:38754895
|
G | GATTATTA others(14): Show |
1 | a0046c0083t0002g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5264-9407_5264-940 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754895 | |||||
| chr13:38754895
|
G | T | 32 | a0001c0001t0001g0178a0001c0001t0001g0190a0001c0001t0027g0110others(29): Show | 32 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.5264-9409G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754895 | ||||||
| chr13:38754898
|
G | GATT | 6 | a0001c0029t0025g0003a0003c0005t0024g0062a0006c0095t0037g0152others(3): Show | 6 | HG01516.hp2 HG02027.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5264-9404_5264-940 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754898 | |||||
| chr13:38754898
|
G | GATTATT | 18 | a0001c0001t0001g0058a0001c0002t0001g0156a0001c0002t0005g0176others(15): Show | 18 | HG00741.hp1 HG01070.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.5264-9404_5264-940 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754898 | |||||
| chr13:38754898
|
G | GATTATTA others(2): Show |
22 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0177others(19): Show | 22 | HG00741.hp2 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.5264-9404_5264-940 others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754898 | |||||
| chr13:38754898
|
G | GATTATTA others(5): Show |
2 | a0004c0004t0012g0196a0020c0040t0003g0005 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5264-9404_5264-940 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754898 | |||||
| chr13:38754898
|
G | GATTATTA others(14): Show |
2 | a0013c0023t0002g0049a0047c0087t0003g0199 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-9404_5264-940 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754898 | |||||
| chr13:38754898
|
G | T | 103 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0161others(100): Show | 103 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.5264-9406G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754898 | ||||||
| chr13:38754901
|
G | GATGATGA others(8): Show |
1 | a0007c0024t0006g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5264-9401_5264-940 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATGATGA others(17): Show |
1 | a0005c0014t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5264-9401_5264-940 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATGATTA others(14): Show |
1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5264-9401_5264-940 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATT | 23 | a0001c0009t0008g0247a0001c0009t0008g0253a0001c0012t0050g0258others(20): Show | 23 | HG00423.hp2 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.5264-9386_5264-938 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATT | 5 | a0001c0001t0002g0159a0002c0006t0001g0079a0029c0049t0002g0119others(2): Show | 5 | HG00735.hp1 HG02486.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.5264-9389_5264-938 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(2): Show |
15 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0002t0003g0138others(12): Show | 15 | HG00438.hp1 HG01175.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.5264-9392_5264-938 others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(5): Show |
8 | a0003c0005t0002g0092a0003c0078t0001g0019a0007c0024t0006g0044others(5): Show | 8 | HG01496.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5264-9395_5264-938 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(8): Show |
8 | a0003c0003t0004g0083a0003c0003t0005g0070a0003c0003t0005g0082others(5): Show | 8 | HG00423.hp1 HG00639.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.5264-9398_5264-938 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(11): Show |
15 | a0001c0029t0002g0150a0002c0006t0013g0032a0002c0077t0009g0139others(12): Show | 15 | HG02129.hp1 HG02735.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.5264-9401_5264-938 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(14): Show |
9 | a0001c0002t0004g0231a0002c0010t0004g0034a0002c0010t0004g0068others(6): Show | 9 | HG00673.hp1 HG01433.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.5264-9384_5264-938 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | GATTATTA others(17): Show |
7 | a0003c0003t0004g0069a0003c0003t0004g0090a0003c0003t0007g0076others(4): Show | 7 | HG02071.hp2 HG02723.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.5264-9384_5264-938 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38754901 | |||||
| chr13:38754901
|
G | T | 157 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(154): Show | 157 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.5264-9403G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754901 | ||||||
| chr13:38754966
|
G | A | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-9338G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754966 | ||||||
| chr13:38754981
|
C | G | 3 | a0002c0006t0001g0079a0005c0090t0002g0099a0008c0050t0001g0123 | 3 | HG00735.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.5264-9323C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38754981 | ||||||
| chr13:38755109
|
G | T | 10 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.5264-9195G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755109 | ||||||
| chr13:38755142
|
C | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-9162C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755142 | ||||||
| chr13:38755191
|
A | G | 231 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(228): Show | 231 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.5264-9113A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755191 | ||||||
| chr13:38755271
|
A | G | 1 | a0002c0011t0004g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5264-9033A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755271 | ||||||
| chr13:38755318
|
C | A | 2 | a0001c0001t0001g0181a0001c0002t0004g0184 | 2 | HG01361.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5264-8986C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755318 | ||||||
| chr13:38755555
|
A | G | 242 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(239): Show | 242 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.5264-8749A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755555 | ||||||
| chr13:38755578
|
T | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-8726T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755578 | ||||||
| chr13:38755591
|
A | G | 3 | a0012c0020t0002g0126a0037c0063t0014g0104a0038c0064t0033g0103 | 3 | HG02965.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5264-8713A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755591 | ||||||
| chr13:38755629
|
A | G | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-8675A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755629 | ||||||
| chr13:38755635
|
A | G | 3 | a0001c0002t0032g0238a0016c0059t0043g0101a0036c0061t0003g0102 | 3 | HG02257.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5264-8669A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755635 | ||||||
| chr13:38755723
|
C | T | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5264-8581C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755723 | ||||||
| chr13:38755859
|
C | T | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5264-8445C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755859 | ||||||
| chr13:38755921
|
C | T | 1 | a0003c0003t0004g0084 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5264-8383C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755921 | ||||||
| chr13:38755978
|
T | A | 82 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(79): Show | 82 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.5264-8326T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38755978 | ||||||
| chr13:38756277
|
G | A | 17 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(14): Show | 17 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.5264-8027G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38756277 | ||||||
| chr13:38756280
|
G | T | 1 | a0029c0049t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5264-8024G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38756280 | ||||||
| chr13:38756524
|
CT | C | 110 | a0001c0001t0002g0185a0001c0002t0003g0138a0001c0002t0004g0231others(107): Show | 110 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.5264-7759delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38756524 | |||||
| chr13:38756524
|
CTT | C | 5 | a0001c0002t0004g0232a0002c0010t0045g0023a0006c0021t0002g0186others(2): Show | 5 | HG02602.hp2 HG02735.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-7760_5264-775 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38756524 | |||||
| chr13:38756587
|
G | A | 1 | a0002c0027t0001g0029 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5264-7717G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38756587 | ||||||
| chr13:38756843
|
T | A | 1 | a0004c0007t0001g0046 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5264-7461T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38756843 | ||||||
| chr13:38756922
|
G | C | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5264-7382G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38756922 | ||||||
| chr13:38757056
|
C | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-7248C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757056 | ||||||
| chr13:38757164
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0002g0159 | 2 | NA18944.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.5264-7140G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757164 | ||||||
| chr13:38757188
|
T | A | 1 | a0002c0006t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5264-7116T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757188 | ||||||
| chr13:38757217
|
G | T | 3 | a0001c0002t0032g0238a0016c0059t0043g0101a0036c0061t0003g0102 | 3 | HG02257.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5264-7087G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757217 | ||||||
| chr13:38757359
|
C | G | 1 | a0007c0024t0006g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5264-6945C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757359 | ||||||
| chr13:38757541
|
G | A | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5264-6763G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757541 | ||||||
| chr13:38757586
|
C | T | 38 | a0001c0001t0002g0185a0001c0002t0003g0138a0001c0030t0003g0144others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.5264-6718C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757586 | ||||||
| chr13:38757588
|
CCTCTTTT others(5): Show |
C | 1 | a0003c0003t0003g0086 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5264-6703_5264-669 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38757588 | |||||
| chr13:38757637
|
C | T | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-6667C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757637 | ||||||
| chr13:38757723
|
T | C | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5264-6581T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757723 | ||||||
| chr13:38757782
|
G | A | 1 | a0001c0029t0025g0003 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5264-6522G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757782 | ||||||
| chr13:38757841
|
G | A | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5264-6463G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757841 | ||||||
| chr13:38757951
|
A | G | 1 | a0002c0011t0004g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5264-6353A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757951 | ||||||
| chr13:38757997
|
G | A | 1 | a0005c0015t0002g0207 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5264-6307G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38757997 | ||||||
| chr13:38758529
|
T | C | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-5775T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38758529 | ||||||
| chr13:38758532
|
C | T | 1 | a0002c0006t0007g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5264-5772C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38758532 | ||||||
| chr13:38758533
|
G | T | 197 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(194): Show | 197 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.5264-5771G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38758533 | ||||||
| chr13:38758745
|
T | A | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-5559T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38758745 | ||||||
| chr13:38758855
|
T | C | 10 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.5264-5449T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38758855 | ||||||
| chr13:38759010
|
T | C | 1 | a0010c0013t0003g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5264-5294T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759010 | ||||||
| chr13:38759045
|
G | C | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5264-5259G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759045 | ||||||
| chr13:38759271
|
A | G | 2 | a0011c0018t0003g0114a0027c0053t0041g0116 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5264-5033A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759271 | ||||||
| chr13:38759363
|
G | T | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5264-4941G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759363 | ||||||
| chr13:38759406
|
G | A | 1 | a0005c0035t0038g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5264-4898G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759406 | ||||||
| chr13:38759433
|
G | C | 1 | a0031c0056t0015g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5264-4871G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759433 | ||||||
| chr13:38759439
|
C | T | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5264-4865C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759439 | ||||||
| chr13:38759450
|
T | TA | 33 | a0001c0001t0027g0110a0001c0002t0032g0238a0001c0012t0050g0258others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.5264-4839dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38759450 | |||||
| chr13:38759454
|
A | G | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-4850A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759454 | ||||||
| chr13:38759461
|
A | C | 16 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.5264-4843A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759461 | ||||||
| chr13:38759557
|
G | A | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-4747G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38759557 | ||||||
| chr13:38760177
|
T | C | 2 | a0003c0003t0007g0076a0003c0003t0036g0073 | 2 | NA18940.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.5264-4127T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760177 | ||||||
| chr13:38760231
|
C | T | 3 | a0004c0007t0018g0039a0012c0020t0017g0130a0025c0048t0003g0225 | 3 | HG01243.hp1 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5264-4073C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760231 | ||||||
| chr13:38760342
|
C | T | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5264-3962C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760342 | ||||||
| chr13:38760387
|
A | T | 3 | a0007c0024t0006g0044a0007c0024t0006g0059a0026c0052t0003g0122 | 3 | HG01496.hp2 HG01993.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5264-3917A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760387 | ||||||
| chr13:38760624
|
G | GT | 5 | a0001c0033t0010g0136a0002c0008t0001g0208a0002c0008t0001g0230others(2): Show | 5 | HG00642.hp2 HG01192.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.5264-3674dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38760624 | |||||
| chr13:38760660
|
T | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-3644T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760660 | ||||||
| chr13:38760831
|
C | CA | 26 | a0001c0001t0027g0110a0001c0002t0032g0238a0001c0033t0010g0136others(23): Show | 26 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.5264-3463dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38760831 | |||||
| chr13:38760831
|
CA | C | 5 | a0001c0001t0018g0057a0001c0070t0003g0095a0003c0005t0001g0087others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-3463delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38760831 | |||||
| chr13:38760909
|
G | A | 88 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(85): Show | 88 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.5264-3395G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760909 | ||||||
| chr13:38760910
|
T | C | 2 | a0003c0005t0002g0092a0041c0079t0039g0093 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5264-3394T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760910 | ||||||
| chr13:38760955
|
T | G | 11 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.5264-3349T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38760955 | ||||||
| chr13:38761203
|
G | A | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-3101G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38761203 | ||||||
| chr13:38761351
|
G | GC | 13 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.5264-2952dupC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38761351 | |||||
| chr13:38761393
|
G | A | 2 | a0045c0085t0009g0200a0047c0087t0003g0199 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5264-2911G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38761393 | ||||||
| chr13:38761442
|
A | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-2862A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38761442 | ||||||
| chr13:38761476
|
G | A | 1 | a0004c0004t0044g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5264-2828G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38761476 | ||||||
| chr13:38762030
|
T | C | 1 | a0001c0002t0001g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5264-2274T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762030 | ||||||
| chr13:38762347
|
A | G | 2 | a0004c0004t0011g0061a0004c0007t0001g0043 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5264-1957A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762347 | ||||||
| chr13:38762412
|
G | A | 1 | a0004c0089t0001g0239 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5264-1892G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762412 | ||||||
| chr13:38762431
|
T | G | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-1873T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762431 | ||||||
| chr13:38762445
|
C | CT | 101 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(98): Show | 101 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.5264-1848dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38762445 | |||||
| chr13:38762564
|
C | T | 8 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.5264-1740C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762564 | ||||||
| chr13:38762759
|
G | C | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5264-1545G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38762759 | ||||||
| chr13:38763050
|
G | T | 24 | a0001c0001t0027g0110a0001c0002t0032g0238a0002c0008t0001g0208others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.5264-1254G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763050 | ||||||
| chr13:38763342
|
AT | A | 11 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.5264-952delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763342 | |||||
| chr13:38763359
|
T | C | 1 | a0031c0056t0015g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5264-945T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763359 | ||||||
| chr13:38763442
|
C | T | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5264-862C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763442 | ||||||
| chr13:38763464
|
C | CTTTTTTT others(3): Show |
71 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.5264-836_5264-827d others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763464 | |||||
| chr13:38763464
|
C | CTTTTTTT others(4): Show |
28 | a0001c0001t0001g0155a0001c0001t0001g0172a0001c0002t0005g0163others(25): Show | 28 | HG00423.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.5264-837_5264-827d others(13): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763464 | |||||
| chr13:38763464
|
C | CTTTTTTT others(5): Show |
121 | a0001c0001t0001g0168a0001c0001t0001g0190a0001c0001t0001g0192others(118): Show | 121 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.5264-838_5264-827d others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763464 | |||||
| chr13:38763464
|
C | CTTTTTTT others(6): Show |
18 | a0001c0001t0001g0175a0001c0002t0004g0232a0001c0033t0010g0204others(15): Show | 18 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.5264-839_5264-827d others(15): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763464 | |||||
| chr13:38763464
|
C | CTTTTTTT others(7): Show |
1 | a0018c0073t0002g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5264-827_5264-826i others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr13 | 38763464 | |||||
| chr13:38763481
|
C | G | 103 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(100): Show | 103 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.5264-823C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763481 | ||||||
| chr13:38763549
|
T | C | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5264-755T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763549 | ||||||
| chr13:38763780
|
G | A | 5 | a0004c0004t0003g0198a0004c0004t0012g0196a0012c0020t0049g0124others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5264-524G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763780 | ||||||
| chr13:38763925
|
A | G | 38 | a0001c0001t0002g0185a0001c0002t0003g0138a0001c0030t0003g0144others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.5264-379A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38763925 | ||||||
| chr13:38764285
|
T | G | 2 | a0016c0060t0029g0106a0035c0062t0009g0105 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5264-19T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 2/23 | chr13 | 38764285 | ||||||
| chr13:38764475
|
T | C | 241 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(238): Show | 241 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(238): Show |
intron_variant | MODIFIER | c.5410+25T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764475 | ||||||
| chr13:38764597
|
A | T | 3 | a0001c0001t0018g0057a0001c0070t0003g0095a0054c0066t0003g0051 | 3 | HG01891.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.5410+147A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764597 | ||||||
| chr13:38764599
|
G | C | 1 | a0001c0002t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5410+149G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764599 | ||||||
| chr13:38764716
|
T | G | 4 | a0020c0040t0003g0005a0045c0085t0009g0200a0046c0083t0002g0201others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.5410+266T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764716 | ||||||
| chr13:38764844
|
G | A | 71 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.5410+394G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764844 | ||||||
| chr13:38764904
|
A | G | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5410+454A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764904 | ||||||
| chr13:38764995
|
C | T | 1 | a0001c0009t0008g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5410+545C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38764995 | ||||||
| chr13:38765006
|
G | A | 68 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(65): Show | 68 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.5410+556G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765006 | ||||||
| chr13:38765146
|
G | A | 1 | a0003c0005t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5410+696G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765146 | ||||||
| chr13:38765208
|
C | A | 24 | a0001c0001t0027g0110a0001c0002t0032g0238a0002c0008t0001g0208others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.5410+758C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765208 | ||||||
| chr13:38765365
|
T | C | 1 | a0002c0006t0001g0038 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5410+915T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765365 | ||||||
| chr13:38765380
|
A | G | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5410+930A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765380 | ||||||
| chr13:38765391
|
A | G | 1 | a0009c0028t0001g0146 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.5410+941A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765391 | ||||||
| chr13:38765395
|
G | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5410+945G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765395 | ||||||
| chr13:38765852
|
G | C | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5410+1402G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38765852 | ||||||
| chr13:38766074
|
A | G | 220 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(217): Show | 220 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.5410+1624A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766074 | ||||||
| chr13:38766155
|
A | G | 3 | a0004c0007t0018g0039a0012c0020t0017g0130a0025c0048t0003g0225 | 3 | HG01243.hp1 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5410+1705A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766155 | ||||||
| chr13:38766218
|
C | T | 3 | a0001c0002t0032g0238a0016c0059t0043g0101a0036c0061t0003g0102 | 3 | HG02257.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5410+1768C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766218 | ||||||
| chr13:38766281
|
T | G | 71 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.5410+1831T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766281 | ||||||
| chr13:38766452
|
G | A | 8 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.5410+2002G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766452 | ||||||
| chr13:38766524
|
A | G | 20 | a0001c0009t0008g0262a0001c0029t0001g0149a0001c0029t0025g0003others(17): Show | 20 | HG00423.hp2 HG01109.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.5410+2074A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766524 | ||||||
| chr13:38766638
|
C | T | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5410+2188C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766638 | ||||||
| chr13:38766691
|
T | C | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5410+2241T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766691 | ||||||
| chr13:38766847
|
A | G | 5 | a0004c0004t0003g0198a0004c0004t0012g0196a0012c0020t0049g0124others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5410+2397A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38766847 | ||||||
| chr13:38767095
|
A | G | 1 | a0001c0002t0007g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5411-2483A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767095 | ||||||
| chr13:38767389
|
T | C | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5411-2189T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767389 | ||||||
| chr13:38767453
|
T | C | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5411-2125T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767453 | ||||||
| chr13:38767501
|
C | A | 38 | a0001c0001t0002g0185a0001c0002t0003g0138a0001c0030t0003g0144others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.5411-2077C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767501 | ||||||
| chr13:38767505
|
A | C | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5411-2073A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767505 | ||||||
| chr13:38767794
|
T | G | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5411-1784T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767794 | ||||||
| chr13:38767877
|
T | C | 220 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(217): Show | 220 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.5411-1701T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38767877 | ||||||
| chr13:38768016
|
G | A | 2 | a0019c0039t0011g0004a0030c0055t0003g0131 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.5411-1562G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768016 | ||||||
| chr13:38768225
|
T | C | 2 | a0005c0015t0002g0213a0007c0025t0006g0221 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.5411-1353T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768225 | ||||||
| chr13:38768507
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5411-1071G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768507 | ||||||
| chr13:38768543
|
C | G | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5411-1035C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768543 | ||||||
| chr13:38768617
|
T | G | 3 | a0045c0085t0009g0200a0046c0083t0002g0201a0047c0087t0003g0199 | 3 | HG02055.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5411-961T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768617 | ||||||
| chr13:38768832
|
G | A | 1 | a0003c0005t0024g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5411-746G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768832 | ||||||
| chr13:38768834
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5411-744T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768834 | ||||||
| chr13:38768887
|
T | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5411-691T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768887 | ||||||
| chr13:38768891
|
A | G | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5411-687A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38768891 | ||||||
| chr13:38769031
|
A | G | 1 | a0006c0016t0021g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5411-547A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38769031 | ||||||
| chr13:38769127
|
G | A | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5411-451G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38769127 | ||||||
| chr13:38769249
|
T | C | 66 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(63): Show | 66 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.5411-329T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38769249 | ||||||
| chr13:38769340
|
T | G | 24 | a0001c0001t0027g0110a0001c0002t0032g0238a0002c0008t0001g0208others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.5411-238T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 3/23 | chr13 | 38769340 | ||||||
| chr13:38769920
|
G | A | 36 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5641+112G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38769920 | ||||||
| chr13:38770064
|
T | C | 196 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(193): Show | 196 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(193): Show |
intron_variant | MODIFIER | c.5641+256T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770064 | ||||||
| chr13:38770182
|
A | C | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5641+374A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770182 | ||||||
| chr13:38770207
|
G | T | 220 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(217): Show | 220 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.5641+399G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770207 | ||||||
| chr13:38770249
|
G | A | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5641+441G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770249 | ||||||
| chr13:38770292
|
G | A | 3 | a0001c0001t0028g0056a0001c0002t0004g0054a0010c0013t0006g0055 | 3 | HG00642.hp1 HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.5641+484G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770292 | ||||||
| chr13:38770311
|
G | A | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5641+503G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770311 | ||||||
| chr13:38770772
|
C | G | 23 | a0001c0001t0027g0110a0001c0002t0032g0238a0002c0008t0001g0208others(20): Show | 23 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.5641+964C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770772 | ||||||
| chr13:38770949
|
AT | A | 5 | a0004c0004t0003g0198a0004c0004t0012g0196a0012c0020t0049g0124others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5641+1142delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770949 | ||||||
| chr13:38770950
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5641+1142T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38770950 | ||||||
| chr13:38771051
|
G | A | 3 | a0004c0004t0003g0198a0004c0004t0012g0196a0044c0084t0009g0197 | 3 | HG01496.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5641+1243G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771051 | ||||||
| chr13:38771246
|
T | C | 5 | a0004c0004t0003g0198a0004c0004t0012g0196a0012c0020t0049g0124others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5641+1438T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771246 | ||||||
| chr13:38771511
|
T | C | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5641+1703T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771511 | ||||||
| chr13:38771568
|
A | G | 1 | a0003c0005t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5641+1760A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771568 | ||||||
| chr13:38771607
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5641+1799A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771607 | ||||||
| chr13:38771624
|
G | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5641+1816G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771624 | ||||||
| chr13:38771650
|
A | C | 238 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(235): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.5641+1842A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38771650 | ||||||
| chr13:38772050
|
T | C | 106 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(103): Show | 106 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.5641+2242T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772050 | ||||||
| chr13:38772055
|
T | A | 38 | a0001c0001t0002g0185a0001c0002t0003g0138a0001c0030t0003g0144others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.5641+2247T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772055 | ||||||
| chr13:38772160
|
T | C | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5641+2352T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772160 | ||||||
| chr13:38772306
|
G | C | 188 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0161others(185): Show | 188 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(185): Show |
intron_variant | MODIFIER | c.5641+2498G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772306 | ||||||
| chr13:38772371
|
C | T | 1 | a0003c0005t0002g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5641+2563C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772371 | ||||||
| chr13:38772586
|
A | G | 1 | a0001c0033t0010g0136 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5641+2778A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772586 | ||||||
| chr13:38772615
|
G | A | 21 | a0001c0009t0008g0247a0001c0009t0008g0260a0001c0009t0020g0248others(18): Show | 21 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.5641+2807G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772615 | ||||||
| chr13:38772625
|
A | G | 1 | a0001c0002t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5641+2817A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772625 | ||||||
| chr13:38772659
|
C | A | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5641+2851C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772659 | ||||||
| chr13:38772701
|
CT | C | 218 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(215): Show | 218 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.5641+2906delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38772701 | |||||
| chr13:38772701
|
CTT | C | 21 | a0001c0009t0008g0262a0001c0029t0001g0149a0001c0029t0025g0003others(18): Show | 21 | HG00423.hp2 HG01109.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.5641+2905_5641+290 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38772701 | |||||
| chr13:38772719
|
G | A | 44 | a0001c0009t0008g0247a0001c0009t0008g0260a0001c0009t0008g0262others(41): Show | 44 | HG00423.hp2 HG01109.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.5641+2911G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772719 | ||||||
| chr13:38772859
|
G | T | 1 | a0016c0060t0029g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5641+3051G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772859 | ||||||
| chr13:38772911
|
G | A | 18 | a0002c0008t0001g0208a0002c0008t0001g0212a0002c0008t0001g0214others(15): Show | 18 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.5641+3103G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772911 | ||||||
| chr13:38772974
|
G | A | 13 | a0001c0029t0001g0149a0001c0029t0025g0003a0002c0006t0001g0096others(10): Show | 13 | HG00423.hp2 HG01109.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.5641+3166G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772974 | ||||||
| chr13:38772988
|
T | C | 17 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.5641+3180T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38772988 | ||||||
| chr13:38773052
|
T | C | 2 | a0032c0058t0003g0195a0050c0075t0003g0194 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5641+3244T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773052 | ||||||
| chr13:38773214
|
C | G | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5641+3406C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773214 | ||||||
| chr13:38773235
|
C | T | 1 | a0013c0023t0002g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5641+3427C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773235 | ||||||
| chr13:38773281
|
A | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5641+3473A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773281 | ||||||
| chr13:38773402
|
T | A | 1 | a0002c0008t0001g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.5641+3594T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773402 | ||||||
| chr13:38773444
|
G | A | 70 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(67): Show | 70 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.5641+3636G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773444 | ||||||
| chr13:38773458
|
A | G | 3 | a0002c0006t0001g0079a0005c0090t0002g0099a0008c0050t0001g0123 | 3 | HG00735.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.5641+3650A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773458 | ||||||
| chr13:38773473
|
C | G | 1 | a0001c0009t0008g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5641+3665C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773473 | ||||||
| chr13:38773565
|
C | T | 238 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(235): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.5641+3757C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773565 | ||||||
| chr13:38773595
|
A | G | 258 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(255): Show | 258 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.5641+3787A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773595 | ||||||
| chr13:38773747
|
G | A | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5641+3939G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773747 | ||||||
| chr13:38773751
|
A | C | 3 | a0001c0001t0013g0202a0001c0033t0010g0204a0005c0014t0003g0203 | 3 | HG01255.hp2 HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5641+3943A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773751 | ||||||
| chr13:38773867
|
A | T | 2 | a0018c0073t0002g0132a0048c0065t0003g0100 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5641+4059A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773867 | ||||||
| chr13:38773903
|
G | A | 18 | a0002c0008t0001g0208a0002c0008t0001g0212a0002c0008t0001g0214others(15): Show | 18 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.5641+4095G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773903 | ||||||
| chr13:38773970
|
A | T | 3 | a0014c0022t0014g0193a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5641+4162A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773970 | ||||||
| chr13:38773972
|
T | A | 2 | a0003c0003t0003g0086a0003c0003t0004g0084 | 2 | NA19004.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.5641+4164T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773972 | ||||||
| chr13:38773975
|
G | A | 196 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(193): Show | 196 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(193): Show |
intron_variant | MODIFIER | c.5641+4167G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773975 | ||||||
| chr13:38773980
|
A | T | 72 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0190others(69): Show | 72 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5641+4172A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38773980 | ||||||
| chr13:38774224
|
T | C | 10 | a0002c0027t0001g0021a0002c0027t0001g0027a0002c0036t0007g0017others(7): Show | 10 | HG00741.hp2 HG01070.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.5641+4416T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38774224 | ||||||
| chr13:38774228
|
G | A | 1 | a0004c0007t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5641+4420G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38774228 | ||||||
| chr13:38774514
|
A | G | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5641+4706A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38774514 | ||||||
| chr13:38774640
|
A | G | 2 | a0012c0020t0049g0124a0034c0088t0011g0226 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5641+4832A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38774640 | ||||||
| chr13:38775227
|
G | A | 2 | a0004c0004t0011g0061a0004c0007t0001g0043 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5641+5419G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775227 | ||||||
| chr13:38775239
|
G | C | 1 | a0003c0005t0002g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5641+5431G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775239 | ||||||
| chr13:38775300
|
A | G | 1 | a0003c0003t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5641+5492A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775300 | ||||||
| chr13:38775322
|
G | A | 236 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(233): Show | 236 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.5641+5514G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775322 | ||||||
| chr13:38775330
|
T | G | 68 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(65): Show | 68 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.5641+5522T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775330 | ||||||
| chr13:38775355
|
G | T | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0033c0057t0022g0127 | 3 | HG01884.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5641+5547G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38775355 | ||||||
| chr13:38776031
|
T | C | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5641+6223T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776031 | ||||||
| chr13:38776240
|
T | A | 8 | a0001c0001t0002g0185a0002c0006t0001g0033a0002c0010t0004g0034others(5): Show | 8 | NA18747.hp2 NA18963.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.5641+6432T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776240 | ||||||
| chr13:38776266
|
C | G | 1 | a0001c0002t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5641+6458C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776266 | ||||||
| chr13:38776431
|
G | A | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5641+6623G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776431 | ||||||
| chr13:38776753
|
A | G | 72 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(69): Show | 72 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.5642-6317A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776753 | ||||||
| chr13:38776787
|
G | GA | 7 | a0001c0067t0001g0182a0003c0005t0026g0091a0005c0035t0002g0018others(4): Show | 7 | HG01255.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5642-6271dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38776787 | |||||
| chr13:38776787
|
GA | G | 27 | a0001c0001t0028g0056a0001c0002t0004g0054a0001c0009t0008g0247others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.5642-6271delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38776787 | |||||
| chr13:38776840
|
G | A | 258 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(255): Show | 258 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.5642-6230G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776840 | ||||||
| chr13:38776882
|
C | T | 1 | a0001c0012t0050g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5642-6188C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776882 | ||||||
| chr13:38776884
|
AC | A | 3 | a0022c0043t0012g0234a0023c0042t0048g0236a0024c0041t0003g0235 | 3 | HG01981.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5642-6183delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38776884 | |||||
| chr13:38776989
|
A | G | 238 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(235): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.5642-6081A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38776989 | ||||||
| chr13:38777041
|
T | C | 1 | a0002c0006t0007g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5642-6029T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777041 | ||||||
| chr13:38777249
|
T | A | 148 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(145): Show | 148 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(145): Show |
intron_variant | MODIFIER | c.5642-5821T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777249 | ||||||
| chr13:38777295
|
C | T | 10 | a0001c0009t0008g0262a0001c0030t0003g0144a0001c0030t0003g0145others(7): Show | 10 | HG02486.hp1 HG02896.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.5642-5775C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777295 | ||||||
| chr13:38777452
|
C | A | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5642-5618C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777452 | ||||||
| chr13:38777568
|
A | G | 1 | a0002c0008t0001g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5642-5502A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777568 | ||||||
| chr13:38777570
|
C | G | 6 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.5642-5500C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777570 | ||||||
| chr13:38777746
|
T | A | 2 | a0002c0008t0001g0230a0007c0025t0003g0229 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.5642-5324T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777746 | ||||||
| chr13:38777751
|
A | G | 10 | a0004c0004t0003g0198a0004c0004t0012g0196a0004c0007t0018g0039others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.5642-5319A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38777751 | ||||||
| chr13:38778257
|
C | T | 1 | a0003c0003t0005g0089 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.5642-4813C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778257 | ||||||
| chr13:38778284
|
G | A | 1 | a0007c0025t0006g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5642-4786G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778284 | ||||||
| chr13:38778397
|
G | C | 1 | a0040c0081t0006g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5642-4673G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778397 | ||||||
| chr13:38778449
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5642-4621C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778449 | ||||||
| chr13:38778533
|
G | A | 20 | a0002c0008t0001g0208a0002c0008t0001g0212a0002c0008t0001g0214others(17): Show | 20 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.5642-4537G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778533 | ||||||
| chr13:38778600
|
T | C | 16 | a0001c0009t0008g0247a0001c0009t0008g0262a0001c0017t0008g0249others(13): Show | 16 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.5642-4470T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778600 | ||||||
| chr13:38778615
|
C | T | 1 | a0029c0049t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5642-4455C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778615 | ||||||
| chr13:38778707
|
C | T | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5642-4363C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778707 | ||||||
| chr13:38778729
|
G | A | 1 | a0003c0078t0001g0019 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.5642-4341G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778729 | ||||||
| chr13:38778768
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5642-4302A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778768 | ||||||
| chr13:38778790
|
T | TA | 16 | a0002c0008t0001g0212a0002c0008t0001g0214a0002c0008t0001g0219others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.5642-4271dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38778790 | |||||
| chr13:38778791
|
A | T | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5642-4279A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778791 | ||||||
| chr13:38778895
|
C | T | 4 | a0003c0003t0002g0067a0003c0003t0004g0083a0003c0003t0005g0082others(1): Show | 4 | HG00423.hp1 HG01934.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.5642-4175C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778895 | ||||||
| chr13:38778896
|
G | T | 2 | a0001c0001t0027g0110a0006c0021t0016g0111 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5642-4174G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38778896 | ||||||
| chr13:38779101
|
G | A | 23 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0018g0057others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.5642-3969G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779101 | ||||||
| chr13:38779208
|
C | T | 1 | a0001c0029t0002g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.5642-3862C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779208 | ||||||
| chr13:38779396
|
TTTAAAAA others(7): Show |
T | 1 | a0054c0066t0003g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5642-3664_5642-365 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38779396 | |||||
| chr13:38779412
|
T | TA | 83 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(80): Show | 83 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.5642-3647dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38779412 | |||||
| chr13:38779413
|
A | T | 1 | a0054c0066t0003g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5642-3657A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779413 | ||||||
| chr13:38779444
|
C | T | 247 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(244): Show | 247 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.5642-3626C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779444 | ||||||
| chr13:38779600
|
A | G | 19 | a0001c0009t0008g0260a0001c0012t0019g0259a0001c0012t0053g0251others(16): Show | 19 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.5642-3470A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779600 | ||||||
| chr13:38779610
|
C | G | 1 | a0001c0001t0018g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5642-3460C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779610 | ||||||
| chr13:38779666
|
C | T | 5 | a0003c0005t0002g0092a0007c0025t0003g0229a0013c0023t0016g0077others(2): Show | 5 | HG00639.hp2 HG01192.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.5642-3404C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779666 | ||||||
| chr13:38779692
|
C | T | 1 | a0006c0096t0015g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5642-3378C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779692 | ||||||
| chr13:38779885
|
A | G | 61 | a0001c0001t0001g0158a0001c0001t0001g0192a0001c0001t0023g0167others(58): Show | 61 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.5642-3185A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779885 | ||||||
| chr13:38779955
|
G | A | 1 | a0004c0004t0007g0015 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.5642-3115G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38779955 | ||||||
| chr13:38780024
|
A | G | 18 | a0001c0012t0053g0251a0001c0017t0008g0249a0001c0017t0055g0256others(15): Show | 18 | HG01243.hp1 HG01981.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.5642-3046A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780024 | ||||||
| chr13:38780058
|
T | C | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5642-3012T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780058 | ||||||
| chr13:38780350
|
G | A | 212 | a0001c0001t0001g0058a0001c0001t0001g0155a0001c0001t0001g0158others(209): Show | 212 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.5642-2720G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780350 | ||||||
| chr13:38780847
|
C | A | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5642-2223C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780847 | ||||||
| chr13:38780855
|
A | G | 3 | a0001c0001t0001g0181a0001c0002t0004g0184a0004c0089t0001g0239 | 3 | HG01169.hp1 HG01361.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5642-2215A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780855 | ||||||
| chr13:38780879
|
G | A | 2 | a0022c0043t0012g0234a0026c0052t0003g0122 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5642-2191G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38780879 | ||||||
| chr13:38781024
|
T | G | 3 | a0001c0009t0020g0248a0001c0009t0020g0250a0044c0084t0009g0197 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5642-2046T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781024 | ||||||
| chr13:38781112
|
C | T | 3 | a0001c0002t0004g0054a0007c0037t0030g0041a0010c0013t0006g0055 | 3 | HG00642.hp1 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.5642-1958C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781112 | ||||||
| chr13:38781179
|
C | G | 212 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0158others(209): Show | 212 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.5642-1891C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781179 | ||||||
| chr13:38781280
|
T | A | 200 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0155others(197): Show | 200 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.5642-1790T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781280 | ||||||
| chr13:38781284
|
A | G | 200 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0155others(197): Show | 200 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.5642-1786A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781284 | ||||||
| chr13:38781295
|
C | T | 3 | a0008c0051t0003g0120a0039c0086t0003g0050a0043c0082t0017g0048 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5642-1775C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781295 | ||||||
| chr13:38781354
|
C | T | 1 | a0003c0003t0036g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5642-1716C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781354 | ||||||
| chr13:38781576
|
T | C | 6 | a0001c0009t0020g0248a0001c0009t0020g0250a0001c0012t0019g0252others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5642-1494T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781576 | ||||||
| chr13:38781705
|
T | G | 24 | a0001c0001t0001g0052a0001c0001t0001g0158a0001c0001t0001g0178others(21): Show | 24 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.5642-1365T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38781705 | ||||||
| chr13:38782020
|
G | A | 3 | a0001c0002t0005g0170a0002c0077t0009g0139a0007c0024t0006g0045 | 3 | HG01109.hp1 HG03486.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.5642-1050G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782020 | ||||||
| chr13:38782173
|
G | C | 2 | a0003c0005t0026g0091a0006c0016t0021g0255 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5642-897G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782173 | ||||||
| chr13:38782203
|
G | C | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5642-867G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782203 | ||||||
| chr13:38782370
|
A | G | 122 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(119): Show | 122 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.5642-700A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782370 | ||||||
| chr13:38782463
|
T | C | 1 | a0003c0003t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5642-607T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782463 | ||||||
| chr13:38782672
|
T | C | 1 | a0014c0022t0014g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5642-398T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782672 | ||||||
| chr13:38782833
|
G | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5642-237G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782833 | ||||||
| chr13:38782882
|
C | T | 1 | a0004c0007t0001g0014 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5642-188C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38782882 | ||||||
| chr13:38782993
|
AT | A | 10 | a0001c0017t0008g0249a0002c0077t0009g0139a0004c0004t0012g0196others(7): Show | 10 | HG01243.hp2 HG01496.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.5642-73delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr13 | 38782993 | |||||
| chr13:38783008
|
G | A | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5642-62G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38783008 | ||||||
| chr13:38783051
|
A | G | 4 | a0006c0016t0052g0244a0029c0049t0002g0119a0041c0079t0039g0093others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.5642-19A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 4/23 | chr13 | 38783051 | ||||||
| chr13:38783247
|
C | A | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5767+52C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783247 | ||||||
| chr13:38783473
|
TA | T | 89 | a0001c0001t0001g0058a0001c0001t0001g0164a0001c0001t0001g0177others(86): Show | 89 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.5767+299delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr13 | 38783473 | |||||
| chr13:38783473
|
TAA | T | 21 | a0001c0001t0027g0110a0001c0017t0008g0249a0001c0030t0047g0151others(18): Show | 21 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.5767+298_5767+299d others(4): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr13 | 38783473 | |||||
| chr13:38783473
|
TAAAA | T | 5 | a0012c0020t0049g0124a0020c0040t0003g0005a0026c0052t0003g0122others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5767+296_5767+299d others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr13 | 38783473 | |||||
| chr13:38783473
|
TAAAAA | T | 98 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(95): Show | 98 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.5767+295_5767+299d others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr13 | 38783473 | |||||
| chr13:38783474
|
A | T | 1 | a0001c0068t0005g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5767+279A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783474 | ||||||
| chr13:38783498
|
G | A | 1 | a0005c0026t0002g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5767+303G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783498 | ||||||
| chr13:38783542
|
G | C | 3 | a0004c0004t0012g0196a0010c0013t0003g0107a0031c0056t0015g0125 | 3 | HG01496.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.5767+347G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783542 | ||||||
| chr13:38783878
|
C | T | 3 | a0020c0040t0003g0005a0026c0052t0003g0122a0044c0084t0009g0197 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.5768-679C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783878 | ||||||
| chr13:38783963
|
C | T | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5768-594C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783963 | ||||||
| chr13:38783972
|
G | C | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5768-585G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783972 | ||||||
| chr13:38783981
|
C | G | 1 | a0029c0049t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5768-576C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38783981 | ||||||
| chr13:38784198
|
G | A | 2 | a0005c0026t0002g0240a0005c0026t0002g0241 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.5768-359G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38784198 | ||||||
| chr13:38784278
|
GGGGCTAT others(6): Show |
G | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5768-277_5768-265d others(15): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr13 | 38784278 | |||||
| chr13:38784372
|
T | C | 18 | a0001c0009t0008g0247a0001c0009t0008g0253a0004c0004t0003g0198others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.5768-185T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38784372 | ||||||
| chr13:38784426
|
C | T | 1 | a0007c0025t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5768-131C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 5/23 | chr13 | 38784426 | ||||||
| chr13:38784842
|
C | T | 2 | a0001c0012t0050g0258a0001c0017t0055g0256 | 2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.6019+34C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38784842 | ||||||
| chr13:38784996
|
T | C | 1 | a0002c0008t0001g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6019+188T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38784996 | ||||||
| chr13:38785195
|
G | C | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6019+387G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785195 | ||||||
| chr13:38785281
|
C | G | 1 | a0002c0006t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6019+473C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785281 | ||||||
| chr13:38785372
|
T | C | 3 | a0015c0031t0003g0128a0015c0031t0003g0129a0055c0071t0031g0109 | 3 | HG03453.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6019+564T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785372 | ||||||
| chr13:38785398
|
G | A | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6019+590G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785398 | ||||||
| chr13:38785571
|
A | G | 125 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(122): Show | 125 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.6019+763A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785571 | ||||||
| chr13:38785588
|
G | C | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6019+780G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785588 | ||||||
| chr13:38785721
|
C | T | 1 | a0004c0004t0012g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6019+913C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785721 | ||||||
| chr13:38785834
|
T | C | 1 | a0012c0020t0049g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6019+1026T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785834 | ||||||
| chr13:38785866
|
C | T | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6019+1058C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785866 | ||||||
| chr13:38785965
|
G | A | 1 | a0023c0042t0048g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6019+1157G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785965 | ||||||
| chr13:38785973
|
T | A | 1 | a0004c0004t0012g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6019+1165T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38785973 | ||||||
| chr13:38786096
|
T | C | 87 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(84): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.6019+1288T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38786096 | ||||||
| chr13:38786388
|
T | A | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6019+1580T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38786388 | ||||||
| chr13:38786434
|
C | A | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6019+1626C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38786434 | ||||||
| chr13:38786675
|
G | GT | 4 | a0001c0001t0001g0058a0002c0011t0004g0211a0012c0020t0017g0130others(1): Show | 4 | HG01243.hp1 HG03492.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+1875dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38786675 | |||||
| chr13:38786694
|
T | A | 4 | a0003c0003t0004g0069a0009c0028t0001g0143a0009c0028t0001g0146others(1): Show | 4 | HG02071.hp2 NA19003.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+1886T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38786694 | ||||||
| chr13:38786832
|
A | G | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6019+2024A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38786832 | ||||||
| chr13:38787038
|
C | G | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+2230C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38787038 | ||||||
| chr13:38787333
|
C | T | 1 | a0047c0087t0003g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6019+2525C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38787333 | ||||||
| chr13:38787543
|
G | A | 92 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.6019+2735G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38787543 | ||||||
| chr13:38787615
|
A | G | 5 | a0001c0009t0008g0247a0013c0023t0002g0049a0018c0073t0002g0132others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+2807A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38787615 | ||||||
| chr13:38787854
|
A | G | 1 | a0001c0017t0008g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6019+3046A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38787854 | ||||||
| chr13:38788080
|
G | A | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6019+3272G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788080 | ||||||
| chr13:38788080
|
G | T | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6019+3272G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788080 | ||||||
| chr13:38788100
|
C | T | 92 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.6019+3292C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788100 | ||||||
| chr13:38788125
|
T | C | 2 | a0004c0004t0012g0196a0010c0013t0003g0107 | 2 | HG01496.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.6019+3317T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788125 | ||||||
| chr13:38788158
|
C | T | 92 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.6019+3350C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788158 | ||||||
| chr13:38788497
|
C | T | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6019+3689C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788497 | ||||||
| chr13:38788579
|
G | A | 16 | a0001c0009t0008g0247a0001c0009t0008g0253a0004c0004t0012g0196others(13): Show | 16 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6019+3771G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38788579 | ||||||
| chr13:38789006
|
G | A | 1 | a0001c0033t0010g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6019+4198G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789006 | ||||||
| chr13:38789224
|
G | A | 93 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(90): Show | 93 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.6019+4416G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789224 | ||||||
| chr13:38789385
|
A | T | 2 | a0003c0005t0002g0092a0013c0023t0016g0077 | 2 | HG00639.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.6019+4577A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789385 | ||||||
| chr13:38789413
|
A | C | 93 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(90): Show | 93 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.6019+4605A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789413 | ||||||
| chr13:38789732
|
ATC | A | 3 | a0006c0016t0052g0244a0029c0049t0002g0119a0041c0079t0039g0093 | 3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.6019+4926_6019+492 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38789732 | |||||
| chr13:38789792
|
A | G | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6019+4984A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789792 | ||||||
| chr13:38789823
|
T | G | 1 | a0057c0076t0002g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6019+5015T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789823 | ||||||
| chr13:38789928
|
C | A | 1 | a0007c0025t0006g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6019+5120C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789928 | ||||||
| chr13:38789938
|
A | T | 93 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(90): Show | 93 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.6019+5130A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38789938 | ||||||
| chr13:38790348
|
A | T | 14 | a0001c0009t0008g0247a0001c0009t0008g0253a0013c0023t0002g0049others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.6019+5540A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38790348 | ||||||
| chr13:38790706
|
A | G | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6019+5898A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38790706 | ||||||
| chr13:38790968
|
C | G | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6019+6160C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38790968 | ||||||
| chr13:38791189
|
A | G | 1 | a0003c0003t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6019+6381A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791189 | ||||||
| chr13:38791328
|
G | A | 5 | a0011c0018t0003g0112a0011c0018t0003g0113a0014c0022t0003g0001others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+6520G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791328 | ||||||
| chr13:38791613
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6019+6805A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791613 | ||||||
| chr13:38791754
|
C | G | 2 | a0001c0017t0008g0249a0008c0051t0003g0120 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.6019+6946C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791754 | ||||||
| chr13:38791785
|
A | G | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6019+6977A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791785 | ||||||
| chr13:38791816
|
T | C | 2 | a0004c0004t0005g0009a0004c0004t0044g0016 | 2 | HG02135.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.6019+7008T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791816 | ||||||
| chr13:38791925
|
C | T | 1 | a0030c0055t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6019+7117C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791925 | ||||||
| chr13:38791935
|
A | G | 1 | a0001c0009t0008g0260 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6019+7127A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791935 | ||||||
| chr13:38791940
|
A | G | 1 | a0029c0049t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6019+7132A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791940 | ||||||
| chr13:38791980
|
T | C | 1 | a0001c0033t0010g0136 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6019+7172T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38791980 | ||||||
| chr13:38792073
|
G | A | 1 | a0002c0006t0002g0022 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6019+7265G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792073 | ||||||
| chr13:38792206
|
G | A | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6019+7398G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792206 | ||||||
| chr13:38792307
|
C | T | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6019+7499C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792307 | ||||||
| chr13:38792357
|
A | G | 83 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(80): Show | 83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.6019+7549A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792357 | ||||||
| chr13:38792360
|
T | A | 2 | a0001c0001t0007g0174a0006c0021t0016g0111 | 2 | HG02717.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6019+7552T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792360 | ||||||
| chr13:38792362
|
A | T | 2 | a0005c0026t0002g0240a0005c0026t0002g0241 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.6019+7554A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792362 | ||||||
| chr13:38792390
|
T | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0029t0025g0003others(2): Show | 5 | HG00438.hp1 HG02129.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+7582T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792390 | ||||||
| chr13:38792772
|
AT | A | 116 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(113): Show | 116 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.6019+7973delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38792772 | |||||
| chr13:38792956
|
A | G | 2 | a0001c0030t0003g0144a0001c0030t0003g0145 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6019+8148A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38792956 | ||||||
| chr13:38793191
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6019+8383A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793191 | ||||||
| chr13:38793310
|
A | T | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6019+8502A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793310 | ||||||
| chr13:38793316
|
G | A | 2 | a0001c0001t0028g0056a0001c0002t0004g0054 | 2 | HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.6019+8508G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793316 | ||||||
| chr13:38793580
|
T | C | 118 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0161others(115): Show | 118 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.6019+8772T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793580 | ||||||
| chr13:38793581
|
G | A | 1 | a0004c0007t0001g0010 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.6019+8773G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793581 | ||||||
| chr13:38793702
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.6019+8894G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793702 | ||||||
| chr13:38793875
|
T | G | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.6019+9067T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793875 | ||||||
| chr13:38793980
|
AC | A | 85 | a0001c0001t0001g0053a0001c0001t0001g0161a0001c0001t0001g0165others(82): Show | 85 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.6019+9173delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38793980 | ||||||
| chr13:38794213
|
G | A | 237 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(234): Show | 237 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.6019+9405G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38794213 | ||||||
| chr13:38794324
|
G | T | 1 | a0008c0019t0012g0115 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.6019+9516G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38794324 | ||||||
| chr13:38794556
|
C | T | 6 | a0001c0012t0019g0252a0001c0030t0003g0144a0001c0030t0003g0145others(3): Show | 6 | HG01981.hp1 HG02723.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+9748C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38794556 | ||||||
| chr13:38794655
|
C | T | 7 | a0001c0012t0019g0252a0001c0030t0003g0144a0001c0030t0003g0145others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.6019+9847C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38794655 | ||||||
| chr13:38794696
|
C | T | 6 | a0001c0012t0019g0252a0001c0030t0003g0144a0001c0030t0003g0145others(3): Show | 6 | HG01981.hp1 HG02723.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+9888C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38794696 | ||||||
| chr13:38795326
|
AT | A | 85 | a0001c0001t0001g0053a0001c0001t0001g0161a0001c0001t0001g0165others(82): Show | 85 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.6019+10529delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38795326 | |||||
| chr13:38795360
|
G | A | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6019+10552G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795360 | ||||||
| chr13:38795385
|
C | T | 1 | a0033c0057t0022g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6019+10577C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795385 | ||||||
| chr13:38795491
|
T | C | 1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6019+10683T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795491 | ||||||
| chr13:38795555
|
T | C | 1 | a0010c0013t0006g0205 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6019+10747T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795555 | ||||||
| chr13:38795556
|
C | T | 2 | a0001c0017t0008g0261a0035c0062t0009g0105 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6019+10748C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795556 | ||||||
| chr13:38795655
|
C | A | 1 | a0003c0003t0002g0067 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.6019+10847C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795655 | ||||||
| chr13:38795878
|
C | T | 2 | a0001c0030t0047g0151a0021c0044t0056g0254 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.6019+11070C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38795878 | ||||||
| chr13:38796191
|
T | A | 1 | a0007c0025t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6019+11383T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796191 | ||||||
| chr13:38796428
|
T | C | 65 | a0001c0001t0001g0053a0001c0001t0001g0158a0001c0001t0001g0172others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.6019+11620T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796428 | ||||||
| chr13:38796444
|
A | G | 63 | a0001c0001t0001g0053a0001c0001t0001g0158a0001c0001t0001g0172others(60): Show | 63 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.6019+11636A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796444 | ||||||
| chr13:38796458
|
G | A | 56 | a0001c0001t0001g0053a0001c0001t0001g0158a0001c0001t0001g0172others(53): Show | 56 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.6019+11650G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796458 | ||||||
| chr13:38796536
|
C | T | 2 | a0002c0006t0007g0237a0002c0011t0004g0218 | 2 | HG02738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6019+11728C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796536 | ||||||
| chr13:38796609
|
T | TAATG | 2 | a0005c0014t0001g0025a0006c0021t0002g0186 | 2 | HG01261.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.6019+11802_6019+11 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38796609 | |||||
| chr13:38796670
|
A | G | 1 | a0031c0056t0015g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6019+11862A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796670 | ||||||
| chr13:38796700
|
G | C | 2 | a0001c0001t0001g0052a0001c0029t0001g0149 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.6019+11892G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796700 | ||||||
| chr13:38796774
|
A | T | 111 | a0001c0001t0001g0053a0001c0001t0001g0158a0001c0001t0001g0172others(108): Show | 111 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.6019+11966A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796774 | ||||||
| chr13:38796847
|
G | GT | 4 | a0011c0018t0003g0112a0011c0018t0003g0113a0024c0041t0003g0235others(1): Show | 4 | HG02895.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+12045dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38796847 | |||||
| chr13:38796982
|
T | A | 79 | a0001c0001t0001g0053a0001c0001t0001g0158a0001c0001t0001g0172others(76): Show | 79 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.6019+12174T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38796982 | ||||||
| chr13:38797063
|
A | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+12255A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797063 | ||||||
| chr13:38797076
|
C | T | 17 | a0001c0001t0001g0175a0001c0001t0023g0167a0001c0002t0001g0156others(14): Show | 17 | HG00621.hp1 HG02083.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.6019+12268C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797076 | ||||||
| chr13:38797078
|
A | G | 2 | a0044c0084t0009g0197a0052c0045t0054g0257 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6019+12270A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797078 | ||||||
| chr13:38797141
|
A | AC | 160 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0158others(157): Show | 160 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.6019+12333_6019+12 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797141 | ||||||
| chr13:38797237
|
C | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+12429C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797237 | ||||||
| chr13:38797248
|
G | A | 2 | a0011c0018t0003g0112a0011c0018t0003g0113 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6019+12440G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797248 | ||||||
| chr13:38797366
|
T | G | 5 | a0001c0002t0032g0238a0001c0030t0047g0151a0021c0044t0056g0254others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+12558T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797366 | ||||||
| chr13:38797382
|
T | C | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6019+12574T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797382 | ||||||
| chr13:38797461
|
A | T | 162 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0158others(159): Show | 162 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.6019+12653A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797461 | ||||||
| chr13:38797462
|
A | T | 1 | a0003c0003t0003g0086 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.6019+12654A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797462 | ||||||
| chr13:38797742
|
C | T | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.6019+12934C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797742 | ||||||
| chr13:38797984
|
G | T | 1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6019+13176G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38797984 | ||||||
| chr13:38798311
|
C | A | 2 | a0002c0006t0007g0020a0005c0026t0002g0242 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.6019+13503C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38798311 | ||||||
| chr13:38798416
|
A | G | 13 | a0001c0009t0008g0260a0001c0012t0053g0251a0001c0017t0008g0261others(10): Show | 13 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.6019+13608A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38798416 | ||||||
| chr13:38798587
|
A | G | 1 | a0016c0059t0043g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6019+13779A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38798587 | ||||||
| chr13:38798629
|
T | C | 1 | a0001c0001t0027g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6019+13821T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38798629 | ||||||
| chr13:38798719
|
A | G | 141 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0158others(138): Show | 141 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.6019+13911A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38798719 | ||||||
| chr13:38799091
|
A | G | 1 | a0005c0026t0002g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6019+14283A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799091 | ||||||
| chr13:38799103
|
T | C | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+14295T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799103 | ||||||
| chr13:38799339
|
T | C | 1 | a0002c0011t0004g0228 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6019+14531T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799339 | ||||||
| chr13:38799384
|
A | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+14576A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799384 | ||||||
| chr13:38799415
|
G | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+14607G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799415 | ||||||
| chr13:38799416
|
A | G | 84 | a0001c0001t0001g0058a0001c0001t0001g0155a0001c0001t0001g0161others(81): Show | 84 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.6019+14608A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799416 | ||||||
| chr13:38799593
|
C | T | 82 | a0001c0001t0001g0058a0001c0001t0001g0155a0001c0001t0001g0161others(79): Show | 82 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.6019+14785C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799593 | ||||||
| chr13:38799659
|
A | G | 1 | a0015c0031t0003g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6019+14851A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799659 | ||||||
| chr13:38799971
|
A | G | 6 | a0001c0001t0001g0166a0001c0001t0002g0183a0002c0008t0002g0215others(3): Show | 6 | HG00438.hp1 HG02074.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+15163A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38799971 | ||||||
| chr13:38800004
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6019+15196T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800004 | ||||||
| chr13:38800164
|
T | C | 1 | a0009c0028t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.6019+15356T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800164 | ||||||
| chr13:38800166
|
G | A | 1 | a0005c0014t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6019+15358G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800166 | ||||||
| chr13:38800179
|
A | T | 1 | a0003c0003t0004g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6019+15371A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800179 | ||||||
| chr13:38800191
|
G | A | 1 | a0001c0012t0019g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6019+15383G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800191 | ||||||
| chr13:38800208
|
T | C | 2 | a0001c0001t0001g0177a0003c0003t0004g0094 | 2 | HG02027.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.6019+15400T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800208 | ||||||
| chr13:38800272
|
T | G | 73 | a0001c0001t0001g0052a0001c0001t0001g0166a0001c0001t0001g0168others(70): Show | 73 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.6019+15464T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800272 | ||||||
| chr13:38800286
|
T | G | 260 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(257): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.6019+15478T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800286 | ||||||
| chr13:38800374
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0028g0056a0007c0024t0006g0044 | 3 | HG01433.hp1 HG01496.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.6019+15566A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800374 | ||||||
| chr13:38800615
|
TTTTCGTC others(10): Show |
T | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+15810_6019+15 others(23): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38800615 | |||||
| chr13:38800619
|
C | T | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6019+15811C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800619 | ||||||
| chr13:38800704
|
A | C | 4 | a0001c0002t0032g0238a0001c0030t0047g0151a0021c0044t0056g0254others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+15896A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800704 | ||||||
| chr13:38800917
|
A | C | 1 | a0041c0079t0039g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6019+16109A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38800917 | ||||||
| chr13:38801091
|
C | T | 91 | a0001c0001t0001g0058a0001c0001t0001g0155a0001c0001t0001g0161others(88): Show | 91 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.6019+16283C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801091 | ||||||
| chr13:38801354
|
G | A | 3 | a0020c0040t0003g0005a0022c0043t0012g0234a0027c0053t0041g0116 | 3 | HG02723.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6019+16546G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801354 | ||||||
| chr13:38801467
|
T | C | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6019+16659T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801467 | ||||||
| chr13:38801547
|
T | C | 1 | a0006c0021t0002g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6019+16739T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801547 | ||||||
| chr13:38801602
|
A | G | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.6019+16794A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801602 | ||||||
| chr13:38801737
|
C | T | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+16929C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801737 | ||||||
| chr13:38801807
|
G | C | 1 | a0001c0012t0019g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6019+16999G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801807 | ||||||
| chr13:38801822
|
G | A | 1 | a0036c0061t0003g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6019+17014G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801822 | ||||||
| chr13:38801878
|
G | C | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6019+17070G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38801878 | ||||||
| chr13:38802163
|
G | A | 65 | a0001c0001t0001g0052a0001c0001t0001g0166a0001c0001t0001g0168others(62): Show | 65 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.6019+17355G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802163 | ||||||
| chr13:38802287
|
G | T | 151 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(148): Show | 151 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.6019+17479G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802287 | ||||||
| chr13:38802301
|
C | T | 6 | a0001c0009t0008g0253a0001c0017t0008g0249a0001c0070t0003g0095others(3): Show | 6 | HG02145.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+17493C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802301 | ||||||
| chr13:38802321
|
G | A | 2 | a0001c0002t0007g0179a0013c0023t0002g0074 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.6019+17513G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802321 | ||||||
| chr13:38802371
|
G | A | 1 | a0035c0062t0009g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6019+17563G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802371 | ||||||
| chr13:38802380
|
G | C | 1 | a0001c0002t0005g0176 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.6019+17572G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802380 | ||||||
| chr13:38802400
|
C | T | 2 | a0028c0054t0009g0117a0051c0046t0051g0245 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.6019+17592C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802400 | ||||||
| chr13:38802663
|
A | G | 188 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(185): Show | 188 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.6019+17855A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802663 | ||||||
| chr13:38802684
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.6019+17876G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802684 | ||||||
| chr13:38802771
|
G | A | 1 | a0002c0006t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6019+17963G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802771 | ||||||
| chr13:38802879
|
C | T | 3 | a0001c0029t0025g0003a0003c0003t0007g0076a0049c0097t0007g0006 | 3 | NA18940.hp2 NA18960.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.6019+18071C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802879 | ||||||
| chr13:38802954
|
G | A | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+18146G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38802954 | ||||||
| chr13:38803001
|
TTC | T | 4 | a0001c0001t0001g0058a0001c0001t0002g0159a0004c0004t0005g0009others(1): Show | 4 | HG02135.hp2 NA18946.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+18197_6019+18 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38803001 | |||||
| chr13:38803011
|
A | C | 4 | a0001c0001t0001g0058a0001c0001t0002g0159a0004c0004t0005g0009others(1): Show | 4 | HG02135.hp2 NA18946.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+18203A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803011 | ||||||
| chr13:38803030
|
A | G | 1 | a0036c0061t0003g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6019+18222A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803030 | ||||||
| chr13:38803050
|
G | A | 67 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.6019+18242G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803050 | ||||||
| chr13:38803110
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+18302G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803110 | ||||||
| chr13:38803175
|
G | A | 30 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(27): Show | 30 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.6019+18367G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803175 | ||||||
| chr13:38803200
|
C | T | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+18392C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803200 | ||||||
| chr13:38803362
|
G | A | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6019+18554G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803362 | ||||||
| chr13:38803466
|
T | C | 3 | a0006c0016t0021g0246a0010c0013t0003g0107a0026c0052t0003g0122 | 3 | HG02145.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.6019+18658T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803466 | ||||||
| chr13:38803560
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+18752G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803560 | ||||||
| chr13:38803593
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6019+18785A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803593 | ||||||
| chr13:38803700
|
T | C | 31 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(28): Show | 31 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.6019+18892T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803700 | ||||||
| chr13:38803840
|
C | T | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+19032C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803840 | ||||||
| chr13:38803938
|
T | C | 3 | a0022c0043t0012g0234a0025c0048t0003g0225a0027c0053t0041g0116 | 3 | HG01243.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6019+19130T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38803938 | ||||||
| chr13:38804212
|
T | C | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+19404T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38804212 | ||||||
| chr13:38804624
|
A | G | 2 | a0001c0017t0008g0261a0053c0069t0003g0108 | 2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6019+19816A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38804624 | ||||||
| chr13:38804801
|
G | A | 1 | a0003c0005t0001g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6019+19993G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38804801 | ||||||
| chr13:38804885
|
T | C | 29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6019+20077T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38804885 | ||||||
| chr13:38804901
|
A | G | 63 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(60): Show | 63 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.6019+20093A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38804901 | ||||||
| chr13:38805122
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6019+20314C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805122 | ||||||
| chr13:38805148
|
GGAAGCAC others(4124): Show |
G | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6019+20343_6019+24 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38805148 | |||||
| chr13:38805228
|
C | A | 21 | a0001c0002t0032g0238a0001c0009t0008g0253a0001c0012t0050g0258others(18): Show | 21 | HG01243.hp2 HG01261.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.6019+20420C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805228 | ||||||
| chr13:38805632
|
G | A | 1 | a0001c0030t0003g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6019+20824G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805632 | ||||||
| chr13:38805782
|
T | A | 1 | a0026c0052t0003g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6019+20974T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805782 | ||||||
| chr13:38805818
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6019+21010C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805818 | ||||||
| chr13:38805860
|
C | A | 20 | a0001c0001t0007g0174a0001c0017t0008g0261a0001c0030t0003g0144others(17): Show | 20 | HG01109.hp2 HG01496.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.6019+21052C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38805860 | ||||||
| chr13:38806002
|
CT | C | 5 | a0001c0030t0003g0144a0004c0007t0001g0047a0009c0028t0001g0146others(2): Show | 5 | HG03139.hp2 NA18906.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+21207delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38806002 | |||||
| chr13:38806436
|
G | A | 2 | a0006c0016t0021g0246a0026c0052t0003g0122 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.6019+21628G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806436 | ||||||
| chr13:38806493
|
G | A | 14 | a0001c0030t0003g0144a0001c0030t0003g0145a0004c0004t0012g0196others(11): Show | 14 | HG01109.hp2 HG01496.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.6019+21685G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806493 | ||||||
| chr13:38806570
|
C | A | 25 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0009t0008g0253others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.6019+21762C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806570 | ||||||
| chr13:38806612
|
CTAA | C | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+21806_6019+21 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38806612 | |||||
| chr13:38806748
|
A | G | 1 | a0002c0092t0046g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6019+21940A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806748 | ||||||
| chr13:38806900
|
T | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+22092T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806900 | ||||||
| chr13:38806908
|
C | G | 148 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(145): Show | 148 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.6019+22100C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38806908 | ||||||
| chr13:38807011
|
A | G | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+22203A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807011 | ||||||
| chr13:38807054
|
T | A | 3 | a0001c0001t0001g0053a0001c0029t0002g0150a0004c0007t0001g0010 | 3 | HG00558.hp1 HG01934.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.6019+22246T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807054 | ||||||
| chr13:38807106
|
T | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+22298T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807106 | ||||||
| chr13:38807164
|
C | A | 63 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(60): Show | 63 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.6019+22356C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807164 | ||||||
| chr13:38807188
|
G | GAT | 5 | a0001c0001t0001g0172a0001c0001t0002g0183a0001c0002t0004g0169others(2): Show | 5 | HG02071.hp1 HG02074.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATAT | 11 | a0001c0001t0002g0185a0001c0033t0010g0204a0002c0006t0007g0237others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATAT | 24 | a0001c0001t0013g0202a0001c0002t0005g0176a0001c0002t0032g0238others(21): Show | 24 | HG01255.hp1 HG01255.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(1): Show |
27 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0027g0110others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(3): Show |
15 | a0001c0001t0001g0177a0001c0002t0003g0138a0001c0002t0003g0180others(12): Show | 15 | HG00642.hp2 HG01261.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(5): Show |
18 | a0001c0001t0001g0052a0001c0001t0001g0192a0001c0001t0023g0167others(15): Show | 18 | HG00621.hp2 HG00738.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(7): Show |
15 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0010t0001g0026others(12): Show | 15 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(9): Show |
11 | a0001c0002t0001g0135a0001c0002t0004g0232a0001c0033t0010g0136others(8): Show | 11 | HG00741.hp1 HG01433.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(11): Show |
3 | a0001c0001t0001g0158a0003c0003t0004g0084a0007c0025t0003g0229 | 3 | HG01192.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(13): Show |
3 | a0001c0001t0001g0168a0002c0010t0045g0023a0002c0011t0004g0206 | 3 | HG00438.hp2 HG02735.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(15): Show |
2 | a0001c0002t0004g0154a0001c0009t0008g0262 | 2 | HG03139.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6019+22380_6019+22 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
G | GATATATA others(17): Show |
1 | a0007c0037t0006g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6019+22380_6019+22 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
GTTATATA others(3): Show |
G | 7 | a0001c0030t0003g0144a0001c0030t0003g0145a0014c0022t0003g0001others(4): Show | 7 | HG01109.hp2 HG02280.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.6019+22381_6019+22 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
GTTATATA others(5): Show |
G | 7 | a0002c0008t0002g0209a0004c0004t0011g0061a0004c0004t0012g0196others(4): Show | 7 | HG01496.hp1 HG01981.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.6019+22381_6019+22 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
GTTATATA others(7): Show |
G | 5 | a0001c0001t0018g0057a0001c0017t0008g0261a0004c0007t0018g0039others(2): Show | 5 | HG01891.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+22381_6019+22 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
GTTATATA others(9): Show |
G | 3 | a0003c0003t0003g0086a0004c0007t0001g0012a0004c0007t0001g0047 | 3 | NA19010.hp1 NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.6019+22381_6019+22 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807188
|
GTTATATA others(15): Show |
G | 5 | a0006c0096t0015g0153a0014c0022t0014g0193a0016c0059t0043g0101others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+22381_6019+22 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807188 | ||||||
| chr13:38807189
|
T | A | 140 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(137): Show | 140 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.6019+22381T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807189 | ||||||
| chr13:38807189
|
T | TTA | 9 | a0001c0012t0053g0251a0002c0006t0001g0096a0003c0005t0026g0091others(6): Show | 9 | HG00639.hp2 HG01243.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.6019+22419_6019+22 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATA | 5 | a0001c0001t0001g0190a0001c0009t0008g0247a0004c0004t0005g0009others(2): Show | 5 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+22417_6019+22 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATA | 11 | a0001c0001t0001g0181a0001c0001t0002g0159a0001c0002t0004g0184others(8): Show | 11 | HG00423.hp1 HG00735.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.6019+22415_6019+22 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(1): Show |
8 | a0001c0001t0001g0161a0001c0001t0001g0165a0002c0006t0002g0022others(5): Show | 8 | HG00639.hp1 HG00738.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.6019+22413_6019+22 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0001g0171a0001c0001t0028g0056a0001c0009t0008g0260 | 3 | HG01515.hp1 HG01943.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.6019+22411_6019+22 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0053a0001c0029t0025g0003a0002c0008t0001g0219others(3): Show | 6 | HG00558.hp1 HG01516.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.6019+22409_6019+22 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0058a0001c0029t0002g0150a0009c0028t0001g0143others(2): Show | 5 | NA18953.hp1 NA19003.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+22407_6019+22 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(9): Show |
7 | a0001c0002t0001g0162a0001c0017t0055g0256a0002c0036t0007g0017others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.6019+22405_6019+22 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0164a0003c0003t0007g0076 | 2 | HG00673.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.6019+22403_6019+22 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
TTATA | T | 4 | a0001c0001t0007g0174a0001c0002t0007g0179a0018c0073t0002g0132others(1): Show | 4 | HG02572.hp1 HG03017.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+22417_6019+22 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
TTATATAT others(3): Show |
T | 2 | a0004c0007t0001g0046a0038c0064t0033g0103 | 2 | HG03195.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.6019+22411_6019+22 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
TTATATAT others(5): Show |
T | 1 | a0006c0021t0016g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6019+22409_6019+22 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
TTATATAT others(7): Show |
T | 2 | a0001c0012t0019g0259a0015c0031t0003g0129 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6019+22407_6019+22 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807189
|
TTATATAT others(11): Show |
T | 2 | a0041c0079t0039g0093a0049c0097t0007g0006 | 2 | HG02559.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.6019+22403_6019+22 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807189 | |||||
| chr13:38807190
|
T | TATATATA others(9): Show |
1 | a0012c0020t0002g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6019+22397_6019+22 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807190 | |||||
| chr13:38807199
|
ATATATAT others(23): Show |
A | 3 | a0001c0002t0005g0140a0003c0005t0002g0075a0005c0014t0040g0098 | 3 | HG00621.hp1 NA18962.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.6019+22395_6019+22 others(36): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807199 | |||||
| chr13:38807229
|
G | A | 64 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0172others(61): Show | 64 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.6019+22421G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807229 | ||||||
| chr13:38807442
|
T | C | 1 | a0001c0033t0010g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6019+22634T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807442 | ||||||
| chr13:38807447
|
A | T | 67 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.6019+22639A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807447 | ||||||
| chr13:38807507
|
A | AT | 6 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0181others(3): Show | 6 | HG00735.hp1 HG01361.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+22705dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807507 | |||||
| chr13:38807553
|
A | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+22745A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807553 | ||||||
| chr13:38807741
|
C | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0168others(9): Show | 12 | HG00438.hp2 HG00642.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.6019+22933C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807741 | ||||||
| chr13:38807843
|
G | A | 1 | a0038c0064t0033g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6019+23035G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807843 | ||||||
| chr13:38807903
|
G | A | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+23095G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38807903 | ||||||
| chr13:38807961
|
GCTT | G | 7 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(4): Show | 7 | HG01192.hp2 HG01891.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.6019+23161_6019+23 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38807961 | |||||
| chr13:38808061
|
C | T | 63 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(60): Show | 63 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.6019+23253C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808061 | ||||||
| chr13:38808063
|
A | G | 1 | a0008c0019t0003g0121 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6019+23255A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808063 | ||||||
| chr13:38808163
|
A | G | 65 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.6019+23355A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808163 | ||||||
| chr13:38808513
|
A | T | 173 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(170): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.6019+23705A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808513 | ||||||
| chr13:38808552
|
T | A | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+23744T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808552 | ||||||
| chr13:38808560
|
C | G | 168 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(165): Show | 168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.6019+23752C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808560 | ||||||
| chr13:38808728
|
C | G | 3 | a0001c0001t0002g0159a0004c0004t0005g0009a0004c0004t0044g0016 | 3 | HG02135.hp2 NA18946.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.6019+23920C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808728 | ||||||
| chr13:38808751
|
C | A | 81 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(78): Show | 81 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.6019+23943C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808751 | ||||||
| chr13:38808965
|
G | A | 2 | a0012c0020t0017g0130a0012c0020t0049g0124 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6019+24157G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38808965 | ||||||
| chr13:38809109
|
C | T | 2 | a0005c0014t0001g0025a0008c0019t0003g0121 | 2 | HG01261.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.6019+24301C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809109 | ||||||
| chr13:38809197
|
A | G | 5 | a0004c0004t0003g0198a0006c0016t0052g0244a0012c0020t0017g0130others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+24389A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809197 | ||||||
| chr13:38809315
|
T | A | 9 | a0001c0001t0001g0190a0001c0001t0028g0056a0001c0030t0047g0151others(6): Show | 9 | HG01433.hp1 HG01496.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.6019+24507T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809315 | ||||||
| chr13:38809503
|
A | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+24695A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809503 | ||||||
| chr13:38809509
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6019+24701C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809509 | ||||||
| chr13:38809514
|
G | T | 1 | a0006c0032t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6019+24706G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809514 | ||||||
| chr13:38809536
|
T | A | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.6019+24728T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809536 | ||||||
| chr13:38809641
|
C | T | 2 | a0014c0022t0014g0193a0052c0045t0054g0257 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.6019+24833C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809641 | ||||||
| chr13:38809642
|
G | A | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+24834G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809642 | ||||||
| chr13:38809647
|
G | A | 95 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(92): Show | 95 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.6019+24839G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809647 | ||||||
| chr13:38809694
|
A | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+24886A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809694 | ||||||
| chr13:38809787
|
T | C | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+24979T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809787 | ||||||
| chr13:38809907
|
G | T | 2 | a0002c0077t0009g0139a0020c0040t0003g0005 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.6019+25099G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809907 | ||||||
| chr13:38809959
|
G | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6019+25151G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809959 | ||||||
| chr13:38809961
|
A | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6019+25153A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809961 | ||||||
| chr13:38809962
|
C | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6019+25154C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809962 | ||||||
| chr13:38809963
|
A | C | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6019+25155A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809963 | ||||||
| chr13:38809964
|
TGAAATAT others(10649): Show |
T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6019+25159_6020-25 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38809964 | |||||
| chr13:38809993
|
A | G | 16 | a0001c0017t0008g0261a0001c0030t0003g0144a0001c0030t0003g0145others(13): Show | 16 | HG01109.hp2 HG01496.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.6019+25185A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38809993 | ||||||
| chr13:38810014
|
T | C | 1 | a0001c0002t0001g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.6019+25206T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810014 | ||||||
| chr13:38810030
|
C | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+25222C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810030 | ||||||
| chr13:38810030
|
C | G | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6019+25222C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810030 | ||||||
| chr13:38810123
|
T | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6019+25315T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810123 | ||||||
| chr13:38810129
|
A | G | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6019+25321A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810129 | ||||||
| chr13:38810229
|
T | TA | 94 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(91): Show | 94 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.6019+25421_6019+25 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810229 | ||||||
| chr13:38810382
|
T | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+25574T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810382 | ||||||
| chr13:38810476
|
A | G | 2 | a0028c0054t0009g0117a0051c0046t0051g0245 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.6019+25668A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810476 | ||||||
| chr13:38810758
|
A | G | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+25950A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38810758 | ||||||
| chr13:38811100
|
G | C | 5 | a0001c0012t0053g0251a0003c0005t0026g0091a0006c0016t0021g0255others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+26292G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811100 | ||||||
| chr13:38811105
|
A | T | 68 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.6019+26297A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811105 | ||||||
| chr13:38811135
|
G | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+26327G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811135 | ||||||
| chr13:38811161
|
C | T | 62 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.6019+26353C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811161 | ||||||
| chr13:38811298
|
A | T | 2 | a0005c0090t0002g0099a0006c0032t0002g0142 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.6019+26490A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811298 | ||||||
| chr13:38811571
|
G | A | 4 | a0001c0002t0001g0135a0022c0043t0012g0234a0025c0048t0003g0225others(1): Show | 4 | HG01243.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+26763G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811571 | ||||||
| chr13:38811603
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+26795G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811603 | ||||||
| chr13:38811719
|
G | A | 92 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(89): Show | 92 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.6019+26911G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811719 | ||||||
| chr13:38811736
|
G | A | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6019+26928G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811736 | ||||||
| chr13:38811800
|
A | G | 1 | a0001c0002t0005g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6019+26992A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811800 | ||||||
| chr13:38811908
|
G | A | 62 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.6019+27100G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38811908 | ||||||
| chr13:38812179
|
G | A | 62 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.6019+27371G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812179 | ||||||
| chr13:38812189
|
A | T | 1 | a0001c0033t0010g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6019+27381A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812189 | ||||||
| chr13:38812198
|
G | A | 3 | a0002c0006t0001g0096a0004c0004t0005g0064a0006c0095t0037g0152 | 3 | HG02027.hp1 NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.6019+27390G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812198 | ||||||
| chr13:38812241
|
G | A | 1 | a0001c0033t0010g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6019+27433G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812241 | ||||||
| chr13:38812318
|
A | T | 3 | a0003c0003t0005g0070a0003c0003t0005g0082a0009c0038t0005g0133 | 3 | NA18955.hp1 NA18992.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.6019+27510A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812318 | ||||||
| chr13:38812422
|
G | A | 1 | a0023c0042t0048g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6019+27614G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812422 | ||||||
| chr13:38812443
|
T | C | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+27635T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812443 | ||||||
| chr13:38812605
|
G | T | 6 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.6019+27797G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812605 | ||||||
| chr13:38812706
|
C | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6019+27898C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812706 | ||||||
| chr13:38812781
|
G | T | 62 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.6019+27973G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812781 | ||||||
| chr13:38812798
|
G | A | 20 | a0001c0001t0001g0192a0001c0017t0008g0261a0001c0030t0003g0144others(17): Show | 20 | HG00621.hp2 HG01109.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.6019+27990G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812798 | ||||||
| chr13:38812807
|
C | T | 1 | a0002c0006t0013g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6019+27999C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812807 | ||||||
| chr13:38812882
|
C | CA | 4 | a0001c0002t0003g0138a0001c0002t0003g0180a0002c0008t0001g0230others(1): Show | 4 | HG00642.hp2 HG00741.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+28081dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38812882 | |||||
| chr13:38812890
|
C | A | 52 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(49): Show | 52 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.6019+28082C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38812890 | ||||||
| chr13:38812916
|
C | CA | 8 | a0001c0002t0032g0238a0001c0030t0047g0151a0002c0006t0001g0033others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.6019+28120dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38812916 | |||||
| chr13:38813025
|
T | A | 1 | a0056c0074t0010g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6019+28217T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813025 | ||||||
| chr13:38813032
|
G | T | 1 | a0006c0021t0002g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6019+28224G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813032 | ||||||
| chr13:38813101
|
A | G | 1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6019+28293A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813101 | ||||||
| chr13:38813222
|
T | C | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+28414T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813222 | ||||||
| chr13:38813350
|
G | GT | 5 | a0001c0009t0008g0247a0001c0029t0002g0150a0004c0004t0012g0196others(2): Show | 5 | HG01175.hp2 HG01496.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+28550dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813350 | |||||
| chr13:38813351
|
T | G | 62 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.6019+28543T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813351 | ||||||
| chr13:38813406
|
G | T | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+28598G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813406 | ||||||
| chr13:38813442
|
G | A | 3 | a0006c0016t0021g0246a0010c0013t0003g0107a0026c0052t0003g0122 | 3 | HG02145.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.6019+28634G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813442 | ||||||
| chr13:38813463
|
TTTCTCTC others(20): Show |
T | 1 | a0003c0003t0036g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6019+28657_6019+28 others(33): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813463 | |||||
| chr13:38813464
|
TTCTC | T | 5 | a0001c0002t0001g0162a0002c0011t0004g0211a0003c0003t0007g0076others(2): Show | 5 | HG03098.hp2 HG03492.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+28707_6019+28 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTC | T | 4 | a0001c0001t0028g0056a0001c0002t0004g0141a0002c0008t0001g0219others(1): Show | 4 | HG01934.hp2 HG01943.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28705_6019+28 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(1): Show |
T | 4 | a0001c0001t0018g0057a0001c0002t0005g0163a0003c0005t0001g0071others(1): Show | 4 | HG01891.hp1 HG02135.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28703_6019+28 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(3): Show |
T | 2 | a0002c0010t0004g0068a0004c0004t0044g0016 | 2 | HG01433.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.6019+28701_6019+28 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0002g0185a0003c0005t0001g0080 | 2 | HG02129.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.6019+28699_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(7): Show |
T | 6 | a0002c0006t0001g0096a0002c0006t0007g0020a0008c0019t0003g0121others(3): Show | 6 | HG00738.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.6019+28697_6019+28 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(11): Show |
T | 1 | a0057c0076t0002g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6019+28693_6019+28 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(15): Show |
T | 1 | a0004c0004t0012g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6019+28689_6019+28 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(48): Show |
T | 2 | a0001c0002t0004g0169a0002c0010t0004g0034 | 2 | HG02129.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.6019+28702_6019+28 others(61): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813464
|
TTCTCTCT others(50): Show |
T | 1 | a0020c0040t0003g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6019+28700_6019+28 others(63): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813464 | |||||
| chr13:38813465
|
TCTCTCTC others(46): Show |
T | 1 | a0001c0009t0008g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6019+28704_6019+28 others(59): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813465 | |||||
| chr13:38813467
|
TCTCTCTC others(44): Show |
T | 1 | a0030c0055t0003g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6019+28706_6019+28 others(57): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813467 | |||||
| chr13:38813471
|
TCTCTCTC others(40): Show |
T | 1 | a0001c0070t0003g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6019+28710_6019+28 others(53): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813471 | |||||
| chr13:38813473
|
TCTCTCTC others(38): Show |
T | 2 | a0001c0012t0050g0258a0001c0017t0008g0249 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(51): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813473 | |||||
| chr13:38813479
|
TCTCTCTC others(32): Show |
T | 1 | a0004c0004t0011g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6019+28711_6019+28 others(45): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813479 | |||||
| chr13:38813481
|
TCTCTCTC others(30): Show |
T | 2 | a0002c0011t0035g0227a0008c0051t0003g0120 | 2 | HG00558.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(43): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813481 | |||||
| chr13:38813483
|
TCTCTCTC others(28): Show |
T | 7 | a0001c0002t0004g0154a0002c0006t0001g0030a0002c0010t0004g0035others(4): Show | 7 | HG00423.hp2 HG00735.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(41): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813483 | |||||
| chr13:38813485
|
TCTCTCTC others(26): Show |
T | 6 | a0001c0002t0001g0135a0001c0030t0047g0151a0002c0006t0007g0237others(3): Show | 6 | HG01167.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(39): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813485 | |||||
| chr13:38813487
|
TCTCTCTC others(24): Show |
T | 3 | a0001c0001t0001g0158a0001c0002t0004g0054a0002c0011t0004g0218 | 3 | HG01952.hp1 HG02738.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(37): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813487 | |||||
| chr13:38813489
|
TCTCTCTC others(22): Show |
T | 5 | a0002c0011t0004g0217a0002c0092t0046g0036a0003c0003t0004g0090others(2): Show | 5 | HG01361.hp1 HG02004.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(35): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813489 | |||||
| chr13:38813490
|
CTCTCTCT others(16): Show |
C | 1 | a0001c0009t0008g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6019+28683_6019+28 others(29): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813490 | ||||||
| chr13:38813491
|
TCTCTCTC others(20): Show |
T | 7 | a0001c0001t0013g0202a0001c0002t0003g0180a0002c0006t0001g0038others(4): Show | 7 | HG01109.hp1 HG01255.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(33): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813491 | |||||
| chr13:38813493
|
TCTCTCTC others(18): Show |
T | 9 | a0001c0001t0001g0177a0001c0002t0003g0138a0001c0002t0004g0232others(6): Show | 9 | HG00741.hp2 HG01346.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(31): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813493 | |||||
| chr13:38813494
|
CT | C | 3 | a0006c0016t0021g0246a0022c0043t0012g0234a0026c0052t0003g0122 | 3 | HG02145.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6019+28687delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813494 | ||||||
| chr13:38813494
|
CTCTCTCT others(8): Show |
C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6019+28687_6019+28 others(21): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813494 | ||||||
| chr13:38813494
|
CTCTCTCT others(10): Show |
C | 1 | a0028c0054t0009g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6019+28687_6019+28 others(23): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813494 | ||||||
| chr13:38813496
|
CTCTCTCT others(6): Show |
C | 2 | a0044c0084t0009g0197a0052c0045t0054g0257 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6019+28689_6019+28 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813496
|
CTCTCTCT others(10): Show |
C | 2 | a0008c0019t0012g0115a0014c0022t0014g0193 | 2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6019+28689_6019+28 others(23): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813496
|
CTCTCTCT others(12): Show |
C | 1 | a0006c0096t0015g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6019+28689_6019+28 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813496
|
CTCTCTCT others(17): Show |
C | 1 | a0023c0042t0048g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6019+28689_6019+28 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813496
|
CTCTCTCT others(21): Show |
C | 2 | a0016c0059t0043g0101a0031c0056t0015g0125 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.6019+28689_6019+28 others(34): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813496
|
CTCTCTCT others(29): Show |
C | 1 | a0037c0063t0014g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6019+28689_6019+28 others(42): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813496 | ||||||
| chr13:38813497
|
TCTCTCTC others(14): Show |
T | 5 | a0001c0002t0004g0231a0003c0003t0003g0086a0003c0003t0005g0089others(2): Show | 5 | HG00673.hp1 NA18946.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(27): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813497 | |||||
| chr13:38813498
|
CTCTCTCT others(17): Show |
C | 1 | a0001c0017t0008g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6019+28691_6019+28 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813498 | ||||||
| chr13:38813498
|
CTCTCTCT others(19): Show |
C | 3 | a0001c0030t0003g0144a0001c0030t0003g0145a0014c0022t0003g0001 | 3 | HG03579.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.6019+28691_6019+28 others(32): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813498 | ||||||
| chr13:38813498
|
CTCTCTCT others(21): Show |
C | 1 | a0050c0075t0003g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6019+28691_6019+28 others(34): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813498 | ||||||
| chr13:38813499
|
TCTCTCTC others(12): Show |
T | 2 | a0002c0011t0004g0206a0004c0007t0001g0043 | 2 | HG00438.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(25): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813499 | |||||
| chr13:38813500
|
CTCTCTCT others(8): Show |
C | 1 | a0003c0005t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6019+28693_6019+28 others(21): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813500 | ||||||
| chr13:38813500
|
CTCTCTCT others(13): Show |
C | 1 | a0009c0038t0007g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.6019+28693_6019+28 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813500 | ||||||
| chr13:38813500
|
CTCTCTCT others(15): Show |
C | 1 | a0004c0089t0001g0239 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.6019+28693_6019+28 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813500 | ||||||
| chr13:38813500
|
CTCTCTCT others(17): Show |
C | 2 | a0014c0022t0003g0002a0032c0058t0003g0195 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6019+28693_6019+28 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813500 | ||||||
| chr13:38813500
|
CTCTCTCT others(19): Show |
C | 1 | a0002c0027t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.6019+28693_6019+28 others(32): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813500 | ||||||
| chr13:38813501
|
TCTCTCTC others(10): Show |
T | 4 | a0002c0008t0001g0230a0003c0003t0004g0094a0003c0003t0005g0070others(1): Show | 4 | HG00642.hp2 NA18947.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(23): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813501 | |||||
| chr13:38813503
|
TCTCTCTC others(8): Show |
T | 3 | a0001c0001t0001g0155a0001c0002t0006g0188a0002c0006t0001g0033 | 3 | HG01358.hp1 NA19056.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(21): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813503 | |||||
| chr13:38813504
|
CTCTCTCT others(4): Show |
C | 3 | a0001c0002t0005g0170a0002c0010t0045g0023a0002c0027t0001g0021 | 3 | HG01070.hp1 HG02735.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.6019+28697_6019+28 others(17): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813504 | ||||||
| chr13:38813504
|
CTCTCTCT others(9): Show |
C | 2 | a0001c0029t0001g0149a0010c0013t0006g0055 | 2 | HG00642.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.6019+28697_6019+28 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813504 | ||||||
| chr13:38813504
|
CTCTCTCT others(11): Show |
C | 5 | a0001c0001t0001g0175a0001c0002t0005g0176a0001c0033t0010g0136others(2): Show | 5 | HG02083.hp1 NA18944.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+28697_6019+28 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813504 | ||||||
| chr13:38813504
|
CTCTCTCT others(13): Show |
C | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6019+28697_6019+28 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813504 | ||||||
| chr13:38813505
|
TCTCTCTC others(6): Show |
T | 4 | a0001c0001t0002g0183a0001c0001t0023g0167a0004c0007t0001g0047others(1): Show | 4 | HG02074.hp1 NA19004.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(19): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813505 | |||||
| chr13:38813506
|
CT | C | 4 | a0001c0001t0027g0110a0001c0012t0019g0252a0004c0007t0018g0039others(1): Show | 4 | HG01192.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28699delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813506 | ||||||
| chr13:38813506
|
CTCTCTCT others(2): Show |
C | 4 | a0001c0001t0001g0166a0002c0008t0001g0208a0038c0064t0033g0103others(1): Show | 4 | HG00438.hp1 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.6019+28699_6019+28 others(15): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813506 | ||||||
| chr13:38813506
|
CTCTCTCT others(7): Show |
C | 4 | a0001c0001t0001g0052a0001c0067t0001g0182a0004c0007t0001g0014others(1): Show | 4 | HG01981.hp2 HG02074.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28699_6019+28 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813506 | ||||||
| chr13:38813506
|
CTCTCTCT others(9): Show |
C | 1 | a0007c0037t0006g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6019+28699_6019+28 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813506 | ||||||
| chr13:38813506
|
CTCTCTCT others(13): Show |
C | 1 | a0005c0035t0002g0018 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6019+28699_6019+28 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813506 | ||||||
| chr13:38813506
|
CTCTCTCT others(52): Show |
C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6019+28700_6019+28 others(65): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813506 | |||||
| chr13:38813507
|
TCTCTCTC others(4): Show |
T | 4 | a0005c0026t0002g0242a0008c0019t0003g0118a0018c0072t0002g0134others(1): Show | 4 | HG00741.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(17): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813507 | |||||
| chr13:38813508
|
CT | C | 3 | a0001c0002t0001g0156a0001c0068t0005g0160a0016c0060t0029g0106 | 3 | NA18951.hp1 NA19057.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6019+28701delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813508 | ||||||
| chr13:38813508
|
CTCTCTCT others(5): Show |
C | 2 | a0001c0001t0007g0174a0043c0082t0017g0048 | 2 | HG02976.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6019+28701_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813508 | ||||||
| chr13:38813508
|
CTCTCTCT others(7): Show |
C | 2 | a0001c0001t0001g0168a0001c0009t0020g0250 | 2 | HG02896.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.6019+28701_6019+28 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813508 | ||||||
| chr13:38813508
|
CTCTCTCT others(11): Show |
C | 1 | a0008c0050t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6019+28701_6019+28 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813508 | ||||||
| chr13:38813508
|
CTCTCTCT others(27): Show |
C | 3 | a0003c0003t0034g0081a0003c0005t0002g0085a0004c0004t0004g0063 | 3 | HG03834.hp2 NA19070.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.6019+28701_6019+28 others(40): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813508 | ||||||
| chr13:38813510
|
CTCTCTCT others(5): Show |
C | 2 | a0001c0009t0020g0248a0003c0003t0004g0084 | 2 | HG02897.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.6019+28703_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813510 | ||||||
| chr13:38813510
|
CTCTCTCT others(25): Show |
C | 2 | a0003c0003t0002g0067a0004c0004t0004g0008 | 2 | NA18962.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.6019+28703_6019+28 others(38): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813510 | ||||||
| chr13:38813511
|
T | TCTC | 3 | a0001c0029t0002g0150a0005c0014t0040g0098a0015c0031t0003g0129 | 3 | HG00621.hp1 NA19009.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6019+28704_6019+28 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813511 | |||||
| chr13:38813512
|
CTCTCTCC others(48): Show |
C | 2 | a0001c0001t0001g0172a0003c0003t0004g0069 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.6019+28706_6019+28 others(61): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813512 | |||||
| chr13:38813513
|
TCTCTC | T | 5 | a0001c0001t0001g0164a0002c0006t0001g0079a0011c0018t0003g0112others(2): Show | 5 | HG00673.hp2 HG00735.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813513 | |||||
| chr13:38813514
|
CT | C | 3 | a0002c0036t0007g0017a0006c0016t0052g0244a0054c0066t0003g0051 | 3 | HG01169.hp2 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.6019+28707delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813514 | ||||||
| chr13:38813516
|
CTCCTCTC others(48): Show |
C | 1 | a0022c0043t0012g0234 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6019+28710_6019+28 others(61): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813516 | |||||
| chr13:38813517
|
T | C | 8 | a0001c0002t0005g0140a0001c0012t0019g0259a0001c0029t0025g0003others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.6019+28709T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813517 | ||||||
| chr13:38813517
|
TC | T | 54 | a0001c0001t0001g0058a0001c0001t0001g0166a0001c0001t0001g0178others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.6019+28711delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813517 | |||||
| chr13:38813518
|
C | CT | 16 | a0001c0001t0001g0181a0001c0001t0002g0159a0001c0029t0002g0150others(13): Show | 16 | HG00621.hp1 HG01175.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.6019+28710_6019+28 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
C | CTCT | 3 | a0001c0001t0001g0053a0001c0001t0001g0161a0040c0081t0006g0066 | 3 | HG00558.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.6019+28710_6019+28 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
C | CTCTCTCT others(7): Show |
1 | a0001c0009t0008g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6019+28710_6019+28 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
C | CTCTCTCT others(4): Show |
1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6019+28710_6019+28 others(17): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
C | T | 8 | a0001c0002t0005g0140a0001c0012t0019g0259a0001c0029t0025g0003others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.6019+28710C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
CCTCTCTC others(44): Show |
C | 1 | a0010c0013t0003g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6019+28711_6019+28 others(57): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
CCTCTCTC others(46): Show |
C | 1 | a0027c0053t0041g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6019+28711_6019+28 others(59): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813518
|
CCTCTCTC others(50): Show |
C | 2 | a0006c0016t0021g0246a0026c0052t0003g0122 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.6019+28711_6019+28 others(63): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813518 | ||||||
| chr13:38813527
|
CTCTCTCT others(41): Show |
C | 1 | a0035c0062t0009g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6019+28721_6019+28 others(54): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813527 | |||||
| chr13:38813527
|
CTCTCTCT others(45): Show |
C | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6019+28721_6019+28 others(58): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813527 | |||||
| chr13:38813529
|
CTCTCTCT others(39): Show |
C | 4 | a0001c0001t0027g0110a0001c0012t0019g0252a0004c0007t0018g0039others(1): Show | 4 | HG01192.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+28723_6019+28 others(52): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813529 | |||||
| chr13:38813529
|
CTCTCTCT others(41): Show |
C | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6019+28723_6019+28 others(54): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813529 | |||||
| chr13:38813531
|
CTCTCTCT others(37): Show |
C | 1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6019+28725_6019+28 others(50): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813531 | |||||
| chr13:38813533
|
C | A | 1 | a0003c0003t0005g0089 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6019+28725C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813533 | ||||||
| chr13:38813533
|
CTCTCTCT others(33): Show |
C | 2 | a0001c0002t0001g0156a0002c0010t0004g0097 | 2 | NA18951.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.6019+28727_6019+28 others(46): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813533 | |||||
| chr13:38813535
|
C | A | 2 | a0003c0003t0005g0089a0004c0007t0001g0047 | 2 | NA18946.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.6019+28727C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813535 | ||||||
| chr13:38813535
|
CTCTCTCT others(33): Show |
C | 1 | a0001c0068t0005g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.6019+28729_6019+28 others(46): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813535 | |||||
| chr13:38813537
|
C | A | 3 | a0003c0003t0005g0089a0004c0007t0001g0047a0008c0051t0003g0120 | 3 | HG03130.hp2 NA18946.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.6019+28729C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813537 | ||||||
| chr13:38813537
|
CTCTCTCT others(25): Show |
C | 1 | a0002c0011t0004g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.6019+28731_6019+28 others(38): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813537 | |||||
| chr13:38813539
|
C | A | 12 | a0001c0002t0001g0135a0001c0002t0004g0231a0002c0006t0001g0038others(9): Show | 12 | HG00673.hp1 HG00741.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.6019+28731C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813539 | ||||||
| chr13:38813539
|
CTCTCTCT others(25): Show |
C | 1 | a0001c0002t0004g0141 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.6019+28733_6019+28 others(38): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813539 | |||||
| chr13:38813539
|
CTCTCTCT others(29): Show |
C | 2 | a0001c0001t0018g0057a0034c0088t0011g0226 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6019+28733_6019+28 others(42): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813539 | |||||
| chr13:38813541
|
C | A | 15 | a0001c0002t0001g0135a0001c0002t0004g0231a0002c0006t0001g0038others(12): Show | 15 | HG00673.hp1 HG00741.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.6019+28733C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813541 | ||||||
| chr13:38813541
|
CTCTCTCT others(25): Show |
C | 2 | a0003c0005t0001g0071a0042c0080t0004g0088 | 2 | HG02135.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.6019+28735_6019+28 others(38): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813541 | |||||
| chr13:38813543
|
C | A | 26 | a0001c0001t0001g0178a0001c0002t0001g0135a0001c0002t0004g0231others(23): Show | 26 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.6019+28735C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813543 | ||||||
| chr13:38813543
|
CTCTCTCT others(25): Show |
C | 1 | a0001c0002t0005g0163 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.6019+28737_6019+28 others(38): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813543 | |||||
| chr13:38813545
|
C | A | 32 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0002t0001g0135others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.6019+28737C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813545 | ||||||
| chr13:38813547
|
C | A | 41 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0002t0001g0135others(38): Show | 41 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.6019+28739C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813547 | ||||||
| chr13:38813549
|
C | A | 47 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0002t0001g0135others(44): Show | 47 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.6019+28741C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813549 | ||||||
| chr13:38813551
|
C | A | 58 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0002t0001g0135others(55): Show | 58 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.6019+28743C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813551 | ||||||
| chr13:38813553
|
C | A | 65 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.6019+28745C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813553 | ||||||
| chr13:38813555
|
C | A | 81 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0175others(78): Show | 81 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.6019+28747C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813555 | ||||||
| chr13:38813555
|
C | CTATATAT others(5): Show |
1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+28748_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813555 | |||||
| chr13:38813557
|
C | A | 117 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(114): Show | 117 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.6019+28749C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813557 | ||||||
| chr13:38813557
|
C | CTATATAT others(5): Show |
1 | a0039c0086t0003g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6019+28750_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813557 | |||||
| chr13:38813559
|
C | A | 140 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(137): Show | 140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.6019+28751C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813559 | ||||||
| chr13:38813561
|
C | A | 160 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.6019+28753C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813561 | ||||||
| chr13:38813561
|
C | CTATATAT others(5): Show |
1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6019+28754_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813561 | |||||
| chr13:38813563
|
C | A | 178 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(175): Show | 178 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.6019+28755C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813563 | ||||||
| chr13:38813563
|
C | CTATA | 5 | a0001c0001t0002g0159a0001c0029t0025g0003a0004c0004t0003g0198others(2): Show | 5 | HG01175.hp2 HG01891.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.6019+28781_6019+28 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813563
|
C | CTATATA | 6 | a0001c0009t0008g0247a0001c0017t0055g0256a0006c0016t0021g0255others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.6019+28779_6019+28 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813563
|
C | CTATATAT others(7): Show |
2 | a0015c0031t0003g0129a0049c0097t0007g0006 | 2 | NA19010.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6019+28771_6019+28 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813563
|
C | CTCTATAT others(15): Show |
1 | a0001c0012t0019g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6019+28756_6019+28 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813563
|
C | CTCTCTCT others(5): Show |
1 | a0003c0005t0002g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6019+28756_6019+28 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813563
|
CTATATAT others(1): Show |
C | 7 | a0003c0003t0002g0067a0003c0003t0034g0081a0003c0005t0002g0085others(4): Show | 7 | HG00639.hp2 HG00738.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.6019+28777_6019+28 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38813563 | |||||
| chr13:38813565
|
A | C | 10 | a0001c0001t0001g0190a0001c0002t0006g0188a0002c0008t0001g0212others(7): Show | 10 | HG01358.hp1 HG01433.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+28757A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813565 | ||||||
| chr13:38813567
|
A | C | 5 | a0001c0001t0001g0190a0007c0024t0006g0044a0009c0028t0001g0143others(2): Show | 5 | HG01433.hp1 HG01496.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.6019+28759A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813567 | ||||||
| chr13:38813569
|
A | C | 3 | a0009c0028t0001g0143a0009c0028t0001g0146a0009c0028t0001g0148 | 3 | NA19003.hp2 NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.6019+28761A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813569 | ||||||
| chr13:38813981
|
A | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+29173A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38813981 | ||||||
| chr13:38814140
|
C | T | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6019+29332C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814140 | ||||||
| chr13:38814207
|
T | C | 1 | a0002c0027t0001g0029 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6019+29399T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814207 | ||||||
| chr13:38814225
|
G | A | 67 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.6019+29417G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814225 | ||||||
| chr13:38814254
|
A | C | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+29446A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814254 | ||||||
| chr13:38814362
|
G | C | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+29554G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814362 | ||||||
| chr13:38814440
|
C | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6019+29632C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814440 | ||||||
| chr13:38814446
|
C | A | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6019+29638C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814446 | ||||||
| chr13:38814456
|
G | C | 2 | a0028c0054t0009g0117a0051c0046t0051g0245 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.6019+29648G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814456 | ||||||
| chr13:38814485
|
C | G | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.6019+29677C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814485 | ||||||
| chr13:38814871
|
A | G | 1 | a0048c0065t0003g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6019+30063A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38814871 | ||||||
| chr13:38815182
|
A | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6019+30374A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815182 | ||||||
| chr13:38815286
|
C | A | 4 | a0011c0018t0003g0114a0022c0043t0012g0234a0025c0048t0003g0225others(1): Show | 4 | HG01243.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6019+30478C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815286 | ||||||
| chr13:38815420
|
A | C | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6019+30612A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815420 | ||||||
| chr13:38815556
|
T | A | 109 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(106): Show | 109 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.6019+30748T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815556 | ||||||
| chr13:38815607
|
C | G | 2 | a0006c0016t0021g0246a0026c0052t0003g0122 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.6019+30799C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815607 | ||||||
| chr13:38815684
|
C | T | 12 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0190others(9): Show | 12 | HG00673.hp2 HG01433.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.6019+30876C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815684 | ||||||
| chr13:38815757
|
G | A | 1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6020-30816G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815757 | ||||||
| chr13:38815928
|
A | G | 1 | a0008c0050t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6020-30645A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38815928 | ||||||
| chr13:38816014
|
C | T | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6020-30559C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816014 | ||||||
| chr13:38816236
|
G | T | 1 | a0002c0010t0004g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.6020-30337G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816236 | ||||||
| chr13:38816372
|
A | G | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6020-30201A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816372 | ||||||
| chr13:38816411
|
T | C | 3 | a0006c0016t0021g0246a0010c0013t0003g0107a0026c0052t0003g0122 | 3 | HG02145.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.6020-30162T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816411 | ||||||
| chr13:38816463
|
G | A | 1 | a0056c0074t0010g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6020-30110G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816463 | ||||||
| chr13:38816526
|
A | G | 7 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(4): Show | 7 | HG01192.hp2 HG01891.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.6020-30047A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816526 | ||||||
| chr13:38816542
|
C | T | 1 | a0005c0014t0040g0098 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6020-30031C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816542 | ||||||
| chr13:38816562
|
C | T | 1 | a0001c0012t0053g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6020-30011C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816562 | ||||||
| chr13:38816587
|
C | G | 1 | a0001c0001t0007g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6020-29986C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816587 | ||||||
| chr13:38816657
|
G | GTC | 29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-29915_6020-29 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38816657 | |||||
| chr13:38816724
|
G | A | 29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-29849G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816724 | ||||||
| chr13:38816727
|
G | C | 2 | a0007c0037t0006g0028a0008c0050t0001g0123 | 2 | HG01175.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6020-29846G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38816727 | ||||||
| chr13:38817110
|
A | G | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6020-29463A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817110 | ||||||
| chr13:38817382
|
T | C | 68 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.6020-29191T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817382 | ||||||
| chr13:38817486
|
G | A | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6020-29087G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817486 | ||||||
| chr13:38817512
|
G | A | 2 | a0006c0016t0021g0246a0026c0052t0003g0122 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.6020-29061G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817512 | ||||||
| chr13:38817536
|
C | T | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6020-29037C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817536 | ||||||
| chr13:38817585
|
A | G | 68 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.6020-28988A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817585 | ||||||
| chr13:38817629
|
A | G | 68 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.6020-28944A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817629 | ||||||
| chr13:38817782
|
G | T | 1 | a0005c0015t0042g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6020-28791G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817782 | ||||||
| chr13:38817785
|
A | C | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-28788A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817785 | ||||||
| chr13:38817811
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-28762G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817811 | ||||||
| chr13:38817817
|
G | A | 1 | a0040c0081t0006g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6020-28756G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817817 | ||||||
| chr13:38817819
|
G | A | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-28754G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817819 | ||||||
| chr13:38817862
|
A | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-28711A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38817862 | ||||||
| chr13:38818125
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-28448G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818125 | ||||||
| chr13:38818221
|
G | A | 2 | a0001c0009t0008g0260a0033c0057t0022g0127 | 2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6020-28352G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818221 | ||||||
| chr13:38818323
|
T | TAAAAACC others(313): Show |
1 | a0001c0030t0047g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6020-28236_6020-28 others(326): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38818323 | |||||
| chr13:38818323
|
T | TAAAAACC others(314): Show |
1 | a0021c0044t0056g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6020-28236_6020-28 others(327): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38818323 | |||||
| chr13:38818653
|
A | G | 1 | a0002c0010t0045g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6020-27920A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818653 | ||||||
| chr13:38818672
|
A | T | 1 | a0028c0054t0009g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6020-27901A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818672 | ||||||
| chr13:38818725
|
G | A | 1 | a0003c0005t0002g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6020-27848G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818725 | ||||||
| chr13:38818792
|
G | A | 28 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.6020-27781G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818792 | ||||||
| chr13:38818880
|
A | G | 2 | a0001c0009t0008g0260a0033c0057t0022g0127 | 2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6020-27693A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818880 | ||||||
| chr13:38818886
|
C | T | 12 | a0001c0002t0032g0238a0001c0009t0008g0253a0001c0012t0050g0258others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.6020-27687C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818886 | ||||||
| chr13:38818968
|
A | G | 3 | a0022c0043t0012g0234a0025c0048t0003g0225a0027c0053t0041g0116 | 3 | HG01243.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6020-27605A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38818968 | ||||||
| chr13:38819002
|
A | G | 1 | a0002c0008t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6020-27571A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819002 | ||||||
| chr13:38819506
|
A | T | 4 | a0001c0002t0005g0163a0001c0068t0005g0160a0003c0005t0001g0071others(1): Show | 4 | HG02135.hp1 HG03834.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-27067A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819506 | ||||||
| chr13:38819544
|
A | G | 1 | a0001c0002t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6020-27029A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819544 | ||||||
| chr13:38819566
|
G | A | 1 | a0008c0019t0003g0121 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6020-27007G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819566 | ||||||
| chr13:38819834
|
G | A | 1 | a0004c0004t0003g0198 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6020-26739G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819834 | ||||||
| chr13:38819956
|
T | C | 67 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.6020-26617T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38819956 | ||||||
| chr13:38820139
|
C | A | 11 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.6020-26434C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820139 | ||||||
| chr13:38820139
|
C | T | 2 | a0002c0027t0001g0021a0011c0018t0003g0114 | 2 | HG01070.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6020-26434C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820139 | ||||||
| chr13:38820140
|
A | G | 109 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(106): Show | 109 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.6020-26433A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820140 | ||||||
| chr13:38820220
|
G | C | 1 | a0045c0085t0009g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6020-26353G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820220 | ||||||
| chr13:38820235
|
G | C | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-26338G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820235 | ||||||
| chr13:38820621
|
G | A | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6020-25952G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820621 | ||||||
| chr13:38820688
|
C | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6020-25885C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820688 | ||||||
| chr13:38820695
|
T | G | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-25878T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820695 | ||||||
| chr13:38820902
|
A | T | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.6020-25671A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38820902 | ||||||
| chr13:38821172
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-25401G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821172 | ||||||
| chr13:38821263
|
T | C | 1 | a0004c0004t0004g0063 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6020-25310T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821263 | ||||||
| chr13:38821266
|
AT | A | 11 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.6020-25297delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38821266 | |||||
| chr13:38821691
|
C | T | 1 | a0001c0033t0010g0136 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6020-24882C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821691 | ||||||
| chr13:38821782
|
A | G | 12 | a0001c0002t0032g0238a0001c0009t0008g0253a0001c0012t0050g0258others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.6020-24791A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821782 | ||||||
| chr13:38821791
|
C | T | 41 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(38): Show | 41 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.6020-24782C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821791 | ||||||
| chr13:38821951
|
T | C | 42 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(39): Show | 42 | HG01192.hp2 HG01243.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.6020-24622T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821951 | ||||||
| chr13:38821997
|
G | C | 3 | a0016c0059t0043g0101a0031c0056t0015g0125a0037c0063t0014g0104 | 3 | HG02257.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-24576G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38821997 | ||||||
| chr13:38822046
|
A | G | 16 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.6020-24527A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822046 | ||||||
| chr13:38822053
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6020-24520A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822053 | ||||||
| chr13:38822072
|
A | G | 6 | a0001c0030t0003g0144a0001c0030t0003g0145a0014c0022t0003g0001others(3): Show | 6 | HG01109.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-24501A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822072 | ||||||
| chr13:38822197
|
T | C | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-24376T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822197 | ||||||
| chr13:38822347
|
CT | C | 35 | a0001c0001t0001g0058a0001c0001t0001g0161a0001c0001t0002g0159others(32): Show | 35 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.6020-24202delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38822347 | |||||
| chr13:38822347
|
CTT | C | 12 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.6020-24203_6020-24 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38822347 | |||||
| chr13:38822352
|
T | C | 7 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(4): Show | 7 | HG01192.hp2 HG01891.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.6020-24221T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822352 | ||||||
| chr13:38822353
|
T | C | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6020-24220T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822353 | ||||||
| chr13:38822366
|
T | G | 56 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(53): Show | 56 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.6020-24207T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822366 | ||||||
| chr13:38822366
|
T | TG | 4 | a0006c0096t0015g0153a0014c0022t0014g0193a0023c0042t0048g0236others(1): Show | 4 | HG01981.hp1 HG02109.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-24207_6020-24 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822366 | ||||||
| chr13:38822380
|
C | T | 2 | a0005c0014t0002g0031a0005c0035t0038g0037 | 2 | HG01175.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.6020-24193C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822380 | ||||||
| chr13:38822453
|
C | T | 65 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.6020-24120C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822453 | ||||||
| chr13:38822502
|
T | G | 1 | a0010c0013t0003g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6020-24071T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822502 | ||||||
| chr13:38822559
|
C | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-24014C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822559 | ||||||
| chr13:38822657
|
T | TA | 3 | a0001c0001t0001g0053a0001c0029t0002g0150a0004c0007t0001g0010 | 3 | HG00558.hp1 HG01934.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.6020-23915dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38822657 | |||||
| chr13:38822777
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6020-23796A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822777 | ||||||
| chr13:38822808
|
C | T | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-23765C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38822808 | ||||||
| chr13:38822861
|
A | AGAAGGAA others(2): Show |
29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-23711_6020-23 others(15): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38822861 | |||||
| chr13:38823031
|
A | G | 1 | a0005c0015t0042g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6020-23542A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823031 | ||||||
| chr13:38823089
|
G | T | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-23484G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823089 | ||||||
| chr13:38823107
|
T | C | 3 | a0003c0003t0003g0086a0004c0007t0001g0012a0004c0007t0001g0047 | 3 | NA19010.hp1 NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.6020-23466T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823107 | ||||||
| chr13:38823127
|
G | A | 1 | a0002c0006t0001g0033 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6020-23446G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823127 | ||||||
| chr13:38823155
|
A | G | 1 | a0013c0023t0016g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6020-23418A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823155 | ||||||
| chr13:38823312
|
C | G | 1 | a0003c0005t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6020-23261C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823312 | ||||||
| chr13:38823453
|
G | A | 65 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.6020-23120G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823453 | ||||||
| chr13:38823489
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6020-23084A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823489 | ||||||
| chr13:38823675
|
A | AAAT | 13 | a0001c0002t0001g0156a0001c0002t0004g0141a0001c0002t0005g0163others(10): Show | 13 | HG02135.hp1 HG03492.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.6020-22883_6020-22 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38823675 | |||||
| chr13:38823850
|
G | A | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-22723G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38823850 | ||||||
| chr13:38824082
|
A | G | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-22491A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824082 | ||||||
| chr13:38824105
|
G | A | 39 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(36): Show | 39 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.6020-22468G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824105 | ||||||
| chr13:38824196
|
C | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-22377C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824196 | ||||||
| chr13:38824202
|
T | C | 7 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(4): Show | 7 | HG01192.hp2 HG01891.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.6020-22371T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824202 | ||||||
| chr13:38824279
|
C | T | 29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-22294C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824279 | ||||||
| chr13:38824493
|
G | A | 4 | a0003c0005t0026g0091a0006c0016t0021g0255a0006c0021t0016g0111others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-22080G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824493 | ||||||
| chr13:38824570
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0028g0056a0007c0024t0006g0044 | 3 | HG01433.hp1 HG01496.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.6020-22003G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824570 | ||||||
| chr13:38824674
|
A | G | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-21899A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824674 | ||||||
| chr13:38824714
|
T | C | 13 | a0001c0017t0008g0261a0001c0030t0003g0144a0001c0030t0003g0145others(10): Show | 13 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.6020-21859T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824714 | ||||||
| chr13:38824810
|
T | G | 109 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(106): Show | 109 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.6020-21763T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824810 | ||||||
| chr13:38824918
|
C | G | 96 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0177others(93): Show | 96 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.6020-21655C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824918 | ||||||
| chr13:38824977
|
G | C | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-21596G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824977 | ||||||
| chr13:38824992
|
C | T | 67 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0166others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.6020-21581C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38824992 | ||||||
| chr13:38825171
|
C | T | 67 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(64): Show | 67 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.6020-21402C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825171 | ||||||
| chr13:38825276
|
A | C | 2 | a0001c0002t0032g0238a0036c0061t0003g0102 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6020-21297A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825276 | ||||||
| chr13:38825298
|
A | G | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6020-21275A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825298 | ||||||
| chr13:38825417
|
A | T | 11 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0019g0252others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.6020-21156A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825417 | ||||||
| chr13:38825434
|
TA | T | 29 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0156others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-21130delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38825434 | |||||
| chr13:38825459
|
T | C | 1 | a0001c0001t0007g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6020-21114T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825459 | ||||||
| chr13:38825461
|
C | T | 67 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(64): Show | 67 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.6020-21112C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825461 | ||||||
| chr13:38825544
|
G | A | 1 | a0035c0062t0009g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6020-21029G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825544 | ||||||
| chr13:38825684
|
C | A | 10 | a0001c0009t0008g0253a0001c0012t0050g0258a0001c0017t0008g0249others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6020-20889C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825684 | ||||||
| chr13:38825837
|
C | T | 5 | a0011c0018t0003g0114a0022c0043t0012g0234a0025c0048t0003g0225others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6020-20736C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825837 | ||||||
| chr13:38825894
|
G | C | 1 | a0011c0018t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6020-20679G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38825894 | ||||||
| chr13:38826032
|
A | C | 135 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0158others(132): Show | 135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.6020-20541A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826032 | ||||||
| chr13:38826290
|
A | G | 1 | a0001c0002t0004g0154 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.6020-20283A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826290 | ||||||
| chr13:38826345
|
A | G | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-20228A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826345 | ||||||
| chr13:38826385
|
A | AT | 5 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0029t0002g0150others(2): Show | 5 | HG00558.hp1 HG01934.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-20179dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38826385 | |||||
| chr13:38826469
|
A | G | 1 | a0015c0031t0003g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6020-20104A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826469 | ||||||
| chr13:38826520
|
C | T | 1 | a0013c0023t0002g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6020-20053C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826520 | ||||||
| chr13:38826966
|
A | G | 95 | a0001c0001t0001g0058a0001c0001t0001g0158a0001c0001t0001g0164others(92): Show | 95 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.6020-19607A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826966 | ||||||
| chr13:38826979
|
G | A | 2 | a0005c0014t0002g0031a0005c0035t0038g0037 | 2 | HG01175.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.6020-19594G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38826979 | ||||||
| chr13:38827194
|
G | A | 1 | a0041c0079t0039g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6020-19379G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827194 | ||||||
| chr13:38827468
|
T | C | 1 | a0002c0077t0009g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6020-19105T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827468 | ||||||
| chr13:38827587
|
A | T | 3 | a0035c0062t0009g0105a0041c0079t0039g0093a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-18986A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827587 | ||||||
| chr13:38827628
|
A | G | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6020-18945A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827628 | ||||||
| chr13:38827636
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6020-18937A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827636 | ||||||
| chr13:38827859
|
A | T | 110 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0168others(107): Show | 110 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.6020-18714A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827859 | ||||||
| chr13:38827969
|
C | A | 42 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(39): Show | 42 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.6020-18604C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38827969 | ||||||
| chr13:38828001
|
G | C | 3 | a0001c0030t0003g0144a0020c0040t0003g0005a0044c0084t0009g0197 | 3 | HG02723.hp2 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.6020-18572G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828001 | ||||||
| chr13:38828113
|
A | G | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6020-18460A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828113 | ||||||
| chr13:38828292
|
A | C | 1 | a0001c0001t0013g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6020-18281A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828292 | ||||||
| chr13:38828611
|
T | C | 3 | a0001c0030t0003g0144a0014c0022t0014g0193a0037c0063t0014g0104 | 3 | HG02109.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-17962T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828611 | ||||||
| chr13:38828715
|
TTAATAA | T | 35 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.6020-17851_6020-17 others(12): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38828715 | |||||
| chr13:38828783
|
G | T | 35 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.6020-17790G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828783 | ||||||
| chr13:38828800
|
A | G | 38 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(35): Show | 38 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.6020-17773A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828800 | ||||||
| chr13:38828875
|
C | T | 213 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(210): Show | 213 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.6020-17698C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828875 | ||||||
| chr13:38828905
|
A | C | 70 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(67): Show | 70 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.6020-17668A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828905 | ||||||
| chr13:38828933
|
T | C | 74 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0003g0138others(71): Show | 74 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.6020-17640T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38828933 | ||||||
| chr13:38829025
|
C | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-17548C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829025 | ||||||
| chr13:38829205
|
A | C | 2 | a0020c0040t0003g0005a0044c0084t0009g0197 | 2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.6020-17368A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829205 | ||||||
| chr13:38829241
|
G | A | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-17332G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829241 | ||||||
| chr13:38829315
|
G | A | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6020-17258G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829315 | ||||||
| chr13:38829331
|
T | A | 33 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(30): Show | 33 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.6020-17242T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829331 | ||||||
| chr13:38829472
|
A | G | 3 | a0001c0030t0003g0144a0014c0022t0014g0193a0037c0063t0014g0104 | 3 | HG02109.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-17101A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829472 | ||||||
| chr13:38829520
|
G | A | 1 | a0003c0003t0036g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6020-17053G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829520 | ||||||
| chr13:38829538
|
A | G | 13 | a0002c0008t0001g0208a0007c0024t0006g0044a0007c0024t0006g0045others(10): Show | 13 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.6020-17035A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829538 | ||||||
| chr13:38829645
|
C | CT | 6 | a0001c0030t0003g0144a0014c0022t0014g0193a0028c0054t0009g0117others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6020-16915dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38829645 | |||||
| chr13:38829666
|
A | C | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-16907A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829666 | ||||||
| chr13:38829721
|
AT | A | 23 | a0001c0002t0001g0162a0001c0002t0005g0140a0001c0002t0005g0163others(20): Show | 23 | HG01243.hp2 HG02083.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.6020-16845delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38829721 | |||||
| chr13:38829776
|
T | C | 17 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6020-16797T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829776 | ||||||
| chr13:38829866
|
G | C | 2 | a0014c0022t0003g0001a0014c0022t0003g0002 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6020-16707G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38829866 | ||||||
| chr13:38830004
|
T | C | 2 | a0020c0040t0003g0005a0044c0084t0009g0197 | 2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.6020-16569T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830004 | ||||||
| chr13:38830079
|
A | G | 1 | a0003c0005t0026g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6020-16494A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830079 | ||||||
| chr13:38830197
|
T | C | 1 | a0006c0095t0037g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6020-16376T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830197 | ||||||
| chr13:38830550
|
G | C | 17 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6020-16023G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830550 | ||||||
| chr13:38830621
|
GCT | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-15948_6020-15 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38830621 | |||||
| chr13:38830702
|
C | T | 1 | a0002c0006t0001g0096 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.6020-15871C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830702 | ||||||
| chr13:38830730
|
TTTTCCTC others(17): Show |
T | 9 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(6): Show | 9 | HG01496.hp1 HG01981.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.6020-15840_6020-15 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38830730 | |||||
| chr13:38830788
|
G | A | 1 | a0010c0013t0006g0205 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6020-15785G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830788 | ||||||
| chr13:38830950
|
C | G | 1 | a0002c0006t0001g0038 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6020-15623C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38830950 | ||||||
| chr13:38831015
|
C | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-15558C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38831015 | ||||||
| chr13:38831033
|
A | T | 44 | a0001c0001t0001g0166a0001c0002t0003g0138a0001c0002t0003g0180others(41): Show | 44 | HG00438.hp1 HG01109.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.6020-15540A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38831033 | ||||||
| chr13:38831525
|
T | C | 17 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6020-15048T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38831525 | ||||||
| chr13:38831613
|
A | AT | 189 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(186): Show | 189 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.6020-14946dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831613 | |||||
| chr13:38831613
|
A | ATT | 23 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(20): Show | 23 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.6020-14947_6020-14 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831613 | |||||
| chr13:38831613
|
A | ATTT | 39 | a0001c0001t0001g0166a0001c0002t0003g0138a0001c0002t0003g0180others(36): Show | 39 | HG00438.hp1 HG01261.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.6020-14948_6020-14 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831613 | |||||
| chr13:38831613
|
A | ATTTT | 7 | a0007c0025t0003g0229a0022c0043t0012g0234a0026c0052t0003g0122others(4): Show | 7 | HG01109.hp2 HG01192.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6020-14949_6020-14 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831613 | |||||
| chr13:38831649
|
G | A | 1 | a0001c0067t0001g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.6020-14924G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38831649 | ||||||
| chr13:38831762
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-14811T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38831762 | ||||||
| chr13:38831776
|
A | AT | 186 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.6020-14783dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831776 | |||||
| chr13:38831776
|
AT | A | 10 | a0001c0009t0020g0248a0004c0004t0012g0196a0008c0019t0012g0115others(7): Show | 10 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.6020-14783delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38831776 | |||||
| chr13:38832071
|
C | T | 1 | a0001c0002t0007g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6020-14502C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832071 | ||||||
| chr13:38832242
|
C | T | 1 | a0005c0014t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6020-14331C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832242 | ||||||
| chr13:38832393
|
A | G | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6020-14180A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832393 | ||||||
| chr13:38832492
|
C | T | 43 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(40): Show | 43 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.6020-14081C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832492 | ||||||
| chr13:38832585
|
A | T | 39 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(36): Show | 39 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.6020-13988A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832585 | ||||||
| chr13:38832635
|
G | A | 1 | a0005c0014t0003g0203 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6020-13938G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832635 | ||||||
| chr13:38832645
|
C | A | 69 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(66): Show | 69 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.6020-13928C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832645 | ||||||
| chr13:38832713
|
T | G | 1 | a0004c0007t0001g0010 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.6020-13860T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832713 | ||||||
| chr13:38832771
|
T | G | 81 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(78): Show | 81 | HG00438.hp1 HG01109.hp2 HG01192.hp1 others(78): Show |
intron_variant | MODIFIER | c.6020-13802T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832771 | ||||||
| chr13:38832912
|
G | A | 44 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(41): Show | 44 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.6020-13661G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832912 | ||||||
| chr13:38832947
|
A | G | 81 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(78): Show | 81 | HG00438.hp1 HG01109.hp2 HG01192.hp1 others(78): Show |
intron_variant | MODIFIER | c.6020-13626A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38832947 | ||||||
| chr13:38833039
|
G | A | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.6020-13534G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833039 | ||||||
| chr13:38833056
|
A | T | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-13517A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833056 | ||||||
| chr13:38833089
|
A | G | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-13484A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833089 | ||||||
| chr13:38833403
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-13170C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833403 | ||||||
| chr13:38833555
|
A | G | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6020-13018A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833555 | ||||||
| chr13:38833654
|
C | T | 4 | a0001c0030t0047g0151a0021c0044t0056g0254a0038c0064t0033g0103others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.6020-12919C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833654 | ||||||
| chr13:38833687
|
GATTT | G | 5 | a0001c0033t0010g0136a0001c0033t0010g0204a0017c0034t0010g0222others(2): Show | 5 | HG00738.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.6020-12873_6020-12 others(10): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38833687 | |||||
| chr13:38833875
|
T | C | 1 | a0001c0029t0002g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6020-12698T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833875 | ||||||
| chr13:38833900
|
T | A | 5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-12673T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833900 | ||||||
| chr13:38833925
|
T | C | 57 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(54): Show | 57 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(54): Show |
intron_variant | MODIFIER | c.6020-12648T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833925 | ||||||
| chr13:38833960
|
C | T | 1 | a0040c0081t0006g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6020-12613C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38833960 | ||||||
| chr13:38834023
|
T | C | 5 | a0006c0016t0021g0246a0006c0016t0021g0255a0006c0021t0016g0111others(2): Show | 5 | HG00639.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.6020-12550T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834023 | ||||||
| chr13:38834029
|
T | A | 83 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(80): Show | 83 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.6020-12544T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834029 | ||||||
| chr13:38834126
|
A | G | 89 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(86): Show | 89 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.6020-12447A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834126 | ||||||
| chr13:38834193
|
A | G | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6020-12380A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834193 | ||||||
| chr13:38834201
|
A | T | 58 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(55): Show | 58 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(55): Show |
intron_variant | MODIFIER | c.6020-12372A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834201 | ||||||
| chr13:38834218
|
C | T | 4 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0012t0050g0258others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.6020-12355C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834218 | ||||||
| chr13:38834380
|
G | A | 2 | a0009c0028t0001g0146a0009c0028t0001g0148 | 2 | NA19003.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.6020-12193G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834380 | ||||||
| chr13:38834613
|
T | C | 115 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(112): Show | 115 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.6020-11960T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834613 | ||||||
| chr13:38834767
|
A | G | 1 | a0010c0013t0003g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6020-11806A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834767 | ||||||
| chr13:38834903
|
G | A | 53 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(50): Show | 53 | HG01243.hp2 HG01261.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.6020-11670G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834903 | ||||||
| chr13:38834918
|
A | G | 2 | a0001c0001t0002g0183a0003c0005t0002g0060 | 2 | HG00423.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.6020-11655A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38834918 | ||||||
| chr13:38835075
|
T | C | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6020-11498T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835075 | ||||||
| chr13:38835238
|
G | T | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-11335G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835238 | ||||||
| chr13:38835428
|
C | T | 5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-11145C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835428 | ||||||
| chr13:38835534
|
G | A | 1 | a0014c0022t0014g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6020-11039G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835534 | ||||||
| chr13:38835794
|
G | A | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6020-10779G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835794 | ||||||
| chr13:38835813
|
A | G | 1 | a0006c0021t0002g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6020-10760A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835813 | ||||||
| chr13:38835876
|
A | G | 87 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(84): Show | 87 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.6020-10697A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38835876 | ||||||
| chr13:38836102
|
T | C | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6020-10471T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836102 | ||||||
| chr13:38836137
|
C | T | 92 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(89): Show | 92 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.6020-10436C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836137 | ||||||
| chr13:38836139
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-10434T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836139 | ||||||
| chr13:38836237
|
A | G | 1 | a0002c0006t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6020-10336A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836237 | ||||||
| chr13:38836302
|
G | A | 3 | a0026c0052t0003g0122a0032c0058t0003g0195a0050c0075t0003g0194 | 3 | HG01109.hp2 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.6020-10271G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836302 | ||||||
| chr13:38836350
|
T | A | 17 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6020-10223T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836350 | ||||||
| chr13:38836463
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.6020-10110T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836463 | ||||||
| chr13:38836586
|
G | A | 28 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6020-9987G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836586 | ||||||
| chr13:38836683
|
G | A | 28 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(25): Show | 28 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.6020-9890G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836683 | ||||||
| chr13:38836720
|
GTTTA | G | 3 | a0016c0059t0043g0101a0041c0079t0039g0093a0052c0045t0054g0257 | 3 | HG02257.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6020-9847_6020-984 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38836720 | |||||
| chr13:38836757
|
G | T | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-9816G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836757 | ||||||
| chr13:38836789
|
T | C | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.6020-9784T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836789 | ||||||
| chr13:38836833
|
C | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-9740C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836833 | ||||||
| chr13:38836851
|
G | C | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.6020-9722G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836851 | ||||||
| chr13:38836858
|
G | C | 1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6020-9715G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836858 | ||||||
| chr13:38836932
|
C | T | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.6020-9641C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836932 | ||||||
| chr13:38836984
|
T | C | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-9589T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38836984 | ||||||
| chr13:38837041
|
T | A | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6020-9532T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837041 | ||||||
| chr13:38837059
|
G | A | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-9514G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837059 | ||||||
| chr13:38837063
|
T | G | 3 | a0001c0030t0003g0144a0014c0022t0014g0193a0037c0063t0014g0104 | 3 | HG02109.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-9510T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837063 | ||||||
| chr13:38837087
|
A | C | 2 | a0001c0012t0019g0252a0002c0077t0009g0139 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.6020-9486A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837087 | ||||||
| chr13:38837090
|
T | A | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6020-9483T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837090 | ||||||
| chr13:38837098
|
A | G | 17 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6020-9475A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837098 | ||||||
| chr13:38837236
|
C | T | 2 | a0001c0001t0001g0192a0004c0007t0001g0010 | 2 | HG00621.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.6020-9337C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837236 | ||||||
| chr13:38837311
|
T | C | 2 | a0001c0001t0002g0185a0057c0076t0002g0224 | 2 | NA18977.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.6020-9262T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837311 | ||||||
| chr13:38837440
|
T | C | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6020-9133T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837440 | ||||||
| chr13:38837758
|
A | G | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-8815A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837758 | ||||||
| chr13:38837769
|
T | TTTTTTTG | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(13): Show | 16 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.6020-8799_6020-879 others(11): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38837769 | |||||
| chr13:38837770
|
T | G | 1 | a0004c0004t0007g0015 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6020-8803T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837770 | ||||||
| chr13:38837772
|
T | TTTTG | 6 | a0007c0025t0003g0229a0022c0043t0012g0234a0026c0052t0003g0122others(3): Show | 6 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-8799_6020-879 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38837772 | |||||
| chr13:38837775
|
G | T | 26 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(23): Show | 26 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.6020-8798G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837775 | ||||||
| chr13:38837780
|
G | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-8793G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837780 | ||||||
| chr13:38837785
|
G | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-8788G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837785 | ||||||
| chr13:38837790
|
G | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-8783G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837790 | ||||||
| chr13:38837861
|
G | C | 1 | a0001c0009t0008g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6020-8712G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837861 | ||||||
| chr13:38837930
|
A | C | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6020-8643A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38837930 | ||||||
| chr13:38838059
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-8514A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838059 | ||||||
| chr13:38838139
|
C | T | 1 | a0001c0002t0006g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6020-8434C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838139 | ||||||
| chr13:38838215
|
A | G | 6 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-8358A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838215 | ||||||
| chr13:38838220
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6020-8353G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838220 | ||||||
| chr13:38838257
|
T | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-8316T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838257 | ||||||
| chr13:38838369
|
T | G | 94 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(91): Show | 94 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.6020-8204T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838369 | ||||||
| chr13:38838384
|
C | T | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6020-8189C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838384 | ||||||
| chr13:38838531
|
C | T | 1 | a0010c0013t0003g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6020-8042C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838531 | ||||||
| chr13:38838559
|
A | C | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-8014A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838559 | ||||||
| chr13:38838692
|
C | T | 53 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(50): Show | 53 | HG01243.hp2 HG01261.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.6020-7881C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838692 | ||||||
| chr13:38838852
|
A | G | 1 | a0002c0010t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.6020-7721A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838852 | ||||||
| chr13:38838915
|
T | G | 90 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(87): Show | 90 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.6020-7658T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838915 | ||||||
| chr13:38838936
|
C | T | 1 | a0005c0090t0002g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6020-7637C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38838936 | ||||||
| chr13:38839060
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0028g0056a0002c0008t0001g0212others(4): Show | 7 | HG01433.hp1 HG01943.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.6020-7513G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839060 | ||||||
| chr13:38839064
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7509C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839064 | ||||||
| chr13:38839090
|
G | A | 1 | a0001c0070t0003g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6020-7483G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839090 | ||||||
| chr13:38839117
|
T | C | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7456T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839117 | ||||||
| chr13:38839152
|
G | A | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-7421G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839152 | ||||||
| chr13:38839189
|
T | C | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-7384T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839189 | ||||||
| chr13:38839263
|
C | T | 1 | a0002c0006t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6020-7310C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839263 | ||||||
| chr13:38839303
|
C | T | 1 | a0006c0095t0037g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6020-7270C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839303 | ||||||
| chr13:38839336
|
T | C | 5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-7237T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839336 | ||||||
| chr13:38839348
|
G | A | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.6020-7225G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839348 | ||||||
| chr13:38839360
|
C | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7213C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839360 | ||||||
| chr13:38839383
|
A | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7190A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839383 | ||||||
| chr13:38839399
|
C | T | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6020-7174C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839399 | ||||||
| chr13:38839519
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7054A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839519 | ||||||
| chr13:38839524
|
C | G | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.6020-7049C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839524 | ||||||
| chr13:38839565
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-7008C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839565 | ||||||
| chr13:38839595
|
G | A | 12 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0009t0008g0247others(9): Show | 12 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.6020-6978G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839595 | ||||||
| chr13:38839613
|
C | T | 3 | a0001c0033t0010g0136a0017c0034t0010g0222a0017c0034t0010g0223 | 3 | HG01516.hp1 HG01517.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.6020-6960C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839613 | ||||||
| chr13:38839699
|
C | T | 1 | a0005c0015t0042g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6020-6874C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839699 | ||||||
| chr13:38839759
|
G | T | 28 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6020-6814G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839759 | ||||||
| chr13:38839767
|
C | T | 1 | a0002c0006t0002g0022 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6020-6806C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839767 | ||||||
| chr13:38839815
|
T | C | 4 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-6758T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839815 | ||||||
| chr13:38839841
|
T | A | 1 | a0003c0003t0004g0084 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6020-6732T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839841 | ||||||
| chr13:38839847
|
G | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6726G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839847 | ||||||
| chr13:38839972
|
T | C | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6601T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38839972 | ||||||
| chr13:38840087
|
G | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6486G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840087 | ||||||
| chr13:38840169
|
C | G | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6020-6404C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840169 | ||||||
| chr13:38840172
|
G | A | 1 | a0039c0086t0003g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6020-6401G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840172 | ||||||
| chr13:38840180
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6393C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840180 | ||||||
| chr13:38840194
|
C | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6379C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840194 | ||||||
| chr13:38840247
|
G | A | 5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-6326G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840247 | ||||||
| chr13:38840269
|
T | C | 98 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(95): Show | 98 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.6020-6304T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840269 | ||||||
| chr13:38840270
|
C | G | 1 | a0001c0012t0053g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6020-6303C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840270 | ||||||
| chr13:38840284
|
T | C | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6289T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840284 | ||||||
| chr13:38840345
|
G | C | 6 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-6228G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840345 | ||||||
| chr13:38840349
|
G | A | 1 | a0058c0047t0002g0210 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6020-6224G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840349 | ||||||
| chr13:38840354
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-6219C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840354 | ||||||
| chr13:38840357
|
C | T | 1 | a0001c0009t0008g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6020-6216C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840357 | ||||||
| chr13:38840359
|
T | A | 6 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-6214T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840359 | ||||||
| chr13:38840422
|
CT | C | 92 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(89): Show | 92 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.6020-6134delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840422 | |||||
| chr13:38840424
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-6149T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840424 | ||||||
| chr13:38840478
|
A | G | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6020-6095A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840478 | ||||||
| chr13:38840625
|
A | AAT | 3 | a0005c0035t0038g0037a0006c0021t0002g0186a0018c0072t0002g0134 | 3 | HG01175.hp2 HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.6020-5929_6020-592 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(3): Show |
5 | a0001c0002t0001g0156a0001c0002t0005g0163a0003c0003t0005g0070others(2): Show | 5 | HG02083.hp1 NA18951.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.6020-5937_6020-592 others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(5): Show |
9 | a0001c0002t0001g0162a0001c0002t0005g0140a0001c0002t0005g0170others(6): Show | 9 | HG02135.hp2 NA18747.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.6020-5939_6020-592 others(16): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(7): Show |
4 | a0001c0068t0005g0160a0003c0003t0007g0076a0004c0004t0007g0015others(1): Show | 4 | NA18940.hp2 NA18963.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.6020-5941_6020-592 others(18): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(9): Show |
2 | a0025c0048t0003g0225a0049c0097t0007g0006 | 2 | HG01243.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.6020-5943_6020-592 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(13): Show |
5 | a0001c0002t0032g0238a0001c0017t0008g0249a0001c0070t0003g0095others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-5947_6020-592 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(15): Show |
1 | a0016c0059t0043g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
A | AATATATA others(17): Show |
2 | a0001c0017t0008g0261a0052c0045t0054g0257 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840625
|
AAT | A | 143 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(140): Show | 143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.6020-5929_6020-592 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840625 | |||||
| chr13:38840636
|
A | ATATATAT others(13): Show |
1 | a0016c0060t0029g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840636 | |||||
| chr13:38840636
|
A | G | 25 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-5937A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840636 | ||||||
| chr13:38840638
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5935A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840638 | ||||||
| chr13:38840640
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5933A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840640 | ||||||
| chr13:38840642
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5931A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840642 | ||||||
| chr13:38840644
|
A | ATATATAT others(25): Show |
1 | a0001c0002t0007g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(36): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(23): Show |
1 | a0015c0031t0003g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(34): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(19): Show |
3 | a0001c0009t0008g0262a0001c0009t0020g0248a0001c0009t0020g0250 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(30): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(17): Show |
4 | a0001c0009t0008g0247a0001c0030t0047g0151a0019c0039t0011g0004others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(28): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(15): Show |
1 | a0004c0004t0003g0198 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(26): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(13): Show |
6 | a0001c0030t0003g0145a0014c0022t0003g0002a0030c0055t0003g0131others(3): Show | 6 | HG02976.hp1 HG03195.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(11): Show |
9 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0009t0008g0260others(6): Show | 9 | HG01261.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(22): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(13): Show |
1 | a0008c0019t0003g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6020-5928_6020-592 others(24): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | ATATATAT others(9): Show |
2 | a0001c0009t0008g0253a0015c0031t0003g0129 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6020-5928_6020-592 others(20): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840644 | |||||
| chr13:38840644
|
A | G | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5929A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840644 | ||||||
| chr13:38840680
|
ATG | A | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5887_6020-588 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840680 | |||||
| chr13:38840703
|
T | C | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6020-5870T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840703 | ||||||
| chr13:38840703
|
TAC | T | 30 | a0001c0002t0032g0238a0001c0033t0010g0136a0001c0033t0010g0204others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6020-5856_6020-585 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840703 | |||||
| chr13:38840729
|
T | C | 6 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-5844T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840729 | ||||||
| chr13:38840731
|
T | C | 25 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(22): Show | 25 | HG01496.hp1 HG01981.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-5842T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840731 | ||||||
| chr13:38840731
|
TAC | T | 30 | a0001c0033t0010g0136a0001c0033t0010g0204a0003c0005t0002g0075others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6020-5828_6020-582 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38840731 | |||||
| chr13:38840745
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5828C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840745 | ||||||
| chr13:38840787
|
G | A | 6 | a0001c0002t0001g0135a0001c0002t0004g0169a0001c0002t0004g0231others(3): Show | 6 | HG00673.hp1 HG02129.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.6020-5786G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840787 | ||||||
| chr13:38840838
|
C | T | 4 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-5735C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840838 | ||||||
| chr13:38840978
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-5595T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38840978 | ||||||
| chr13:38841248
|
C | T | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5325C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841248 | ||||||
| chr13:38841319
|
G | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-5254G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841319 | ||||||
| chr13:38841363
|
G | T | 1 | a0002c0011t0004g0228 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6020-5210G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841363 | ||||||
| chr13:38841386
|
G | A | 29 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.6020-5187G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841386 | ||||||
| chr13:38841398
|
G | A | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.6020-5175G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841398 | ||||||
| chr13:38841564
|
GA | G | 6 | a0001c0017t0055g0256a0002c0006t0001g0096a0004c0004t0012g0196others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.6020-4999delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38841564 | |||||
| chr13:38841594
|
A | G | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6020-4979A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841594 | ||||||
| chr13:38841617
|
C | T | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6020-4956C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841617 | ||||||
| chr13:38841678
|
A | G | 6 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6020-4895A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841678 | ||||||
| chr13:38841728
|
G | A | 30 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6020-4845G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841728 | ||||||
| chr13:38841842
|
A | G | 30 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6020-4731A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841842 | ||||||
| chr13:38841880
|
T | C | 30 | a0001c0033t0010g0136a0001c0033t0010g0204a0007c0024t0006g0044others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6020-4693T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841880 | ||||||
| chr13:38841895
|
T | C | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-4678T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38841895 | ||||||
| chr13:38842007
|
T | A | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6020-4566T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842007 | ||||||
| chr13:38842022
|
G | A | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.6020-4551G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842022 | ||||||
| chr13:38842035
|
T | A | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.6020-4538T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842035 | ||||||
| chr13:38842054
|
G | A | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.6020-4519G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842054 | ||||||
| chr13:38842437
|
T | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-4136T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842437 | ||||||
| chr13:38842496
|
G | A | 2 | a0020c0040t0003g0005a0053c0069t0003g0108 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6020-4077G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842496 | ||||||
| chr13:38842572
|
G | A | 1 | a0003c0005t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6020-4001G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842572 | ||||||
| chr13:38842652
|
C | T | 13 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(10): Show | 13 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.6020-3921C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842652 | ||||||
| chr13:38842695
|
C | T | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6020-3878C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842695 | ||||||
| chr13:38842928
|
T | G | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6020-3645T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38842928 | ||||||
| chr13:38843132
|
A | G | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6020-3441A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843132 | ||||||
| chr13:38843167
|
T | C | 1 | a0004c0007t0018g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6020-3406T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843167 | ||||||
| chr13:38843185
|
G | A | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6020-3388G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843185 | ||||||
| chr13:38843270
|
CT | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-3302delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843270 | ||||||
| chr13:38843294
|
G | A | 2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6020-3279G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843294 | ||||||
| chr13:38843301
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-3272A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843301 | ||||||
| chr13:38843364
|
G | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-3209G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843364 | ||||||
| chr13:38843440
|
C | CAAA | 18 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(15): Show | 18 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.6020-3123_6020-312 others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38843440 | |||||
| chr13:38843440
|
C | CAAAA | 7 | a0007c0025t0003g0229a0010c0013t0003g0107a0028c0054t0009g0117others(4): Show | 7 | HG01192.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.6020-3124_6020-312 others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38843440 | |||||
| chr13:38843522
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-3051T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843522 | ||||||
| chr13:38843623
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2950A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843623 | ||||||
| chr13:38843688
|
A | G | 1 | a0003c0003t0004g0084 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6020-2885A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843688 | ||||||
| chr13:38843745
|
G | T | 13 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(10): Show | 13 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.6020-2828G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843745 | ||||||
| chr13:38843765
|
C | A | 1 | a0002c0010t0004g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.6020-2808C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843765 | ||||||
| chr13:38843841
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2732C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843841 | ||||||
| chr13:38843890
|
GT | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2672delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38843890 | |||||
| chr13:38843904
|
T | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-2669T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38843904 | ||||||
| chr13:38844109
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2464C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844109 | ||||||
| chr13:38844201
|
G | A | 4 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6020-2372G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844201 | ||||||
| chr13:38844273
|
G | A | 26 | a0002c0008t0001g0230a0007c0024t0006g0044a0007c0024t0006g0045others(23): Show | 26 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.6020-2300G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844273 | ||||||
| chr13:38844274
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2299C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844274 | ||||||
| chr13:38844286
|
T | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2287T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844286 | ||||||
| chr13:38844344
|
A | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2229A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844344 | ||||||
| chr13:38844390
|
G | A | 2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6020-2183G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844390 | ||||||
| chr13:38844483
|
A | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-2090A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844483 | ||||||
| chr13:38844484
|
C | A | 2 | a0005c0026t0002g0242a0018c0072t0002g0134 | 2 | HG00741.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6020-2089C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844484 | ||||||
| chr13:38844485
|
G | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-2088G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844485 | ||||||
| chr13:38844633
|
G | A | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-1940G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844633 | ||||||
| chr13:38844654
|
C | G | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6020-1919C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844654 | ||||||
| chr13:38844810
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-1763C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844810 | ||||||
| chr13:38844817
|
C | T | 1 | a0006c0021t0002g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6020-1756C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844817 | ||||||
| chr13:38844835
|
A | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6020-1738A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844835 | ||||||
| chr13:38844951
|
T | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-1622T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38844951 | ||||||
| chr13:38845017
|
T | C | 98 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(95): Show | 98 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.6020-1556T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845017 | ||||||
| chr13:38845018
|
G | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-1555G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845018 | ||||||
| chr13:38845076
|
C | CT | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-1497_6020-149 others(5): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845076 | ||||||
| chr13:38845247
|
CAACTT | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-1325_6020-132 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845247 | ||||||
| chr13:38845324
|
T | A | 5 | a0006c0016t0021g0246a0006c0016t0021g0255a0006c0021t0016g0111others(2): Show | 5 | HG00639.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.6020-1249T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845324 | ||||||
| chr13:38845341
|
G | A | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-1232G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845341 | ||||||
| chr13:38845386
|
C | T | 1 | a0001c0070t0003g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6020-1187C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845386 | ||||||
| chr13:38845478
|
C | G | 98 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(95): Show | 98 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.6020-1095C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845478 | ||||||
| chr13:38845501
|
C | T | 1 | a0003c0003t0004g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.6020-1072C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845501 | ||||||
| chr13:38845781
|
T | C | 68 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(65): Show | 68 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(65): Show |
intron_variant | MODIFIER | c.6020-792T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845781 | ||||||
| chr13:38845827
|
G | A | 98 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(95): Show | 98 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.6020-746G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845827 | ||||||
| chr13:38845938
|
A | G | 68 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(65): Show | 68 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(65): Show |
intron_variant | MODIFIER | c.6020-635A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38845938 | ||||||
| chr13:38846012
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-561A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846012 | ||||||
| chr13:38846095
|
T | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-478T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846095 | ||||||
| chr13:38846104
|
T | C | 93 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(90): Show | 93 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.6020-469T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846104 | ||||||
| chr13:38846139
|
G | A | 1 | a0004c0007t0001g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6020-434G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846139 | ||||||
| chr13:38846208
|
T | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-365T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846208 | ||||||
| chr13:38846217
|
T | TA | 5 | a0001c0001t0002g0185a0004c0004t0004g0008a0004c0004t0004g0063others(2): Show | 5 | NA18977.hp1 NA18977.hp2 NA19081.hp1 others(2): Show |
intron_variant | MODIFIER | c.6020-341dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38846217 | |||||
| chr13:38846217
|
TA | T | 45 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(42): Show | 45 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.6020-341delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr13 | 38846217 | |||||
| chr13:38846314
|
T | C | 56 | a0001c0001t0001g0166a0001c0002t0003g0138a0001c0002t0003g0180others(53): Show | 56 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.6020-259T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846314 | ||||||
| chr13:38846370
|
C | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6020-203C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846370 | ||||||
| chr13:38846383
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-190C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846383 | ||||||
| chr13:38846424
|
A | G | 93 | a0001c0001t0001g0166a0001c0002t0001g0156a0001c0002t0001g0162others(90): Show | 93 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.6020-149A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846424 | ||||||
| chr13:38846443
|
A | G | 1 | a0016c0060t0029g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6020-130A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846443 | ||||||
| chr13:38846462
|
G | A | 29 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(26): Show | 29 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.6020-111G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846462 | ||||||
| chr13:38846526
|
T | C | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6020-47T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 6/23 | chr13 | 38846526 | ||||||
| chr13:38846786
|
T | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+64T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38846786 | ||||||
| chr13:38846834
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+112A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38846834 | ||||||
| chr13:38846959
|
G | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+237G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38846959 | ||||||
| chr13:38847038
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+316A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847038 | ||||||
| chr13:38847054
|
T | A | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+332T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847054 | ||||||
| chr13:38847192
|
G | A | 1 | a0041c0079t0039g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6169+470G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847192 | ||||||
| chr13:38847202
|
A | AT | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+480_6169+481i others(3): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847202 | ||||||
| chr13:38847279
|
C | G | 26 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(23): Show | 26 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.6169+557C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847279 | ||||||
| chr13:38847305
|
TC | T | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.6169+584delC | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847305 | ||||||
| chr13:38847373
|
A | T | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6169+651A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847373 | ||||||
| chr13:38847388
|
C | G | 4 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+666C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847388 | ||||||
| chr13:38847433
|
G | C | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6169+711G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847433 | ||||||
| chr13:38847539
|
A | G | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+817A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847539 | ||||||
| chr13:38847545
|
C | T | 25 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.6169+823C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847545 | ||||||
| chr13:38847547
|
G | A | 2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6169+825G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847547 | ||||||
| chr13:38847582
|
G | A | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6169+860G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847582 | ||||||
| chr13:38847627
|
G | A | 1 | a0001c0029t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.6170-834G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847627 | ||||||
| chr13:38847680
|
T | A | 1 | a0005c0035t0002g0018 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6170-781T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847680 | ||||||
| chr13:38847696
|
A | G | 2 | a0007c0025t0003g0229a0033c0057t0022g0127 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.6170-765A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38847696 | ||||||
| chr13:38848002
|
A | G | 1 | a0004c0004t0011g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6170-459A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38848002 | ||||||
| chr13:38848006
|
C | T | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.6170-455C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38848006 | ||||||
| chr13:38848067
|
T | A | 1 | a0003c0003t0034g0081 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6170-394T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38848067 | ||||||
| chr13:38848136
|
A | AT | 6 | a0001c0001t0001g0166a0003c0005t0001g0080a0003c0078t0001g0019others(3): Show | 6 | HG00438.hp1 HG02129.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.6170-320dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr13 | 38848136 | |||||
| chr13:38848277
|
C | T | 1 | a0028c0054t0009g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6170-184C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 7/23 | chr13 | 38848277 | ||||||
| chr13:38848708
|
T | G | 2 | a0005c0026t0002g0242a0018c0072t0002g0134 | 2 | HG00741.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6379+38T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38848708 | ||||||
| chr13:38848803
|
C | T | 1 | a0004c0004t0004g0008 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6379+133C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38848803 | ||||||
| chr13:38848804
|
G | A | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6379+134G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38848804 | ||||||
| chr13:38849302
|
G | A | 1 | a0018c0072t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6379+632G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849302 | ||||||
| chr13:38849369
|
C | T | 5 | a0001c0033t0010g0136a0001c0033t0010g0204a0017c0034t0010g0222others(2): Show | 5 | HG00738.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.6380-669C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849369 | ||||||
| chr13:38849389
|
A | G | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6380-649A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849389 | ||||||
| chr13:38849429
|
C | T | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6380-609C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849429 | ||||||
| chr13:38849441
|
C | A | 1 | a0007c0024t0006g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6380-597C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849441 | ||||||
| chr13:38849759
|
T | C | 5 | a0001c0033t0010g0136a0001c0033t0010g0204a0017c0034t0010g0222others(2): Show | 5 | HG00738.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.6380-279T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849759 | ||||||
| chr13:38849797
|
CT | C | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6380-236delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr13 | 38849797 | |||||
| chr13:38849850
|
G | A | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6380-188G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849850 | ||||||
| chr13:38849951
|
C | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6380-87C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 8/23 | chr13 | 38849951 | ||||||
| chr13:38850299
|
A | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6577+64A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850299 | ||||||
| chr13:38850710
|
C | T | 88 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(85): Show | 88 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.6578-234C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850710 | ||||||
| chr13:38850741
|
G | A | 88 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(85): Show | 88 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.6578-203G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850741 | ||||||
| chr13:38850852
|
A | G | 3 | a0002c0011t0004g0206a0002c0011t0004g0228a0004c0004t0011g0061 | 3 | HG00438.hp2 HG02083.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.6578-92A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850852 | ||||||
| chr13:38850854
|
A | G | 1 | a0001c0001t0002g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6578-90A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850854 | ||||||
| chr13:38850901
|
A | G | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6578-43A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 9/23 | chr13 | 38850901 | ||||||
| chr13:38851368
|
C | T | 21 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(18): Show | 21 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6742+260C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 10/23 | chr13 | 38851368 | ||||||
| chr13:38851596
|
C | G | 1 | a0004c0007t0001g0010 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.6743-90C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 10/23 | chr13 | 38851596 | ||||||
| chr13:38851875
|
G | T | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.6925+7G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38851875 | ||||||
| chr13:38851893
|
C | T | 1 | a0002c0008t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6925+25C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38851893 | ||||||
| chr13:38852101
|
C | T | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6925+233C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852101 | ||||||
| chr13:38852118
|
A | G | 1 | a0001c0002t0004g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6925+250A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852118 | ||||||
| chr13:38852188
|
G | A | 1 | a0001c0002t0006g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6925+320G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852188 | ||||||
| chr13:38852353
|
A | G | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.6925+485A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852353 | ||||||
| chr13:38852508
|
A | G | 1 | a0001c0009t0008g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6925+640A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852508 | ||||||
| chr13:38852567
|
A | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6925+699A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852567 | ||||||
| chr13:38852704
|
C | CT | 30 | a0001c0001t0001g0181a0001c0001t0013g0202a0001c0017t0008g0249others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6925+854dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38852704 | |||||
| chr13:38852717
|
T | G | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.6925+849T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852717 | ||||||
| chr13:38852770
|
T | C | 1 | a0016c0060t0029g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6925+902T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852770 | ||||||
| chr13:38852842
|
C | G | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.6925+974C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38852842 | ||||||
| chr13:38853156
|
C | T | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6925+1288C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853156 | ||||||
| chr13:38853201
|
G | A | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6925+1333G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853201 | ||||||
| chr13:38853313
|
G | A | 5 | a0001c0033t0010g0136a0001c0033t0010g0204a0017c0034t0010g0222others(2): Show | 5 | HG00738.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.6925+1445G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853313 | ||||||
| chr13:38853317
|
G | GA | 6 | a0001c0070t0003g0095a0002c0011t0004g0218a0003c0003t0036g0073others(3): Show | 6 | HG02145.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.6925+1468dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38853317 | |||||
| chr13:38853495
|
C | A | 1 | a0049c0097t0007g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.6925+1627C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853495 | ||||||
| chr13:38853531
|
C | A | 1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6925+1663C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853531 | ||||||
| chr13:38853790
|
A | G | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.6925+1922A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853790 | ||||||
| chr13:38853857
|
T | C | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6925+1989T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38853857 | ||||||
| chr13:38854017
|
A | G | 2 | a0036c0061t0003g0102a0048c0065t0003g0100 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6926-2109A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854017 | ||||||
| chr13:38854038
|
T | C | 1 | a0001c0029t0002g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6926-2088T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854038 | ||||||
| chr13:38854116
|
G | A | 20 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(17): Show | 20 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.6926-2010G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854116 | ||||||
| chr13:38854129
|
C | A | 1 | a0001c0002t0004g0154 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.6926-1997C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854129 | ||||||
| chr13:38854330
|
C | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6926-1796C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854330 | ||||||
| chr13:38854373
|
G | A | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6926-1753G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854373 | ||||||
| chr13:38854406
|
A | G | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.6926-1720A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854406 | ||||||
| chr13:38854513
|
A | C | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6926-1613A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854513 | ||||||
| chr13:38854569
|
A | G | 1 | a0003c0003t0005g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.6926-1557A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854569 | ||||||
| chr13:38854586
|
C | A | 1 | a0007c0025t0006g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6926-1540C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854586 | ||||||
| chr13:38854612
|
T | C | 2 | a0014c0022t0014g0193a0037c0063t0014g0104 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6926-1514T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38854612 | ||||||
| chr13:38855005
|
T | C | 1 | a0002c0006t0013g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6926-1121T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38855005 | ||||||
| chr13:38855138
|
AT | A | 105 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(102): Show | 105 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.6926-978delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38855138 | |||||
| chr13:38855378
|
A | G | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.6926-748A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38855378 | ||||||
| chr13:38855656
|
A | G | 1 | a0052c0045t0054g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6926-470A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38855656 | ||||||
| chr13:38855736
|
T | G | 1 | a0002c0092t0046g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6926-390T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38855736 | ||||||
| chr13:38855771
|
G | A | 1 | a0041c0079t0039g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6926-355G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | chr13 | 38855771 | ||||||
| chr13:38856045
|
T | TA | 6 | a0001c0001t0001g0192a0001c0001t0002g0183a0003c0003t0003g0086others(3): Show | 6 | HG00621.hp2 HG02074.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.6926-59dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38856045 | |||||
| chr13:38856045
|
TA | T | 20 | a0001c0002t0005g0140a0001c0017t0055g0256a0001c0033t0010g0136others(17): Show | 20 | HG00738.hp1 HG01070.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.6926-59delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38856045 | |||||
| chr13:38856045
|
TAA | T | 73 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(70): Show | 73 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.6926-60_6926-59del others(2): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38856045 | |||||
| chr13:38856045
|
TAAA | T | 5 | a0001c0009t0008g0247a0001c0009t0020g0250a0027c0053t0041g0116others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.6926-61_6926-59del others(3): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr13 | 38856045 | |||||
| chr13:38856306
|
G | A | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.7056+50G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856306 | ||||||
| chr13:38856368
|
G | A | 2 | a0003c0003t0005g0082a0009c0038t0005g0133 | 2 | NA18955.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.7056+112G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856368 | ||||||
| chr13:38856393
|
T | C | 1 | a0046c0083t0002g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.7056+137T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856393 | ||||||
| chr13:38856442
|
T | C | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.7056+186T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856442 | ||||||
| chr13:38856619
|
A | G | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.7056+363A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856619 | ||||||
| chr13:38856681
|
T | C | 2 | a0002c0011t0004g0211a0002c0011t0035g0227 | 2 | HG00558.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.7056+425T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856681 | ||||||
| chr13:38856720
|
A | G | 88 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(85): Show | 88 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.7056+464A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856720 | ||||||
| chr13:38856738
|
T | TCCTAAAT others(314): Show |
5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.7056+499_7056+500i others(323): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTAAAT others(319): Show |
15 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(12): Show | 15 | NA18747.hp1 NA18940.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.7056+499_7056+500i others(328): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTAAAT others(320): Show |
4 | a0003c0003t0005g0089a0004c0004t0005g0009a0004c0004t0005g0065others(1): Show | 4 | HG02083.hp1 HG02135.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.7056+499_7056+500i others(329): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(315): Show |
1 | a0001c0030t0003g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7056+485_7056+486i others(324): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(315): Show |
3 | a0020c0040t0003g0005a0038c0064t0033g0103a0053c0069t0003g0108 | 3 | HG02723.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7056+485_7056+486i others(324): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(315): Show |
19 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0007g0179others(16): Show | 19 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.7056+485_7056+486i others(324): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(316): Show |
1 | a0036c0061t0003g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7056+485_7056+486i others(325): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(316): Show |
2 | a0015c0031t0003g0129a0048c0065t0003g0100 | 2 | HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7056+485_7056+486i others(325): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(333): Show |
2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7056+485_7056+486i others(342): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856738
|
T | TCCTGAAT others(340): Show |
1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7056+485_7056+486i others(349): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr13 | 38856738 | |||||
| chr13:38856828
|
C | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7056+572C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856828 | ||||||
| chr13:38856931
|
C | T | 4 | a0001c0002t0005g0140a0001c0068t0005g0160a0004c0004t0005g0009others(1): Show | 4 | HG02135.hp2 NA18947.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.7056+675C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856931 | ||||||
| chr13:38856960
|
G | A | 5 | a0001c0009t0008g0247a0001c0030t0003g0145a0004c0004t0003g0198others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.7056+704G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38856960 | ||||||
| chr13:38857119
|
A | G | 1 | a0002c0008t0001g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.7057-756A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857119 | ||||||
| chr13:38857174
|
A | G | 93 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(90): Show | 93 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.7057-701A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857174 | ||||||
| chr13:38857188
|
G | A | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.7057-687G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857188 | ||||||
| chr13:38857210
|
A | G | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7057-665A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857210 | ||||||
| chr13:38857309
|
T | G | 1 | a0006c0032t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7057-566T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857309 | ||||||
| chr13:38857321
|
A | G | 2 | a0001c0002t0003g0138a0001c0002t0003g0180 | 2 | HG01261.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.7057-554A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857321 | ||||||
| chr13:38857503
|
T | C | 1 | a0008c0050t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7057-372T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857503 | ||||||
| chr13:38857698
|
C | T | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0022c0043t0012g0234others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.7057-177C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857698 | ||||||
| chr13:38857808
|
T | C | 63 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0003g0138others(60): Show | 63 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(60): Show |
intron_variant | MODIFIER | c.7057-67T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857808 | ||||||
| chr13:38857824
|
A | C | 1 | a0001c0002t0007g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.7057-51A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 12/23 | chr13 | 38857824 | ||||||
| chr13:38858203
|
T | C | 5 | a0001c0033t0010g0136a0001c0033t0010g0204a0017c0034t0010g0222others(2): Show | 5 | HG00738.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.7215+170T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858203 | ||||||
| chr13:38858364
|
A | G | 2 | a0007c0025t0003g0229a0033c0057t0022g0127 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.7215+331A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858364 | ||||||
| chr13:38858423
|
G | C | 71 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0164others(68): Show | 71 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.7215+390G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858423 | ||||||
| chr13:38858589
|
CTAAGTT | C | 5 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.7215+561_7215+566d others(8): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr13 | 38858589 | |||||
| chr13:38858602
|
C | T | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7215+569C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858602 | ||||||
| chr13:38858645
|
C | T | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7215+612C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858645 | ||||||
| chr13:38858772
|
G | A | 4 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.7216-515G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858772 | ||||||
| chr13:38858964
|
G | A | 6 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(3): Show | 6 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.7216-323G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858964 | ||||||
| chr13:38858987
|
C | G | 257 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(254): Show | 257 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.7216-300C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858987 | ||||||
| chr13:38858987
|
C | T | 4 | a0002c0010t0004g0034a0002c0011t0004g0217a0003c0003t0004g0078others(1): Show | 4 | HG00423.hp1 NA18963.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.7216-300C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858987 | ||||||
| chr13:38858992
|
G | A | 116 | a0001c0001t0001g0172a0001c0002t0001g0135a0001c0002t0001g0156others(113): Show | 116 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.7216-295G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38858992 | ||||||
| chr13:38859141
|
C | A | 1 | a0002c0006t0013g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7216-146C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 13/23 | chr13 | 38859141 | ||||||
| chr13:38859652
|
A | G | 73 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.7519+62A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859652 | ||||||
| chr13:38859676
|
A | G | 86 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(83): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.7519+86A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859676 | ||||||
| chr13:38859825
|
A | G | 1 | a0007c0025t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.7519+235A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859825 | ||||||
| chr13:38859865
|
A | AG | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+276dupG | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr13 | 38859865 | |||||
| chr13:38859868
|
T | A | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+278T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859868 | ||||||
| chr13:38859872
|
GA | G | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+283delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859872 | ||||||
| chr13:38859876
|
C | T | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+286C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859876 | ||||||
| chr13:38859878
|
G | C | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+288G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859878 | ||||||
| chr13:38859880
|
CACATTTT others(20): Show |
C | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+292_7519+318d others(29): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr13 | 38859880 | |||||
| chr13:38859908
|
A | T | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7519+318A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38859908 | ||||||
| chr13:38860048
|
A | T | 2 | a0003c0005t0024g0062a0008c0050t0001g0123 | 2 | HG01175.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.7519+458A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860048 | ||||||
| chr13:38860053
|
G | C | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.7519+463G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860053 | ||||||
| chr13:38860334
|
G | A | 4 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.7519+744G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860334 | ||||||
| chr13:38860420
|
C | T | 1 | a0004c0007t0001g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7519+830C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860420 | ||||||
| chr13:38860530
|
G | C | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.7520-901G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860530 | ||||||
| chr13:38860671
|
T | C | 124 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(121): Show | 124 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.7520-760T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860671 | ||||||
| chr13:38860694
|
C | T | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7520-737C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860694 | ||||||
| chr13:38860712
|
G | T | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7520-719G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860712 | ||||||
| chr13:38860714
|
C | T | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7520-717C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860714 | ||||||
| chr13:38860745
|
C | T | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7520-686C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860745 | ||||||
| chr13:38860960
|
G | A | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.7520-471G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38860960 | ||||||
| chr13:38861262
|
C | T | 10 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.7520-169C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38861262 | ||||||
| chr13:38861288
|
G | A | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.7520-143G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38861288 | ||||||
| chr13:38861323
|
A | G | 2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7520-108A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38861323 | ||||||
| chr13:38861402
|
G | A | 1 | a0003c0005t0002g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.7520-29G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38861402 | ||||||
| chr13:38861415
|
C | CG | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.7520-16_7520-15ins others(1): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | chr13 | 38861415 | ||||||
| chr13:38861415
|
C | CT | 9 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(6): Show | 9 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.7520-5dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr13 | 38861415 | |||||
| chr13:38861415
|
C | CTT | 9 | a0010c0013t0003g0107a0014c0022t0014g0193a0022c0043t0012g0234others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.7520-6_7520-5dupTT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr13 | 38861415 | |||||
| chr13:38861609
|
C | T | 1 | a0002c0011t0035g0227 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.7651+47C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38861609 | ||||||
| chr13:38861674
|
C | A | 1 | a0001c0001t0023g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.7651+112C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38861674 | ||||||
| chr13:38861746
|
G | A | 135 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(132): Show | 135 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.7651+184G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38861746 | ||||||
| chr13:38861856
|
C | T | 3 | a0001c0009t0008g0260a0015c0031t0003g0129a0048c0065t0003g0100 | 3 | HG02109.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7651+294C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38861856 | ||||||
| chr13:38861876
|
A | G | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7651+314A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38861876 | ||||||
| chr13:38862015
|
G | T | 1 | a0005c0015t0042g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.7651+453G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862015 | ||||||
| chr13:38862034
|
A | G | 8 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(5): Show | 8 | HG01496.hp1 HG01981.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.7651+472A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862034 | ||||||
| chr13:38862114
|
G | A | 1 | a0004c0004t0004g0007 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.7651+552G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862114 | ||||||
| chr13:38862262
|
A | T | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+700A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862262 | ||||||
| chr13:38862263
|
G | A | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+701G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862263 | ||||||
| chr13:38862264
|
A | T | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+702A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862264 | ||||||
| chr13:38862277
|
G | A | 10 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.7651+715G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862277 | ||||||
| chr13:38862278
|
C | A | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+716C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862278 | ||||||
| chr13:38862280
|
A | G | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+718A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862280 | ||||||
| chr13:38862282
|
G | T | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+720G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862282 | ||||||
| chr13:38862283
|
T | C | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+721T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862283 | ||||||
| chr13:38862284
|
C | A | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+722C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862284 | ||||||
| chr13:38862436
|
G | A | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7651+874G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862436 | ||||||
| chr13:38862511
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.7651+949G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862511 | ||||||
| chr13:38862599
|
G | A | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7651+1037G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862599 | ||||||
| chr13:38862799
|
G | GA | 10 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.7651+1246dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr13 | 38862799 | |||||
| chr13:38862809
|
G | A | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.7651+1247G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862809 | ||||||
| chr13:38862888
|
G | T | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7651+1326G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38862888 | ||||||
| chr13:38863001
|
A | G | 107 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(104): Show | 107 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.7652-1274A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863001 | ||||||
| chr13:38863018
|
C | G | 2 | a0002c0011t0004g0211a0002c0011t0035g0227 | 2 | HG00558.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.7652-1257C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863018 | ||||||
| chr13:38863103
|
G | T | 5 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.7652-1172G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863103 | ||||||
| chr13:38863113
|
G | A | 1 | a0002c0006t0002g0022 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7652-1162G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863113 | ||||||
| chr13:38863223
|
C | T | 123 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(120): Show | 123 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.7652-1052C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863223 | ||||||
| chr13:38863390
|
T | G | 1 | a0003c0003t0007g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7652-885T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863390 | ||||||
| chr13:38863393
|
A | G | 1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7652-882A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863393 | ||||||
| chr13:38863416
|
T | C | 4 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.7652-859T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863416 | ||||||
| chr13:38863536
|
T | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7652-739T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863536 | ||||||
| chr13:38863557
|
C | CA | 261 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.7652-711dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr13 | 38863557 | |||||
| chr13:38863611
|
C | A | 4 | a0007c0024t0006g0059a0007c0025t0006g0221a0010c0013t0006g0205others(1): Show | 4 | HG01167.hp1 HG01346.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.7652-664C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863611 | ||||||
| chr13:38863820
|
A | G | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7652-455A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863820 | ||||||
| chr13:38863822
|
T | A | 1 | a0001c0030t0003g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7652-453T>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863822 | ||||||
| chr13:38863870
|
A | T | 138 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(135): Show | 138 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.7652-405A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863870 | ||||||
| chr13:38863886
|
G | T | 138 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(135): Show | 138 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.7652-389G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863886 | ||||||
| chr13:38863896
|
G | T | 1 | a0005c0014t0003g0203 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.7652-379G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38863896 | ||||||
| chr13:38864082
|
ACCTCCCA others(5): Show |
A | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7652-190_7652-179d others(14): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr13 | 38864082 | |||||
| chr13:38864084
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7652-191C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38864084 | ||||||
| chr13:38864086
|
C | T | 1 | a0005c0015t0042g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.7652-189C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38864086 | ||||||
| chr13:38864094
|
G | A | 2 | a0001c0001t0001g0155a0001c0067t0001g0182 | 2 | NA19079.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.7652-181G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38864094 | ||||||
| chr13:38864123
|
C | T | 37 | a0001c0002t0001g0135a0001c0002t0004g0054a0001c0002t0004g0141others(34): Show | 37 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.7652-152C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38864123 | ||||||
| chr13:38864246
|
C | A | 123 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(120): Show | 123 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.7652-29C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 15/23 | chr13 | 38864246 | ||||||
| chr13:38864701
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7983+95A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38864701 | ||||||
| chr13:38864743
|
A | G | 1 | a0007c0025t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.7983+137A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38864743 | ||||||
| chr13:38864827
|
CATT | C | 107 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(104): Show | 107 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.7983+224_7983+226d others(5): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38864827 | |||||
| chr13:38865108
|
T | C | 137 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(134): Show | 137 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.7983+502T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865108 | ||||||
| chr13:38865137
|
G | A | 1 | a0015c0031t0003g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7983+531G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865137 | ||||||
| chr13:38865260
|
T | TAC | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.7983+664_7983+665d others(4): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38865260 | |||||
| chr13:38865313
|
A | G | 2 | a0005c0026t0002g0240a0005c0026t0002g0241 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.7983+707A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865313 | ||||||
| chr13:38865341
|
G | T | 4 | a0004c0004t0004g0007a0004c0004t0004g0008a0004c0004t0004g0063others(1): Show | 4 | NA18977.hp2 NA19065.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.7983+735G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865341 | ||||||
| chr13:38865528
|
C | T | 107 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(104): Show | 107 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.7983+922C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865528 | ||||||
| chr13:38865593
|
A | G | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.7983+987A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865593 | ||||||
| chr13:38865698
|
C | T | 1 | a0003c0003t0004g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7983+1092C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865698 | ||||||
| chr13:38865831
|
G | T | 4 | a0016c0059t0043g0101a0016c0060t0029g0106a0041c0079t0039g0093others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7983+1225G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865831 | ||||||
| chr13:38865879
|
C | T | 4 | a0001c0017t0055g0256a0004c0004t0012g0196a0008c0019t0012g0115others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.7983+1273C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865879 | ||||||
| chr13:38865944
|
G | A | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7983+1338G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38865944 | ||||||
| chr13:38866125
|
C | T | 107 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(104): Show | 107 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.7983+1519C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866125 | ||||||
| chr13:38866175
|
T | C | 143 | a0001c0001t0018g0057a0001c0001t0027g0110a0001c0002t0001g0135others(140): Show | 143 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.7983+1569T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866175 | ||||||
| chr13:38866176
|
G | A | 14 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0009t0008g0247others(11): Show | 14 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.7983+1570G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866176 | ||||||
| chr13:38866195
|
G | C | 85 | a0001c0002t0001g0135a0001c0002t0003g0138a0001c0002t0003g0180others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.7983+1589G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866195 | ||||||
| chr13:38866204
|
G | A | 136 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0162others(133): Show | 136 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.7983+1598G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866204 | ||||||
| chr13:38866266
|
G | A | 1 | a0009c0038t0007g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.7983+1660G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866266 | ||||||
| chr13:38866537
|
G | A | 10 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.7983+1931G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866537 | ||||||
| chr13:38866616
|
G | A | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7983+2010G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866616 | ||||||
| chr13:38866622
|
G | A | 1 | a0043c0082t0017g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7983+2016G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866622 | ||||||
| chr13:38866624
|
G | A | 10 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.7983+2018G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866624 | ||||||
| chr13:38866667
|
C | CA | 94 | a0001c0001t0001g0177a0001c0002t0001g0135a0001c0002t0003g0138others(91): Show | 94 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.7983+2079dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38866667 | |||||
| chr13:38866667
|
C | CAA | 22 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0004g0141others(19): Show | 22 | HG02083.hp1 HG02135.hp2 HG02738.hp1 others(19): Show |
intron_variant | MODIFIER | c.7983+2078_7983+207 others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38866667 | |||||
| chr13:38866667
|
CA | C | 20 | a0001c0001t0001g0161a0001c0033t0010g0136a0001c0033t0010g0204others(17): Show | 20 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.7983+2079delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38866667 | |||||
| chr13:38866711
|
G | T | 12 | a0007c0024t0006g0044a0007c0024t0006g0045a0007c0024t0006g0059others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.7983+2105G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866711 | ||||||
| chr13:38866869
|
A | G | 2 | a0003c0005t0024g0062a0008c0050t0001g0123 | 2 | HG01175.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.7983+2263A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866869 | ||||||
| chr13:38866936
|
T | C | 1 | a0026c0052t0003g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7983+2330T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866936 | ||||||
| chr13:38866979
|
A | T | 3 | a0004c0004t0012g0196a0008c0019t0012g0115a0023c0042t0048g0236 | 3 | HG01496.hp1 HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7983+2373A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38866979 | ||||||
| chr13:38867228
|
A | G | 1 | a0001c0009t0008g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7983+2622A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867228 | ||||||
| chr13:38867368
|
C | A | 1 | a0006c0096t0015g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7983+2762C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867368 | ||||||
| chr13:38867374
|
C | G | 1 | a0001c0012t0053g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7983+2768C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867374 | ||||||
| chr13:38867487
|
C | T | 1 | a0040c0081t0006g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7983+2881C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867487 | ||||||
| chr13:38867511
|
G | T | 16 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.7983+2905G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867511 | ||||||
| chr13:38867516
|
C | T | 1 | a0012c0020t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7983+2910C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867516 | ||||||
| chr13:38867727
|
G | C | 16 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(13): Show | 16 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.7983+3121G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867727 | ||||||
| chr13:38867839
|
G | T | 1 | a0003c0005t0024g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.7983+3233G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867839 | ||||||
| chr13:38867913
|
C | T | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7983+3307C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38867913 | ||||||
| chr13:38868040
|
G | A | 1 | a0001c0012t0050g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7983+3434G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868040 | ||||||
| chr13:38868056
|
A | G | 18 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(15): Show | 18 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.7983+3450A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868056 | ||||||
| chr13:38868133
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.7983+3527G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868133 | ||||||
| chr13:38868222
|
C | T | 1 | a0004c0004t0044g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.7983+3616C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868222 | ||||||
| chr13:38868314
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7983+3708C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868314 | ||||||
| chr13:38868330
|
A | T | 20 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(17): Show | 20 | HG02083.hp1 HG02135.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.7983+3724A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868330 | ||||||
| chr13:38868411
|
A | C | 71 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.7983+3805A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868411 | ||||||
| chr13:38868451
|
C | A | 1 | a0001c0012t0053g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7983+3845C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868451 | ||||||
| chr13:38868452
|
G | A | 6 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(3): Show | 6 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.7983+3846G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868452 | ||||||
| chr13:38868569
|
G | A | 207 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(204): Show | 207 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.7983+3963G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868569 | ||||||
| chr13:38868638
|
A | G | 1 | a0025c0048t0003g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7983+4032A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868638 | ||||||
| chr13:38868922
|
G | C | 1 | a0007c0025t0006g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7984-3820G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38868922 | ||||||
| chr13:38869019
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7984-3723C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869019 | ||||||
| chr13:38869053
|
T | C | 4 | a0004c0004t0012g0196a0008c0019t0012g0115a0022c0043t0012g0234others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7984-3689T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869053 | ||||||
| chr13:38869251
|
G | A | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.7984-3491G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869251 | ||||||
| chr13:38869267
|
A | G | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7984-3475A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869267 | ||||||
| chr13:38869279
|
T | C | 211 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(208): Show | 211 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.7984-3463T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869279 | ||||||
| chr13:38869344
|
T | G | 13 | a0001c0002t0006g0188a0007c0024t0006g0044a0007c0024t0006g0045others(10): Show | 13 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.7984-3398T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869344 | ||||||
| chr13:38869376
|
A | G | 211 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(208): Show | 211 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.7984-3366A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869376 | ||||||
| chr13:38869440
|
T | C | 1 | a0004c0089t0001g0239 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.7984-3302T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869440 | ||||||
| chr13:38869509
|
C | T | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.7984-3233C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869509 | ||||||
| chr13:38869553
|
A | T | 145 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(142): Show | 145 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.7984-3189A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869553 | ||||||
| chr13:38869678
|
A | G | 6 | a0006c0016t0021g0246a0006c0016t0021g0255a0006c0016t0052g0244others(3): Show | 6 | HG00639.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.7984-3064A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869678 | ||||||
| chr13:38869795
|
G | T | 9 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0017t0055g0256others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.7984-2947G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869795 | ||||||
| chr13:38869799
|
A | T | 9 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0017t0055g0256others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.7984-2943A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38869799 | ||||||
| chr13:38870232
|
T | C | 2 | a0016c0059t0043g0101a0052c0045t0054g0257 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7984-2510T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870232 | ||||||
| chr13:38870457
|
A | G | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7984-2285A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870457 | ||||||
| chr13:38870525
|
TTTAAG | T | 53 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(50): Show | 53 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.7984-2214_7984-221 others(9): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38870525 | |||||
| chr13:38870583
|
G | T | 1 | a0006c0032t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7984-2159G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870583 | ||||||
| chr13:38870688
|
G | A | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.7984-2054G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870688 | ||||||
| chr13:38870717
|
A | C | 4 | a0004c0004t0012g0196a0008c0019t0012g0115a0022c0043t0012g0234others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7984-2025A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870717 | ||||||
| chr13:38870922
|
A | G | 1 | a0044c0084t0009g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7984-1820A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870922 | ||||||
| chr13:38870929
|
A | G | 1 | a0040c0081t0006g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7984-1813A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870929 | ||||||
| chr13:38870960
|
T | C | 3 | a0014c0022t0014g0193a0033c0057t0022g0127a0037c0063t0014g0104 | 3 | HG01884.hp1 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7984-1782T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38870960 | ||||||
| chr13:38871007
|
C | A | 4 | a0004c0004t0012g0196a0008c0019t0012g0115a0022c0043t0012g0234others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7984-1735C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871007 | ||||||
| chr13:38871014
|
A | C | 1 | a0002c0006t0007g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7984-1728A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871014 | ||||||
| chr13:38871016
|
C | T | 52 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(49): Show | 52 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.7984-1726C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871016 | ||||||
| chr13:38871046
|
G | A | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.7984-1696G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871046 | ||||||
| chr13:38871068
|
G | A | 2 | a0006c0096t0015g0153a0031c0056t0015g0125 | 2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.7984-1674G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871068 | ||||||
| chr13:38871086
|
C | T | 1 | a0002c0010t0004g0097 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.7984-1656C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871086 | ||||||
| chr13:38871380
|
G | A | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.7984-1362G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871380 | ||||||
| chr13:38871606
|
G | A | 54 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(51): Show | 54 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.7984-1136G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871606 | ||||||
| chr13:38871637
|
G | A | 1 | a0005c0015t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7984-1105G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871637 | ||||||
| chr13:38871713
|
A | C | 6 | a0001c0001t0002g0183a0001c0001t0002g0185a0003c0005t0002g0060others(3): Show | 6 | HG00423.hp2 HG02074.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.7984-1029A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38871713 | ||||||
| chr13:38872463
|
C | CTAAAG | 62 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(59): Show | 62 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.7984-278_7984-274d others(7): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr13 | 38872463 | |||||
| chr13:38872560
|
C | A | 1 | a0006c0021t0002g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7984-182C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38872560 | ||||||
| chr13:38872659
|
G | A | 6 | a0001c0033t0010g0136a0001c0033t0010g0204a0002c0092t0046g0036others(3): Show | 6 | HG00738.hp1 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.7984-83G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38872659 | ||||||
| chr13:38872732
|
G | A | 62 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(59): Show | 62 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.7984-10G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 16/23 | chr13 | 38872732 | ||||||
| chr13:38873306
|
A | G | 3 | a0014c0022t0014g0193a0033c0057t0022g0127a0037c0063t0014g0104 | 3 | HG01884.hp1 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8176+372A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38873306 | ||||||
| chr13:38873320
|
GA | G | 4 | a0004c0004t0012g0196a0008c0019t0012g0115a0022c0043t0012g0234others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.8176+393delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr13 | 38873320 | |||||
| chr13:38873528
|
G | T | 213 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(210): Show | 213 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.8176+594G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38873528 | ||||||
| chr13:38873626
|
T | TAATA | 211 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(208): Show | 211 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.8176+695_8176+696i others(6): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr13 | 38873626 | |||||
| chr13:38873740
|
A | C | 8 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0070t0003g0095others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.8177-742A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38873740 | ||||||
| chr13:38873804
|
C | A | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.8177-678C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38873804 | ||||||
| chr13:38874152
|
T | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.8177-330T>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874152 | ||||||
| chr13:38874172
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.8177-310G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874172 | ||||||
| chr13:38874196
|
CA | C | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8177-285delA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874196 | ||||||
| chr13:38874207
|
A | G | 71 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0004g0054others(68): Show | 71 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.8177-275A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874207 | ||||||
| chr13:38874318
|
A | G | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.8177-164A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874318 | ||||||
| chr13:38874339
|
T | C | 62 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(59): Show | 62 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.8177-143T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 17/23 | chr13 | 38874339 | ||||||
| chr13:38874756
|
C | T | 2 | a0016c0059t0043g0101a0052c0045t0054g0257 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.8281+170C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38874756 | ||||||
| chr13:38874866
|
A | G | 1 | a0003c0005t0024g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.8281+280A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38874866 | ||||||
| chr13:38875146
|
A | G | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(72): Show | 75 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.8281+560A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875146 | ||||||
| chr13:38875171
|
A | AG | 212 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(209): Show | 212 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.8281+587dupG | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr13 | 38875171 | |||||
| chr13:38875195
|
A | AT | 3 | a0001c0002t0004g0169a0001c0002t0004g0231a0003c0003t0003g0086 | 3 | HG00673.hp1 HG02129.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.8281+615dupT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr13 | 38875195 | |||||
| chr13:38875229
|
T | C | 4 | a0004c0004t0012g0196a0008c0019t0012g0115a0022c0043t0012g0234others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.8281+643T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875229 | ||||||
| chr13:38875230
|
A | G | 2 | a0016c0059t0043g0101a0052c0045t0054g0257 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.8281+644A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875230 | ||||||
| chr13:38875233
|
A | G | 53 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(50): Show | 53 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.8281+647A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875233 | ||||||
| chr13:38875291
|
G | A | 53 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(50): Show | 53 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.8281+705G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875291 | ||||||
| chr13:38875432
|
C | T | 212 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(209): Show | 212 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.8282-590C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875432 | ||||||
| chr13:38875465
|
C | T | 2 | a0001c0001t0001g0168a0002c0008t0001g0214 | 2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.8282-557C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875465 | ||||||
| chr13:38875584
|
A | G | 9 | a0001c0017t0008g0249a0001c0017t0008g0261a0001c0017t0055g0256others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.8282-438A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875584 | ||||||
| chr13:38875652
|
A | G | 1 | a0002c0027t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.8282-370A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875652 | ||||||
| chr13:38875989
|
A | G | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.8282-33A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38875989 | ||||||
| chr13:38876002
|
A | C | 62 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(59): Show | 62 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.8282-20A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 18/23 | chr13 | 38876002 | ||||||
| chr13:38876152
|
A | C | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.8409+3A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 19/23 | chr13 | 38876152 | ||||||
| chr13:38876430
|
G | C | 1 | a0051c0046t0051g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.8544+48G>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876430 | ||||||
| chr13:38876446
|
T | TA | 83 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(80): Show | 83 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.8544+78dupA | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr13 | 38876446 | |||||
| chr13:38876446
|
T | TTAA | 7 | a0010c0013t0003g0107a0014c0022t0014g0193a0026c0052t0003g0122others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.8544+64_8544+65ins others(3): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876446 | ||||||
| chr13:38876447
|
A | T | 20 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(17): Show | 20 | HG02083.hp1 HG02135.hp2 HG02976.hp2 others(17): Show |
intron_variant | MODIFIER | c.8544+65A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876447 | ||||||
| chr13:38876525
|
C | A | 21 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(18): Show | 21 | HG02083.hp1 HG02135.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.8544+143C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876525 | ||||||
| chr13:38876850
|
T | C | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.8545-267T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876850 | ||||||
| chr13:38876936
|
T | C | 13 | a0001c0002t0006g0188a0007c0024t0006g0044a0007c0024t0006g0045others(10): Show | 13 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.8545-181T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38876936 | ||||||
| chr13:38877025
|
C | T | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.8545-92C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 20/23 | chr13 | 38877025 | ||||||
| chr13:38877296
|
G | A | 4 | a0001c0009t0008g0260a0015c0031t0003g0129a0036c0061t0003g0102others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.8671+53G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877296 | ||||||
| chr13:38877420
|
A | T | 52 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(49): Show | 52 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.8671+177A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877420 | ||||||
| chr13:38877490
|
T | C | 15 | a0001c0030t0047g0151a0005c0014t0003g0203a0011c0018t0003g0112others(12): Show | 15 | HG02257.hp1 HG02486.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.8671+247T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877490 | ||||||
| chr13:38877600
|
T | C | 2 | a0001c0009t0020g0248a0001c0009t0020g0250 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.8671+357T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877600 | ||||||
| chr13:38877709
|
A | G | 1 | a0004c0007t0001g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.8672-425A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877709 | ||||||
| chr13:38877829
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8672-305C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877829 | ||||||
| chr13:38877863
|
C | T | 1 | a0002c0011t0004g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8672-271C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877863 | ||||||
| chr13:38877887
|
T | C | 52 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(49): Show | 52 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.8672-247T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38877887 | ||||||
| chr13:38878026
|
G | T | 1 | a0004c0004t0005g0065 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.8672-108G>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38878026 | ||||||
| chr13:38878081
|
G | A | 1 | a0001c0002t0004g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8672-53G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38878081 | ||||||
| chr13:38878098
|
T | C | 212 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(209): Show | 212 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.8672-36T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38878098 | ||||||
| chr13:38878127
|
A | G | 1 | a0001c0002t0005g0140 | 1 | NA18962.hp1 | splice_region_variant&intron_variant | LOW | c.8672-7A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 21/23 | chr13 | 38878127 | ||||||
| chr13:38878389
|
T | TAAAAACA others(310): Show |
1 | a0001c0001t0023g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.8859+82_8859+83ins others(317): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr13 | 38878389 | |||||
| chr13:38878389
|
T | TAAAAACA others(309): Show |
1 | a0001c0001t0001g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.8859+82_8859+83ins others(316): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr13 | 38878389 | |||||
| chr13:38878389
|
T | TAAAAACA others(310): Show |
48 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0155others(45): Show | 48 | HG00558.hp1 HG00735.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.8859+82_8859+83ins others(317): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr13 | 38878389 | |||||
| chr13:38878389
|
T | TAAAAACA others(311): Show |
24 | a0001c0001t0001g0052a0001c0001t0001g0164a0001c0001t0001g0166others(21): Show | 24 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.8859+82_8859+83ins others(318): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr13 | 38878389 | |||||
| chr13:38878389
|
T | TAAAAACA others(312): Show |
1 | a0002c0008t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8859+82_8859+83ins others(319): Show |
FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr13 | 38878389 | |||||
| chr13:38878443
|
C | G | 1 | a0055c0071t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8859+122C>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878443 | ||||||
| chr13:38878525
|
A | T | 6 | a0001c0030t0047g0151a0004c0004t0012g0196a0008c0019t0012g0115others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.8859+204A>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878525 | ||||||
| chr13:38878530
|
A | G | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.8859+209A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878530 | ||||||
| chr13:38878558
|
G | A | 1 | a0001c0002t0032g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8859+237G>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878558 | ||||||
| chr13:38878663
|
C | T | 87 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0004g0054others(84): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.8860-168C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878663 | ||||||
| chr13:38878797
|
C | T | 67 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(64): Show | 67 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.8860-34C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878797 | ||||||
| chr13:38878800
|
C | T | 3 | a0028c0054t0009g0117a0035c0062t0009g0105a0045c0085t0009g0200 | 3 | HG02055.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8860-31C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 22/23 | chr13 | 38878800 | ||||||
| chr13:38879136
|
A | G | 213 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(210): Show | 213 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.9006+159A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879136 | ||||||
| chr13:38879139
|
C | T | 1 | a0001c0012t0053g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.9006+162C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879139 | ||||||
| chr13:38879164
|
C | A | 19 | a0001c0002t0001g0156a0001c0002t0001g0162a0001c0002t0005g0140others(16): Show | 19 | HG02083.hp1 HG02135.hp2 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.9006+187C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879164 | ||||||
| chr13:38879252
|
A | G | 1 | a0004c0007t0001g0014 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.9006+275A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879252 | ||||||
| chr13:38879256
|
C | T | 1 | a0003c0003t0004g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.9006+279C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879256 | ||||||
| chr13:38879396
|
T | C | 1 | a0001c0017t0055g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.9006+419T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879396 | ||||||
| chr13:38879423
|
C | T | 78 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(75): Show | 78 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.9006+446C>T | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879423 | ||||||
| chr13:38879646
|
A | G | 84 | a0001c0002t0003g0138a0001c0002t0003g0180a0001c0002t0004g0054others(81): Show | 84 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.9007-638A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879646 | ||||||
| chr13:38879695
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.9007-589A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879695 | ||||||
| chr13:38879834
|
AT | A | 6 | a0001c0002t0001g0156a0001c0002t0001g0162a0003c0003t0007g0076others(3): Show | 6 | NA18940.hp2 NA18951.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.9007-444delT | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr13 | 38879834 | |||||
| chr13:38879840
|
T | C | 67 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0058others(64): Show | 67 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.9007-444T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879840 | ||||||
| chr13:38879906
|
T | C | 34 | a0001c0002t0004g0054a0001c0002t0004g0141a0001c0002t0004g0154others(31): Show | 34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.9007-378T>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879906 | ||||||
| chr13:38879990
|
A | C | 8 | a0007c0025t0003g0229a0010c0013t0003g0107a0014c0022t0014g0193others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.9007-294A>C | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38879990 | ||||||
| chr13:38880175
|
A | G | 3 | a0004c0004t0003g0198a0019c0039t0011g0004a0030c0055t0003g0131 | 3 | HG01891.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.9007-109A>G | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38880175 | ||||||
| chr13:38880211
|
C | A | 1 | a0035c0062t0009g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9007-73C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38880211 | ||||||
| chr13:38880225
|
C | A | 1 | a0006c0016t0052g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.9007-59C>A | FREM2 | ENSG00000150893.11 | transcript | ENST00000280481.9 | protein_coding | 23/23 | chr13 | 38880225 |