Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0002 | 1/0 | 1073 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0003 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0004 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0005 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0006 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0007 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| a0008 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | MKTLL others(1068): Show |
chr12 | 14607632 | 14701599 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3219 | 160 | 18 | 48 | 59 | 8 | 26 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0002 | 0/0 | 3219 | 32 | 29 | 2 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0003 | 0/0 | 3219 | 16 | 14 | 1 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0004 | 0/0 | 3219 | 6 | 4 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0005 | 0/0 | 3219 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0007 | 0/0 | 3219 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0008 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0011 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0012 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0016 | 0/0 | 3219 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0017 | 0/0 | 3219 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0001c0018 | 0/0 | 3219 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0002c0006 | 1/0 | 3219 | 4 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0003c0013 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0004c0019 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0005c0010 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0006c0014 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0007c0015 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
chr12 | 14607632 | 14701599 | ||
| a0008c0009 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | ATGAA others(3214): Show |
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 | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0001t0003 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0002t0001 | 0/0 | 3858 | 31 | 28 | 2 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0002t0004 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0003t0001 | 0/0 | 3858 | 16 | 14 | 1 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0004t0001 | 0/0 | 3858 | 6 | 4 | 0 | 2 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0005t0002 | 0/0 | 3858 | 4 | 4 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0007t0001 | 0/0 | 3858 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0008t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0011t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0012t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0016t0001 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0017t0001 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0001c0018t0001 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0002c0006t0001 | 1/0 | 3858 | 4 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0003c0013t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0004c0019t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0005c0010t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0006c0014t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0007c0015t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| a0008c0009t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | GACCA others(3853): Show |
chr12 | 14607632 | 14701599 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| 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 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0098 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0194 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0202 | 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 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0007 | 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 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0122 | 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 |
| 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 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0147 | 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 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0002t0001g0215 | 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 |
| a0001c0003t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0016 | 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 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0120 | 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 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0005t0002g0130 | 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 |
| a0001c0005t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0007t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0008t0001g0133 | 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 |
| a0001c0012t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0016t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0017t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0001c0018t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0002c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0003c0013t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0004c0019t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0005c0010t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0006c0014t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0007c0015t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| a0008c0009t0001g0064 | 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 | g0059 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0074 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0044 | 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 | g0095 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | 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 | g0001 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0079 | 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 | g0050 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01255 | hp2 | a0001 | c0018 | t0001 | g0096 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | 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 | g0164 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01884 | hp1 | a0001 | c0005 | t0002 | g0132 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0200 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01891 | hp2 | a0001 | c0005 | t0002 | g0177 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0181 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0101 | 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 | g0093 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | 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 | g0180 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0119 | 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 | g0024 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02258 | hp2 | a0001 | c0005 | t0002 | g0131 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0006 | 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 | g0066 | 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 | g0144 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02523 | hp2 | a0003 | c0013 | t0001 | g0033 | EAS | KHV | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02572 | hp2 | a0004 | c0019 | t0001 | g0186 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0124 | 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 | g0212 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0209 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | 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 | g0187 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0117 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02897 | hp2 | a0001 | c0012 | t0001 | g0094 | AFR | GWD | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0006 | 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 | g0017 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0016 | 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 | g0147 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0012 | 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 | g0062 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03041 | hp1 | a0002 | c0006 | t0001 | g0183 | 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 | g0089 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0121 | 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 | g0051 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0034 | 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 | g0006 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ESN | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0118 | 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 | g0042 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0063 | 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 | g0173 | SAS | BEB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0102 | 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 | g0087 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04199 | hp2 | a0001 | c0017 | t0001 | g0111 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0184 | AFR | YRI | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18952 | hp1 | a0005 | c0010 | t0001 | g0192 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18972 | hp1 | a0006 | c0014 | t0001 | g0046 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | 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 | g0203 | 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 | g0020 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18986 | hp2 | a0007 | c0015 | t0001 | g0142 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18993 | hp1 | a0008 | 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 | g0178 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0076 | 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 | g0196 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19030 | hp1 | a0001 | c0007 | t0001 | g0216 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | LWK | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20129 | hp1 | a0001 | c0008 | t0001 | g0133 | 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 | g0069 | SAS | GIH | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| NA20905 | hp2 | a0001 | c0016 | t0001 | g0067 | SAS | GIH | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0002 | 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 | g0150 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02486 | hp2 | a0001 | c0005 | t0002 | g0130 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| homoSapiens | grch38p0 | a0002 | c0006 | t0001 | g0055 | REF | REF | GUCY2C_chr12_14607632_14701599 | GUCY2C | chr12 | 14607632 | 14701599 |
| view | 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 | a0006 | 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 | a0007 | 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 | a0003 | 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 | a0008 | 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 | a0001 a0003 a0005 others(3): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0004 | 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 |
| view | 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 | a0001c0005 a0001c0007 |
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 | a0001c0005 a0001c0007 |
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 | a0001c0001 a0001c0004 a0001c0007 others(8): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0003 a0001c0004 a0001c0008 |
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 |
| view | 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 |
| view | 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 | a0001c0001t0001g0178 | 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | a0001c0003t0001g0017 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0061 | 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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0002t0001g0153 | 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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 7 | a0001c0001t0001g0103 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0005 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0109 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 33 | a0001c0001t0001g0103 a0001c0002t0001g0002 a0001c0002t0001g0007 others(30): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 12 | a0001c0001t0001g0103 a0001c0002t0001g0146 a0001c0002t0001g0153 others(9): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0211 | 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 | a0003c0013t0001g0033 | 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 | 18 | a0001c0001t0001g0103 a0001c0001t0001g0191 a0001c0002t0001g0002 others(15): 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 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0004g0028 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0003t0001g0016 a0001c0003t0001g0018 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0198 |
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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0105 | 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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0001t0001g0124 | 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 | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0065 | 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 | 8 | a0001c0001t0001g0103 a0001c0002t0001g0146 a0001c0002t0001g0153 others(5): 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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0129 a0001c0003t0001g0175 a0001c0003t0001g0181 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0174 |
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 | a0001c0002t0001g0129 a0001c0003t0001g0175 a0001c0003t0001g0181 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0181 a0001c0008t0001g0133 |
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 | a0001c0001t0001g0036 | 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 | a0001c0003t0001g0181 a0001c0005t0002g0130 a0001c0005t0002g0131 others(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 | a0001c0001t0001g0102 | 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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0057 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0070 | 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 | 4 | a0001c0001t0001g0103 a0001c0003t0001g0012 a0001c0003t0001g0213 others(1): 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 | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2777-597A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 23/26 | chr12 | 14619906 | |||||||
| chr12:14620347 | T | G | 4 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0167 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0087 | 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 | a0001c0002t0001g0215 | 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0017 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0051 others(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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 a0001c0005t0002g0177 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0163 |
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 | a0001c0005t0002g0177 | 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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2601+90A>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 22/26 | chr12 | 14621915 | |||||||
| chr12:14622280 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0002t0001g0146 | 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): 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 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0098 others(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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | 25 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(22): 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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0006c0014t0001g0046 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0107 | 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 | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2409-1180A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 21/26 | chr12 | 14623377 | |||||||
| chr12:14623398 | T | C | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0001t0001g0197 | 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0057 others(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 | a0001c0002t0001g0056 a0001c0003t0001g0016 a0001c0003t0001g0018 |
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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0002t0001g0215 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0165 | 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 | 16 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(13): 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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0002t0001g0056 a0001c0003t0001g0006 a0001c0003t0001g0016 others(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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 35 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0097 others(32): 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0003t0001g0181 a0001c0008t0001g0133 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0005 | 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0001t0001g0188 | 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 | a0001c0003t0001g0017 | 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 | a0001c0004t0001g0015 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0001g0170 others(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 | 16 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(13): 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0017 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0089 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0161 | 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | a0001c0004t0001g0117 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0159 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2250-1362C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14627277 | |||||||
| chr12:14627368 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0001g0141 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0089 a0001c0001t0001g0208 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0001t0001g0103 | 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2249+77T>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 20/26 | chr12 | 14628569 | |||||||
| chr12:14628744 | G | GA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): 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 | 1 | a0001c0002t0001g0002 | 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 | a0001c0001t0001g0180 | 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0051 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0002c0006t0001g0200 | 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2158-517G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14629254 | |||||||
| chr12:14629264 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0001t0001g0080 | 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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 11 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0002t0001g0002 others(8): 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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0215 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0075 | 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 | a0001c0002t0001g0030 a0001c0002t0001g0122 a0001c0002t0001g0123 |
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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0008t0001g0133 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(34): 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 | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0145 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 |
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 | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): 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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0166 | 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 | a0001c0003t0001g0017 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0165 a0001c0003t0001g0181 a0001c0008t0001g0133 |
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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0164 | 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 | a0001c0008t0001g0133 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0158 others(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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2158-4580C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633317 | |||||||
| chr12:14633424 | A | C | 16 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(13): 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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2158-4739C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633476 | |||||||
| chr12:14633477 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.2158-4740T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633477 | |||||||
| chr12:14633665 | T | TA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2158-4929dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14633665 | |||||||
| chr12:14633774 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): 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 | a0001c0001t0001g0083 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0074 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2157+4489C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14635373 | |||||||
| chr12:14635871 | C | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 |
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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0001t0001g0160 | 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 | a0001c0002t0001g0215 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0085 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0172 a0001c0001t0003g0171 |
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 | a0001c0001t0001g0061 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2157+2838G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14637024 | |||||||
| chr12:14637196 | C | CA | 14 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0002t0001g0029 others(11): 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 | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0162 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 17 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(14): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0002t0001g0056 a0001c0003t0001g0006 a0001c0003t0001g0016 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0215 | 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 | a0001c0008t0001g0133 | 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2157+1516delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638345 | |||||||
| chr12:14638655 | G | T | 2 | a0001c0002t0001g0147 a0001c0002t0001g0151 |
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 | a0001c0016t0001g0067 | 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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2157+897A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14638965 | |||||||
| chr12:14638991 | A | G | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 15 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(12): 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 | 18 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(15): 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0087 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): 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 | 10 | a0001c0001t0001g0035 a0001c0001t0001g0100 a0001c0001t0001g0145 others(7): 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 | a0005c0010t0001g0192 | 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 | 105 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.2157+145C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 19/26 | chr12 | 14639717 | |||||||
| chr12:14640180 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2069-230T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 18/26 | chr12 | 14640180 | |||||||
| chr12:14640220 | C | T | 39 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(36): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0003t0001g0006 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0097 a0001c0001t0001g0109 others(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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0008c0009t0001g0064 | 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 | a0001c0001t0001g0098 | 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 | a0001c0003t0001g0017 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 22 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(19): 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 | a0001c0001t0001g0113 a0001c0001t0001g0195 a0001c0004t0001g0019 others(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 | a0001c0001t0001g0063 | 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 | a0001c0004t0001g0118 a0001c0004t0001g0119 |
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 | 60 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1931-352A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641571 | |||||||
| chr12:14641809 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1931-590A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14641809 | |||||||
| chr12:14641885 | C | T | 14 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(11): 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 | 41 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(38): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0158 | 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 19 | a0001c0002t0001g0056 a0001c0002t0001g0070 a0001c0002t0001g0129 others(16): 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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0003t0001g0181 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 19 | a0001c0002t0001g0056 a0001c0002t0001g0070 a0001c0002t0001g0129 others(16): 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0146 | 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 | a0001c0001t0001g0065 | 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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1930+652T>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 17/26 | chr12 | 14642922 | |||||||
| chr12:14643067 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(31): 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 | 12 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(9): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0207 |
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 | a0002c0006t0001g0183 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): 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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0003t0001g0021 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0097 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1797+553A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 16/26 | chr12 | 14644676 | |||||||
| chr12:14644680 | T | C | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0079 others(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 | 17 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0147 others(14): 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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0044 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0146 | 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0050 |
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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1711-276G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14645591 | |||||||
| chr12:14645592 | G | A | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | 36 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(33): 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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0187 a0001c0001t0001g0191 others(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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0003t0001g0017 | 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0002c0006t0001g0183 a0002c0006t0001g0184 |
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 | 6 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0004g0028 others(3): 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0001t0001g0178 | 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0001t0001g0180 | 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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0012t0001g0094 | 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 | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): 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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 8 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(5): 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 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1711-2958delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 15/26 | chr12 | 14648272 | |||||||
| chr12:14648272 | TAA | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0139 a0001c0002t0001g0002 |
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 | a0001c0001t0001g0077 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0017t0001g0111 | 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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0193 | 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0001t0001g0101 | 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 | a0001c0005t0002g0131 | 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 | a0001c0005t0002g0177 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0185 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 19 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0002t0001g0129 others(16): 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0001g0146 | 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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | a0001c0001t0001g0201 | 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 | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): 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 | a0001c0001t0001g0069 | 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0140 | 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0002t0001g0215 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0136 | 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 | 16 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0002t0001g0129 others(13): 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 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0003t0001g0016 a0001c0003t0001g0018 |
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 | a0001c0001t0001g0182 | 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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 |
153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): 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 | a0001c0004t0001g0117 | 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 | a0001c0001t0001g0172 a0001c0001t0003g0171 |
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 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0122 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0085 | 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 | a0001c0007t0001g0209 | 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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | 16 | a0001c0001t0001g0189 a0001c0002t0001g0070 a0001c0002t0001g0129 others(13): 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 | a0001c0004t0001g0117 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0140 | 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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): 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 | a0001c0001t0001g0140 | 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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): 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 | a0001c0002t0001g0215 | 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 | a0001c0002t0001g0215 | 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 | a0001c0007t0001g0209 | 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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0114 |
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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0001t0001g0194 | 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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0003t0001g0017 | 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 | a0001c0001t0001g0180 | 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 | 1 | a0001c0002t0001g0002 | 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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0078 | 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0146 | 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 | a0001c0003t0001g0017 | 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 | a0001c0001t0001g0102 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0002t0001g0129 a0001c0003t0001g0175 |
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 | a0001c0001t0001g0080 | 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 | a0001c0003t0001g0108 | 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 | a0003c0013t0001g0033 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0079 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0215 | 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 | 140 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 7 | a0001c0002t0001g0146 a0001c0002t0001g0153 a0001c0002t0001g0154 others(4): 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 | a0001c0001t0001g0058 | 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 | a0001c0003t0001g0016 a0001c0003t0001g0018 |
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 | a0001c0001t0001g0109 | 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0005t0002g0177 | 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | a0001c0003t0001g0018 | 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 | a0001c0003t0001g0181 a0001c0008t0001g0133 a0001c0011t0001g0014 |
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 | 6 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0004g0028 others(3): 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0159 | 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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0001t0001g0041 | 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 | a0001c0016t0001g0067 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0082 | 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0099 others(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 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0029 others(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 | 44 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(41): 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 | a0001c0001t0001g0105 | 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 | 20 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0129 others(17): 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 | a0001c0001t0001g0071 | 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 | a0001c0004t0001g0117 | 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 | a0001c0008t0001g0133 | 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 | 14 | a0001c0002t0001g0070 a0001c0002t0001g0129 a0001c0002t0001g0153 others(11): 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 | a0001c0003t0001g0017 | 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 | a0001c0002t0001g0056 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 others(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 | a0001c0001t0001g0025 | 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 | a0001c0002t0001g0070 a0001c0003t0001g0021 |
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 | 14 | a0001c0002t0001g0070 a0001c0002t0001g0129 a0001c0002t0001g0153 others(11): 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 | a0001c0001t0001g0178 | 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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1283-2567C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14663629 | |||||||
| chr12:14663846 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): 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 | a0001c0007t0001g0209 a0001c0007t0001g0216 |
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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0002t0001g0150 | 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 | a0001c0003t0001g0017 | 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 | 22 | a0001c0001t0001g0167 a0001c0001t0001g0180 a0001c0001t0001g0190 others(19): 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 | 32 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0026 others(29): 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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): 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 | a0001c0005t0002g0177 | 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 | a0001c0003t0001g0175 | 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 | 29 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0060 others(26): 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 | a0001c0001t0001g0036 a0001c0001t0001g0134 a0001c0002t0001g0090 others(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 | a0001c0002t0001g0056 a0001c0005t0002g0130 a0001c0005t0002g0131 others(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 | 6 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0004g0028 others(3): 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 | 5 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0003t0001g0012 others(2): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0003t0001g0006 a0001c0003t0001g0021 a0001c0003t0001g0120 others(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 | a0001c0003t0001g0017 a0001c0003t0001g0175 |
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 | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0155 others(18): 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 | a0001c0001t0001g0092 | 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 | a0001c0002t0001g0147 | 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1282+2986delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14666735 | |||||||
| chr12:14666738 | A | G | 6 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
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 | 10 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(7): 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): 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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(47): Show |
57 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(54): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | a0001c0001t0001g0024 | 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): 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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(45): Show |
55 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(52): 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 | a0001c0001t0001g0089 a0001c0005t0002g0130 a0001c0005t0002g0131 others(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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0004t0001g0118 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1282+1326C>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668396 | |||||||
| chr12:14668632 | CT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1282+1089delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668632 | |||||||
| chr12:14668826 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1282+896C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14668826 | |||||||
| chr12:14668856 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0001g0057 a0001c0001t0001g0124 a0001c0001t0001g0170 others(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 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0018 others(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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(64): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1282+511dupA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 10/26 | chr12 | 14669210 | |||||||
| chr12:14669345 | C | T | 1 | a0002c0006t0001g0200 | 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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0208 a0001c0001t0001g0212 |
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 | a0001c0001t0001g0136 | 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0003t0001g0016 a0001c0003t0001g0018 a0001c0004t0001g0015 |
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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0016t0001g0067 |
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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0054 | 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0001g0036 | 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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0003t0001g0175 | 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0044 others(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 | GAA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0135 others(13): Show |
17 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(14): 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 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0018 others(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 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0003t0001g0017 others(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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0145 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1085-295G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14673253 | |||||||
| chr12:14673270 | T | A | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0031 |
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 | a0001c0003t0001g0175 | 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 | a0001c0003t0001g0175 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0031 | 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084+512G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 8/26 | chr12 | 14674113 | |||||||
| chr12:14674120 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): 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 | 10 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(7): 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 | a0001c0001t0001g0158 a0001c0001t0001g0198 |
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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(47): Show |
57 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(54): 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 | a0001c0001t0001g0180 | 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 | 32 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0088 others(29): 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 | 27 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0136 others(24): Show |
29 | HG00609.hp1 HG01934.hp2 HG02027.hp2 others(26): 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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0102 | 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0002t0001g0056 a0001c0002t0001g0146 |
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 | 44 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(41): Show |
49 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.949-490delC | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14675249 | |||||||
| chr12:14675250 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(47): Show |
57 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(54): 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 | a0001c0004t0001g0117 a0001c0004t0001g0118 a0001c0004t0001g0119 |
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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(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 | a0001c0001t0001g0061 | 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 | a0001c0002t0001g0090 | 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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.948+812G>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676042 | |||||||
| chr12:14676101 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
16 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(13): 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 | a0001c0001t0001g0063 | 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.948+384T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 7/26 | chr12 | 14676470 | |||||||
| chr12:14676524 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0003t0001g0175 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0100 others(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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0003t0001g0017 a0001c0003t0001g0108 a0001c0003t0001g0175 |
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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): 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 | a0001c0001t0001g0091 | 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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | a0001c0001t0001g0097 a0001c0001t0001g0156 a0001c0001t0001g0170 others(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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): 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 | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0012t0001g0094 | 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 | a0001c0001t0001g0095 | 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0008t0001g0133 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.830+328C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 6/26 | chr12 | 14679329 | |||||||
| chr12:14679360 | C | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): 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 | a0001c0001t0001g0206 | 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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.734-144delA | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 5/26 | chr12 | 14679896 | |||||||
| chr12:14679953 | T | A | 14 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(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 | a0001c0003t0001g0016 a0001c0003t0001g0018 a0001c0003t0001g0181 others(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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): 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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): 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 | a0001c0001t0001g0201 | 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 | a0001c0002t0001g0125 a0001c0002t0001g0129 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(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 | a0001c0001t0001g0189 | 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 | a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(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 | a0001c0001t0001g0205 | 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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.612-11delT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681487 | |||||||
| chr12:14681493 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.612-16C>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681493 | |||||||
| chr12:14681764 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.612-287C>T | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 4/26 | chr12 | 14681764 | |||||||
| chr12:14681925 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): 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 | a0001c0004t0001g0119 | 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 | 10 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(7): 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 | 15 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
16 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(13): 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 | a0001c0001t0001g0208 a0001c0001t0001g0212 |
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 | a0001c0001t0001g0043 | 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 | a0001c0003t0001g0017 a0001c0003t0001g0108 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0003t0001g0016 a0001c0003t0001g0018 a0001c0004t0001g0015 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 10 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(7): 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 | 3 | a0001c0003t0001g0012 a0001c0003t0001g0213 a0001c0003t0001g0214 |
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 | a0001c0001t0001g0176 | 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 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.396-167T>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 3/26 | chr12 | 14683424 | |||||||
| chr12:14683617 | G | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0110 |
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 | a0001c0008t0001g0133 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0146 |
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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | 15 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
16 | HG00609.hp1 HG02027.hp2 HG02083.hp2 others(13): 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 | a0001c0001t0001g0173 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0107 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0002c0006t0001g0184 | 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 | a0001c0001t0001g0047 a0001c0002t0001g0146 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0003t0001g0175 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0003t0001g0213 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0173 a0001c0003t0001g0017 others(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 | a0001c0001t0001g0115 | 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 | 4 | a0001c0001t0001g0166 a0001c0003t0001g0012 a0001c0003t0001g0021 others(1): 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 | 17 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(14): 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 | 5 | a0001c0001t0001g0166 a0001c0002t0001g0123 a0001c0003t0001g0012 others(2): 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 | 18 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0001g0104 others(15): Show |
18 | HG02273.hp1 HG02451.hp2 HG02486.hp1 others(15): 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 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0043 others(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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0170 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0097 others(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 | a0001c0002t0001g0123 a0001c0008t0001g0133 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0136 others(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 | 2 | a0001c0003t0001g0012 a0001c0003t0001g0214 |
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 | 2 | a0001c0003t0001g0012 a0001c0003t0001g0214 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(49): Show |
54 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(51): 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0140 others(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 | 38 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0136 others(35): 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 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): 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 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0003t0001g0012 |
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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0104 others(44): 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 | 4 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0003t0001g0012 others(1): 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 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0097 others(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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0104 others(44): 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 | a0001c0001t0001g0013 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(49): 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 | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): 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 | 5 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0003t0001g0012 others(2): 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 | 5 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0003t0001g0012 others(2): 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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): 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 | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): 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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): 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 | 5 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0003t0001g0012 others(2): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0005t0002g0132 | 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 | a0001c0017t0001g0111 | 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 | a0001c0001t0001g0144 | 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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0155 a0001c0003t0001g0213 |
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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | 1 | a0001c0002t0001g0002 | 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 4 | a0001c0001t0001g0208 a0001c0003t0001g0012 a0001c0003t0001g0213 others(1): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0040 others(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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 38 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(35): Show |
43 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(40): 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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.218-361A>C | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688424 | |||||||
| chr12:14688551 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0155 others(19): 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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.218-527A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14688590 | |||||||
| chr12:14688631 | A | G | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0149 others(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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): 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 | a0001c0001t0001g0212 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | a0001c0001t0001g0212 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0191 | 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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0212 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | a0001c0001t0001g0212 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0197 | 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 | a0001c0003t0001g0181 | 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 | 9 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(6): 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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0109 | 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 | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(68): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): 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 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0132 |
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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): 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 | a0001c0001t0001g0173 | 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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.218-3289G>A | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691352 | |||||||
| chr12:14691562 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.218-3499A>G | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14691562 | |||||||
| chr12:14691619 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(97): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): 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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0110 | 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 | a0001c0002t0001g0146 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0124 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0017t0001g0111 | 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 | a0001c0001t0001g0212 a0001c0002t0001g0210 a0001c0002t0001g0211 others(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 | 4 | a0001c0001t0001g0208 a0001c0003t0001g0012 a0001c0003t0001g0213 others(1): 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 | a0003c0013t0001g0033 | 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 | a0001c0001t0001g0185 a0002c0006t0001g0183 a0002c0006t0001g0184 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | 4 | a0001c0001t0001g0208 a0001c0003t0001g0012 a0001c0003t0001g0213 others(1): 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 | a0001c0001t0001g0185 a0002c0006t0001g0183 a0002c0006t0001g0184 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(96): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): 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 | a0001c0001t0001g0182 | 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0040 | 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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0003t0001g0006 a0001c0003t0001g0120 a0001c0003t0001g0121 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(96): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | |||||||
| chr12:14694664 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0155 others(19): 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 | a0002c0006t0001g0200 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(96): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(69): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.217+631dupT | GUCY2C | ENSG00000070019.5 | transcript | ENST00000261170.5 | protein_coding | 1/26 | chr12 | 14695600 | |||||||
| chr12:14695600 | C | CAA | 27 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0208 | 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 | a0001c0003t0001g0021 a0001c0004t0001g0019 a0001c0004t0001g0020 |
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 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0210 others(7): 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 |