Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285172 |
| ensemblid | ENSG00000155744.10 |
| hgncid | 28593 |
| symbol | HYCC2 |
| name | hyccin PI4KA lipid kinase complex subunit 2 |
| refseq_nuc | NM_001321623.1 |
| refseq_prot | NP_001308552.1 |
| ensembl_nuc | ENST00000681958.1 |
| ensembl_prot | ENSP00000507218.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 200973718 |
| end | 201071671 |
| strand | - |
| ver | v1.2 |
| region | chr2:200973718-201071671 |
| region5000 | chr2:200968718-201076671 |
| regionname0 | HYCC2_chr2_200973718_201071671 |
| regionname5000 | HYCC2_chr2_200968718_201076671 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 586 | 175 | 85 | 38 | 24 | 10 | 16 | 8 | HYCC2_chr2_200968718_201076671 | HYCC2 | MLGTD others(581): Show |
chr2 | 200968718 | 201076671 |
| a0002 | 0/0 | 586 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | MLGTD others(581): Show |
chr2 | 200968718 | 201076671 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1758 | 175 | 85 | 38 | 24 | 10 | 16 | HYCC2_chr2_200968718_201076671 | HYCC2 | ATGCT others(1753): Show |
chr2 | 200968718 | 201076671 | ||
| a0002c0002 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | ATGCT others(1753): Show |
chr2 | 200968718 | 201076671 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 9503 | 44 | 9 | 17 | 11 | 2 | 3 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0002 | 0/0 | 9501 | 16 | 3 | 2 | 5 | 1 | 5 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9496): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0003 | 0/0 | 9498 | 14 | 14 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0004 | 0/0 | 9498 | 12 | 8 | 2 | 1 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0005 | 0/0 | 9493 | 8 | 8 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9488): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0006 | 0/0 | 9498 | 8 | 0 | 5 | 1 | 2 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0007 | 0/0 | 9504 | 8 | 3 | 3 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9499): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0008 | 0/0 | 9500 | 8 | 5 | 3 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9495): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0009 | 0/0 | 9505 | 6 | 6 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0010 | 0/0 | 9499 | 4 | 2 | 1 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9494): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0011 | 0/0 | 9497 | 4 | 4 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9492): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0012 | 0/0 | 9502 | 3 | 2 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9497): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0013 | 0/0 | 9500 | 3 | 0 | 1 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9495): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0014 | 0/0 | 9496 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9491): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0015 | 0/0 | 9503 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0016 | 0/0 | 9503 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0017 | 0/0 | 9500 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9495): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0018 | 0/0 | 9505 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0019 | 0/0 | 9497 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9492): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0020 | 0/0 | 9501 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9496): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0021 | 0/0 | 9491 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9486): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0022 | 0/0 | 9497 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9492): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0023 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9494): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0024 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0025 | 0/0 | 9496 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9491): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0026 | 0/0 | 9501 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9496): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0027 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9494): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0028 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9494): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0029 | 0/0 | 9498 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0030 | 0/0 | 9503 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0031 | 0/0 | 9501 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9496): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0032 | 0/0 | 9501 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9496): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0033 | 0/0 | 9500 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9495): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0034 | 0/0 | 9506 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9501): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0035 | 0/0 | 9505 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0036 | 0/0 | 9506 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9501): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0037 | 0/0 | 9505 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0038 | 0/0 | 9505 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0039 | 0/0 | 9505 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9500): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0040 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0041 | 0/0 | 9497 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9492): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0042 | 0/0 | 9503 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0043 | 0/0 | 9496 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9491): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0044 | 0/0 | 9503 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9498): Show |
chr2 | 200968718 | 201076671 |
| a0001c0001t0045 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9493): Show |
chr2 | 200968718 | 201076671 |
| a0002c0002t0005 | 0/0 | 9493 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | GCAGT others(9488): Show |
chr2 | 200968718 | 201076671 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0013g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0015g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0018g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0019g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0020g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0022g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0023g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0024g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0025g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0026g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0027g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0028g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0029g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0030g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0033g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0034g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0035g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0036g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0037g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0038g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0039g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0040g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0041g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0042g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0043g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0044g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0001c0001t0045g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| a0002c0002t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0037 | g0062 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0026 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00140 | hp2 | a0001 | c0001 | t0042 | g0049 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0107 | EUR | FIN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00408 | hp1 | a0001 | c0001 | t0018 | g0056 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00408 | hp2 | a0001 | c0001 | t0020 | g0046 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0034 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00741 | hp1 | a0001 | c0001 | t0036 | g0048 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0116 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01069 | hp2 | a0001 | c0001 | t0035 | g0122 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0121 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0058 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0028 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0136 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0106 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0104 | EUR | IBS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0008 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0105 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0040 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02055 | hp1 | a0001 | c0001 | t0023 | g0126 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0075 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02080 | hp1 | a0001 | c0001 | t0029 | g0118 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02132 | hp1 | a0001 | c0001 | t0030 | g0033 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02145 | hp1 | a0001 | c0001 | t0044 | g0047 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02145 | hp2 | a0001 | c0001 | t0028 | g0135 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0117 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0173 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0094 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02622 | hp1 | a0001 | c0001 | t0040 | g0165 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02630 | hp1 | a0001 | c0001 | t0041 | g0158 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0095 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02717 | hp2 | a0001 | c0001 | t0043 | g0134 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0138 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0061 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02735 | hp2 | a0001 | c0001 | t0033 | g0123 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0161 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0148 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0050 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0160 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0120 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03130 | hp2 | a0001 | c0001 | t0038 | g0140 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03195 | hp1 | a0002 | c0002 | t0005 | g0150 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03209 | hp1 | a0001 | c0001 | t0025 | g0097 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03225 | hp1 | a0001 | c0001 | t0034 | g0171 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0168 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0006 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0115 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0157 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0139 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03927 | hp1 | a0001 | c0001 | t0039 | g0042 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03942 | hp1 | a0001 | c0001 | t0022 | g0031 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03942 | hp2 | a0001 | c0001 | t0032 | g0005 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0041 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | YRI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18944 | hp2 | a0001 | c0001 | t0016 | g0027 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA18979 | hp2 | a0001 | c0001 | t0016 | g0019 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0144 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19043 | hp2 | a0001 | c0001 | t0031 | g0018 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0004 | EUR | TSI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0029 | EUR | TSI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02109 | hp1 | a0001 | c0001 | t0027 | g0143 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02486 | hp1 | a0001 | c0001 | t0026 | g0137 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02486 | hp2 | a0001 | c0001 | t0045 | g0133 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0169 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0096 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0149 | AFR | USA | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0145 | REF | REF | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0085 | REF | REF | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200992939 | C | A | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.691G>T | p.Val231Leu | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/13 | 881/9503 | 691/1761 | 231/586 | chr2 | 200992939 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200974210 | TA | T | 3 | a0001c0001t0011 a0001c0001t0040 a0001c0001t0041 |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7059delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 7059 | chr2 | 200974210 | ||||||
| chr2:200974268 | G | A | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7002C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 7002 | chr2 | 200974268 | ||||||
| chr2:200974355 | G | C | 1 | a0001c0001t0024 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6915C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6915 | chr2 | 200974355 | ||||||
| chr2:200974482 | A | G | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6788T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6788 | chr2 | 200974482 | ||||||
| chr2:200974529 | A | G | 1 | a0001c0001t0016 | 2 | NA18944.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6741T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6741 | chr2 | 200974529 | ||||||
| chr2:200974797 | T | C | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6473A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6473 | chr2 | 200974797 | ||||||
| chr2:200974872 | A | G | 2 | a0001c0001t0021 a0001c0001t0034 |
2 | HG02280.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6398T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6398 | chr2 | 200974872 | ||||||
| chr2:200974931 | T | C | 2 | a0001c0001t0014 a0001c0001t0043 |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6339A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6339 | chr2 | 200974931 | ||||||
| chr2:200975057 | T | A | 1 | a0001c0001t0029 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6213A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6213 | chr2 | 200975057 | ||||||
| chr2:200975232 | T | C | 1 | a0001c0001t0037 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6038A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6038 | chr2 | 200975232 | ||||||
| chr2:200975252 | C | T | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6018G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6018 | chr2 | 200975252 | ||||||
| chr2:200975360 | C | T | 1 | a0001c0001t0033 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5910G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5910 | chr2 | 200975360 | ||||||
| chr2:200975370 | T | C | 2 | a0001c0001t0005 a0002c0002t0005 |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5900A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5900 | chr2 | 200975370 | ||||||
| chr2:200975541 | T | A | 1 | a0001c0001t0038 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5729A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5729 | chr2 | 200975541 | ||||||
| chr2:200975669 | A | G | 1 | a0001c0001t0026 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5601T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5601 | chr2 | 200975669 | ||||||
| chr2:200975968 | T | A | 1 | a0001c0001t0026 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5302A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5302 | chr2 | 200975968 | ||||||
| chr2:200976197 | A | C | 2 | a0001c0001t0005 a0002c0002t0005 |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5073T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5073 | chr2 | 200976197 | ||||||
| chr2:200976207 | T | G | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5063A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5063 | chr2 | 200976207 | ||||||
| chr2:200976757 | A | G | 2 | a0001c0001t0027 a0001c0001t0031 |
2 | HG02109.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4513T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4513 | chr2 | 200976757 | ||||||
| chr2:200976782 | T | C | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4488A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4488 | chr2 | 200976782 | ||||||
| chr2:200977128 | T | C | 1 | a0001c0001t0039 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4142A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4142 | chr2 | 200977128 | ||||||
| chr2:200977285 | G | C | 1 | a0001c0001t0030 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3985C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3985 | chr2 | 200977285 | ||||||
| chr2:200977287 | G | A | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(5): Show |
33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3983C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3983 | chr2 | 200977287 | ||||||
| chr2:200977778 | G | A | 3 | a0001c0001t0011 a0001c0001t0040 a0001c0001t0041 |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3492C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3492 | chr2 | 200977778 | ||||||
| chr2:200977991 | C | T | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3279G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3279 | chr2 | 200977991 | ||||||
| chr2:200978126 | T | A | 1 | a0001c0001t0006 | 8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3144A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3144 | chr2 | 200978126 | ||||||
| chr2:200978127 | A | C | 1 | a0001c0001t0006 | 8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3143T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3143 | chr2 | 200978127 | ||||||
| chr2:200978464 | C | CT | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0034 others(1): Show |
13 | HG00140.hp1 HG00741.hp1 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2805dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2805 | chr2 | 200978464 | ||||||
| chr2:200978464 | CTT | C | 10 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0021 others(7): Show |
12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805delAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2804 | chr2 | 200978464 | ||||||
| chr2:200978464 | CTTT | C | 5 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0013 others(2): Show |
23 | HG01261.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2803_*2805delAAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2803 | chr2 | 200978464 | ||||||
| chr2:200978464 | CTTTT | C | 2 | a0001c0001t0005 a0002c0002t0005 |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2802_*2805delAAAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2802 | chr2 | 200978464 | ||||||
| chr2:200978464 | CTTTTT | C | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(5): Show |
34 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2801_*2805delAAAA others(1): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2801 | chr2 | 200978464 | ||||||
| chr2:200978534 | A | G | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(18): Show |
72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2736T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2736 | chr2 | 200978534 | ||||||
| chr2:200978761 | C | T | 1 | a0001c0001t0033 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2509G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2509 | chr2 | 200978761 | ||||||
| chr2:200978807 | G | A | 4 | a0001c0001t0013 a0001c0001t0019 a0001c0001t0028 others(1): Show |
6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2463C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2463 | chr2 | 200978807 | ||||||
| chr2:200979247 | T | C | 1 | a0001c0001t0022 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2023 | chr2 | 200979247 | ||||||
| chr2:200979264 | T | TAC | 11 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0017 others(8): Show |
24 | HG00099.hp1 HG00408.hp1 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2005dupGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2005 | chr2 | 200979264 | ||||||
| chr2:200979264 | TAC | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(10): Show |
46 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2005delGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2004 | chr2 | 200979264 | ||||||
| chr2:200979264 | TACAC | T | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(1): Show |
9 | HG01071.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2005delGTGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2002 | chr2 | 200979264 | ||||||
| chr2:200979264 | TACACAC | T | 3 | a0001c0001t0005 a0001c0001t0022 a0002c0002t0005 |
10 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2000_*2005delGTGT others(2): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2000 | chr2 | 200979264 | ||||||
| chr2:200979264 | TACACACA others(3): Show |
T | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996_*2005delGTGT others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1996 | chr2 | 200979264 | ||||||
| chr2:200979286 | C | T | 1 | a0001c0001t0020 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1984 | chr2 | 200979286 | ||||||
| chr2:200979525 | T | C | 1 | a0001c0001t0014 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1745 | chr2 | 200979525 | ||||||
| chr2:200979828 | C | A | 3 | a0001c0001t0011 a0001c0001t0040 a0001c0001t0041 |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1442 | chr2 | 200979828 | ||||||
| chr2:200979929 | G | A | 1 | a0001c0001t0042 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1341 | chr2 | 200979929 | ||||||
| chr2:200979948 | A | G | 1 | a0001c0001t0043 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1322 | chr2 | 200979948 | ||||||
| chr2:200980061 | CT | C | 2 | a0001c0001t0014 a0001c0001t0043 |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1208 | chr2 | 200980061 | ||||||
| chr2:200980485 | T | A | 1 | a0001c0001t0044 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 785 | chr2 | 200980485 | ||||||
| chr2:200980533 | C | T | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 737 | chr2 | 200980533 | ||||||
| chr2:200980680 | G | T | 1 | a0001c0001t0015 | 2 | HG00642.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*590C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 590 | chr2 | 200980680 | ||||||
| chr2:200980933 | C | G | 1 | a0001c0001t0018 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 337 | chr2 | 200980933 | ||||||
| chr2:200980986 | T | C | 1 | a0001c0001t0045 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 284 | chr2 | 200980986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200982084 | T | C | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1160-213A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982084 | |||||||
| chr2:200982196 | ATTC | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0017 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1160-328_1160-326d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982196 | |||||||
| chr2:200982204 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-333A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982204 | |||||||
| chr2:200982214 | C | T | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-343G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982214 | |||||||
| chr2:200982230 | GAAAAA | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-364_1160-360d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982230 | |||||||
| chr2:200982308 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1160-437A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982308 | |||||||
| chr2:200982536 | T | C | 4 | a0001c0001t0004g0001 a0001c0001t0004g0111 a0001c0001t0004g0112 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-665A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982536 | |||||||
| chr2:200982703 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1160-832G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982703 | |||||||
| chr2:200982883 | G | A | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1160-1012C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982883 | |||||||
| chr2:200982979 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0018g0056 |
2 | HG00408.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1160-1108C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982979 | |||||||
| chr2:200983047 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1160-1176G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983047 | |||||||
| chr2:200983154 | A | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160-1283T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983154 | |||||||
| chr2:200983163 | G | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(120): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1160-1292C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983163 | |||||||
| chr2:200983167 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-1296T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983167 | |||||||
| chr2:200983666 | CAT | C | 54 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(51): Show |
56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1160-1797_1160-179 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983666 | |||||||
| chr2:200983797 | G | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 others(3): Show |
6 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-1926C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983797 | |||||||
| chr2:200984390 | C | G | 23 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(20): Show |
23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.1160-2519G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984390 | |||||||
| chr2:200984545 | G | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-2674C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984545 | |||||||
| chr2:200984987 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1159+2378A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984987 | |||||||
| chr2:200985532 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1159+1833C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985532 | |||||||
| chr2:200985591 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1159+1774C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985591 | |||||||
| chr2:200985792 | A | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1159+1573T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985792 | |||||||
| chr2:200985833 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1159+1532G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985833 | |||||||
| chr2:200985834 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1159+1531A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985834 | |||||||
| chr2:200985873 | T | C | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1159+1492A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985873 | |||||||
| chr2:200985932 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+1433T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985932 | |||||||
| chr2:200986382 | T | C | 10 | a0001c0001t0003g0016 a0001c0001t0003g0110 a0001c0001t0003g0124 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1159+983A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986382 | |||||||
| chr2:200986508 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1159+857A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986508 | |||||||
| chr2:200986834 | T | C | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+531A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986834 | |||||||
| chr2:200987043 | A | G | 3 | a0001c0001t0004g0113 a0001c0001t0004g0119 a0001c0001t0025g0097 |
3 | HG02922.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1159+322T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200987043 | |||||||
| chr2:200988734 | A | G | 54 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(51): Show |
56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.832-313T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200988734 | |||||||
| chr2:200989107 | A | G | 6 | a0001c0001t0002g0030 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-686T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989107 | |||||||
| chr2:200989222 | A | G | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-801T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989222 | |||||||
| chr2:200989350 | T | C | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-929A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989350 | |||||||
| chr2:200989452 | C | A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-1031G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989452 | |||||||
| chr2:200989471 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-1050A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989471 | |||||||
| chr2:200989651 | A | G | 1 | a0001c0001t0010g0058 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.832-1230T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989651 | |||||||
| chr2:200989913 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.832-1492T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989913 | |||||||
| chr2:200990277 | T | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-1856A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990277 | |||||||
| chr2:200990475 | T | C | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+1806A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990475 | |||||||
| chr2:200990579 | CT | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+1701delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990579 | |||||||
| chr2:200990590 | T | C | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+1691A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990590 | |||||||
| chr2:200990621 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+1660C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990621 | |||||||
| chr2:200990665 | C | T | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+1616G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990665 | |||||||
| chr2:200990680 | C | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+1601G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990680 | |||||||
| chr2:200990831 | G | A | 79 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(76): Show |
81 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+1450C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990831 | |||||||
| chr2:200991315 | C | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.831+966G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991315 | |||||||
| chr2:200991420 | T | C | 1 | a0001c0001t0038g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+861A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991420 | |||||||
| chr2:200991568 | C | CA | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0037 others(10): Show |
13 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+712dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991568 | |||||||
| chr2:200991645 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+636C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991645 | |||||||
| chr2:200991645 | G | T | 1 | a0001c0001t0038g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+636C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991645 | |||||||
| chr2:200991754 | A | AAAAT | 71 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(68): Show |
73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.831+523_831+526dup others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991754 | |||||||
| chr2:200991784 | G | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+497C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991784 | |||||||
| chr2:200991896 | C | A | 1 | a0001c0001t0012g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.831+385G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991896 | |||||||
| chr2:200991937 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+344C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991937 | |||||||
| chr2:200992008 | T | G | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+273A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200992008 | |||||||
| chr2:200992143 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.831+138C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200992143 | |||||||
| chr2:200992379 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.744-11C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992379 | |||||||
| chr2:200992413 | C | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-45G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992413 | |||||||
| chr2:200992599 | A | T | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.744-231T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992599 | |||||||
| chr2:200992809 | G | A | 1 | a0002c0002t0005g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.743+78C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992809 | |||||||
| chr2:200993106 | A | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.627-103T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993106 | |||||||
| chr2:200993194 | A | G | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-191T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993194 | |||||||
| chr2:200993818 | A | G | 1 | a0001c0001t0042g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.627-815T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993818 | |||||||
| chr2:200993925 | A | G | 71 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(68): Show |
73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.627-922T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993925 | |||||||
| chr2:200993999 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.627-996C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993999 | |||||||
| chr2:200994192 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-1189C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994192 | |||||||
| chr2:200994277 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.627-1274G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994277 | |||||||
| chr2:200994527 | G | A | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.627-1524C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994527 | |||||||
| chr2:200994687 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.627-1684C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994687 | |||||||
| chr2:200994836 | A | G | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.627-1833T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994836 | |||||||
| chr2:200995290 | T | C | 1 | a0001c0001t0029g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.626+2155A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995290 | |||||||
| chr2:200995366 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.626+2079T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995366 | |||||||
| chr2:200995401 | TC | T | 4 | a0001c0001t0006g0098 a0001c0001t0006g0106 a0001c0001t0006g0108 others(1): Show |
4 | HG00741.hp2 HG01168.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+2043delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995401 | |||||||
| chr2:200995426 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+2019G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995426 | |||||||
| chr2:200996028 | C | CT | 24 | a0001c0001t0001g0054 a0001c0001t0001g0090 a0001c0001t0002g0015 others(21): Show |
24 | HG00408.hp2 HG00738.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+1416dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996028 | |||||||
| chr2:200996028 | CT | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0005g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+1416delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996028 | |||||||
| chr2:200996093 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.626+1352C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996093 | |||||||
| chr2:200996465 | T | TA | 11 | a0001c0001t0001g0024 a0001c0001t0005g0144 a0001c0001t0005g0146 others(8): Show |
11 | HG01192.hp2 HG01261.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+979dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996465 | |||||||
| chr2:200996581 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.626+864G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996581 | |||||||
| chr2:200996769 | T | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+676A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996769 | |||||||
| chr2:200996824 | C | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.626+621G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996824 | |||||||
| chr2:200996899 | C | G | 1 | a0001c0001t0004g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.626+546G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996899 | |||||||
| chr2:200996971 | A | G | 23 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(20): Show |
23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.626+474T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996971 | |||||||
| chr2:200997272 | C | T | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.626+173G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200997272 | |||||||
| chr2:200997429 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0007g0077 |
3 | HG01069.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.626+16A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200997429 | |||||||
| chr2:200997705 | A | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-165T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200997705 | |||||||
| chr2:200997813 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-273C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200997813 | |||||||
| chr2:200998245 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.531-705A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998245 | |||||||
| chr2:200998412 | T | C | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.531-872A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998412 | |||||||
| chr2:200998491 | C | T | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.531-951G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998491 | |||||||
| chr2:200998577 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-1037G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998577 | |||||||
| chr2:200998618 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.531-1078C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998618 | |||||||
| chr2:200998807 | T | C | 83 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(80): Show |
85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.531-1267A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998807 | |||||||
| chr2:200999080 | C | A | 71 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(68): Show |
73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.531-1540G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999080 | |||||||
| chr2:200999454 | C | G | 1 | a0001c0001t0007g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.531-1914G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999454 | |||||||
| chr2:200999472 | G | A | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-1932C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999472 | |||||||
| chr2:200999575 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.531-2035G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999575 | |||||||
| chr2:200999818 | C | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 others(3): Show |
6 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-2278G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999818 | |||||||
| chr2:200999834 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.531-2294G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999834 | |||||||
| chr2:200999927 | G | A | 19 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0053 others(16): Show |
19 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(16): Show |
intron_variant | MODIFIER | c.531-2387C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999927 | |||||||
| chr2:200999977 | G | A | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.531-2437C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999977 | |||||||
| chr2:201000057 | C | CA | 12 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0003g0124 others(9): Show |
12 | HG00733.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.531-2518dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | |||||||
| chr2:201000057 | C | CAAA | 7 | a0001c0001t0005g0144 a0001c0001t0005g0147 a0001c0001t0005g0151 others(4): Show |
7 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-2520_531-2518d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | |||||||
| chr2:201000057 | CA | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0052 others(7): Show |
10 | HG00408.hp1 HG01257.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-2518delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | |||||||
| chr2:201000124 | C | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-2584G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000124 | |||||||
| chr2:201000127 | T | C | 1 | a0001c0001t0009g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.531-2587A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000127 | |||||||
| chr2:201000319 | G | T | 2 | a0001c0001t0013g0006 a0001c0001t0032g0005 |
2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.531-2779C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000319 | |||||||
| chr2:201000436 | G | T | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-2896C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000436 | |||||||
| chr2:201000469 | G | A | 163 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.531-2929C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000469 | |||||||
| chr2:201000588 | AG | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.531-3049delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000588 | |||||||
| chr2:201000706 | T | C | 6 | a0001c0001t0008g0002 a0001c0001t0008g0099 a0001c0001t0008g0101 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-3166A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000706 | |||||||
| chr2:201000836 | AG | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-3297delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000836 | |||||||
| chr2:201000960 | C | T | 1 | a0001c0001t0043g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531-3420G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000960 | |||||||
| chr2:201000970 | C | CA | 10 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0003g0166 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-3431dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000970 | |||||||
| chr2:201001022 | C | T | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.531-3482G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001022 | |||||||
| chr2:201001121 | G | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531-3581C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001121 | |||||||
| chr2:201001135 | C | G | 1 | a0001c0001t0044g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531-3595G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001135 | |||||||
| chr2:201001137 | C | CA | 22 | a0001c0001t0001g0082 a0001c0001t0004g0103 a0001c0001t0005g0144 others(19): Show |
22 | HG01261.hp1 HG01515.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-3598dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001137 | |||||||
| chr2:201001147 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531-3607T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001147 | |||||||
| chr2:201001260 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-3720T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001260 | |||||||
| chr2:201001530 | C | T | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-3990G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001530 | |||||||
| chr2:201001642 | T | C | 1 | a0001c0001t0007g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.531-4102A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001642 | |||||||
| chr2:201001685 | T | G | 23 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(20): Show |
23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.531-4145A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001685 | |||||||
| chr2:201001702 | C | A | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-4162G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001702 | |||||||
| chr2:201001987 | T | G | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.531-4447A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001987 | |||||||
| chr2:201002149 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.531-4609A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002149 | |||||||
| chr2:201002273 | C | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-4733G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002273 | |||||||
| chr2:201002281 | C | CA | 26 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
26 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.531-4742dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002281 | |||||||
| chr2:201002629 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.531-5089C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002629 | |||||||
| chr2:201002775 | G | A | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-5235C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002775 | |||||||
| chr2:201002870 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-5330T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002870 | |||||||
| chr2:201002891 | G | A | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.531-5351C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002891 | |||||||
| chr2:201002906 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.531-5366T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002906 | |||||||
| chr2:201003050 | G | A | 1 | a0001c0001t0044g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531-5510C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003050 | |||||||
| chr2:201003317 | A | G | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+5656T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003317 | |||||||
| chr2:201003372 | G | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530+5601C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003372 | |||||||
| chr2:201003439 | G | A | 3 | a0001c0001t0017g0148 a0001c0001t0017g0149 a0001c0001t0034g0171 |
3 | HG02965.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+5534C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003439 | |||||||
| chr2:201003578 | G | A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+5395C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003578 | |||||||
| chr2:201003582 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0007g0040 |
2 | HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.530+5391C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003582 | |||||||
| chr2:201003805 | C | CT | 18 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0036 others(15): Show |
18 | HG00642.hp2 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.530+5167dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | |||||||
| chr2:201003805 | CT | C | 57 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0003g0016 others(54): Show |
59 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.530+5167delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | |||||||
| chr2:201003805 | CTT | C | 9 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(6): Show |
9 | HG01261.hp1 HG02080.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.530+5166_530+5167d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | |||||||
| chr2:201003805 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG01496.hp1 HG01515.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.530+5156_530+5167d others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | |||||||
| chr2:201003970 | C | G | 4 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(1): Show |
4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+5003G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003970 | |||||||
| chr2:201004005 | G | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+4968C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004005 | |||||||
| chr2:201004021 | G | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530+4952C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004021 | |||||||
| chr2:201004134 | C | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+4839G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004134 | |||||||
| chr2:201004307 | G | A | 6 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+4666C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004307 | |||||||
| chr2:201004396 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+4577A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004396 | |||||||
| chr2:201004447 | C | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02615.hp1 HG02615.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+4526G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004447 | |||||||
| chr2:201004679 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.530+4294G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004679 | |||||||
| chr2:201004768 | G | A | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.530+4205C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004768 | |||||||
| chr2:201004799 | C | T | 15 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+4174G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004799 | |||||||
| chr2:201005016 | C | CA | 34 | a0001c0001t0002g0044 a0001c0001t0004g0001 a0001c0001t0004g0100 others(31): Show |
36 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.530+3956dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005016 | |||||||
| chr2:201005096 | G | A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+3877C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005096 | |||||||
| chr2:201005232 | G | A | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.530+3741C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005232 | |||||||
| chr2:201005559 | A | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+3414T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005559 | |||||||
| chr2:201005721 | C | T | 1 | a0001c0001t0011g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+3252G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005721 | |||||||
| chr2:201005765 | G | A | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.530+3208C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005765 | |||||||
| chr2:201006026 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+2947C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006026 | |||||||
| chr2:201006130 | C | CT | 16 | a0001c0001t0003g0110 a0001c0001t0003g0132 a0001c0001t0004g0128 others(13): Show |
16 | HG01975.hp2 HG02027.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.530+2842dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006130 | |||||||
| chr2:201006188 | C | T | 1 | a0001c0001t0014g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530+2785G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006188 | |||||||
| chr2:201006295 | A | AT | 19 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0002g0076 others(16): Show |
19 | HG02080.hp1 HG02145.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+2677dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006295 | |||||||
| chr2:201006295 | AT | A | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+2677delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006295 | |||||||
| chr2:201006426 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.530+2547G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006426 | |||||||
| chr2:201006682 | T | C | 1 | a0001c0001t0004g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.530+2291A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006682 | |||||||
| chr2:201006781 | G | A | 1 | a0001c0001t0009g0003 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.530+2192C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006781 | |||||||
| chr2:201006947 | A | T | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+2026T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006947 | |||||||
| chr2:201007129 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.530+1844G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007129 | |||||||
| chr2:201007222 | A | G | 1 | a0001c0001t0006g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530+1751T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007222 | |||||||
| chr2:201007233 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+1740G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007233 | |||||||
| chr2:201007245 | C | T | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530+1728G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007245 | |||||||
| chr2:201007250 | A | G | 1 | a0001c0001t0004g0111 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.530+1723T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007250 | |||||||
| chr2:201007255 | A | G | 54 | a0001c0001t0002g0162 a0001c0001t0003g0016 a0001c0001t0003g0110 others(51): Show |
56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.530+1718T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007255 | |||||||
| chr2:201007288 | A | G | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1685T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007288 | |||||||
| chr2:201007327 | C | T | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1646G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007327 | |||||||
| chr2:201007457 | T | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1516A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007457 | |||||||
| chr2:201007537 | G | A | 1 | a0001c0001t0011g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+1436C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007537 | |||||||
| chr2:201007641 | C | T | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1332G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007641 | |||||||
| chr2:201007731 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+1242C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007731 | |||||||
| chr2:201007772 | A | G | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+1201T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007772 | |||||||
| chr2:201007784 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.530+1189T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007784 | |||||||
| chr2:201007969 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+1004A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007969 | |||||||
| chr2:201008184 | C | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+789G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008184 | |||||||
| chr2:201008530 | T | G | 1 | a0001c0001t0004g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.530+443A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008530 | |||||||
| chr2:201008595 | T | TAAATAAA others(13): Show |
9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+358_530+377dup others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008595 | |||||||
| chr2:201008687 | G | A | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.530+286C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008687 | |||||||
| chr2:201008918 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+55A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008918 | |||||||
| chr2:201009331 | A | G | 1 | a0001c0001t0043g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415-243T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009331 | |||||||
| chr2:201009648 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.415-560G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009648 | |||||||
| chr2:201009742 | G | A | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415-654C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009742 | |||||||
| chr2:201009852 | C | G | 1 | a0001c0001t0008g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.415-764G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009852 | |||||||
| chr2:201009864 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.415-776C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009864 | |||||||
| chr2:201009997 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.415-909C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009997 | |||||||
| chr2:201010014 | G | A | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-926C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010014 | |||||||
| chr2:201010103 | C | CA | 6 | a0001c0001t0001g0051 a0001c0001t0004g0001 a0001c0001t0004g0111 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-1016dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010103 | |||||||
| chr2:201010104 | A | C | 1 | a0001c0001t0036g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.415-1016T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010104 | |||||||
| chr2:201010196 | T | A | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.415-1108A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010196 | |||||||
| chr2:201010250 | G | C | 4 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(1): Show |
4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+1142C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010250 | |||||||
| chr2:201010307 | T | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+1085A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010307 | |||||||
| chr2:201010767 | A | AG | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+624dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010767 | |||||||
| chr2:201010786 | T | C | 6 | a0001c0001t0008g0002 a0001c0001t0008g0099 a0001c0001t0008g0101 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+606A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010786 | |||||||
| chr2:201010822 | T | A | 1 | a0001c0001t0007g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.414+570A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010822 | |||||||
| chr2:201010917 | C | T | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+475G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010917 | |||||||
| chr2:201010931 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414+461C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010931 | |||||||
| chr2:201011087 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414+305C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201011087 | |||||||
| chr2:201011329 | C | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+63G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201011329 | |||||||
| chr2:201011804 | A | C | 1 | a0001c0001t0013g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-332T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011804 | |||||||
| chr2:201011833 | C | T | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-361G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011833 | |||||||
| chr2:201011954 | A | T | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.334-482T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011954 | |||||||
| chr2:201012259 | A | T | 1 | a0001c0001t0005g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-787T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012259 | |||||||
| chr2:201012347 | G | A | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-875C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012347 | |||||||
| chr2:201012398 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-926A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012398 | |||||||
| chr2:201012593 | A | G | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-1121T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012593 | |||||||
| chr2:201012834 | A | G | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.334-1362T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012834 | |||||||
| chr2:201012952 | T | TAC | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0007g0092 others(3): Show |
6 | HG00408.hp1 HG02132.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1482_334-1481d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | |||||||
| chr2:201012952 | TAC | T | 85 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(82): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.334-1482_334-1481d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | |||||||
| chr2:201012952 | TACAC | T | 17 | a0001c0001t0001g0038 a0001c0001t0001g0156 a0001c0001t0002g0015 others(14): Show |
17 | HG01261.hp1 HG01496.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.334-1484_334-1481d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | |||||||
| chr2:201012952 | TACACAC | T | 10 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(7): Show |
10 | HG02615.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.334-1486_334-1481d others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | |||||||
| chr2:201012952 | TACACACA others(1): Show |
T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-1488_334-1481d others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | |||||||
| chr2:201013158 | G | A | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-1686C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013158 | |||||||
| chr2:201013163 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-1691T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013163 | |||||||
| chr2:201013436 | T | G | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-1964A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013436 | |||||||
| chr2:201013479 | CA | C | 5 | a0001c0001t0006g0104 a0001c0001t0007g0026 a0001c0001t0011g0160 others(2): Show |
5 | HG00140.hp1 HG01069.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2008delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013479 | |||||||
| chr2:201013483 | A | C | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-2011T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013483 | |||||||
| chr2:201013523 | T | A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2051A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013523 | |||||||
| chr2:201013526 | C | CCAAACAC others(1): Show |
2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-2062_334-2055d others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013526 | |||||||
| chr2:201013547 | C | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-2075G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013547 | |||||||
| chr2:201013580 | G | A | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.334-2108C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013580 | |||||||
| chr2:201013593 | A | G | 1 | a0001c0001t0005g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-2121T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013593 | |||||||
| chr2:201013664 | G | A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2192C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013664 | |||||||
| chr2:201013670 | C | G | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-2198G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013670 | |||||||
| chr2:201013829 | G | T | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2357C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013829 | |||||||
| chr2:201014078 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-2606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014078 | |||||||
| chr2:201014205 | A | G | 1 | a0001c0001t0004g0102 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.334-2733T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014205 | |||||||
| chr2:201014366 | C | T | 1 | a0001c0001t0009g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.333+2625G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014366 | |||||||
| chr2:201014669 | G | A | 1 | a0001c0001t0045g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2322C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014669 | |||||||
| chr2:201014732 | T | C | 14 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(11): Show |
14 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+2259A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014732 | |||||||
| chr2:201015058 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0015g0034 |
2 | HG00642.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.333+1933A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015058 | |||||||
| chr2:201015058 | TC | T | 6 | a0001c0001t0011g0157 a0001c0001t0011g0160 a0001c0001t0011g0161 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+1932delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015058 | |||||||
| chr2:201015170 | T | C | 1 | a0001c0001t0014g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+1821A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015170 | |||||||
| chr2:201015225 | A | G | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.333+1766T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015225 | |||||||
| chr2:201015382 | T | TTTC | 14 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(11): Show |
14 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+1608_333+1609i others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015382 | |||||||
| chr2:201015560 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.333+1431C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015560 | |||||||
| chr2:201015661 | T | C | 1 | a0001c0001t0003g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.333+1330A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015661 | |||||||
| chr2:201015790 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+1201G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015790 | |||||||
| chr2:201015833 | G | A | 1 | a0001c0001t0013g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.333+1158C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015833 | |||||||
| chr2:201015834 | C | T | 1 | a0001c0001t0013g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.333+1157G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015834 | |||||||
| chr2:201016201 | AAATAC | A | 21 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(18): Show |
21 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+785_333+789del others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016201 | |||||||
| chr2:201016230 | A | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.333+761T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016230 | |||||||
| chr2:201016392 | G | A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+599C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016392 | |||||||
| chr2:201016592 | A | G | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.333+399T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016592 | |||||||
| chr2:201016765 | A | G | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+226T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016765 | |||||||
| chr2:201016770 | C | T | 83 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(80): Show |
85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.333+221G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016770 | |||||||
| chr2:201016804 | T | A | 1 | a0001c0001t0012g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.333+187A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016804 | |||||||
| chr2:201016893 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+98C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016893 | |||||||
| chr2:201016954 | A | G | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.333+37T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016954 | |||||||
| chr2:201017260 | T | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-90A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017260 | |||||||
| chr2:201017314 | T | G | 1 | a0001c0001t0007g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154-144A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017314 | |||||||
| chr2:201017422 | GATT | G | 3 | a0001c0001t0002g0030 a0001c0001t0002g0045 a0001c0001t0002g0073 |
3 | HG03017.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.154-255_154-253del others(3): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017422 | |||||||
| chr2:201017930 | C | T | 1 | a0001c0001t0014g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-760G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017930 | |||||||
| chr2:201017938 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0015g0034 |
2 | HG00642.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.154-768A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017938 | |||||||
| chr2:201017961 | A | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154-791T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017961 | |||||||
| chr2:201018131 | A | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.154-961T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018131 | |||||||
| chr2:201018642 | T | C | 2 | a0001c0001t0006g0104 a0001c0001t0006g0107 |
2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.154-1472A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018642 | |||||||
| chr2:201018967 | C | G | 1 | a0001c0001t0007g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-1797G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018967 | |||||||
| chr2:201018994 | T | C | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1824A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018994 | |||||||
| chr2:201019197 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.154-2027A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019197 | |||||||
| chr2:201019215 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.154-2045A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019215 | |||||||
| chr2:201019392 | G | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-2222C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019392 | |||||||
| chr2:201019396 | A | AT | 2 | a0001c0001t0006g0104 a0001c0001t0006g0107 |
2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.154-2227dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019396 | |||||||
| chr2:201019418 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154-2248G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019418 | |||||||
| chr2:201019438 | AC | A | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-2269delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019438 | |||||||
| chr2:201019502 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.154-2332G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019502 | |||||||
| chr2:201019537 | G | A | 17 | a0001c0001t0001g0172 a0001c0001t0002g0030 a0001c0001t0002g0043 others(14): Show |
17 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-2367C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019537 | |||||||
| chr2:201019756 | T | TA | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-2587dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019756 | |||||||
| chr2:201019871 | C | A | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2701G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019871 | |||||||
| chr2:201019954 | G | A | 1 | a0002c0002t0005g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-2784C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019954 | |||||||
| chr2:201020422 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+2409C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020422 | |||||||
| chr2:201020543 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153+2288A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020543 | |||||||
| chr2:201020570 | A | T | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.153+2261T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020570 | |||||||
| chr2:201021004 | T | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0037 others(3): Show |
6 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1827A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021004 | |||||||
| chr2:201021288 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.153+1543G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021288 | |||||||
| chr2:201021635 | C | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+1196G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021635 | |||||||
| chr2:201021833 | G | A | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153+998C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021833 | |||||||
| chr2:201021945 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153+886C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021945 | |||||||
| chr2:201022370 | T | G | 1 | a0001c0001t0004g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.153+461A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022370 | |||||||
| chr2:201022443 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.153+388C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022443 | |||||||
| chr2:201022640 | T | G | 1 | a0001c0001t0004g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+191A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022640 | |||||||
| chr2:201023504 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.51+455A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023504 | |||||||
| chr2:201023594 | T | C | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.51+365A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023594 | |||||||
| chr2:201023607 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0017 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.51+352A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023607 | |||||||
| chr2:201023713 | G | A | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.51+246C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023713 | |||||||
| chr2:201023807 | A | T | 1 | a0001c0001t0004g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.51+152T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023807 | |||||||
| chr2:201023810 | C | A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+149G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023810 | |||||||
| chr2:201023852 | TATGTTTC others(15): Show |
T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.51+85_51+106delTAT others(19): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023852 | |||||||
| chr2:201023916 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.51+43C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023916 | |||||||
| chr2:201024217 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-178C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024217 | |||||||
| chr2:201024375 | G | A | 31 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0100 others(28): Show |
33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30-336C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024375 | |||||||
| chr2:201024395 | C | G | 1 | a0001c0001t0007g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30-356G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024395 | |||||||
| chr2:201024418 | G | A | 1 | a0001c0001t0004g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30-379C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024418 | |||||||
| chr2:201024467 | C | T | 6 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-428G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024467 | |||||||
| chr2:201024940 | A | G | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-901T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024940 | |||||||
| chr2:201024966 | A | T | 4 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0154 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-927T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024966 | |||||||
| chr2:201025028 | C | T | 31 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0100 others(28): Show |
33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30-989G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025028 | |||||||
| chr2:201025169 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30-1130A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025169 | |||||||
| chr2:201025387 | A | C | 1 | a0001c0001t0014g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-30-1348T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025387 | |||||||
| chr2:201025457 | G | GAAAGA | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-1423_-30-1419d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025457 | |||||||
| chr2:201025487 | A | G | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-1448T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025487 | |||||||
| chr2:201025751 | T | C | 1 | a0001c0001t0045g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30-1712A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025751 | |||||||
| chr2:201025906 | T | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0017 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-1867A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025906 | |||||||
| chr2:201025928 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0015g0008 |
3 | HG01192.hp1 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-30-1889C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025928 | |||||||
| chr2:201025974 | T | C | 2 | a0001c0001t0002g0074 a0001c0001t0012g0075 |
2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-30-1935A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025974 | |||||||
| chr2:201025994 | G | C | 1 | a0001c0001t0005g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-30-1955C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025994 | |||||||
| chr2:201026081 | A | T | 1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-30-2042T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026081 | |||||||
| chr2:201026134 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-2095A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026134 | |||||||
| chr2:201026169 | C | A | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-2130G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026169 | |||||||
| chr2:201026471 | A | T | 8 | a0001c0001t0006g0098 a0001c0001t0006g0104 a0001c0001t0006g0105 others(5): Show |
8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-2432T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026471 | |||||||
| chr2:201026574 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-2535G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026574 | |||||||
| chr2:201026866 | A | G | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-30-2827T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026866 | |||||||
| chr2:201026983 | T | C | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30-2944A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026983 | |||||||
| chr2:201027014 | T | G | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-2975A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027014 | |||||||
| chr2:201027029 | G | T | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-30-2990C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027029 | |||||||
| chr2:201027070 | G | A | 8 | a0001c0001t0004g0100 a0001c0001t0005g0151 a0001c0001t0005g0152 others(5): Show |
8 | HG02080.hp1 HG02083.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-3031C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027070 | |||||||
| chr2:201027197 | T | G | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-30-3158A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027197 | |||||||
| chr2:201027279 | C | T | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30-3240G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027279 | |||||||
| chr2:201027409 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-3370A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027409 | |||||||
| chr2:201027465 | G | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-3426C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027465 | |||||||
| chr2:201027553 | C | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-30-3514G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027553 | |||||||
| chr2:201027577 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-30-3538G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027577 | |||||||
| chr2:201027766 | C | G | 1 | a0001c0001t0002g0072 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-30-3727G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027766 | |||||||
| chr2:201027792 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3753G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027792 | |||||||
| chr2:201027796 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3757C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027796 | |||||||
| chr2:201027799 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3760A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027799 | |||||||
| chr2:201027812 | A | T | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3773T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027812 | |||||||
| chr2:201027826 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3787G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027826 | |||||||
| chr2:201027833 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3794A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027833 | |||||||
| chr2:201027844 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3805A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027844 | |||||||
| chr2:201027946 | G | A | 1 | a0001c0001t0020g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-30-3907C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027946 | |||||||
| chr2:201027948 | TG | T | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-3910delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027948 | |||||||
| chr2:201027969 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-30-3930A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027969 | |||||||
| chr2:201027993 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30-3954C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027993 | |||||||
| chr2:201028076 | G | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-4037C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028076 | |||||||
| chr2:201028109 | C | G | 1 | a0001c0001t0043g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-30-4070G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028109 | |||||||
| chr2:201028137 | G | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-4098C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028137 | |||||||
| chr2:201028228 | G | C | 1 | a0001c0001t0020g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-30-4189C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028228 | |||||||
| chr2:201028357 | G | C | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-4318C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028357 | |||||||
| chr2:201028436 | T | C | 1 | a0001c0001t0004g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-30-4397A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028436 | |||||||
| chr2:201028465 | T | C | 78 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(75): Show |
80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-30-4426A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028465 | |||||||
| chr2:201028537 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-30-4498C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028537 | |||||||
| chr2:201028611 | C | G | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30-4572G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028611 | |||||||
| chr2:201028636 | A | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-4597T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028636 | |||||||
| chr2:201028693 | G | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-4654C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028693 | |||||||
| chr2:201028709 | G | A | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-4670C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028709 | |||||||
| chr2:201028742 | G | A | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-30-4703C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028742 | |||||||
| chr2:201028882 | A | G | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30-4843T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028882 | |||||||
| chr2:201028902 | G | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-30-4863C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028902 | |||||||
| chr2:201029139 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-30-5100C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029139 | |||||||
| chr2:201029152 | G | T | 1 | a0001c0001t0043g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-30-5113C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029152 | |||||||
| chr2:201029191 | C | A | 6 | a0001c0001t0008g0002 a0001c0001t0008g0099 a0001c0001t0008g0101 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-5152G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029191 | |||||||
| chr2:201029296 | A | G | 70 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(67): Show |
72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-5257T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029296 | |||||||
| chr2:201029735 | C | G | 1 | a0001c0001t0033g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-5696G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029735 | |||||||
| chr2:201029851 | G | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-30-5812C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029851 | |||||||
| chr2:201029963 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0021g0173 a0001c0001t0037g0062 |
3 | HG00099.hp1 HG02080.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-30-5924C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029963 | |||||||
| chr2:201030094 | A | G | 1 | a0001c0001t0011g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30-6055T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030094 | |||||||
| chr2:201030107 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-30-6068G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030107 | |||||||
| chr2:201030220 | A | T | 78 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(75): Show |
80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-30-6181T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030220 | |||||||
| chr2:201030315 | T | A | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30-6276A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030315 | |||||||
| chr2:201030570 | T | G | 6 | a0001c0001t0008g0002 a0001c0001t0008g0099 a0001c0001t0008g0101 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-6531A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030570 | |||||||
| chr2:201030582 | C | CT | 21 | a0001c0001t0001g0065 a0001c0001t0002g0030 a0001c0001t0002g0043 others(18): Show |
21 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30-6544dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030582 | |||||||
| chr2:201030586 | T | C | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30-6547A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030586 | |||||||
| chr2:201030760 | G | A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-6721C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030760 | |||||||
| chr2:201031025 | GTGT | G | 2 | a0001c0001t0004g0100 a0001c0001t0029g0118 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-30-6989_-30-6987d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031025 | |||||||
| chr2:201031344 | A | G | 1 | a0001c0001t0009g0003 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-30-7305T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031344 | |||||||
| chr2:201031592 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-7553C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031592 | |||||||
| chr2:201031644 | T | C | 70 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(67): Show |
72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-7605A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031644 | |||||||
| chr2:201031843 | T | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-7804A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031843 | |||||||
| chr2:201032086 | G | A | 2 | a0001c0001t0008g0121 a0001c0001t0035g0122 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-8047C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201032086 | |||||||
| chr2:201033145 | TTGTA | T | 2 | a0001c0001t0008g0121 a0001c0001t0035g0122 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-9110_-30-9107d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033145 | |||||||
| chr2:201033149 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-30-9126_-30-9111d others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033149 | |||||||
| chr2:201033155 | GTGTA | G | 2 | a0001c0001t0003g0164 a0001c0001t0012g0020 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-30-9120_-30-9117d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033155 | |||||||
| chr2:201033157 | GTA | G | 10 | a0001c0001t0003g0127 a0001c0001t0003g0129 a0001c0001t0003g0130 others(7): Show |
10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-9120_-30-9119d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033157 | |||||||
| chr2:201033159 | A | ATG | 15 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0172 others(12): Show |
15 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-9122_-30-9121d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | |||||||
| chr2:201033159 | A | ATGTG | 9 | a0001c0001t0001g0032 a0001c0001t0001g0079 a0001c0001t0001g0081 others(6): Show |
9 | HG00558.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9124_-30-9121d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | |||||||
| chr2:201033159 | A | G | 45 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(42): Show |
47 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30-9120T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | |||||||
| chr2:201033159 | ATG | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0038 others(9): Show |
12 | HG00741.hp1 HG01243.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-9122_-30-9121d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | |||||||
| chr2:201033159 | ATGTG | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0066 a0001c0001t0001g0087 others(6): Show |
9 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9124_-30-9121d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | |||||||
| chr2:201033188 | T | A | 1 | a0001c0001t0003g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30-9149A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033188 | |||||||
| chr2:201033190 | T | A | 15 | a0001c0001t0003g0131 a0001c0001t0003g0164 a0001c0001t0004g0100 others(12): Show |
16 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30-9151A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033190 | |||||||
| chr2:201033190 | TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9161_-30-9152d others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033190 | |||||||
| chr2:201033192 | T | A | 47 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0125 others(44): Show |
49 | HG00642.hp1 HG00733.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-30-9153A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033192 | |||||||
| chr2:201033192 | T | TGA | 3 | a0001c0001t0006g0107 a0001c0001t0006g0108 a0001c0001t0024g0168 |
3 | HG00280.hp2 HG01168.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30-9154_-30-9153i others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033192 | |||||||
| chr2:201033194 | T | A | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-30-9155A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033194 | |||||||
| chr2:201033194 | T | TGAGA | 2 | a0001c0001t0034g0171 a0001c0001t0041g0158 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30-9156_-30-9155i others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033194 | |||||||
| chr2:201033196 | T | A | 60 | a0001c0001t0001g0038 a0001c0001t0002g0162 a0001c0001t0003g0110 others(57): Show |
62 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30-9157A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033196 | T | TGA | 2 | a0001c0001t0005g0144 a0001c0001t0005g0153 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-30-9159_-30-9158d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033196 | T | TGTGA | 9 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0151 others(6): Show |
9 | HG01071.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033196 | T | TGTGTGAG others(1): Show |
2 | a0001c0001t0007g0026 a0001c0001t0042g0049 |
2 | HG00140.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033196 | T | TGTGTGTG others(1): Show |
2 | a0001c0001t0002g0017 a0001c0001t0003g0016 |
2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033196 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0002g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-30-9158_-30-9157i others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | |||||||
| chr2:201033198 | A | T | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG01952.hp2 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-9159T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033198 | |||||||
| chr2:201033200 | A | T | 2 | a0001c0001t0014g0094 a0001c0001t0014g0096 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-30-9161T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033200 | |||||||
| chr2:201033243 | C | T | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-9204G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033243 | |||||||
| chr2:201033339 | G | C | 9 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0127 others(6): Show |
9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-9300C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033339 | |||||||
| chr2:201033371 | A | ATTTAT | 11 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
11 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-9337_-30-9333d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | |||||||
| chr2:201033371 | ATTTAT | A | 26 | a0001c0001t0001g0022 a0001c0001t0002g0162 a0001c0001t0003g0124 others(23): Show |
26 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30-9337_-30-9333d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | |||||||
| chr2:201033371 | ATTTATTT others(3): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-30-9342_-30-9333d others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | |||||||
| chr2:201033504 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30-9465G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033504 | |||||||
| chr2:201033505 | G | A | 4 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(1): Show |
4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-9466C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033505 | |||||||
| chr2:201033704 | C | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-9665G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033704 | |||||||
| chr2:201033722 | A | AT | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9684dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033722 | |||||||
| chr2:201033731 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-30-9692C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033731 | |||||||
| chr2:201033913 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-9874A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033913 | |||||||
| chr2:201033925 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-30-9886A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033925 | |||||||
| chr2:201034162 | A | ACAT | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-10126_-30-1012 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034162 | |||||||
| chr2:201034415 | A | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-10376T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034415 | |||||||
| chr2:201034477 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30-10438G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034477 | |||||||
| chr2:201034562 | T | C | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-10523A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034562 | |||||||
| chr2:201034801 | G | C | 1 | a0001c0001t0008g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+10695C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034801 | |||||||
| chr2:201034826 | C | T | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-31+10670G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034826 | |||||||
| chr2:201035115 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+10381C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035115 | |||||||
| chr2:201035166 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+10330T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035166 | |||||||
| chr2:201035226 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0120 a0001c0001t0033g0123 |
3 | HG00733.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-31+10270G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035226 | |||||||
| chr2:201035293 | G | C | 1 | a0001c0001t0006g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-31+10203C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035293 | |||||||
| chr2:201035296 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+10200G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035296 | |||||||
| chr2:201035300 | T | A | 1 | a0001c0001t0009g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-31+10196A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035300 | |||||||
| chr2:201035407 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+10089A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035407 | |||||||
| chr2:201035417 | G | A | 14 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0103 others(11): Show |
15 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31+10079C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035417 | |||||||
| chr2:201035763 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-31+9733G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035763 | |||||||
| chr2:201035798 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-31+9698C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035798 | |||||||
| chr2:201035851 | G | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+9645C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035851 | |||||||
| chr2:201036067 | A | G | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+9429T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036067 | |||||||
| chr2:201036447 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-31+9049T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036447 | |||||||
| chr2:201036466 | C | G | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+9030G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036466 | |||||||
| chr2:201036513 | C | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+8983G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036513 | |||||||
| chr2:201036697 | C | G | 1 | a0001c0001t0032g0005 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-31+8799G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036697 | |||||||
| chr2:201036948 | G | A | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+8548C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036948 | |||||||
| chr2:201037194 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+8302C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037194 | |||||||
| chr2:201037251 | A | C | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+8245T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037251 | |||||||
| chr2:201037543 | G | C | 1 | a0001c0001t0004g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31+7953C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037543 | |||||||
| chr2:201037621 | G | C | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+7875C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037621 | |||||||
| chr2:201037650 | T | C | 1 | a0001c0001t0010g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+7846A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037650 | |||||||
| chr2:201037827 | C | T | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+7669G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037827 | |||||||
| chr2:201037938 | C | T | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7558G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037938 | |||||||
| chr2:201037939 | A | G | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7557T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037939 | |||||||
| chr2:201037988 | T | A | 70 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(67): Show |
72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-31+7508A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037988 | |||||||
| chr2:201038074 | T | C | 1 | a0001c0001t0010g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+7422A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038074 | |||||||
| chr2:201038083 | A | C | 1 | a0001c0001t0010g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+7413T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038083 | |||||||
| chr2:201038553 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-31+6943G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038553 | |||||||
| chr2:201038561 | C | T | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+6935G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038561 | |||||||
| chr2:201038618 | T | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+6878A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038618 | |||||||
| chr2:201038845 | G | A | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31+6651C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038845 | |||||||
| chr2:201038913 | T | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6583A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038913 | |||||||
| chr2:201038928 | TA | T | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+6567delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038928 | |||||||
| chr2:201039104 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+6392G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039104 | |||||||
| chr2:201039216 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+6280G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039216 | |||||||
| chr2:201039410 | T | G | 1 | a0001c0001t0008g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+6086A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039410 | |||||||
| chr2:201039578 | C | T | 78 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(75): Show |
80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-31+5918G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039578 | |||||||
| chr2:201039723 | G | A | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+5773C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039723 | |||||||
| chr2:201039736 | C | T | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+5760G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039736 | |||||||
| chr2:201039742 | G | A | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+5754C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039742 | |||||||
| chr2:201039743 | T | C | 83 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(80): Show |
85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-31+5753A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039743 | |||||||
| chr2:201039971 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-31+5525C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039971 | |||||||
| chr2:201040002 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-31+5494C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040002 | |||||||
| chr2:201040130 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0073 |
2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-31+5366C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040130 | |||||||
| chr2:201040441 | T | TTTG | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+5052_-31+5054d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040441 | |||||||
| chr2:201040459 | G | GT | 6 | a0001c0001t0001g0021 a0001c0001t0004g0113 a0001c0001t0004g0119 others(3): Show |
6 | HG00280.hp2 HG01175.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5036dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040459 | |||||||
| chr2:201040459 | G | T | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+5037C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040459 | |||||||
| chr2:201040462 | T | G | 1 | a0001c0001t0011g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-31+5034A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040462 | |||||||
| chr2:201040646 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+4850C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040646 | |||||||
| chr2:201040765 | G | A | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+4731C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040765 | |||||||
| chr2:201040941 | A | G | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+4555T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040941 | |||||||
| chr2:201040996 | T | TAAACCCT others(24): Show |
1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31+4469_-31+4499d others(33): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040996 | |||||||
| chr2:201041139 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-31+4357T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041139 | |||||||
| chr2:201041366 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-31+4130G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041366 | |||||||
| chr2:201041792 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-31+3704T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041792 | |||||||
| chr2:201041845 | T | C | 1 | a0001c0001t0010g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+3651A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041845 | |||||||
| chr2:201041938 | T | C | 83 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(80): Show |
85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-31+3558A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041938 | |||||||
| chr2:201042005 | G | C | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-31+3491C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042005 | |||||||
| chr2:201042046 | C | T | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+3450G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042046 | |||||||
| chr2:201042073 | C | G | 1 | a0001c0001t0015g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-31+3423G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042073 | |||||||
| chr2:201042089 | T | C | 2 | a0001c0001t0003g0159 a0001c0001t0003g0166 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-31+3407A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042089 | |||||||
| chr2:201042102 | A | C | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-31+3394T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042102 | |||||||
| chr2:201042158 | G | T | 1 | a0001c0001t0017g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+3338C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042158 | |||||||
| chr2:201042301 | C | T | 1 | a0001c0001t0007g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31+3195G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042301 | |||||||
| chr2:201042532 | A | AC | 16 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0063 others(13): Show |
16 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+2963dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042532 | |||||||
| chr2:201042598 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+2898C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042598 | |||||||
| chr2:201042632 | G | A | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31+2864C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042632 | |||||||
| chr2:201042664 | G | C | 1 | a0001c0001t0045g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-31+2832C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042664 | |||||||
| chr2:201042692 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+2804C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042692 | |||||||
| chr2:201042741 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2755C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042741 | |||||||
| chr2:201042755 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+2741C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042755 | |||||||
| chr2:201042839 | A | AC | 9 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0068 others(6): Show |
9 | HG01175.hp2 HG01433.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+2656dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042839 | |||||||
| chr2:201042854 | T | TG | 25 | a0001c0001t0001g0065 a0001c0001t0002g0162 a0001c0001t0003g0124 others(22): Show |
25 | HG00408.hp2 HG01192.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31+2641dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042854 | |||||||
| chr2:201042910 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0005g0144 a0001c0001t0005g0146 others(7): Show |
10 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+2586C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042910 | |||||||
| chr2:201042917 | A | AC | 20 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0063 others(17): Show |
20 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-31+2578dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042917 | |||||||
| chr2:201043041 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2455A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043041 | |||||||
| chr2:201043191 | G | C | 1 | a0001c0001t0004g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-31+2305C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043191 | |||||||
| chr2:201043432 | T | TA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+2063dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043432 | |||||||
| chr2:201043432 | T | TAA | 10 | a0001c0001t0005g0144 a0001c0001t0005g0147 a0001c0001t0005g0151 others(7): Show |
10 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31+2062_-31+2063d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043432 | |||||||
| chr2:201043434 | A | T | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2062T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043434 | |||||||
| chr2:201043446 | A | G | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-31+2050T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043446 | |||||||
| chr2:201043447 | A | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31+2049T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043447 | |||||||
| chr2:201043450 | G | A | 3 | a0001c0001t0004g0114 a0001c0001t0008g0121 a0001c0001t0035g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-31+2046C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043450 | |||||||
| chr2:201043466 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-31+2030T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043466 | |||||||
| chr2:201043569 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+1927G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043569 | |||||||
| chr2:201043638 | A | G | 18 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0100 others(15): Show |
19 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-31+1858T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043638 | |||||||
| chr2:201043814 | G | A | 74 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(71): Show |
76 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-31+1682C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043814 | |||||||
| chr2:201044335 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+1161C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044335 | |||||||
| chr2:201044425 | A | G | 1 | a0001c0001t0009g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31+1071T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044425 | |||||||
| chr2:201044556 | G | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+940C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044556 | |||||||
| chr2:201044670 | C | T | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+826G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044670 | |||||||
| chr2:201044792 | A | G | 28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0032 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.-31+704T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044792 | |||||||
| chr2:201044847 | C | T | 1 | a0001c0001t0010g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+649G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044847 | |||||||
| chr2:201044971 | A | G | 1 | a0001c0001t0037g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-31+525T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044971 | |||||||
| chr2:201045172 | C | T | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+324G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045172 | |||||||
| chr2:201045173 | G | A | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+323C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045173 | |||||||
| chr2:201045305 | A | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+191T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045305 | |||||||
| chr2:201045480 | A | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+16T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045480 | |||||||
| chr2:201045607 | A | G | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-128-14T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045607 | |||||||
| chr2:201045665 | T | C | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-128-72A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045665 | |||||||
| chr2:201045936 | T | C | 9 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0127 others(6): Show |
9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-343A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045936 | |||||||
| chr2:201046006 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-128-413G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046006 | |||||||
| chr2:201046118 | A | G | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-525T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046118 | |||||||
| chr2:201046235 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-128-642A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046235 | |||||||
| chr2:201046239 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-128-646T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046239 | |||||||
| chr2:201046371 | T | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-778A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046371 | |||||||
| chr2:201046424 | G | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-831C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046424 | |||||||
| chr2:201046426 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-833C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046426 | |||||||
| chr2:201046441 | A | G | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-848T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046441 | |||||||
| chr2:201046719 | G | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-1126C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046719 | |||||||
| chr2:201046903 | A | T | 1 | a0001c0001t0023g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-128-1310T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046903 | |||||||
| chr2:201046987 | T | C | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-1394A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046987 | |||||||
| chr2:201047199 | A | G | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-1606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047199 | |||||||
| chr2:201047268 | G | T | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-128-1675C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047268 | |||||||
| chr2:201047445 | C | CAT | 5 | a0001c0001t0001g0063 a0001c0001t0002g0071 a0001c0001t0008g0121 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-1854_-128-185 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATAT | 2 | a0001c0001t0004g0114 a0001c0001t0019g0138 |
2 | HG00642.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-128-1856_-128-185 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(1): Show |
11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-128-1860_-128-185 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(3): Show |
4 | a0001c0001t0002g0162 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02647.hp1 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-1862_-128-185 others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(5): Show |
23 | a0001c0001t0003g0110 a0001c0001t0003g0125 a0001c0001t0004g0001 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-128-1864_-128-185 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(7): Show |
12 | a0001c0001t0003g0124 a0001c0001t0003g0129 a0001c0001t0003g0130 others(9): Show |
12 | HG00733.hp1 HG01515.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.-128-1866_-128-185 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(9): Show |
3 | a0001c0001t0003g0127 a0001c0001t0004g0103 a0001c0001t0008g0115 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-128-1868_-128-185 others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(11): Show |
1 | a0001c0001t0003g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-128-1870_-128-185 others(22): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(13): Show |
5 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0004g0100 others(2): Show |
5 | HG02083.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-1872_-128-185 others(24): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(15): Show |
4 | a0001c0001t0003g0159 a0001c0001t0011g0160 a0001c0001t0011g0161 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-1853_-128-185 others(26): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(17): Show |
2 | a0001c0001t0011g0157 a0001c0001t0024g0168 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-128-1853_-128-185 others(28): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | C | CATATATA others(19): Show |
1 | a0001c0001t0003g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-128-1853_-128-185 others(30): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047445 | CAT | C | 2 | a0001c0001t0028g0135 a0001c0001t0044g0047 |
2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-128-1854_-128-185 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | |||||||
| chr2:201047465 | T | TATATATA others(7): Show |
1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-128-1873_-128-187 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047465 | |||||||
| chr2:201047559 | G | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(5): Show |
8 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-1966C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047559 | |||||||
| chr2:201047680 | A | G | 1 | a0001c0001t0028g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-128-2087T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047680 | |||||||
| chr2:201047795 | ACTGTTAA others(5): Show |
A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-2214_-128-220 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047795 | |||||||
| chr2:201047890 | C | CA | 40 | a0001c0001t0001g0081 a0001c0001t0002g0162 a0001c0001t0003g0124 others(37): Show |
41 | HG00099.hp1 HG00741.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.-128-2298dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047890 | |||||||
| chr2:201047890 | C | CAA | 8 | a0001c0001t0001g0021 a0001c0001t0002g0015 a0001c0001t0002g0017 others(5): Show |
8 | HG01175.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-2299_-128-229 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047890 | |||||||
| chr2:201048506 | A | AT | 61 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(58): Show |
63 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-128-2914dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048506 | |||||||
| chr2:201048506 | A | ATTT | 6 | a0001c0001t0005g0146 a0001c0001t0005g0151 a0001c0001t0005g0152 others(3): Show |
6 | HG02886.hp1 HG02897.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-128-2916_-128-291 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048506 | |||||||
| chr2:201048522 | A | T | 78 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(75): Show |
80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-128-2929T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048522 | |||||||
| chr2:201048542 | G | A | 4 | a0001c0001t0002g0074 a0001c0001t0005g0154 a0001c0001t0005g0155 others(1): Show |
4 | HG00099.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-2949C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048542 | |||||||
| chr2:201048561 | A | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-2968T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048561 | |||||||
| chr2:201048706 | C | G | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-3113G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048706 | |||||||
| chr2:201048859 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-3266G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048859 | |||||||
| chr2:201049199 | A | G | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-128-3606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049199 | |||||||
| chr2:201049389 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-3796C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049389 | |||||||
| chr2:201049510 | C | T | 1 | a0001c0001t0004g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-3917G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049510 | |||||||
| chr2:201049517 | T | G | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-3924A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049517 | |||||||
| chr2:201049587 | T | C | 1 | a0001c0001t0002g0010 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-128-3994A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049587 | |||||||
| chr2:201049642 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0015g0008 |
3 | HG01192.hp1 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-128-4049G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049642 | |||||||
| chr2:201049658 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-128-4065A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049658 | |||||||
| chr2:201049891 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-128-4298G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049891 | |||||||
| chr2:201050110 | C | G | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-4517G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050110 | |||||||
| chr2:201050122 | G | A | 6 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-4529C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050122 | |||||||
| chr2:201050159 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-4566T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050159 | |||||||
| chr2:201050212 | T | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-4619A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050212 | |||||||
| chr2:201050213 | CA | C | 6 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-128-4621delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050213 | |||||||
| chr2:201050599 | GA | G | 6 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(3): Show |
6 | HG02486.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-5007delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050599 | |||||||
| chr2:201050607 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-128-5014T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050607 | |||||||
| chr2:201050628 | C | G | 1 | a0001c0001t0042g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-128-5035G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050628 | |||||||
| chr2:201050759 | A | AC | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-5167dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050759 | |||||||
| chr2:201051085 | T | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-5492A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051085 | |||||||
| chr2:201051322 | A | G | 6 | a0001c0001t0011g0157 a0001c0001t0011g0160 a0001c0001t0011g0161 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-5729T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051322 | |||||||
| chr2:201051352 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG01496.hp1 HG01515.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-128-5759C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051352 | |||||||
| chr2:201051695 | G | C | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-6102C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051695 | |||||||
| chr2:201052105 | T | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-6512A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052105 | |||||||
| chr2:201052246 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-6653C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052246 | |||||||
| chr2:201052276 | A | G | 3 | a0001c0001t0011g0160 a0001c0001t0011g0161 a0001c0001t0040g0165 |
3 | HG02622.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-128-6683T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052276 | |||||||
| chr2:201052285 | G | A | 2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-128-6692C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052285 | |||||||
| chr2:201052354 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-128-6761G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052354 | |||||||
| chr2:201052443 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-128-6850T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052443 | |||||||
| chr2:201052900 | G | C | 5 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(2): Show |
5 | HG02486.hp1 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-7307C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052900 | |||||||
| chr2:201053019 | A | G | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-7426T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053019 | |||||||
| chr2:201053209 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-7616C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053209 | |||||||
| chr2:201053215 | T | C | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-7622A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053215 | |||||||
| chr2:201053236 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-128-7643G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053236 | |||||||
| chr2:201053416 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-7823T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053416 | |||||||
| chr2:201053505 | C | G | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-128-7912G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053505 | |||||||
| chr2:201053612 | G | A | 2 | a0001c0001t0004g0100 a0001c0001t0029g0118 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-128-8019C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053612 | |||||||
| chr2:201053736 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-128-8143C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053736 | |||||||
| chr2:201053882 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-8289A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053882 | |||||||
| chr2:201054083 | C | T | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-8490G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054083 | |||||||
| chr2:201054096 | T | G | 3 | a0001c0001t0001g0172 a0001c0001t0002g0069 a0001c0001t0002g0084 |
3 | HG03491.hp1 NA18963.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-128-8503A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054096 | |||||||
| chr2:201054122 | C | G | 1 | a0001c0001t0003g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-128-8529G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054122 | |||||||
| chr2:201054289 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0007g0077 |
3 | HG01069.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-128-8696A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054289 | |||||||
| chr2:201054498 | T | A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-8905A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054498 | |||||||
| chr2:201054629 | C | G | 1 | a0001c0001t0004g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-9036G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054629 | |||||||
| chr2:201054825 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-9232C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054825 | |||||||
| chr2:201055042 | T | C | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-9449A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055042 | |||||||
| chr2:201055243 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-9650G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055243 | |||||||
| chr2:201055337 | G | A | 51 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(48): Show |
53 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-128-9744C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055337 | |||||||
| chr2:201055383 | G | GA | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-9791dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055383 | |||||||
| chr2:201055384 | A | G | 2 | a0001c0001t0027g0143 a0001c0001t0031g0018 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-9791T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055384 | |||||||
| chr2:201055493 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-128-9900C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055493 | |||||||
| chr2:201055494 | T | A | 1 | a0001c0001t0002g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-128-9901A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055494 | |||||||
| chr2:201055500 | A | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0120 a0001c0001t0033g0123 |
3 | HG00733.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-128-9907T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055500 | |||||||
| chr2:201055555 | A | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-9962T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055555 | |||||||
| chr2:201055895 | T | C | 31 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0100 others(28): Show |
33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-128-10302A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055895 | |||||||
| chr2:201056016 | G | A | 4 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(1): Show |
4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-10423C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056016 | |||||||
| chr2:201056060 | G | T | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-128-10467C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056060 | |||||||
| chr2:201056121 | G | T | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-10528C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056121 | |||||||
| chr2:201056143 | G | A | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-128-10550C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056143 | |||||||
| chr2:201056151 | G | A | 1 | a0001c0001t0013g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-128-10558C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056151 | |||||||
| chr2:201056175 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-128-10582C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056175 | |||||||
| chr2:201056188 | C | A | 9 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0127 others(6): Show |
9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-10595G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056188 | |||||||
| chr2:201056201 | A | T | 14 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(11): Show |
14 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128-10608T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056201 | |||||||
| chr2:201056204 | A | AAATAAAT others(4): Show |
2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-10612_-128-10 others(17): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056204 | |||||||
| chr2:201056205 | T | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-10612A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056205 | |||||||
| chr2:201056205 | T | TAAATAAA others(2): Show |
11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-128-10613_-128-10 others(15): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056205 | |||||||
| chr2:201056535 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-10942C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056535 | |||||||
| chr2:201056606 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-128-11013C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056606 | |||||||
| chr2:201056674 | C | CA | 10 | a0001c0001t0005g0144 a0001c0001t0013g0004 a0001c0001t0013g0006 others(7): Show |
10 | HG00741.hp1 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-128-11082dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056674 | |||||||
| chr2:201056718 | T | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-11125A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056718 | |||||||
| chr2:201056739 | T | C | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-11146A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056739 | |||||||
| chr2:201057010 | G | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-11417C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057010 | |||||||
| chr2:201057198 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-128-11605T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057198 | |||||||
| chr2:201057874 | A | C | 1 | a0001c0001t0026g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-12281T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057874 | |||||||
| chr2:201058008 | C | T | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-12415G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058008 | |||||||
| chr2:201058014 | T | C | 1 | a0001c0001t0003g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128-12421A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058014 | |||||||
| chr2:201058262 | A | G | 1 | a0001c0001t0008g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-128-12669T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058262 | |||||||
| chr2:201058298 | A | C | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-12705T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058298 | |||||||
| chr2:201058411 | T | C | 1 | a0001c0001t0007g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-128-12818A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058411 | |||||||
| chr2:201058434 | A | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-12841T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058434 | |||||||
| chr2:201058568 | G | A | 2 | a0001c0001t0016g0019 a0001c0001t0016g0027 |
2 | NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-128-12975C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058568 | |||||||
| chr2:201058599 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-13006C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058599 | |||||||
| chr2:201058621 | C | A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129+12989G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058621 | |||||||
| chr2:201058759 | C | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
8 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-129+12851G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058759 | |||||||
| chr2:201058912 | C | T | 17 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(14): Show |
17 | HG02280.hp1 HG02615.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-129+12698G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058912 | |||||||
| chr2:201059200 | C | T | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+12410G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059200 | |||||||
| chr2:201059231 | T | C | 1 | a0001c0001t0004g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-129+12379A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059231 | |||||||
| chr2:201059335 | T | C | 2 | a0001c0001t0034g0171 a0001c0001t0040g0165 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-129+12275A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059335 | |||||||
| chr2:201059355 | C | T | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-129+12255G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059355 | |||||||
| chr2:201059635 | G | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11975C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059635 | |||||||
| chr2:201059726 | G | C | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11884C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059726 | |||||||
| chr2:201059765 | A | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11845T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059765 | |||||||
| chr2:201059792 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+11818A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059792 | |||||||
| chr2:201059876 | T | A | 2 | a0001c0001t0009g0003 a0001c0001t0009g0141 |
3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-129+11734A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059876 | |||||||
| chr2:201059905 | C | T | 4 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129+11705G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059905 | |||||||
| chr2:201060009 | T | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(120): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-129+11601A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060009 | |||||||
| chr2:201060054 | C | CG | 39 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0032 others(36): Show |
40 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-129+11555dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | |||||||
| chr2:201060054 | C | CGG | 15 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-129+11554_-129+11 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | |||||||
| chr2:201060054 | CGG | C | 18 | a0001c0001t0002g0162 a0001c0001t0003g0127 a0001c0001t0003g0129 others(15): Show |
18 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-129+11554_-129+11 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | |||||||
| chr2:201060059 | G | C | 1 | a0001c0001t0004g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-129+11551C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060059 | |||||||
| chr2:201060060 | G | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+11550C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060060 | |||||||
| chr2:201060065 | G | C | 2 | a0001c0001t0003g0166 a0001c0001t0014g0096 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-129+11545C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | |||||||
| chr2:201060065 | G | GT | 4 | a0001c0001t0004g0100 a0001c0001t0006g0098 a0001c0001t0008g0099 others(1): Show |
4 | HG02027.hp2 HG02083.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129+11544_-129+11 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | |||||||
| chr2:201060065 | G | T | 27 | a0001c0001t0003g0110 a0001c0001t0004g0001 a0001c0001t0004g0102 others(24): Show |
29 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-129+11545C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | |||||||
| chr2:201060066 | G | C | 9 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0151 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+11544C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060066 | |||||||
| chr2:201060066 | G | GC | 2 | a0001c0001t0005g0144 a0002c0002t0005g0150 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-129+11543_-129+11 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060066 | |||||||
| chr2:201060101 | G | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+11509C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060101 | |||||||
| chr2:201060210 | G | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11400C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060210 | |||||||
| chr2:201060562 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+11048A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060562 | |||||||
| chr2:201060619 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+10991A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060619 | |||||||
| chr2:201060738 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+10872T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060738 | |||||||
| chr2:201061072 | CA | C | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02109.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+10537delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061072 | |||||||
| chr2:201061078 | A | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+10532T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061078 | |||||||
| chr2:201061092 | T | C | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+10518A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061092 | |||||||
| chr2:201061127 | G | C | 1 | a0001c0001t0024g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-129+10483C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061127 | |||||||
| chr2:201061627 | GT | G | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+9982delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061627 | |||||||
| chr2:201061635 | T | A | 1 | a0001c0001t0007g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-129+9975A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061635 | |||||||
| chr2:201061641 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-129+9969T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061641 | |||||||
| chr2:201062115 | A | G | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+9495T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062115 | |||||||
| chr2:201062377 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+9233C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062377 | |||||||
| chr2:201062524 | A | G | 163 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-129+9086T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062524 | |||||||
| chr2:201062591 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+9019G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062591 | |||||||
| chr2:201062646 | G | C | 1 | a0001c0001t0033g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-129+8964C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062646 | |||||||
| chr2:201063119 | G | A | 22 | a0001c0001t0002g0162 a0001c0001t0003g0124 a0001c0001t0003g0125 others(19): Show |
22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-129+8491C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063119 | |||||||
| chr2:201063170 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-129+8440C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063170 | |||||||
| chr2:201063197 | C | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+8413G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063197 | |||||||
| chr2:201063198 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-129+8412C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063198 | |||||||
| chr2:201063266 | G | A | 1 | a0001c0001t0045g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-129+8344C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063266 | |||||||
| chr2:201063360 | C | T | 53 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(50): Show |
55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-129+8250G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063360 | |||||||
| chr2:201063563 | G | A | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+8047C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063563 | |||||||
| chr2:201063762 | A | G | 170 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-129+7848T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063762 | |||||||
| chr2:201063878 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-129+7732C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063878 | |||||||
| chr2:201063886 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-129+7724G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063886 | |||||||
| chr2:201063948 | G | T | 2 | a0001c0001t0021g0173 a0001c0001t0034g0171 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-129+7662C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063948 | |||||||
| chr2:201064003 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-129+7607A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064003 | |||||||
| chr2:201064308 | AT | A | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+7301delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064308 | |||||||
| chr2:201064395 | G | T | 3 | a0001c0001t0014g0094 a0001c0001t0014g0095 a0001c0001t0014g0096 |
3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-129+7215C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064395 | |||||||
| chr2:201064483 | T | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+7127A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064483 | |||||||
| chr2:201064496 | T | C | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+7114A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064496 | |||||||
| chr2:201064530 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG00738.hp1 HG01257.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-129+7080C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064530 | |||||||
| chr2:201064530 | G | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+7080C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064530 | |||||||
| chr2:201064909 | T | C | 6 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+6701A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064909 | |||||||
| chr2:201064945 | T | C | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+6665A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064945 | |||||||
| chr2:201064974 | C | G | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+6636G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064974 | |||||||
| chr2:201065043 | G | T | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+6567C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065043 | |||||||
| chr2:201065338 | T | C | 1 | a0001c0001t0007g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-129+6272A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065338 | |||||||
| chr2:201065521 | G | A | 8 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(5): Show |
8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+6089C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065521 | |||||||
| chr2:201065957 | C | T | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-129+5653G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065957 | |||||||
| chr2:201066019 | A | T | 1 | a0001c0001t0016g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-129+5591T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066019 | |||||||
| chr2:201066085 | T | G | 1 | a0001c0001t0010g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-129+5525A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066085 | |||||||
| chr2:201066100 | CAG | C | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+5508_-129+550 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066100 | |||||||
| chr2:201066207 | A | G | 78 | a0001c0001t0002g0162 a0001c0001t0003g0110 a0001c0001t0003g0124 others(75): Show |
80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-129+5403T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066207 | |||||||
| chr2:201066669 | T | C | 1 | a0001c0001t0024g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-129+4941A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066669 | |||||||
| chr2:201066698 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+4912G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066698 | |||||||
| chr2:201066699 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+4911C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066699 | |||||||
| chr2:201066856 | C | T | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+4754G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066856 | |||||||
| chr2:201066887 | T | C | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+4723A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066887 | |||||||
| chr2:201067007 | T | C | 83 | a0001c0001t0001g0156 a0001c0001t0002g0015 a0001c0001t0002g0017 others(80): Show |
85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-129+4603A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067007 | |||||||
| chr2:201067201 | G | T | 9 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(6): Show |
9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+4409C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067201 | |||||||
| chr2:201067233 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+4377G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067233 | |||||||
| chr2:201067385 | T | C | 1 | a0001c0001t0005g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-129+4225A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067385 | |||||||
| chr2:201068050 | C | T | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-129+3560G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068050 | |||||||
| chr2:201068075 | C | T | 1 | a0001c0001t0031g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+3535G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068075 | |||||||
| chr2:201068076 | G | A | 1 | a0001c0001t0019g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-129+3534C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068076 | |||||||
| chr2:201068211 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+3399G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068211 | |||||||
| chr2:201068244 | G | A | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+3366C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068244 | |||||||
| chr2:201068347 | C | T | 2 | a0001c0001t0017g0148 a0001c0001t0017g0149 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+3263G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068347 | |||||||
| chr2:201068398 | G | A | 13 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+3212C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068398 | |||||||
| chr2:201068487 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0003g0016 |
3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+3123G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068487 | |||||||
| chr2:201068920 | C | CA | 5 | a0001c0001t0009g0003 a0001c0001t0009g0139 a0001c0001t0009g0141 others(2): Show |
6 | HG02647.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+2689dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068920 | |||||||
| chr2:201069007 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-129+2603G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069007 | |||||||
| chr2:201069077 | T | G | 1 | a0001c0001t0027g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-129+2533A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069077 | |||||||
| chr2:201069193 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+2417T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069193 | |||||||
| chr2:201069500 | T | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0146 a0001c0001t0005g0147 others(8): Show |
11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+2110A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069500 | |||||||
| chr2:201069542 | AAACAC | A | 2 | a0001c0001t0001g0059 a0001c0001t0002g0076 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-129+2063_-129+206 others(9): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069542 | |||||||
| chr2:201069543 | AAC | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0021 others(16): Show |
19 | HG01175.hp2 HG01192.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-129+2065_-129+206 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACAC | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(15): Show |
18 | HG01496.hp1 HG01496.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.-129+2063_-129+206 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACAC | A | 23 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0032 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.-129+2061_-129+206 others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(1): Show |
A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0055 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(15): Show |
intron_variant | MODIFIER | c.-129+2059_-129+206 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(3): Show |
A | 26 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0051 others(23): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-129+2057_-129+206 others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(5): Show |
A | 28 | a0001c0001t0003g0110 a0001c0001t0003g0124 a0001c0001t0003g0127 others(25): Show |
29 | HG00280.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-129+2055_-129+206 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(7): Show |
A | 8 | a0001c0001t0003g0125 a0001c0001t0003g0130 a0001c0001t0003g0131 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+2053_-129+206 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0052 a0001c0001t0023g0126 |
2 | HG02055.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-129+2051_-129+206 others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(13): Show |
A | 1 | a0001c0001t0006g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-129+2047_-129+206 others(24): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(15): Show |
A | 5 | a0001c0001t0008g0121 a0001c0001t0014g0094 a0001c0001t0014g0095 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129+2045_-129+206 others(26): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(19): Show |
A | 5 | a0001c0001t0013g0004 a0001c0001t0013g0006 a0001c0001t0013g0136 others(2): Show |
5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129+2041_-129+206 others(30): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069543 | AACACACA others(25): Show |
A | 1 | a0001c0001t0043g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-129+2035_-129+206 others(36): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | |||||||
| chr2:201069579 | C | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+2031G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | |||||||
| chr2:201069579 | C | CACAA | 8 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-129+2030_-129+203 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | |||||||
| chr2:201069579 | C | CACACACA others(1): Show |
2 | a0001c0001t0005g0146 a0001c0001t0005g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-129+2030_-129+203 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | |||||||
| chr2:201069614 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(5): Show |
8 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+1996G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069614 | |||||||
| chr2:201070095 | A | G | 1 | a0001c0001t0032g0005 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-129+1515T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070095 | |||||||
| chr2:201070307 | A | G | 2 | a0001c0001t0013g0006 a0001c0001t0032g0005 |
2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-129+1303T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070307 | |||||||
| chr2:201070451 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+1159C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070451 | |||||||
| chr2:201070649 | T | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+961A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070649 | |||||||
| chr2:201070677 | T | C | 13 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0163 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+933A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070677 | |||||||
| chr2:201070781 | T | G | 1 | a0001c0001t0011g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-129+829A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070781 | |||||||
| chr2:201071002 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+608T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071002 | |||||||
| chr2:201071077 | G | C | 1 | a0001c0001t0008g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-129+533C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071077 | |||||||
| chr2:201071138 | G | A | 1 | a0001c0001t0034g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+472C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071138 | |||||||
| chr2:201071279 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+331C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071279 | |||||||
| chr2:201071303 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+307C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071303 | |||||||
| chr2:201071378 | C | G | 1 | a0001c0001t0013g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-129+232G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071378 |