Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2984 |
|---|---|
| ensemblid | ENSG00000070019.5 |
| hgncid | 4688 |
| symbol | GUCY2C |
| name | guanylate cyclase 2C |
| refseq_nuc | NM_004963.4 |
| refseq_prot | NP_004954.2 |
| ensembl_nuc | ENST00000261170.5 |
| ensembl_prot | ENSP00000261170.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 14612632 |
| end | 14696599 |
| strand | - |
| ver | v1.2 |
| region | chr12:14612632-14696599 |
| region5000 | chr12:14607632-14701599 |
| regionname0 | GUCY2C_chr12_14612632_14696599 |
| regionname5000 | GUCY2C_chr12_14607632_14701599 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1073 | 226 | 74 | 52 | 63 | 8 | 28 | 46 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0002 | 1/0 | 1073 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0003 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0004 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0005 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0006 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0007 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0008 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3222 | 160 | 18 | 48 | 59 | 8 | 26 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0002 | 0/0 | 3222 | 32 | 29 | 2 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0003 | 0/0 | 3222 | 16 | 14 | 1 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0004 | 0/0 | 3222 | 6 | 4 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0005 | 0/0 | 3222 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0006 | 1/0 | 3222 | 4 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0007 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0008 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0009 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0010 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0011 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0012 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0013 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0014 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0015 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0016 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0017 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0018 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| c0019 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 637 | 230 | 73 | 52 | 67 | 8 | 28 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| t0002 | 0/0 | 637 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| t0003 | 0/0 | 637 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| t0004 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3222 | 160 | 18 | 48 | 59 | 8 | 26 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0002 | 0/0 | 3222 | 32 | 29 | 2 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0003 | 0/0 | 3222 | 16 | 14 | 1 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0004 | 0/0 | 3222 | 6 | 4 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0005 | 0/0 | 3222 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0007 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0008 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0011 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0012 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0016 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0017 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0018 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0002c0006 | 1/0 | 3222 | 4 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0003c0019 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0004c0009 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0005c0010 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0006c0013 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0007c0014 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0008c0015 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3858 | 159 | 18 | 48 | 58 | 8 | 26 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0001t0003 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0002t0001 | 0/0 | 3858 | 31 | 28 | 2 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0002t0004 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0003t0001 | 0/0 | 3858 | 16 | 14 | 1 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0004t0001 | 0/0 | 3858 | 6 | 4 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0005t0002 | 0/0 | 3858 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0007t0001 | 0/0 | 3858 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0008t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0011t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0012t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0016t0001 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0017t0001 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0001c0018t0001 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0002c0006t0001 | 1/0 | 3858 | 4 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0003c0019t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0004c0009t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0005c0010t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0006c0013t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0007c0014t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| a0008c0015t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | copy fasta | chr12 | 14607632 | 14701599 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0005t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0005t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0007t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0011t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0012t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0016t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0017t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0018t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0003c0019t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0004c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0005c0010t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0006c0013t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0007c0014t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0008c0015t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01255 | hp2 | a0001 | c0018 | t0001 | g0098 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01884 | hp1 | a0001 | c0005 | t0002 | g0133 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0202 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01891 | hp2 | a0001 | c0005 | t0002 | g0179 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0120 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02258 | hp2 | a0001 | c0005 | t0002 | g0132 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02451 | hp2 | a0001 | c0011 | t0001 | g0014 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02523 | hp2 | a0006 | c0013 | t0001 | g0034 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02572 | hp2 | a0003 | c0019 | t0001 | g0188 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0214 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0118 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02897 | hp2 | a0001 | c0012 | t0001 | g0074 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0218 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03041 | hp1 | a0002 | c0006 | t0001 | g0185 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0119 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04199 | hp2 | a0001 | c0017 | t0001 | g0112 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0186 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18952 | hp1 | a0005 | c0010 | t0001 | g0194 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18972 | hp1 | a0007 | c0014 | t0001 | g0047 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18986 | hp2 | a0008 | c0015 | t0001 | g0142 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18993 | hp1 | a0004 | c0009 | t0001 | g0064 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19030 | hp1 | a0001 | c0007 | t0001 | g0219 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20129 | hp1 | a0001 | c0008 | t0001 | g0134 | AFR | ASW | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ASW | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20905 | hp2 | a0001 | c0016 | t0001 | g0079 | SAS | GIH | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02486 | hp2 | a0001 | c0005 | t0002 | g0131 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| homoSapiens_grch38 | hp1 | a0002 | c0006 | t0001 | g0113 | REF | REF | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14613277
|
C | T | 1 | a0007 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.3062G>A | p.Arg1021His | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 27/27 | 3213/3858 | 3062/3222 | 1021/1073 | chr12 | 14613277 | ||
| chr12:14621108
|
T | C | 1 | a0008 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.2710A>G | p.Met904Val | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/27 | 2861/3858 | 2710/3222 | 904/1073 | chr12 | 14621108 | ||
| chr12:14621155
|
C | T | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2663G>A | p.Arg888Gln | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/27 | 2814/3858 | 2663/3222 | 888/1073 | chr12 | 14621155 | ||
| chr12:14669803
|
C | T | 1 | a0005 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1201G>A | p.Val401Ile | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/27 | 1352/3858 | 1201/3222 | 401/1073 | chr12 | 14669803 | ||
| chr12:14672919
|
A | G | 1 | a0004 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1124T>C | p.Val375Ala | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/27 | 1275/3858 | 1124/3222 | 375/1073 | chr12 | 14672919 | ||
| chr12:14676959
|
A | C | 6 | a0001a0004a0005others(3): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
missense_variant | MODERATE | c.843T>G | p.Phe281Leu | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/27 | 994/3858 | 843/3222 | 281/1073 | chr12 | 14676959 | ||
| chr12:14688052
|
T | G | 1 | a0003 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.229A>C | p.Thr77Pro | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/27 | 380/3858 | 229/3222 | 77/1073 | chr12 | 14688052 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14613216
|
C | G | 1 | a0001c0008 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.3123G>C | p.Gly1041Gly | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 27/27 | 3274/3858 | 3123/3222 | 1041/1073 | chr12 | 14613216 | ||
| chr12:14622152
|
T | C | 1 | a0001c0012 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.2454A>G | p.Glu818Glu | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/27 | 2605/3858 | 2454/3222 | 818/1073 | chr12 | 14622152 | ||
| chr12:14625810
|
C | G | 2 | a0001c0005a0001c0007 | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.2355G>C | p.Leu785Leu | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/27 | 2506/3858 | 2355/3222 | 785/1073 | chr12 | 14625810 | ||
| chr12:14628735
|
C | T | 2 | a0001c0005a0001c0007 | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.2160G>A | p.Val720Val | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/27 | 2311/3858 | 2160/3222 | 720/1073 | chr12 | 14628735 | ||
| chr12:14641128
|
G | A | 11 | a0001c0001a0001c0004a0001c0007others(8): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
synonymous_variant | LOW | c.2022C>T | p.Ile674Ile | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/27 | 2173/3858 | 2022/3222 | 674/1073 | chr12 | 14641128 | ||
| chr12:14652973
|
T | C | 1 | a0001c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1512A>G | p.Arg504Arg | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/27 | 1663/3858 | 1512/3222 | 504/1073 | chr12 | 14652973 | ||
| chr12:14669744
|
A | C | 1 | a0001c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1260T>G | p.Leu420Leu | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/27 | 1411/3858 | 1260/3222 | 420/1073 | chr12 | 14669744 | ||
| chr12:14669804
|
G | A | 1 | a0001c0016 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.1200C>T | p.His400His | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/27 | 1351/3858 | 1200/3222 | 400/1073 | chr12 | 14669804 | ||
| chr12:14681426
|
G | C | 1 | a0001c0017 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.663C>G | p.Gly221Gly | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/27 | 814/3858 | 663/3222 | 221/1073 | chr12 | 14681426 | ||
| chr12:14683083
|
C | T | 3 | a0001c0003a0001c0004a0001c0008 | 23 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
synonymous_variant | LOW | c.570G>A | p.Ser190Ser | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/27 | 721/3858 | 570/3222 | 190/1073 | chr12 | 14683083 | ||
| chr12:14683143
|
G | A | 1 | a0001c0018 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.510C>T | p.Phe170Phe | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/27 | 661/3858 | 510/3222 | 170/1073 | chr12 | 14683143 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14612746
|
T | G | 1 | a0001c0001t0003 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*371A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 27/27 | 371 | chr12 | 14612746 | |||||
| chr12:14613061
|
G | A | 1 | a0001c0005t0002 | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*56C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 27/27 | 56 | chr12 | 14613061 | |||||
| chr12:14613090
|
G | A | 1 | a0001c0002t0004 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 27/27 | 27 | chr12 | 14613090 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14613549
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3048-258G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14613549 | ||||||
| chr12:14613657
|
G | A | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3048-366C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14613657 | ||||||
| chr12:14613893
|
A | G | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3048-602T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14613893 | ||||||
| chr12:14613938
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3048-647T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14613938 | ||||||
| chr12:14613978
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3048-687C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14613978 | ||||||
| chr12:14614011
|
C | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.3048-720G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614011 | ||||||
| chr12:14614046
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3048-755A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614046 | ||||||
| chr12:14614220
|
G | A | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.3047+647C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614220 | ||||||
| chr12:14614365
|
ATAAGT | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+497_3047+501d others(7): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614365 | ||||||
| chr12:14614374
|
G | A | 8 | a0001c0001t0001g0105a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3047+493C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614374 | ||||||
| chr12:14614559
|
A | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+308T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614559 | ||||||
| chr12:14614565
|
A | AG | 1 | a0001c0001t0001g0001 | 3 | NA18977.hp1 NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.3047+301_3047+302i others(3): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614565 | ||||||
| chr12:14614603
|
A | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+264T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614603 | ||||||
| chr12:14614604
|
G | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+263C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614604 | ||||||
| chr12:14614606
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3047+261C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614606 | ||||||
| chr12:14614617
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+250C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614617 | ||||||
| chr12:14614625
|
G | C | 35 | a0001c0001t0001g0105a0001c0002t0001g0005a0001c0002t0001g0006others(32): Show | 39 | HG00733.hp2 HG01884.hp2 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.3047+242C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614625 | ||||||
| chr12:14614647
|
A | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047+220T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 26/26 | chr12 | 14614647 | ||||||
| chr12:14614964
|
C | T | 13 | a0001c0001t0001g0105a0001c0002t0001g0148a0001c0002t0001g0149others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2971-21G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14614964 | ||||||
| chr12:14615009
|
T | C | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2971-66A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615009 | ||||||
| chr12:14615016
|
T | C | 1 | a0001c0002t0001g0213 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2971-73A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615016 | ||||||
| chr12:14615045
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2971-102G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615045 | ||||||
| chr12:14615442
|
C | T | 1 | a0006c0013t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2971-499G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615442 | ||||||
| chr12:14615632
|
G | GAT | 20 | a0001c0001t0001g0105a0001c0001t0001g0193a0001c0002t0001g0006others(17): Show | 21 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.2971-691_2971-690d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615632 | ||||||
| chr12:14615632
|
G | GATAT | 3 | a0001c0002t0001g0149a0001c0002t0001g0156a0001c0002t0004g0028 | 3 | HG02451.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2971-693_2971-690d others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615632 | ||||||
| chr12:14615648
|
T | TAA | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2971-707_2971-706d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615648 | ||||||
| chr12:14615660
|
A | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2971-717T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615660 | ||||||
| chr12:14615736
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0201 | 2 | NA18942.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2971-793A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615736 | ||||||
| chr12:14615785
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2971-842C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615785 | ||||||
| chr12:14615812
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2970+821C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615812 | ||||||
| chr12:14615836
|
C | A | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2970+797G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615836 | ||||||
| chr12:14615872
|
C | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2970+761G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14615872 | ||||||
| chr12:14616094
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2970+539G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616094 | ||||||
| chr12:14616280
|
G | A | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2970+353C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616280 | ||||||
| chr12:14616310
|
C | A | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2970+323G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616310 | ||||||
| chr12:14616509
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2970+124C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616509 | ||||||
| chr12:14616534
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2970+99C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616534 | ||||||
| chr12:14616587
|
C | A | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2970+46G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 25/26 | chr12 | 14616587 | ||||||
| chr12:14616770
|
A | G | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876-43T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14616770 | ||||||
| chr12:14616785
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0138 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2876-58G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14616785 | ||||||
| chr12:14616868
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2876-141G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14616868 | ||||||
| chr12:14616971
|
C | T | 9 | a0001c0001t0001g0105a0001c0002t0001g0148a0001c0002t0001g0149others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2876-244G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14616971 | ||||||
| chr12:14616973
|
G | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(201): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.2876-246C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14616973 | ||||||
| chr12:14617189
|
T | C | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876-462A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617189 | ||||||
| chr12:14617424
|
C | T | 4 | a0001c0002t0001g0129a0001c0003t0001g0177a0001c0003t0001g0183others(1): Show | 4 | HG01934.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2876-697G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617424 | ||||||
| chr12:14617483
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01993.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2876-756C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617483 | ||||||
| chr12:14617625
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2876-898G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617625 | ||||||
| chr12:14617795
|
C | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0176 | 3 | HG00733.hp1 HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2876-1068G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617795 | ||||||
| chr12:14617819
|
A | G | 4 | a0001c0002t0001g0129a0001c0003t0001g0177a0001c0003t0001g0183others(1): Show | 4 | HG01934.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2876-1092T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14617819 | ||||||
| chr12:14618033
|
G | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2875+1178C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618033 | ||||||
| chr12:14618172
|
T | C | 2 | a0001c0003t0001g0183a0001c0008t0001g0134 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2875+1039A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618172 | ||||||
| chr12:14618172
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2875+1039A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618172 | ||||||
| chr12:14618177
|
C | T | 8 | a0001c0003t0001g0183a0001c0005t0002g0131a0001c0005t0002g0132others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2875+1034G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618177 | ||||||
| chr12:14618278
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2875+933G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618278 | ||||||
| chr12:14618330
|
TAG | T | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2875+879_2875+880d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618330 | ||||||
| chr12:14618377
|
T | G | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2875+834A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618377 | ||||||
| chr12:14618491
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG01071.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2875+720G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618491 | ||||||
| chr12:14618505
|
C | T | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2875+706G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618505 | ||||||
| chr12:14618687
|
G | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0057others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2875+524C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618687 | ||||||
| chr12:14618688
|
G | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2875+523C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618688 | ||||||
| chr12:14618755
|
C | T | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2875+456G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618755 | ||||||
| chr12:14618792
|
G | A | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2875+419C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618792 | ||||||
| chr12:14618840
|
A | G | 1 | a0001c0002t0001g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2875+371T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618840 | ||||||
| chr12:14618904
|
T | G | 5 | a0001c0001t0001g0105a0001c0003t0001g0215a0001c0003t0001g0216others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2875+307A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618904 | ||||||
| chr12:14618957
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2875+254A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 24/26 | chr12 | 14618957 | ||||||
| chr12:14619906
|
T | C | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2777-597A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14619906 | ||||||
| chr12:14620244
|
C | G | 1 | a0001c0001t0001g0144 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2776+798G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620244 | ||||||
| chr12:14620347
|
T | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2776+695A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620347 | ||||||
| chr12:14620366
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2776+676G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620366 | ||||||
| chr12:14620487
|
A | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2776+555T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620487 | ||||||
| chr12:14620660
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2776+382G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620660 | ||||||
| chr12:14620663
|
A | T | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2776+379T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620663 | ||||||
| chr12:14620771
|
A | G | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2776+271T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620771 | ||||||
| chr12:14620859
|
GTT | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2776+181_2776+182d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620859 | ||||||
| chr12:14620917
|
A | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2776+125T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620917 | ||||||
| chr12:14620999
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2776+43T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14620999 | ||||||
| chr12:14621287
|
TCACATGT others(4): Show |
T | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2602-82_2602-72del others(11): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621287 | ||||||
| chr12:14621315
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2602-99C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621315 | ||||||
| chr12:14621315
|
G | T | 3 | a0001c0002t0001g0129a0001c0003t0001g0177a0001c0005t0002g0179 | 3 | HG01891.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2602-99C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621315 | ||||||
| chr12:14621464
|
T | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2602-248A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621464 | ||||||
| chr12:14621865
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 2 | HG00738.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2601+140G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621865 | ||||||
| chr12:14621913
|
G | A | 1 | a0001c0005t0002g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2601+92C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621913 | ||||||
| chr12:14621915
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2601+90A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621915 | ||||||
| chr12:14622280
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(70): Show | 80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2409-83A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622280 | ||||||
| chr12:14622326
|
G | A | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2409-129C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622326 | ||||||
| chr12:14622400
|
A | G | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2409-203T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622400 | ||||||
| chr12:14622581
|
G | C | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2409-384C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622581 | ||||||
| chr12:14622596
|
T | C | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2409-399A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622596 | ||||||
| chr12:14622791
|
A | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(163): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2409-594T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622791 | ||||||
| chr12:14622795
|
A | C | 5 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01258.hp2 HG01433.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-598T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622795 | ||||||
| chr12:14622888
|
AT | A | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2409-692delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622888 | ||||||
| chr12:14622957
|
G | C | 26 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(23): Show | 30 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2409-760C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14622957 | ||||||
| chr12:14623071
|
G | A | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2409-874C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623071 | ||||||
| chr12:14623076
|
T | C | 1 | a0007c0014t0001g0047 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2409-879A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623076 | ||||||
| chr12:14623155
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0192 | 2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2409-958G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623155 | ||||||
| chr12:14623233
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2409-1036A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623233 | ||||||
| chr12:14623377
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2409-1180A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623377 | ||||||
| chr12:14623398
|
T | C | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2409-1201A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623398 | ||||||
| chr12:14623433
|
C | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-1236G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623433 | ||||||
| chr12:14623463
|
T | G | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2409-1266A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623463 | ||||||
| chr12:14623627
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2409-1430C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623627 | ||||||
| chr12:14623707
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2409-1510C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623707 | ||||||
| chr12:14623831
|
C | T | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-1634G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623831 | ||||||
| chr12:14623858
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2409-1661C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623858 | ||||||
| chr12:14624074
|
T | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0057others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2408+1683A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624074 | ||||||
| chr12:14624183
|
G | A | 3 | a0001c0002t0001g0056a0001c0003t0001g0015a0001c0003t0001g0017 | 3 | HG02965.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2408+1574C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624183 | ||||||
| chr12:14624206
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(1): Show | 5 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2408+1551G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624206 | ||||||
| chr12:14624365
|
C | A | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2408+1392G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624365 | ||||||
| chr12:14624429
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2408+1328C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624429 | ||||||
| chr12:14624452
|
A | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+1305T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624452 | ||||||
| chr12:14624526
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2408+1231A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624526 | ||||||
| chr12:14624653
|
G | A | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(14): Show | 19 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2408+1104C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624653 | ||||||
| chr12:14624666
|
A | G | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2408+1091T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624666 | ||||||
| chr12:14624704
|
G | GT | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2408+1052dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624704 | ||||||
| chr12:14624876
|
A | G | 6 | a0001c0002t0001g0056a0001c0003t0001g0003a0001c0003t0001g0015others(3): Show | 8 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2408+881T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14624876 | ||||||
| chr12:14625105
|
T | C | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2408+652A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625105 | ||||||
| chr12:14625283
|
C | T | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2408+474G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625283 | ||||||
| chr12:14625327
|
AT | A | 36 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0059others(33): Show | 38 | HG00621.hp2 HG00642.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2408+429delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625327 | ||||||
| chr12:14625327
|
ATT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2408+428_2408+429d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625327 | ||||||
| chr12:14625367
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2408+390T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625367 | ||||||
| chr12:14625389
|
G | T | 6 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(3): Show | 7 | HG00733.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2408+368C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625389 | ||||||
| chr12:14625413
|
C | T | 2 | a0001c0003t0001g0183a0001c0008t0001g0134 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2408+344G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625413 | ||||||
| chr12:14625475
|
G | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2408+282C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625475 | ||||||
| chr12:14625477
|
G | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2408+280C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625477 | ||||||
| chr12:14625554
|
T | C | 1 | a0001c0001t0001g0001 | 3 | NA18977.hp1 NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2408+203A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625554 | ||||||
| chr12:14625637
|
G | A | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2408+120C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14625637 | ||||||
| chr12:14626105
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2250-190G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626105 | ||||||
| chr12:14626110
|
C | T | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2250-195G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626110 | ||||||
| chr12:14626111
|
G | A | 1 | a0001c0004t0001g0016 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2250-196C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626111 | ||||||
| chr12:14626112
|
G | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0087a0001c0001t0001g0174others(9): Show | 12 | HG00140.hp2 HG00673.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2250-197C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626112 | ||||||
| chr12:14626200
|
C | T | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(14): Show | 19 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2250-285G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626200 | ||||||
| chr12:14626208
|
C | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2250-293G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626208 | ||||||
| chr12:14626233
|
G | C | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250-318C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626233 | ||||||
| chr12:14626243
|
A | AAG | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250-329_2250-328i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626243 | ||||||
| chr12:14626271
|
A | G | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2250-356T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626271 | ||||||
| chr12:14626320
|
TAAAC | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0210others(1): Show | 5 | HG02630.hp1 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2250-409_2250-406d others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626320 | ||||||
| chr12:14626358
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2250-443C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626358 | ||||||
| chr12:14626374
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2250-459T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626374 | ||||||
| chr12:14626412
|
C | T | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2250-497G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626412 | ||||||
| chr12:14626777
|
A | T | 1 | a0001c0004t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2250-862T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14626777 | ||||||
| chr12:14627113
|
C | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250-1198G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627113 | ||||||
| chr12:14627173
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2250-1258A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627173 | ||||||
| chr12:14627277
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(72): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2250-1362C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627277 | ||||||
| chr12:14627368
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2249+1278A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627368 | ||||||
| chr12:14627551
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2249+1095T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627551 | ||||||
| chr12:14627587
|
A | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2249+1059T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627587 | ||||||
| chr12:14627775
|
A | C | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+871T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627775 | ||||||
| chr12:14627814
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0210others(1): Show | 5 | HG02630.hp1 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+832G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627814 | ||||||
| chr12:14627912
|
G | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+734C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627912 | ||||||
| chr12:14627941
|
T | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+705A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627941 | ||||||
| chr12:14628105
|
T | A | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2249+541A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628105 | ||||||
| chr12:14628150
|
C | CT | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+495dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628150 | ||||||
| chr12:14628170
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2249+476C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628170 | ||||||
| chr12:14628328
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2249+318G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628328 | ||||||
| chr12:14628357
|
A | G | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2249+289T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628357 | ||||||
| chr12:14628446
|
G | T | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+200C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628446 | ||||||
| chr12:14628448
|
A | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+198T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628448 | ||||||
| chr12:14628569
|
A | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2249+77T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628569 | ||||||
| chr12:14628744
|
G | GA | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(119): Show | 133 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
splice_region_variant&intron_variant | LOW | c.2158-8dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628744 | ||||||
| chr12:14628755
|
G | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0031 | 3 | HG01884.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2158-18C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628755 | ||||||
| chr12:14628885
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2158-148G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628885 | ||||||
| chr12:14628906
|
A | G | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2158-169T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628906 | ||||||
| chr12:14628934
|
C | T | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-197G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628934 | ||||||
| chr12:14628982
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2158-245C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14628982 | ||||||
| chr12:14629080
|
C | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-343G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629080 | ||||||
| chr12:14629139
|
G | A | 1 | a0002c0006t0001g0202 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2158-402C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629139 | ||||||
| chr12:14629254
|
C | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2158-517G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629254 | ||||||
| chr12:14629264
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2158-527C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629264 | ||||||
| chr12:14629433
|
C | T | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2158-696G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629433 | ||||||
| chr12:14629453
|
T | G | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2158-716A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629453 | ||||||
| chr12:14629717
|
G | A | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2158-980C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629717 | ||||||
| chr12:14629846
|
T | G | 1 | a0001c0001t0001g0068 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2158-1109A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629846 | ||||||
| chr12:14629932
|
C | T | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158-1195G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629932 | ||||||
| chr12:14630027
|
GGAGGTAT others(13): Show |
G | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-1310_2158-129 others(24): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630027 | ||||||
| chr12:14630092
|
T | C | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2158-1355A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630092 | ||||||
| chr12:14630097
|
C | CT | 12 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0002t0001g0006others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2158-1361dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630097 | ||||||
| chr12:14630097
|
CT | C | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158-1361delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630097 | ||||||
| chr12:14630109
|
T | A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-1372A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630109 | ||||||
| chr12:14630147
|
A | G | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2158-1410T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630147 | ||||||
| chr12:14630195
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2158-1458C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630195 | ||||||
| chr12:14630201
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2158-1464T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630201 | ||||||
| chr12:14630330
|
A | C | 3 | a0001c0002t0001g0030a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG02109.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2158-1593T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630330 | ||||||
| chr12:14630340
|
G | A | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158-1603C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630340 | ||||||
| chr12:14630463
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2158-1726C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630463 | ||||||
| chr12:14630477
|
T | G | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2158-1740A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630477 | ||||||
| chr12:14630689
|
G | C | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158-1952C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630689 | ||||||
| chr12:14630751
|
C | T | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2158-2014G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630751 | ||||||
| chr12:14630781
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158-2044C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630781 | ||||||
| chr12:14630848
|
A | C | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2158-2111T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630848 | ||||||
| chr12:14630864
|
A | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(35): Show | 42 | HG00438.hp1 HG00639.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.2158-2127T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630864 | ||||||
| chr12:14630890
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2158-2153T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630890 | ||||||
| chr12:14630958
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2158-2221G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630958 | ||||||
| chr12:14630967
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2158-2230C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14630967 | ||||||
| chr12:14631343
|
T | C | 2 | a0001c0003t0001g0183a0001c0008t0001g0134 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2158-2606A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631343 | ||||||
| chr12:14631395
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(178): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2158-2658A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631395 | ||||||
| chr12:14631465
|
A | G | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2158-2728T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631465 | ||||||
| chr12:14631672
|
A | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158-2935T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631672 | ||||||
| chr12:14631680
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2158-2943C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631680 | ||||||
| chr12:14631800
|
T | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2158-3063A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631800 | ||||||
| chr12:14631917
|
G | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158-3180C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14631917 | ||||||
| chr12:14632005
|
G | GT | 3 | a0001c0001t0001g0172a0001c0003t0001g0183a0001c0008t0001g0134 | 3 | HG00280.hp1 HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2158-3269dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632005 | ||||||
| chr12:14632135
|
T | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(2): Show | 6 | HG00733.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-3398A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632135 | ||||||
| chr12:14632483
|
G | T | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2158-3746C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632483 | ||||||
| chr12:14632563
|
C | A | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158-3826G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632563 | ||||||
| chr12:14632637
|
G | T | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2158-3900C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632637 | ||||||
| chr12:14632826
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2158-4089G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632826 | ||||||
| chr12:14632958
|
C | T | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2158-4221G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14632958 | ||||||
| chr12:14633140
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2158-4403C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633140 | ||||||
| chr12:14633143
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0130a0001c0001t0001g0163others(3): Show | 6 | HG01167.hp1 HG02622.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2158-4406C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633143 | ||||||
| chr12:14633241
|
C | T | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2158-4504G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633241 | ||||||
| chr12:14633249
|
C | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158-4512G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633249 | ||||||
| chr12:14633317
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(86): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2158-4580C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633317 | ||||||
| chr12:14633424
|
A | C | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(14): Show | 19 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2158-4687T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633424 | ||||||
| chr12:14633476
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(69): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2158-4739C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633476 | ||||||
| chr12:14633477
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2158-4740T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633477 | ||||||
| chr12:14633665
|
T | TA | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(178): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2158-4929dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633665 | ||||||
| chr12:14633774
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2158-5037A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633774 | ||||||
| chr12:14634026
|
T | C | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2158-5289A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14634026 | ||||||
| chr12:14634250
|
A | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158-5513T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14634250 | ||||||
| chr12:14634699
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2157+5163C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14634699 | ||||||
| chr12:14634711
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2157+5151G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14634711 | ||||||
| chr12:14635033
|
T | G | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2157+4829A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635033 | ||||||
| chr12:14635211
|
G | A | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2157+4651C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635211 | ||||||
| chr12:14635229
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2157+4633T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635229 | ||||||
| chr12:14635295
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2157+4567G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635295 | ||||||
| chr12:14635350
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2157+4512A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635350 | ||||||
| chr12:14635373
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2157+4489C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635373 | ||||||
| chr12:14635871
|
C | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2157+3991G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635871 | ||||||
| chr12:14636068
|
A | G | 2 | a0001c0003t0001g0183a0001c0008t0001g0134 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2157+3794T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636068 | ||||||
| chr12:14636187
|
A | T | 7 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(4): Show | 8 | HG00733.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2157+3675T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636187 | ||||||
| chr12:14636254
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2157+3608G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636254 | ||||||
| chr12:14636331
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2157+3531G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636331 | ||||||
| chr12:14636332
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2157+3530C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636332 | ||||||
| chr12:14636681
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2157+3181T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636681 | ||||||
| chr12:14636725
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2157+3137C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636725 | ||||||
| chr12:14636817
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2157+3045C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636817 | ||||||
| chr12:14636861
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0003g0158 | 2 | NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2157+3001C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636861 | ||||||
| chr12:14636887
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2157+2975C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14636887 | ||||||
| chr12:14637024
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2157+2838G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637024 | ||||||
| chr12:14637196
|
C | CA | 15 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0002t0001g0029others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2157+2665dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637196 | ||||||
| chr12:14637196
|
C | CAA | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2157+2664_2157+266 others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637196 | ||||||
| chr12:14637196
|
C | CAAA | 22 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(19): Show | 22 | HG00597.hp2 HG00673.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2157+2663_2157+266 others(7): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637196 | ||||||
| chr12:14637212
|
C | A | 9 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(6): Show | 11 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2157+2650G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637212 | ||||||
| chr12:14637234
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2157+2628T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637234 | ||||||
| chr12:14637412
|
T | C | 10 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(7): Show | 12 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2157+2450A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637412 | ||||||
| chr12:14637646
|
C | G | 18 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(15): Show | 20 | HG00733.hp2 HG01884.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.2157+2216G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637646 | ||||||
| chr12:14637748
|
C | T | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2157+2114G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637748 | ||||||
| chr12:14637800
|
T | C | 6 | a0001c0002t0001g0056a0001c0003t0001g0003a0001c0003t0001g0015others(3): Show | 8 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2157+2062A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637800 | ||||||
| chr12:14637887
|
A | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2157+1975T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637887 | ||||||
| chr12:14637933
|
A | G | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2157+1929T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637933 | ||||||
| chr12:14637992
|
C | T | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2157+1870G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637992 | ||||||
| chr12:14638028
|
A | T | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2157+1834T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638028 | ||||||
| chr12:14638345
|
AT | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(83): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.2157+1516delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638345 | ||||||
| chr12:14638655
|
G | T | 2 | a0001c0002t0001g0150a0001c0002t0001g0154 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2157+1207C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638655 | ||||||
| chr12:14638880
|
A | C | 1 | a0001c0016t0001g0079 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2157+982T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638880 | ||||||
| chr12:14638965
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2157+897A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638965 | ||||||
| chr12:14638991
|
A | G | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2157+871T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638991 | ||||||
| chr12:14639018
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2157+844C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639018 | ||||||
| chr12:14639078
|
G | A | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(13): Show | 18 | HG00733.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2157+784C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639078 | ||||||
| chr12:14639206
|
G | A | 19 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(16): Show | 21 | HG00621.hp2 HG00733.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2157+656C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639206 | ||||||
| chr12:14639292
|
T | G | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2157+570A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639292 | ||||||
| chr12:14639299
|
CA | C | 24 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0072others(21): Show | 24 | HG00609.hp2 HG00639.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2157+562delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639299 | ||||||
| chr12:14639299
|
CAA | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2157+561_2157+562d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639299 | ||||||
| chr12:14639299
|
CAAA | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0102a0001c0001t0001g0147others(8): Show | 11 | HG01070.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2157+560_2157+562d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639299 | ||||||
| chr12:14639436
|
A | G | 1 | a0005c0010t0001g0194 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2157+426T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639436 | ||||||
| chr12:14639717
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(103): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.2157+145C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639717 | ||||||
| chr12:14640180
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2069-230T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640180 | ||||||
| chr12:14640220
|
C | T | 41 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(38): Show | 45 | HG00621.hp2 HG00733.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.2069-270G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640220 | ||||||
| chr12:14640258
|
C | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-308G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640258 | ||||||
| chr12:14640286
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2069-336C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640286 | ||||||
| chr12:14640292
|
A | G | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2069-342T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640292 | ||||||
| chr12:14640300
|
T | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-350A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640300 | ||||||
| chr12:14640381
|
C | T | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2069-431G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640381 | ||||||
| chr12:14640462
|
C | CA | 9 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(6): Show | 10 | HG00733.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2069-513dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640462 | ||||||
| chr12:14640462
|
C | CAAA | 4 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0003t0001g0003others(1): Show | 6 | HG02280.hp1 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-515_2069-513d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640462 | ||||||
| chr12:14640462
|
CA | C | 17 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0110others(14): Show | 17 | HG00738.hp1 HG01109.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.2069-513delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640462 | ||||||
| chr12:14640462
|
CAA | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2069-514_2069-513d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640462 | ||||||
| chr12:14640476
|
A | AG | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2069-527_2069-526i others(3): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640476 | ||||||
| chr12:14640576
|
T | G | 1 | a0004c0009t0001g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2068+506A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640576 | ||||||
| chr12:14640638
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2068+444G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640638 | ||||||
| chr12:14640787
|
G | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2068+295C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640787 | ||||||
| chr12:14640836
|
C | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+246G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640836 | ||||||
| chr12:14640853
|
G | A | 23 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(20): Show | 25 | HG00621.hp2 HG00733.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2068+229C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640853 | ||||||
| chr12:14640944
|
G | A | 4 | a0001c0001t0001g0115a0001c0001t0001g0197a0001c0004t0001g0020others(1): Show | 4 | NA18983.hp1 NA18998.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+138C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640944 | ||||||
| chr12:14641432
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1931-213A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641432 | ||||||
| chr12:14641546
|
G | T | 2 | a0001c0004t0001g0119a0001c0004t0001g0120 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1931-327C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641546 | ||||||
| chr12:14641571
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(58): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1931-352A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641571 | ||||||
| chr12:14641809
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1931-590A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641809 | ||||||
| chr12:14641885
|
C | T | 15 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(12): Show | 17 | HG00733.hp2 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1931-666G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641885 | ||||||
| chr12:14641936
|
C | CA | 43 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(40): Show | 47 | HG00621.hp2 HG00733.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1931-718dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641936 | ||||||
| chr12:14641960
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1931-741C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641960 | ||||||
| chr12:14641962
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1931-743C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641962 | ||||||
| chr12:14641968
|
A | C | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1931-749T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641968 | ||||||
| chr12:14641982
|
A | T | 20 | a0001c0002t0001g0056a0001c0002t0001g0081a0001c0002t0001g0129others(17): Show | 22 | HG00621.hp2 HG02055.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1931-763T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641982 | ||||||
| chr12:14642211
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1931-992A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642211 | ||||||
| chr12:14642287
|
C | T | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1931-1068G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642287 | ||||||
| chr12:14642290
|
G | A | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1931-1071C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642290 | ||||||
| chr12:14642314
|
T | C | 1 | a0001c0003t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1931-1095A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642314 | ||||||
| chr12:14642328
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931-1109C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642328 | ||||||
| chr12:14642360
|
C | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1931-1141G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642360 | ||||||
| chr12:14642424
|
A | G | 20 | a0001c0002t0001g0056a0001c0002t0001g0081a0001c0002t0001g0129others(17): Show | 22 | HG00621.hp2 HG02055.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1930+1150T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642424 | ||||||
| chr12:14642439
|
T | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1930+1135A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642439 | ||||||
| chr12:14642501
|
T | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1930+1073A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642501 | ||||||
| chr12:14642559
|
T | A | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1930+1015A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642559 | ||||||
| chr12:14642682
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1930+892A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642682 | ||||||
| chr12:14642741
|
G | A | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1930+833C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642741 | ||||||
| chr12:14642850
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1930+724G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642850 | ||||||
| chr12:14642870
|
G | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1930+704C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642870 | ||||||
| chr12:14642922
|
A | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1930+652T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642922 | ||||||
| chr12:14643067
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 38 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1930+507G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14643067 | ||||||
| chr12:14643709
|
G | T | 13 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1798-3C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14643709 | ||||||
| chr12:14643779
|
G | C | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1798-73C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14643779 | ||||||
| chr12:14643821
|
A | G | 10 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(7): Show | 12 | HG02055.hp1 HG02280.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1798-115T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14643821 | ||||||
| chr12:14643886
|
CT | C | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1798-181delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14643886 | ||||||
| chr12:14643982
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | HG02083.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1798-276C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14643982 | ||||||
| chr12:14644034
|
G | T | 1 | a0002c0006t0001g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1798-328C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644034 | ||||||
| chr12:14644139
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1798-433A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644139 | ||||||
| chr12:14644154
|
C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1798-448G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644154 | ||||||
| chr12:14644202
|
TGGC | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1798-499_1798-497d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644202 | ||||||
| chr12:14644263
|
A | G | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1798-557T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644263 | ||||||
| chr12:14644321
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1798-615C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644321 | ||||||
| chr12:14644331
|
A | G | 1 | a0001c0003t0001g0019 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1798-625T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644331 | ||||||
| chr12:14644509
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1797+720A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644509 | ||||||
| chr12:14644659
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1797+570T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644659 | ||||||
| chr12:14644676
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1797+553A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644676 | ||||||
| chr12:14644680
|
T | C | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1797+549A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644680 | ||||||
| chr12:14644740
|
C | CT | 25 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0058others(22): Show | 27 | HG00597.hp2 HG00621.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1797+488dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644740 | ||||||
| chr12:14644740
|
C | CTT | 19 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0081others(16): Show | 20 | HG00621.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1797+487_1797+488d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644740 | ||||||
| chr12:14644740
|
CT | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1797+488delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644740 | ||||||
| chr12:14644740
|
CTTTTTTT | C | 10 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(7): Show | 12 | HG02055.hp1 HG02280.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1797+482_1797+488d others(9): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644740 | ||||||
| chr12:14644860
|
G | C | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1797+369C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644860 | ||||||
| chr12:14644935
|
T | A | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+294A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644935 | ||||||
| chr12:14645039
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00738.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1797+190A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14645039 | ||||||
| chr12:14645124
|
A | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(2): Show | 6 | HG00733.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+105T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14645124 | ||||||
| chr12:14645149
|
T | C | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1797+80A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14645149 | ||||||
| chr12:14645154
|
A | G | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1797+75T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14645154 | ||||||
| chr12:14645333
|
A | T | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1711-18T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645333 | ||||||
| chr12:14645466
|
G | T | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1711-151C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645466 | ||||||
| chr12:14645591
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1711-276G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645591 | ||||||
| chr12:14645592
|
G | A | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1711-277C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645592 | ||||||
| chr12:14645730
|
T | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1711-415A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645730 | ||||||
| chr12:14645792
|
A | AT | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1711-478dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645792 | ||||||
| chr12:14645828
|
G | GT | 8 | a0001c0001t0001g0139a0001c0001t0001g0189a0001c0001t0001g0193others(5): Show | 8 | HG00733.hp2 HG01934.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711-514dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645828 | ||||||
| chr12:14645838
|
G | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1711-523C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645838 | ||||||
| chr12:14646028
|
G | A | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711-713C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646028 | ||||||
| chr12:14646324
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1711-1009A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646324 | ||||||
| chr12:14646462
|
C | T | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1711-1147G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646462 | ||||||
| chr12:14646463
|
G | A | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1711-1148C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646463 | ||||||
| chr12:14646574
|
G | C | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711-1259C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646574 | ||||||
| chr12:14646911
|
T | C | 2 | a0002c0006t0001g0185a0002c0006t0001g0186 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1711-1596A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14646911 | ||||||
| chr12:14647028
|
A | C | 7 | a0001c0002t0001g0149a0001c0002t0001g0156a0001c0002t0004g0028others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1711-1713T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647028 | ||||||
| chr12:14647298
|
T | C | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1711-1983A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647298 | ||||||
| chr12:14647497
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1711-2182G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647497 | ||||||
| chr12:14647749
|
T | G | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1711-2434A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647749 | ||||||
| chr12:14647780
|
G | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1711-2465C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647780 | ||||||
| chr12:14647797
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1711-2482G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647797 | ||||||
| chr12:14647816
|
G | C | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1711-2501C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647816 | ||||||
| chr12:14647947
|
C | CTTAT | 5 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(2): Show | 6 | HG00733.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1711-2636_1711-263 others(8): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647947 | ||||||
| chr12:14647947
|
C | CTTATTTA others(5): Show |
1 | a0001c0012t0001g0074 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1711-2644_1711-263 others(16): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647947 | ||||||
| chr12:14647947
|
CTTAT | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1711-2636_1711-263 others(8): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647947 | ||||||
| chr12:14647951
|
T | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1711-2636A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14647951 | ||||||
| chr12:14648053
|
C | T | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1711-2738G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648053 | ||||||
| chr12:14648150
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1711-2835G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648150 | ||||||
| chr12:14648186
|
T | C | 3 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0003t0001g0019 | 3 | HG00621.hp2 HG04228.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1711-2871A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648186 | ||||||
| chr12:14648207
|
G | A | 9 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(6): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1711-2892C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648207 | ||||||
| chr12:14648250
|
G | A | 3 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0003t0001g0019 | 3 | HG00621.hp2 HG04228.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1711-2935C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648250 | ||||||
| chr12:14648272
|
TA | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1711-2958delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648272 | ||||||
| chr12:14648272
|
TAA | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0137a0001c0002t0001g0006others(1): Show | 5 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1711-2959_1711-295 others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648272 | ||||||
| chr12:14648273
|
A | T | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1711-2958T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648273 | ||||||
| chr12:14648344
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1711-3029T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648344 | ||||||
| chr12:14648354
|
A | G | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1711-3039T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648354 | ||||||
| chr12:14648527
|
C | A | 3 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0003t0001g0019 | 3 | HG00621.hp2 HG04228.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1710+2880G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648527 | ||||||
| chr12:14648540
|
T | C | 1 | a0001c0017t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1710+2867A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648540 | ||||||
| chr12:14648596
|
T | A | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+2811A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648596 | ||||||
| chr12:14648680
|
C | G | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1710+2727G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648680 | ||||||
| chr12:14648828
|
G | A | 3 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0003t0001g0019 | 3 | HG00621.hp2 HG04228.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1710+2579C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648828 | ||||||
| chr12:14648846
|
T | C | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1710+2561A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648846 | ||||||
| chr12:14648856
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1710+2551G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648856 | ||||||
| chr12:14649073
|
A | G | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1710+2334T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649073 | ||||||
| chr12:14649145
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1710+2262G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649145 | ||||||
| chr12:14649288
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1710+2119A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649288 | ||||||
| chr12:14649302
|
T | A | 1 | a0001c0005t0002g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1710+2105A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649302 | ||||||
| chr12:14649420
|
A | C | 1 | a0001c0005t0002g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1710+1987T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649420 | ||||||
| chr12:14649424
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1710+1983T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649424 | ||||||
| chr12:14649428
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1710+1979T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649428 | ||||||
| chr12:14649485
|
T | TA | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1710+1921dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649485 | ||||||
| chr12:14649640
|
T | C | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1710+1767A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649640 | ||||||
| chr12:14649686
|
A | G | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1710+1721T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649686 | ||||||
| chr12:14649833
|
G | C | 20 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0002t0001g0129others(17): Show | 20 | HG00621.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1710+1574C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649833 | ||||||
| chr12:14649926
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1710+1481T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14649926 | ||||||
| chr12:14650036
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1710+1371G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650036 | ||||||
| chr12:14650081
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(1): Show | 5 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1710+1326C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650081 | ||||||
| chr12:14650227
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1710+1180A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650227 | ||||||
| chr12:14650448
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1710+959C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650448 | ||||||
| chr12:14650471
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1710+936G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650471 | ||||||
| chr12:14650505
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1710+902A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650505 | ||||||
| chr12:14650535
|
C | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1710+872G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650535 | ||||||
| chr12:14650686
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1710+721T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650686 | ||||||
| chr12:14650877
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1710+530T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650877 | ||||||
| chr12:14650952
|
T | C | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1710+455A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14650952 | ||||||
| chr12:14651708
|
C | A | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1606-197G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651708 | ||||||
| chr12:14651790
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1605+169C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651790 | ||||||
| chr12:14651829
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1605+130T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651829 | ||||||
| chr12:14651873
|
C | T | 17 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0002t0001g0129others(14): Show | 17 | HG00621.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1605+86G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651873 | ||||||
| chr12:14651910
|
G | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1605+49C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651910 | ||||||
| chr12:14651920
|
G | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1605+39C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 14/26 | chr12 | 14651920 | ||||||
| chr12:14652043
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1534-13T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652043 | ||||||
| chr12:14652060
|
G | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1534-30C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652060 | ||||||
| chr12:14652163
|
A | ATATT | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534-137_1534-134d others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652163 | ||||||
| chr12:14652163
|
A | ATATTTAT others(1): Show |
156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1534-141_1534-134d others(10): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652163 | ||||||
| chr12:14652163
|
A | ATATTTAT others(5): Show |
1 | a0001c0004t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1534-145_1534-134d others(14): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652163 | ||||||
| chr12:14652163
|
A | ATATTTAT others(9): Show |
2 | a0001c0001t0001g0159a0001c0001t0003g0158 | 2 | NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1534-149_1534-134d others(18): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652163 | ||||||
| chr12:14652211
|
G | A | 8 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0123others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1534-181C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652211 | ||||||
| chr12:14652294
|
C | T | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1534-264G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652294 | ||||||
| chr12:14652335
|
C | T | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1534-305G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652335 | ||||||
| chr12:14652399
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1534-369A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652399 | ||||||
| chr12:14652410
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1534-380T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652410 | ||||||
| chr12:14652725
|
C | T | 1 | a0001c0007t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1533+227G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652725 | ||||||
| chr12:14652880
|
G | T | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1533+72C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 13/26 | chr12 | 14652880 | ||||||
| chr12:14653149
|
A | G | 17 | a0001c0001t0001g0191a0001c0002t0001g0081a0001c0002t0001g0129others(14): Show | 17 | HG00621.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1471-135T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653149 | ||||||
| chr12:14653199
|
C | T | 1 | a0001c0004t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1471-185G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653199 | ||||||
| chr12:14653206
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1471-192G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653206 | ||||||
| chr12:14653221
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1471-207C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653221 | ||||||
| chr12:14653342
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1471-328C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653342 | ||||||
| chr12:14653505
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1471-491C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653505 | ||||||
| chr12:14653536
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1471-522C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653536 | ||||||
| chr12:14653687
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1471-673T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653687 | ||||||
| chr12:14653937
|
G | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1471-923C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653937 | ||||||
| chr12:14653999
|
A | G | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1471-985T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14653999 | ||||||
| chr12:14654001
|
TTGGACCT others(6): Show |
T | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1471-1000_1471-988 others(16): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654001 | ||||||
| chr12:14654007
|
C | A | 1 | a0001c0007t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1471-993G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654007 | ||||||
| chr12:14654168
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1471-1154C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654168 | ||||||
| chr12:14654338
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0072others(1): Show | 4 | NA18983.hp2 NA18993.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1471-1324G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654338 | ||||||
| chr12:14654381
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0116 | 2 | NA18943.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1471-1367G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654381 | ||||||
| chr12:14654618
|
T | C | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1471-1604A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654618 | ||||||
| chr12:14654634
|
T | C | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1471-1620A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654634 | ||||||
| chr12:14654927
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1470+1585C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14654927 | ||||||
| chr12:14655002
|
A | G | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1470+1510T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655002 | ||||||
| chr12:14655037
|
T | G | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1470+1475A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655037 | ||||||
| chr12:14655277
|
G | C | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1470+1235C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655277 | ||||||
| chr12:14655690
|
C | T | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1470+822G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655690 | ||||||
| chr12:14655753
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1470+759T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655753 | ||||||
| chr12:14655896
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0031 | 3 | HG01884.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1470+616A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655896 | ||||||
| chr12:14655961
|
C | T | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1470+551G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14655961 | ||||||
| chr12:14656344
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1470+168C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 12/26 | chr12 | 14656344 | ||||||
| chr12:14656720
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1365-103A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14656720 | ||||||
| chr12:14656905
|
G | C | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1365-288C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14656905 | ||||||
| chr12:14657032
|
G | A | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 10 | HG02055.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365-415C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657032 | ||||||
| chr12:14657183
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1365-566G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657183 | ||||||
| chr12:14657436
|
T | TAAAAATG others(324): Show |
1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1365-820_1365-819i others(333): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657436 | ||||||
| chr12:14657632
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1365-1015T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657632 | ||||||
| chr12:14657725
|
C | A | 5 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG02723.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365-1108G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657725 | ||||||
| chr12:14657752
|
C | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG00609.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1365-1135G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657752 | ||||||
| chr12:14657755
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1365-1138A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657755 | ||||||
| chr12:14657759
|
C | A | 2 | a0001c0002t0001g0129a0001c0003t0001g0177 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1365-1142G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657759 | ||||||
| chr12:14657949
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1365-1332A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14657949 | ||||||
| chr12:14658003
|
A | C | 1 | a0001c0003t0001g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1365-1386T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658003 | ||||||
| chr12:14658047
|
A | G | 1 | a0006c0013t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1365-1430T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658047 | ||||||
| chr12:14658412
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1365-1795G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658412 | ||||||
| chr12:14658566
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1365-1949G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658566 | ||||||
| chr12:14658580
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1365-1963C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658580 | ||||||
| chr12:14658588
|
A | C | 5 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG02723.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365-1971T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658588 | ||||||
| chr12:14658608
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(98): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1365-1991C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658608 | ||||||
| chr12:14658864
|
A | G | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1364+2117T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14658864 | ||||||
| chr12:14659050
|
CT | C | 8 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(5): Show | 8 | HG01934.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1364+1930delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659050 | ||||||
| chr12:14659233
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1364+1748A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659233 | ||||||
| chr12:14659295
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1364+1686C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659295 | ||||||
| chr12:14659332
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1364+1649A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659332 | ||||||
| chr12:14659338
|
C | T | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1364+1643G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659338 | ||||||
| chr12:14659448
|
G | T | 8 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0156others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1364+1533C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659448 | ||||||
| chr12:14659593
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1364+1388T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659593 | ||||||
| chr12:14659728
|
C | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1364+1253G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659728 | ||||||
| chr12:14659784
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1364+1197A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14659784 | ||||||
| chr12:14660591
|
A | G | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1364+390T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14660591 | ||||||
| chr12:14660725
|
G | A | 1 | a0001c0005t0002g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1364+256C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14660725 | ||||||
| chr12:14660752
|
A | G | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1364+229T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14660752 | ||||||
| chr12:14660814
|
T | C | 1 | a0001c0003t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1364+167A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14660814 | ||||||
| chr12:14660904
|
A | G | 3 | a0001c0003t0001g0183a0001c0008t0001g0134a0001c0011t0001g0014 | 3 | HG01934.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1364+77T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 11/26 | chr12 | 14660904 | ||||||
| chr12:14661069
|
C | T | 7 | a0001c0002t0001g0149a0001c0002t0001g0156a0001c0002t0004g0028others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1283-7G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661069 | ||||||
| chr12:14661110
|
G | A | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1283-48C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661110 | ||||||
| chr12:14661281
|
C | T | 1 | a0001c0003t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1283-219G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661281 | ||||||
| chr12:14661658
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1283-596G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661658 | ||||||
| chr12:14661679
|
A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1283-617T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661679 | ||||||
| chr12:14661679
|
A | T | 6 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02723.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1283-617T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661679 | ||||||
| chr12:14661680
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1283-618T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661680 | ||||||
| chr12:14661762
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1283-700T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661762 | ||||||
| chr12:14661780
|
G | A | 1 | a0001c0016t0001g0079 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1283-718C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661780 | ||||||
| chr12:14661890
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1283-828C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14661890 | ||||||
| chr12:14662403
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1283-1341G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662403 | ||||||
| chr12:14662435
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1283-1373C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662435 | ||||||
| chr12:14662598
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1283-1536G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662598 | ||||||
| chr12:14662635
|
C | G | 1 | a0001c0002t0001g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1283-1573G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662635 | ||||||
| chr12:14662675
|
C | CA | 12 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0071others(9): Show | 12 | HG00621.hp2 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1283-1614dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662675 | ||||||
| chr12:14662675
|
C | CAA | 8 | a0001c0002t0001g0005a0001c0002t0001g0026a0001c0002t0001g0029others(5): Show | 9 | HG00733.hp2 HG01934.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1283-1615_1283-161 others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662675 | ||||||
| chr12:14662675
|
CA | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 49 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1283-1614delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662675 | ||||||
| chr12:14662694
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1283-1632T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662694 | ||||||
| chr12:14662709
|
C | T | 21 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0081others(18): Show | 24 | HG00621.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1283-1647G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662709 | ||||||
| chr12:14662915
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1283-1853G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662915 | ||||||
| chr12:14662946
|
T | C | 1 | a0001c0004t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1283-1884A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662946 | ||||||
| chr12:14662978
|
T | C | 1 | a0001c0002t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1283-1916A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14662978 | ||||||
| chr12:14663143
|
G | T | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1283-2081C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663143 | ||||||
| chr12:14663147
|
C | T | 15 | a0001c0002t0001g0081a0001c0002t0001g0129a0001c0002t0001g0149others(12): Show | 15 | HG00621.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1283-2085G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663147 | ||||||
| chr12:14663162
|
T | C | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1283-2100A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663162 | ||||||
| chr12:14663294
|
T | C | 6 | a0001c0002t0001g0056a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02723.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1283-2232A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663294 | ||||||
| chr12:14663332
|
G | T | 2 | a0001c0002t0001g0149a0001c0002t0001g0156 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1283-2270C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663332 | ||||||
| chr12:14663377
|
G | T | 4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1283-2315C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663377 | ||||||
| chr12:14663387
|
T | A | 1 | a0001c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1283-2325A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663387 | ||||||
| chr12:14663423
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1283-2361T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663423 | ||||||
| chr12:14663438
|
T | C | 2 | a0001c0002t0001g0081a0001c0003t0001g0019 | 2 | HG00621.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1283-2376A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663438 | ||||||
| chr12:14663470
|
G | T | 15 | a0001c0002t0001g0081a0001c0002t0001g0129a0001c0002t0001g0149others(12): Show | 15 | HG00621.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1283-2408C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663470 | ||||||
| chr12:14663519
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1283-2457C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663519 | ||||||
| chr12:14663629
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1283-2567C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663629 | ||||||
| chr12:14663846
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(54): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1283-2784C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663846 | ||||||
| chr12:14664093
|
A | G | 2 | a0001c0007t0001g0214a0001c0007t0001g0219 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1283-3031T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664093 | ||||||
| chr12:14664275
|
C | T | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0150others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1283-3213G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664275 | ||||||
| chr12:14664747
|
G | T | 1 | a0001c0002t0001g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1283-3685C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664747 | ||||||
| chr12:14664821
|
A | G | 1 | a0001c0003t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1283-3759T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664821 | ||||||
| chr12:14664847
|
GTCAT | G | 23 | a0001c0001t0001g0161a0001c0001t0001g0182a0001c0001t0001g0192others(20): Show | 26 | HG00597.hp2 HG01517.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1283-3789_1283-378 others(8): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664847 | ||||||
| chr12:14664895
|
G | T | 33 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0026others(30): Show | 37 | HG00621.hp2 HG01109.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1283-3833C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664895 | ||||||
| chr12:14664946
|
T | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1283-3884A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664946 | ||||||
| chr12:14664984
|
C | T | 1 | a0001c0005t0002g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1283-3922G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14664984 | ||||||
| chr12:14665161
|
A | T | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1283-4099T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665161 | ||||||
| chr12:14665218
|
G | GA | 30 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0059others(27): Show | 33 | HG01192.hp2 HG01243.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.1283-4157dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665218 | ||||||
| chr12:14665218
|
GA | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0145a0001c0002t0001g0094others(7): Show | 10 | HG00733.hp2 HG01891.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1283-4157delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665218 | ||||||
| chr12:14665321
|
C | A | 1 | a0001c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1283-4259G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665321 | ||||||
| chr12:14665481
|
T | C | 4 | a0001c0002t0001g0056a0001c0005t0002g0131a0001c0005t0002g0132others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+4241A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665481 | ||||||
| chr12:14665558
|
TAGC | T | 7 | a0001c0002t0001g0149a0001c0002t0001g0156a0001c0002t0004g0028others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282+4161_1282+416 others(7): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665558 | ||||||
| chr12:14665612
|
C | T | 6 | a0001c0002t0001g0149a0001c0002t0001g0156a0001c0003t0001g0215others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282+4110G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665612 | ||||||
| chr12:14665805
|
A | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+3917T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665805 | ||||||
| chr12:14665837
|
G | T | 11 | a0001c0003t0001g0003a0001c0003t0001g0019a0001c0003t0001g0121others(8): Show | 13 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282+3885C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665837 | ||||||
| chr12:14665859
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0177 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1282+3863C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665859 | ||||||
| chr12:14665884
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1282+3838C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665884 | ||||||
| chr12:14665953
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282+3769G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665953 | ||||||
| chr12:14665957
|
T | A | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1282+3765A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14665957 | ||||||
| chr12:14666135
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1282+3587G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666135 | ||||||
| chr12:14666242
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1282+3480G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666242 | ||||||
| chr12:14666427
|
C | CT | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+3294dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666427 | ||||||
| chr12:14666628
|
G | A | 15 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282+3094C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666628 | ||||||
| chr12:14666713
|
TGATACAG others(6): Show |
T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2996_1282+300 others(17): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666713 | ||||||
| chr12:14666728
|
A | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2994T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666728 | ||||||
| chr12:14666730
|
G | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2992C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666730 | ||||||
| chr12:14666732
|
C | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2990G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666732 | ||||||
| chr12:14666734
|
C | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2988G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666734 | ||||||
| chr12:14666735
|
CA | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1282+2986delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666735 | ||||||
| chr12:14666738
|
A | G | 6 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00673.hp2 HG02040.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282+2984T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666738 | ||||||
| chr12:14666745
|
A | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2977T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666745 | ||||||
| chr12:14666746
|
A | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2976T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666746 | ||||||
| chr12:14666748
|
A | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1282+2974T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666748 | ||||||
| chr12:14666758
|
A | G | 2 | a0001c0002t0001g0149a0001c0002t0001g0156 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1282+2964T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666758 | ||||||
| chr12:14666779
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1282+2943G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666779 | ||||||
| chr12:14666911
|
G | A | 11 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1282+2811C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666911 | ||||||
| chr12:14666943
|
G | A | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+2779C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666943 | ||||||
| chr12:14667277
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(118): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1282+2445G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667277 | ||||||
| chr12:14667309
|
T | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 58 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1282+2413A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667309 | ||||||
| chr12:14667472
|
G | A | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+2250C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667472 | ||||||
| chr12:14667541
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282+2181C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667541 | ||||||
| chr12:14667658
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(118): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1282+2064A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667658 | ||||||
| chr12:14667690
|
A | G | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282+2032T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667690 | ||||||
| chr12:14667694
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282+2028A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667694 | ||||||
| chr12:14667834
|
C | G | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+1888G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667834 | ||||||
| chr12:14667999
|
CT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(142): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1282+1722delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667999 | ||||||
| chr12:14667999
|
CTT | C | 50 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 56 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1282+1721_1282+172 others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14667999 | ||||||
| chr12:14668004
|
T | C | 4 | a0001c0001t0001g0093a0001c0005t0002g0131a0001c0005t0002g0132others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+1718A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668004 | ||||||
| chr12:14668005
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1282+1717A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668005 | ||||||
| chr12:14668241
|
G | A | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+1481C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668241 | ||||||
| chr12:14668283
|
G | A | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282+1439C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668283 | ||||||
| chr12:14668391
|
G | A | 1 | a0001c0004t0001g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282+1331C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668391 | ||||||
| chr12:14668396
|
G | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1282+1326C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668396 | ||||||
| chr12:14668632
|
CT | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1282+1089delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668632 | ||||||
| chr12:14668826
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+896C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668826 | ||||||
| chr12:14668856
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+866C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668856 | ||||||
| chr12:14668886
|
G | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0130a0001c0001t0001g0174others(22): Show | 25 | HG00140.hp2 HG00673.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1282+836C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668886 | ||||||
| chr12:14669195
|
CT | C | 11 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(8): Show | 13 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282+526delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669195 | ||||||
| chr12:14669210
|
C | CT | 70 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1282+511dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669210 | ||||||
| chr12:14669345
|
C | T | 1 | a0002c0006t0001g0202 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1282+377G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669345 | ||||||
| chr12:14669442
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+280A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669442 | ||||||
| chr12:14669461
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1282+261G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669461 | ||||||
| chr12:14669921
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1171-88C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14669921 | ||||||
| chr12:14669931
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-98G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14669931 | ||||||
| chr12:14670341
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1171-508A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670341 | ||||||
| chr12:14670355
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1171-522G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670355 | ||||||
| chr12:14670532
|
G | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1171-699C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670532 | ||||||
| chr12:14670718
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1171-885G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670718 | ||||||
| chr12:14670817
|
T | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1171-984A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670817 | ||||||
| chr12:14670842
|
A | T | 3 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0004t0001g0016 | 3 | HG02965.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1171-1009T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14670842 | ||||||
| chr12:14671044
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1171-1211C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671044 | ||||||
| chr12:14671052
|
A | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0016t0001g0079 | 3 | HG02293.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1171-1219T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671052 | ||||||
| chr12:14671070
|
T | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1237A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671070 | ||||||
| chr12:14671081
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1171-1248C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671081 | ||||||
| chr12:14671337
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1171-1504G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671337 | ||||||
| chr12:14671339
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1171-1506G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671339 | ||||||
| chr12:14671380
|
C | T | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+1493G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671380 | ||||||
| chr12:14671434
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1170+1439A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671434 | ||||||
| chr12:14671628
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1170+1245T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671628 | ||||||
| chr12:14671668
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1170+1205C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671668 | ||||||
| chr12:14671826
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1170+1047C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671826 | ||||||
| chr12:14671855
|
G | A | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1170+1018C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671855 | ||||||
| chr12:14671904
|
A | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+969T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671904 | ||||||
| chr12:14671912
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(107): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1170+961G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14671912 | ||||||
| chr12:14672016
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1170+857G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672016 | ||||||
| chr12:14672069
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0045others(1): Show | 4 | HG00733.hp1 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+804G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672069 | ||||||
| chr12:14672082
|
G | GA | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1170+790dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672082 | ||||||
| chr12:14672082
|
G | GAA | 17 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0136others(14): Show | 18 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1170+789_1170+790d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672082 | ||||||
| chr12:14672193
|
C | T | 10 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(7): Show | 12 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1170+680G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672193 | ||||||
| chr12:14672199
|
T | C | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1170+674A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672199 | ||||||
| chr12:14672277
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0107a0001c0003t0001g0018others(2): Show | 5 | HG02965.hp1 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+596C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672277 | ||||||
| chr12:14672404
|
G | A | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+469C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672404 | ||||||
| chr12:14672533
|
G | T | 6 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00673.hp2 HG02040.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+340C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672533 | ||||||
| chr12:14672858
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1170+15T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 9/26 | chr12 | 14672858 | ||||||
| chr12:14673022
|
C | T | 15 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1085-64G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673022 | ||||||
| chr12:14673031
|
G | C | 2 | a0001c0002t0001g0149a0001c0002t0001g0156 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1085-73C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673031 | ||||||
| chr12:14673037
|
A | G | 15 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1085-79T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673037 | ||||||
| chr12:14673079
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1085-121A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673079 | ||||||
| chr12:14673253
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1085-295G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673253 | ||||||
| chr12:14673270
|
T | A | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-312A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673270 | ||||||
| chr12:14673295
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1085-337A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673295 | ||||||
| chr12:14673353
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0033 | 3 | HG00621.hp1 NA18968.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1085-395A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673353 | ||||||
| chr12:14673609
|
C | T | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1085-651G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673609 | ||||||
| chr12:14673703
|
TAAATGTT others(5): Show |
T | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1085-757_1085-746d others(14): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673703 | ||||||
| chr12:14673866
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1084+759C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673866 | ||||||
| chr12:14673897
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1084+728G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673897 | ||||||
| chr12:14674055
|
A | C | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+570T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674055 | ||||||
| chr12:14674113
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1084+512G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674113 | ||||||
| chr12:14674120
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1084+505A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674120 | ||||||
| chr12:14674206
|
T | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(3): Show | 6 | HG02630.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+419A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674206 | ||||||
| chr12:14674301
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1084+324C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674301 | ||||||
| chr12:14674485
|
AATG | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1084+137_1084+139d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674485 | ||||||
| chr12:14674529
|
AATC | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(132): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1084+93_1084+95del others(3): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674529 | ||||||
| chr12:14674906
|
T | G | 11 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.949-146A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14674906 | ||||||
| chr12:14674984
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0201 | 2 | NA18942.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.949-224G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14674984 | ||||||
| chr12:14675021
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 58 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.949-261G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675021 | ||||||
| chr12:14675118
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.949-358C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675118 | ||||||
| chr12:14675207
|
C | CA | 33 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0051others(30): Show | 38 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.949-448dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675207 | ||||||
| chr12:14675207
|
C | CAA | 29 | a0001c0001t0001g0011a0001c0001t0001g0136a0001c0001t0001g0137others(26): Show | 30 | HG00609.hp1 HG01934.hp2 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.949-449_949-448dup others(2): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675207 | ||||||
| chr12:14675207
|
CA | C | 15 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.949-448delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675207 | ||||||
| chr12:14675222
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.949-462T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675222 | ||||||
| chr12:14675224
|
A | AG | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.949-465_949-464ins others(1): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675224 | ||||||
| chr12:14675225
|
A | G | 2 | a0001c0002t0001g0056a0001c0002t0001g0148 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.949-465T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675225 | ||||||
| chr12:14675249
|
AG | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 50 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.949-490delC | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675249 | ||||||
| chr12:14675250
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(153): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.949-490C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675250 | ||||||
| chr12:14675250
|
GA | G | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.949-491delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675250 | ||||||
| chr12:14675283
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 58 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.949-523T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675283 | ||||||
| chr12:14675458
|
GT | G | 3 | a0001c0004t0001g0118a0001c0004t0001g0119a0001c0004t0001g0120 | 3 | HG02145.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.949-699delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675458 | ||||||
| chr12:14675461
|
G | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.949-701C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675461 | ||||||
| chr12:14675523
|
G | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.949-763C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675523 | ||||||
| chr12:14675614
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.949-854A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675614 | ||||||
| chr12:14675759
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.949-999C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675759 | ||||||
| chr12:14676042
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.948+812G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676042 | ||||||
| chr12:14676101
|
A | G | 16 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0136others(13): Show | 17 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.948+753T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676101 | ||||||
| chr12:14676109
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.948+745G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676109 | ||||||
| chr12:14676150
|
G | T | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.948+704C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676150 | ||||||
| chr12:14676315
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.948+539C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676315 | ||||||
| chr12:14676316
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.948+538G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676316 | ||||||
| chr12:14676470
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.948+384T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676470 | ||||||
| chr12:14676524
|
A | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.948+330T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676524 | ||||||
| chr12:14676547
|
C | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.948+307G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676547 | ||||||
| chr12:14676601
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.948+253A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676601 | ||||||
| chr12:14676678
|
G | A | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.948+176C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676678 | ||||||
| chr12:14676768
|
G | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0102others(1): Show | 5 | HG01070.hp2 HG01978.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+86C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676768 | ||||||
| chr12:14676986
|
A | G | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-15T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14676986 | ||||||
| chr12:14677073
|
A | T | 3 | a0001c0003t0001g0018a0001c0003t0001g0109a0001c0003t0001g0177 | 3 | HG02965.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.831-102T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677073 | ||||||
| chr12:14677131
|
T | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.831-160A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677131 | ||||||
| chr12:14677173
|
G | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.831-202C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677173 | ||||||
| chr12:14677242
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.831-271C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677242 | ||||||
| chr12:14677608
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.831-637A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677608 | ||||||
| chr12:14677734
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.831-763G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677734 | ||||||
| chr12:14677736
|
A | ATT | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.831-767_831-766dup others(2): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677736 | ||||||
| chr12:14677736
|
A | ATTT | 28 | a0001c0001t0001g0059a0001c0001t0001g0160a0001c0001t0001g0174others(25): Show | 28 | HG00140.hp2 HG00673.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.831-768_831-766dup others(3): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677736 | ||||||
| chr12:14677855
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(100): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.831-884G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14677855 | ||||||
| chr12:14678076
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.831-1105T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678076 | ||||||
| chr12:14678211
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.831-1240C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678211 | ||||||
| chr12:14678239
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.831-1268C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678239 | ||||||
| chr12:14678331
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01993.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.830+1326C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678331 | ||||||
| chr12:14678486
|
A | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.830+1171T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678486 | ||||||
| chr12:14678557
|
A | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.830+1100T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678557 | ||||||
| chr12:14678586
|
G | A | 1 | a0001c0012t0001g0074 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.830+1071C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678586 | ||||||
| chr12:14678591
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.830+1066C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678591 | ||||||
| chr12:14678667
|
G | A | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.830+990C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678667 | ||||||
| chr12:14678670
|
C | G | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.830+987G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678670 | ||||||
| chr12:14678695
|
C | T | 1 | a0001c0002t0004g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.830+962G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678695 | ||||||
| chr12:14678698
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.830+959C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14678698 | ||||||
| chr12:14679247
|
A | G | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.830+410T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14679247 | ||||||
| chr12:14679329
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.830+328C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14679329 | ||||||
| chr12:14679360
|
C | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.830+297G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14679360 | ||||||
| chr12:14679473
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.830+184C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14679473 | ||||||
| chr12:14679896
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.734-144delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14679896 | ||||||
| chr12:14679953
|
T | A | 14 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(11): Show | 16 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.734-200A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14679953 | ||||||
| chr12:14679972
|
A | G | 4 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0003t0001g0183others(1): Show | 4 | HG01934.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-219T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14679972 | ||||||
| chr12:14680118
|
TC | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(107): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.734-366delG | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680118 | ||||||
| chr12:14680124
|
A | G | 14 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-371T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680124 | ||||||
| chr12:14680425
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(118): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.734-672T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680425 | ||||||
| chr12:14680434
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.734-681T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680434 | ||||||
| chr12:14680606
|
C | A | 2 | a0001c0002t0001g0125a0001c0002t0001g0129 | 2 | HG00733.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733+750G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680606 | ||||||
| chr12:14680995
|
T | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.733+361A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14680995 | ||||||
| chr12:14681140
|
A | G | 14 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(11): Show | 16 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.733+216T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14681140 | ||||||
| chr12:14681193
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.733+163T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14681193 | ||||||
| chr12:14681224
|
C | T | 2 | a0001c0004t0001g0020a0001c0004t0001g0021 | 2 | NA18983.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.733+132G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14681224 | ||||||
| chr12:14681274
|
G | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+82C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14681274 | ||||||
| chr12:14681484
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | splice_region_variant&intron_variant | LOW | c.612-7A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681484 | ||||||
| chr12:14681487
|
GA | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.612-11delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681487 | ||||||
| chr12:14681493
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.612-16C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681493 | ||||||
| chr12:14681764
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.612-287C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681764 | ||||||
| chr12:14681925
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.612-448C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681925 | ||||||
| chr12:14681930
|
G | A | 1 | a0001c0004t0001g0120 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612-453C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681930 | ||||||
| chr12:14681951
|
C | T | 11 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.612-474G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681951 | ||||||
| chr12:14682102
|
C | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0136others(13): Show | 17 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.612-625G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682102 | ||||||
| chr12:14682114
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.612-637A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682114 | ||||||
| chr12:14682270
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.611+772C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682270 | ||||||
| chr12:14682271
|
T | C | 2 | a0001c0003t0001g0018a0001c0003t0001g0109 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.611+771A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682271 | ||||||
| chr12:14682291
|
G | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.611+751C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682291 | ||||||
| chr12:14682319
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.611+723T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682319 | ||||||
| chr12:14682754
|
T | A | 3 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0004t0001g0016 | 3 | HG02965.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.611+288A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682754 | ||||||
| chr12:14682773
|
T | C | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.611+269A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682773 | ||||||
| chr12:14682782
|
G | T | 11 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.611+260C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682782 | ||||||
| chr12:14682866
|
A | C | 4 | a0001c0003t0001g0215a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+176T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682866 | ||||||
| chr12:14682888
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.611+154G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14682888 | ||||||
| chr12:14683289
|
A | C | 1 | a0001c0002t0001g0125 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.396-32T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683289 | ||||||
| chr12:14683371
|
G | A | 14 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(11): Show | 16 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.396-114C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683371 | ||||||
| chr12:14683424
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.396-167T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683424 | ||||||
| chr12:14683617
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.396-360C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683617 | ||||||
| chr12:14683653
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.396-396C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683653 | ||||||
| chr12:14683716
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.396-459G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683716 | ||||||
| chr12:14683807
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0111 | 2 | HG00639.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.396-550G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683807 | ||||||
| chr12:14683898
|
G | C | 1 | a0001c0008t0001g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.396-641C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683898 | ||||||
| chr12:14683944
|
A | G | 15 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.396-687T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683944 | ||||||
| chr12:14684045
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0148 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.396-788G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684045 | ||||||
| chr12:14684262
|
A | G | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.396-1005T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684262 | ||||||
| chr12:14684333
|
C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0136others(13): Show | 17 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.396-1076G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684333 | ||||||
| chr12:14684389
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396-1132T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684389 | ||||||
| chr12:14684432
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.396-1175C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684432 | ||||||
| chr12:14684445
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.396-1188A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684445 | ||||||
| chr12:14684532
|
C | CTCTT | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.396-1279_396-1276d others(6): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684532 | ||||||
| chr12:14684563
|
CCCTTCCT others(5): Show |
C | 1 | a0002c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.396-1318_396-1307d others(14): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684563 | ||||||
| chr12:14684582
|
TTCCTTCC others(4): Show |
T | 2 | a0001c0001t0001g0050a0001c0002t0001g0148 | 2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.396-1336_396-1326d others(13): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684582 | ||||||
| chr12:14684582
|
TTCCTTCC others(12): Show |
T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG00099.hp1 HG01243.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.396-1344_396-1326d others(21): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684582 | ||||||
| chr12:14684582
|
TTCCTTCC others(28): Show |
T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.396-1360_396-1326d others(37): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684582 | ||||||
| chr12:14684582
|
TTCCTTCC others(36): Show |
T | 1 | a0001c0003t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.396-1368_396-1326d others(45): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684582 | ||||||
| chr12:14684585
|
C | CT | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0003t0001g0215 | 3 | HG00597.hp2 HG02559.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.396-1329dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684585 | ||||||
| chr12:14684586
|
TTCC | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(4): Show | 7 | HG00438.hp2 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-1332_396-1330d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684586
|
TTCCTTCC | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0038others(29): Show | 34 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.396-1336_396-1330d others(9): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684586
|
TTCCTTCC others(8): Show |
T | 51 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 56 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.396-1344_396-1330d others(17): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684586
|
TTCCTTCC others(20): Show |
T | 18 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0102others(15): Show | 19 | HG00438.hp1 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.396-1356_396-1330d others(29): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684586
|
TTCCTTCC others(24): Show |
T | 4 | a0001c0001t0001g0130a0001c0001t0001g0175a0001c0003t0001g0018others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-1360_396-1330d others(33): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684586
|
TTCCTTCC others(32): Show |
T | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.396-1368_396-1330d others(41): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684586 | ||||||
| chr12:14684587
|
T | TTC | 5 | a0001c0001t0001g0170a0001c0003t0001g0019a0001c0003t0001g0216others(2): Show | 5 | HG02976.hp1 NA19030.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-1331_396-1330i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684587 | ||||||
| chr12:14684589
|
C | CT | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.396-1333dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684589 | ||||||
| chr12:14684589
|
C | T | 6 | a0001c0001t0001g0170a0001c0002t0001g0123a0001c0003t0001g0019others(3): Show | 6 | HG02976.hp1 HG03130.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-1332G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684589 | ||||||
| chr12:14684590
|
TTCC | T | 19 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0062others(16): Show | 19 | HG02273.hp1 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.396-1336_396-1334d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684590 | ||||||
| chr12:14684590
|
TTCCTTCC others(4): Show |
T | 10 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0042others(7): Show | 11 | HG00621.hp1 HG01934.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.396-1344_396-1334d others(13): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684590 | ||||||
| chr12:14684590
|
TTCCTTCC others(12): Show |
T | 3 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-1352_396-1334d others(21): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684590 | ||||||
| chr12:14684590
|
TTCCTTCC others(20): Show |
T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.396-1360_396-1334d others(29): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684590 | ||||||
| chr12:14684590
|
TTCCTTCC others(28): Show |
T | 12 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0184others(9): Show | 12 | HG00140.hp2 HG00673.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.396-1368_396-1334d others(37): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684590 | ||||||
| chr12:14684591
|
T | TTC | 20 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0139others(17): Show | 22 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.396-1335_396-1334i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684591 | ||||||
| chr12:14684593
|
C | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0139others(18): Show | 23 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.396-1336G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684593 | ||||||
| chr12:14684594
|
TTCC | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(2): Show | 5 | HG00438.hp2 HG01433.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-1340_396-1338d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684594 | ||||||
| chr12:14684594
|
TTCCTTCC others(16): Show |
T | 2 | a0001c0002t0001g0123a0001c0008t0001g0134 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.396-1360_396-1338d others(25): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684594 | ||||||
| chr12:14684595
|
T | TTC | 6 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-1339_396-1338i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684595 | ||||||
| chr12:14684595
|
TCC | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0141others(13): Show | 19 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.396-1340_396-1339d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684595 | ||||||
| chr12:14684596
|
C | T | 3 | a0001c0003t0001g0216a0001c0003t0001g0217a0001c0003t0001g0218 | 3 | HG02976.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.396-1339G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684596 | ||||||
| chr12:14684597
|
C | CCTT | 3 | a0001c0003t0001g0216a0001c0003t0001g0217a0001c0003t0001g0218 | 3 | HG02976.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.396-1341_396-1340i others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684597 | ||||||
| chr12:14684597
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-1340G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684597 | ||||||
| chr12:14684598
|
TTCC | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0032others(50): Show | 55 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.396-1344_396-1342d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684598 | ||||||
| chr12:14684599
|
T | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0141others(13): Show | 19 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.396-1342A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684599 | ||||||
| chr12:14684599
|
T | TTC | 21 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0139others(18): Show | 23 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.396-1343_396-1342i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684599 | ||||||
| chr12:14684601
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 45 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.396-1344G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684601 | ||||||
| chr12:14684602
|
TTCC | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(2): Show | 5 | HG00438.hp2 HG01433.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-1348_396-1346d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684602 | ||||||
| chr12:14684603
|
T | TTC | 6 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-1347_396-1346i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684603 | ||||||
| chr12:14684605
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG00738.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-1348G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684605 | ||||||
| chr12:14684606
|
TTCC | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(101): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.396-1352_396-1350d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684606 | ||||||
| chr12:14684607
|
T | TTC | 3 | a0001c0001t0001g0159a0001c0001t0003g0158a0001c0003t0001g0218 | 3 | HG02976.hp1 NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.396-1351_396-1350i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684607 | ||||||
| chr12:14684607
|
TCC | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(45): Show | 53 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.396-1352_396-1351d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684607 | ||||||
| chr12:14684609
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0003g0158a0001c0003t0001g0216others(2): Show | 5 | HG02976.hp1 NA18971.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-1352G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684609 | ||||||
| chr12:14684610
|
TTCC | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(2): Show | 5 | HG00438.hp2 HG01433.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-1356_396-1354d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684610 | ||||||
| chr12:14684611
|
T | C | 48 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(45): Show | 53 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.396-1354A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684611 | ||||||
| chr12:14684611
|
T | TTC | 6 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-1355_396-1354i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684611 | ||||||
| chr12:14684613
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(51): Show | 59 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.396-1356G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684613 | ||||||
| chr12:14684614
|
TTCC | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(104): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.396-1360_396-1358d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684614 | ||||||
| chr12:14684615
|
T | TTC | 6 | a0001c0001t0001g0159a0001c0001t0003g0158a0001c0003t0001g0215others(3): Show | 6 | HG02559.hp1 HG02976.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-1359_396-1358i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684615 | ||||||
| chr12:14684617
|
C | T | 6 | a0001c0001t0001g0159a0001c0001t0003g0158a0001c0003t0001g0215others(3): Show | 6 | HG02559.hp1 HG02976.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-1360G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684617 | ||||||
| chr12:14684619
|
TCC | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 83 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.396-1364_396-1363d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684619 | ||||||
| chr12:14684622
|
TTCC | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(115): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.396-1368_396-1366d others(5): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684622 | ||||||
| chr12:14684623
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 83 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.396-1366A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684623 | ||||||
| chr12:14684623
|
T | TTC | 6 | a0001c0001t0001g0159a0001c0001t0003g0158a0001c0003t0001g0215others(3): Show | 6 | HG02559.hp1 HG02976.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-1367_396-1366i others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684623 | ||||||
| chr12:14684625
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.396-1368G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684625 | ||||||
| chr12:14684648
|
C | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.396-1391G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684648 | ||||||
| chr12:14684695
|
T | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.396-1438A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684695 | ||||||
| chr12:14684929
|
G | A | 1 | a0001c0005t0002g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.395+1232C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14684929 | ||||||
| chr12:14685272
|
C | T | 1 | a0001c0017t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395+889G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685272 | ||||||
| chr12:14685273
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.395+888C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685273 | ||||||
| chr12:14685417
|
G | T | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+744C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685417 | ||||||
| chr12:14685457
|
C | T | 2 | a0001c0001t0001g0157a0001c0003t0001g0215 | 2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.395+704G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685457 | ||||||
| chr12:14685535
|
T | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(107): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.395+626A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685535 | ||||||
| chr12:14685578
|
A | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.395+583T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14685578 | ||||||
| chr12:14686074
|
T | C | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.395+87A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14686074 | ||||||
| chr12:14686077
|
G | C | 13 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0017others(10): Show | 15 | HG01934.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.395+84C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14686077 | ||||||
| chr12:14686596
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.331-371G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14686596 | ||||||
| chr12:14686689
|
A | G | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-464T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14686689 | ||||||
| chr12:14686778
|
G | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0031 | 3 | HG01884.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.331-553C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14686778 | ||||||
| chr12:14686802
|
T | A | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-577A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14686802 | ||||||
| chr12:14686916
|
TTGA | T | 5 | a0001c0001t0001g0210a0001c0003t0001g0215a0001c0003t0001g0216others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-694_331-692del others(3): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14686916 | ||||||
| chr12:14687435
|
C | T | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.330+516G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14687435 | ||||||
| chr12:14687692
|
T | A | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.330+259A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 2/26 | chr12 | 14687692 | ||||||
| chr12:14688080
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG03490.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.218-17T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688080 | ||||||
| chr12:14688121
|
T | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-58A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688121 | ||||||
| chr12:14688192
|
C | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0041others(7): Show | 10 | HG00733.hp1 HG01175.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.218-129G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688192 | ||||||
| chr12:14688218
|
T | C | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-155A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688218 | ||||||
| chr12:14688260
|
T | TTCTC | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 44 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.218-201_218-198dup others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688260 | ||||||
| chr12:14688276
|
C | T | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-213G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688276 | ||||||
| chr12:14688424
|
T | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.218-361A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688424 | ||||||
| chr12:14688551
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.218-488C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688551 | ||||||
| chr12:14688590
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.218-527A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688590 | ||||||
| chr12:14688631
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-568T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688631 | ||||||
| chr12:14688647
|
G | A | 6 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00673.hp2 HG02040.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-584C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688647 | ||||||
| chr12:14688678
|
C | T | 8 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0151others(5): Show | 8 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-615G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688678 | ||||||
| chr12:14688710
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-647A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688710 | ||||||
| chr12:14689135
|
A | G | 6 | a0001c0001t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-1072T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14689135 | ||||||
| chr12:14689267
|
G | A | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-1204C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14689267 | ||||||
| chr12:14689641
|
G | A | 6 | a0001c0001t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-1578C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14689641 | ||||||
| chr12:14689708
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.218-1645T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14689708 | ||||||
| chr12:14689756
|
T | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-1693A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14689756 | ||||||
| chr12:14690110
|
T | C | 6 | a0001c0001t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-2047A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690110 | ||||||
| chr12:14690170
|
C | T | 6 | a0001c0001t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-2107G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690170 | ||||||
| chr12:14690207
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.218-2144G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690207 | ||||||
| chr12:14690237
|
A | T | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.218-2174T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690237 | ||||||
| chr12:14690351
|
A | G | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 8 | HG00609.hp2 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-2288T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690351 | ||||||
| chr12:14690361
|
A | C | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-2298T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690361 | ||||||
| chr12:14690398
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.218-2335C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690398 | ||||||
| chr12:14690505
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.218-2442T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690505 | ||||||
| chr12:14690516
|
C | A | 1 | a0001c0003t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.218-2453G>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690516 | ||||||
| chr12:14690532
|
C | CT | 10 | a0001c0002t0001g0006a0001c0002t0001g0031a0001c0002t0001g0149others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-2470dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690532 | ||||||
| chr12:14690648
|
T | C | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-2585A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690648 | ||||||
| chr12:14690703
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218-2640C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690703 | ||||||
| chr12:14690901
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.218-2838G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14690901 | ||||||
| chr12:14691023
|
C | G | 3 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133 | 3 | HG01884.hp1 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.218-2960G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691023 | ||||||
| chr12:14691059
|
G | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-2996C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691059 | ||||||
| chr12:14691111
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.218-3048T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691111 | ||||||
| chr12:14691208
|
T | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-3145A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691208 | ||||||
| chr12:14691294
|
G | C | 7 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG00673.hp2 HG02040.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-3231C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691294 | ||||||
| chr12:14691352
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.218-3289G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691352 | ||||||
| chr12:14691562
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.218-3499A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691562 | ||||||
| chr12:14691619
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(101): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.218-3556G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691619 | ||||||
| chr12:14691645
|
A | G | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-3582T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691645 | ||||||
| chr12:14691646
|
C | T | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.218-3583G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691646 | ||||||
| chr12:14691669
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218-3606C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691669 | ||||||
| chr12:14691827
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218-3764C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691827 | ||||||
| chr12:14692128
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.218-4065C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692128 | ||||||
| chr12:14692201
|
C | T | 8 | a0001c0001t0001g0130a0001c0002t0001g0123a0001c0002t0001g0124others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+4031G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692201 | ||||||
| chr12:14692404
|
T | A | 1 | a0001c0017t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217+3828A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692404 | ||||||
| chr12:14692426
|
A | AT | 6 | a0001c0001t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+3805dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692426 | ||||||
| chr12:14692426
|
A | ATT | 5 | a0001c0001t0001g0210a0001c0003t0001g0215a0001c0003t0001g0216others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+3804_217+3805d others(4): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692426 | ||||||
| chr12:14692534
|
T | A | 1 | a0006c0013t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.217+3698A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692534 | ||||||
| chr12:14692575
|
C | T | 5 | a0001c0001t0001g0187a0002c0006t0001g0185a0002c0006t0001g0186others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+3657G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692575 | ||||||
| chr12:14692585
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217+3647G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692585 | ||||||
| chr12:14692586
|
G | A | 5 | a0001c0001t0001g0210a0001c0003t0001g0215a0001c0003t0001g0216others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+3646C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692586 | ||||||
| chr12:14692618
|
C | T | 5 | a0001c0001t0001g0187a0002c0006t0001g0185a0002c0006t0001g0186others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+3614G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692618 | ||||||
| chr12:14692637
|
C | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG00733.hp1 HG01175.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+3595G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692637 | ||||||
| chr12:14692708
|
A | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG03654.hp1 NA18943.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.217+3524T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692708 | ||||||
| chr12:14692850
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.217+3382C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14692850 | ||||||
| chr12:14693070
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.217+3162T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693070 | ||||||
| chr12:14693079
|
T | C | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.217+3153A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693079 | ||||||
| chr12:14693120
|
T | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.217+3112A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693120 | ||||||
| chr12:14693145
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.217+3087G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693145 | ||||||
| chr12:14693253
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.217+2979G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693253 | ||||||
| chr12:14693392
|
C | G | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.217+2840G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693392 | ||||||
| chr12:14693609
|
A | G | 6 | a0001c0003t0001g0003a0001c0003t0001g0121a0001c0003t0001g0122others(3): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.217+2623T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14693609 | ||||||
| chr12:14694095
|
C | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.217+2137G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694095 | ||||||
| chr12:14694354
|
G | C | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.217+1878C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694354 | ||||||
| chr12:14694426
|
A | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 8 | HG00438.hp2 HG00639.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.217+1806T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694426 | ||||||
| chr12:14694602
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 5 | HG00621.hp1 HG02027.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+1630G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694602 | ||||||
| chr12:14694617
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.217+1615G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694617 | ||||||
| chr12:14694664
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.217+1568C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694664 | ||||||
| chr12:14694711
|
G | A | 1 | a0002c0006t0001g0202 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+1521C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14694711 | ||||||
| chr12:14695027
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.217+1205T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695027 | ||||||
| chr12:14695056
|
G | A | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.217+1176C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695056 | ||||||
| chr12:14695568
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG00597.hp1 NA18998.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+664A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695568 | ||||||
| chr12:14695600
|
C | CA | 75 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.217+631dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695600 | ||||||
| chr12:14695600
|
C | CAA | 27 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.217+630_217+631dup others(2): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695600 | ||||||
| chr12:14695600
|
CA | C | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 11 | HG01496.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+631delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695600 | ||||||
| chr12:14695662
|
G | GGCCCAGA others(7): Show |
1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.217+556_217+569dup others(14): Show |
GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695662 | ||||||
| chr12:14695765
|
G | T | 3 | a0001c0003t0001g0019a0001c0004t0001g0020a0001c0004t0001g0021 | 3 | NA18983.hp1 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.217+467C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695765 | ||||||
| chr12:14695769
|
A | T | 4 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0003t0001g0018others(1): Show | 4 | HG02965.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+463T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695769 | ||||||
| chr12:14695858
|
A | G | 1 | a0001c0011t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.217+374T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695858 | ||||||
| chr12:14695997
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.217+235G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695997 | ||||||
| chr12:14696046
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.217+186C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14696046 | ||||||
| chr12:14696048
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.217+184C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14696048 | ||||||
| chr12:14696197
|
CAG | C | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+33_217+34delCT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14696197 | ||||||
| chr12:14696212
|
T | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+20A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14696212 |