Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 494470 |
|---|---|
| ensemblid | ENSG00000141622.14 |
| hgncid | 31696 |
| symbol | ARK2C |
| name | arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C |
| refseq_nuc | NM_152470.3 |
| refseq_prot | NP_689683.2 |
| ensembl_nuc | ENST00000269439.12 |
| ensembl_prot | ENSP00000269439.6 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 46334018 |
| end | 46463140 |
| strand | + |
| ver | v1.2 |
| region | chr18:46334018-46463140 |
| region5000 | chr18:46329018-46468140 |
| regionname0 | ARK2C_chr18_46334018_46463140 |
| regionname5000 | ARK2C_chr18_46329018_46468140 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 346 | 259 | 80 | 52 | 84 | 8 | 33 | 60 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0002 | 0/0 | 346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1041 | 252 | 79 | 48 | 83 | 8 | 33 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| c0002 | 0/1 | 1041 | 5 | 0 | 4 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| c0003 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| c0004 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| c0005 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6756 | 51 | 5 | 7 | 31 | 1 | 7 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0002 | 0/0 | 6762 | 34 | 0 | 7 | 18 | 3 | 6 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0003 | 1/0 | 6762 | 22 | 18 | 2 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0004 | 0/0 | 6756 | 16 | 0 | 1 | 15 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0005 | 0/0 | 6762 | 14 | 1 | 7 | 1 | 1 | 4 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0006 | 0/0 | 6763 | 8 | 2 | 1 | 0 | 1 | 4 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0007 | 0/0 | 6762 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0008 | 0/0 | 6762 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0009 | 0/0 | 6756 | 7 | 0 | 2 | 4 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0010 | 0/1 | 6762 | 6 | 0 | 5 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0011 | 0/0 | 6756 | 6 | 0 | 4 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0012 | 0/0 | 6762 | 5 | 5 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0013 | 0/0 | 6756 | 4 | 0 | 3 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0014 | 0/0 | 6764 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0015 | 0/0 | 6756 | 3 | 1 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0016 | 0/0 | 6763 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0017 | 0/0 | 6756 | 3 | 1 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0018 | 0/0 | 6762 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0019 | 0/0 | 6756 | 2 | 0 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0020 | 0/0 | 6762 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0021 | 0/0 | 6762 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0022 | 0/0 | 6756 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0023 | 0/0 | 6756 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0024 | 0/0 | 6762 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0025 | 0/0 | 6763 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0026 | 0/0 | 6757 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0027 | 0/0 | 6762 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0028 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0029 | 0/0 | 6757 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0030 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0031 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0032 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0033 | 0/0 | 6762 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0034 | 0/0 | 6762 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0035 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0036 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0037 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0038 | 0/0 | 6762 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0039 | 0/0 | 6757 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0040 | 0/0 | 6762 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0041 | 0/0 | 6751 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0042 | 0/0 | 6764 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0043 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0044 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0045 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0046 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0047 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0048 | 0/0 | 6762 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0049 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0050 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0051 | 0/0 | 6756 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0052 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0053 | 0/0 | 6762 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0054 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0055 | 0/0 | 6757 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0056 | 0/0 | 6756 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0057 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0058 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0059 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0060 | 0/0 | 6762 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0061 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0062 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0063 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0064 | 0/0 | 6756 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0065 | 0/0 | 6762 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0066 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| t0067 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1041 | 252 | 79 | 48 | 83 | 8 | 33 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0002 | 0/1 | 1041 | 5 | 0 | 4 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0004 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0005 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0002c0003 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7796 | 50 | 5 | 7 | 30 | 1 | 7 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0002 | 0/0 | 7802 | 34 | 0 | 7 | 18 | 3 | 6 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0003 | 1/0 | 7802 | 22 | 18 | 2 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0004 | 0/0 | 7796 | 16 | 0 | 1 | 15 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0005 | 0/0 | 7802 | 13 | 1 | 7 | 1 | 1 | 3 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0006 | 0/0 | 7803 | 8 | 2 | 1 | 0 | 1 | 4 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0007 | 0/0 | 7802 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0008 | 0/0 | 7802 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0009 | 0/0 | 7796 | 7 | 0 | 2 | 4 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0010 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0011 | 0/0 | 7796 | 6 | 0 | 4 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0012 | 0/0 | 7802 | 4 | 4 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0013 | 0/0 | 7796 | 4 | 0 | 3 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0014 | 0/0 | 7804 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0015 | 0/0 | 7796 | 3 | 1 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0016 | 0/0 | 7803 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0017 | 0/0 | 7796 | 3 | 1 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0018 | 0/0 | 7802 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0019 | 0/0 | 7796 | 2 | 0 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0020 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0021 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0022 | 0/0 | 7796 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0023 | 0/0 | 7796 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0024 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0025 | 0/0 | 7803 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0026 | 0/0 | 7797 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0027 | 0/0 | 7802 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0028 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0029 | 0/0 | 7797 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0030 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0031 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0032 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0033 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0034 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0035 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0036 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0037 | 0/0 | 7797 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0038 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0039 | 0/0 | 7797 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0040 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0041 | 0/0 | 7791 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0042 | 0/0 | 7804 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0043 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0044 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0045 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0046 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0047 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0048 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0049 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0050 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0051 | 0/0 | 7796 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0052 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0053 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0054 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0055 | 0/0 | 7797 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0056 | 0/0 | 7796 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0057 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0058 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0059 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0060 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0061 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0062 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0063 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0064 | 0/0 | 7796 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0065 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0066 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0001t0067 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0002t0010 | 0/1 | 7802 | 5 | 0 | 4 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0004t0012 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0001c0005t0001 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| a0002c0003t0005 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | copy fasta | chr18 | 46329018 | 46468140 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0018g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0018g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0019g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0019g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0020g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0021g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0021g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0022g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0022g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0023g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0023g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0024g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0024g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0025g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0025g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0026g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0026g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0027g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0027g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0028g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0029g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0030g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0031g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0032g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0033g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0034g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0035g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0036g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0037g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0038g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0039g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0040g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0041g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0042g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0043g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0044g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0045g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0046g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0047g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0048g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0049g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0050g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0051g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0052g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0053g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0054g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0055g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0056g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0057g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0058g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0059g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0060g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0061g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0062g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0063g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0064g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0065g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0066g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0067g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0002t0010g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0002t0010g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0002t0010g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0004t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0002c0003t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00140 | hp1 | a0001 | c0001 | t0064 | g0084 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0144 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0140 | EUR | FIN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00639 | hp2 | a0001 | c0002 | t0010 | g0001 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00642 | hp1 | a0001 | c0002 | t0010 | g0001 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00733 | hp2 | a0001 | c0001 | t0019 | g0138 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0137 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01069 | hp1 | a0001 | c0001 | t0029 | g0002 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01069 | hp2 | a0001 | c0001 | t0015 | g0041 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01071 | hp1 | a0001 | c0002 | t0010 | g0176 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01071 | hp2 | a0001 | c0001 | t0019 | g0002 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0001 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01099 | hp2 | a0001 | c0001 | t0049 | g0020 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01106 | hp1 | a0001 | c0001 | t0044 | g0166 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0083 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0241 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01109 | hp2 | a0001 | c0001 | t0042 | g0230 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01175 | hp2 | a0001 | c0001 | t0039 | g0040 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0131 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01243 | hp2 | a0001 | c0001 | t0067 | g0179 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01257 | hp2 | a0001 | c0001 | t0013 | g0151 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0227 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01358 | hp2 | a0001 | c0001 | t0010 | g0101 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01361 | hp1 | a0001 | c0001 | t0009 | g0146 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0102 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0256 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01496 | hp2 | a0001 | c0001 | t0050 | g0175 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0057 | EUR | IBS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0079 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0202 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01981 | hp2 | a0001 | c0001 | t0056 | g0172 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02145 | hp1 | a0001 | c0001 | t0025 | g0091 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0167 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02155 | hp2 | a0001 | c0001 | t0034 | g0200 | EAS | CDX | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02257 | hp2 | a0001 | c0001 | t0028 | g0096 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02258 | hp2 | a0001 | c0001 | t0025 | g0030 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0070 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02300 | hp2 | a0001 | c0001 | t0051 | g0248 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02451 | hp2 | a0001 | c0001 | t0021 | g0092 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02523 | hp2 | a0001 | c0001 | t0059 | g0188 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0078 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0013 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02615 | hp1 | a0001 | c0001 | t0043 | g0008 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0220 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0221 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0245 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0226 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02683 | hp2 | a0001 | c0001 | t0033 | g0051 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02717 | hp2 | a0001 | c0001 | t0036 | g0173 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0081 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0232 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02809 | hp2 | a0001 | c0001 | t0065 | g0198 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02818 | hp1 | a0001 | c0004 | t0012 | g0174 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02886 | hp1 | a0001 | c0001 | t0045 | g0075 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0236 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0061 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0156 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0076 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0240 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03098 | hp1 | a0001 | c0001 | t0018 | g0231 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0028 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0077 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0177 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03225 | hp1 | a0001 | c0001 | t0035 | g0196 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03239 | hp1 | a0001 | c0001 | t0011 | g0142 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03486 | hp1 | a0001 | c0001 | t0058 | g0048 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0155 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0153 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03491 | hp2 | a0001 | c0001 | t0027 | g0014 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03492 | hp2 | a0002 | c0003 | t0005 | g0125 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03540 | hp1 | a0001 | c0001 | t0047 | g0027 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0218 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03579 | hp1 | a0001 | c0001 | t0057 | g0080 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03654 | hp2 | a0001 | c0001 | t0040 | g0069 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0056 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03831 | hp1 | a0001 | c0001 | t0027 | g0162 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03942 | hp1 | a0001 | c0001 | t0041 | g0066 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0237 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04199 | hp1 | a0001 | c0001 | t0053 | g0114 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04199 | hp2 | a0001 | c0001 | t0038 | g0133 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0085 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04228 | hp1 | a0001 | c0001 | t0055 | g0082 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18522 | hp1 | a0001 | c0001 | t0046 | g0025 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0235 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18950 | hp2 | a0001 | c0001 | t0026 | g0022 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18960 | hp2 | a0001 | c0001 | t0017 | g0150 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18962 | hp1 | a0001 | c0001 | t0022 | g0214 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18963 | hp2 | a0001 | c0001 | t0026 | g0052 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18964 | hp1 | a0001 | c0001 | t0054 | g0242 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0219 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18970 | hp1 | a0001 | c0001 | t0017 | g0149 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18970 | hp2 | a0001 | c0001 | t0048 | g0141 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0111 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18993 | hp2 | a0001 | c0001 | t0022 | g0216 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19010 | hp2 | a0001 | c0001 | t0013 | g0124 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0193 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19030 | hp2 | a0001 | c0001 | t0066 | g0190 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19060 | hp1 | a0001 | c0005 | t0001 | g0204 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19066 | hp2 | a0001 | c0001 | t0061 | g0128 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19083 | hp1 | a0001 | c0001 | t0052 | g0191 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0163 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19084 | hp2 | a0001 | c0001 | t0060 | g0244 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19085 | hp2 | a0001 | c0001 | t0063 | g0043 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20129 | hp1 | a0001 | c0001 | t0017 | g0239 | AFR | ASW | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | ASW | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20905 | hp1 | a0001 | c0001 | t0023 | g0042 | SAS | GIH | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | GIH | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02109 | hp2 | a0001 | c0001 | t0062 | g0032 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03471 | hp2 | a0001 | c0001 | t0031 | g0063 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | USA | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | USA | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA21309 | hp1 | a0001 | c0001 | t0030 | g0062 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0010 | g0126 | REF | REF | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0046 | REF | REF | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46456066
|
T | G | 1 | a0002 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.909T>G | p.Asp303Glu | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 7/8 | 1166/7802 | 909/1041 | 303/346 | chr18 | 46456066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46435352
|
A | G | 1 | a0001c0002 | 5 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(2): Show |
synonymous_variant | LOW | c.441A>G | p.Gln147Gln | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/8 | 698/7802 | 441/1041 | 147/346 | chr18 | 46435352 | ||
| chr18:46435361
|
A | T | 1 | a0001c0005 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.450A>T | p.Thr150Thr | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/8 | 707/7802 | 450/1041 | 150/346 | chr18 | 46435361 | ||
| chr18:46456570
|
C | G | 1 | a0001c0004 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.975C>G | p.Leu325Leu | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1232/7802 | 975/1041 | 325/346 | chr18 | 46456570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46456858
|
A | G | 3 | a0001c0001t0065a0001c0001t0066a0001c0001t0067 | 3 | HG01243.hp2 HG02809.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*222A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 222 | chr18 | 46456858 | |||||
| chr18:46456965
|
C | T | 1 | a0001c0001t0064 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*329C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 329 | chr18 | 46456965 | |||||
| chr18:46457135
|
C | T | 1 | a0001c0001t0009 | 7 | HG00280.hp2 HG01361.hp1 HG01433.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*499C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 499 | chr18 | 46457135 | |||||
| chr18:46457316
|
G | A | 1 | a0001c0001t0028 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 680 | chr18 | 46457316 | |||||
| chr18:46457371
|
C | T | 1 | a0001c0001t0063 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*735C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 735 | chr18 | 46457371 | |||||
| chr18:46457469
|
A | G | 1 | a0001c0001t0062 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 833 | chr18 | 46457469 | |||||
| chr18:46457635
|
G | A | 2 | a0001c0001t0019a0001c0001t0029 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 999 | chr18 | 46457635 | |||||
| chr18:46457766
|
T | C | 4 | a0001c0001t0014a0001c0001t0020a0001c0001t0030others(1): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1130T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1130 | chr18 | 46457766 | |||||
| chr18:46458030
|
C | A | 1 | a0001c0001t0032 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1394 | chr18 | 46458030 | |||||
| chr18:46458081
|
G | A | 1 | a0001c0001t0032 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1445G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1445 | chr18 | 46458081 | |||||
| chr18:46458087
|
G | A | 1 | a0001c0001t0033 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1451 | chr18 | 46458087 | |||||
| chr18:46458243
|
C | G | 3 | a0001c0001t0011a0001c0001t0060a0001c0001t0061 | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1607C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1607 | chr18 | 46458243 | |||||
| chr18:46458414
|
G | A | 1 | a0001c0001t0034 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1778G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1778 | chr18 | 46458414 | |||||
| chr18:46458480
|
A | G | 31 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(28): Show | 123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1844A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1844 | chr18 | 46458480 | |||||
| chr18:46458594
|
C | T | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(22): Show | 106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1958C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1958 | chr18 | 46458594 | |||||
| chr18:46458595
|
G | A | 1 | a0001c0001t0035 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1959 | chr18 | 46458595 | |||||
| chr18:46458616
|
A | G | 1 | a0001c0001t0061 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 1980 | chr18 | 46458616 | |||||
| chr18:46458667
|
C | T | 1 | a0001c0001t0059 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2031C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2031 | chr18 | 46458667 | |||||
| chr18:46458720
|
T | C | 3 | a0001c0001t0011a0001c0001t0060a0001c0001t0061 | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2084 | chr18 | 46458720 | |||||
| chr18:46458830
|
T | C | 1 | a0001c0001t0028 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2194 | chr18 | 46458830 | |||||
| chr18:46458886
|
G | A | 1 | a0001c0001t0065 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2250G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2250 | chr18 | 46458886 | |||||
| chr18:46458891
|
A | G | 1 | a0001c0001t0046 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2255A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2255 | chr18 | 46458891 | |||||
| chr18:46459110
|
C | G | 3 | a0001c0001t0011a0001c0001t0060a0001c0001t0061 | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2474C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2474 | chr18 | 46459110 | |||||
| chr18:46459262
|
C | T | 4 | a0001c0001t0014a0001c0001t0030a0001c0001t0047others(1): Show | 6 | HG02896.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2626C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2626 | chr18 | 46459262 | |||||
| chr18:46459414
|
A | G | 4 | a0001c0001t0011a0001c0001t0028a0001c0001t0060others(1): Show | 9 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2778A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2778 | chr18 | 46459414 | |||||
| chr18:46459471
|
G | C | 3 | a0001c0001t0011a0001c0001t0060a0001c0001t0061 | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2835G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2835 | chr18 | 46459471 | |||||
| chr18:46459569
|
G | A | 2 | a0001c0001t0021a0001c0001t0036 | 3 | HG02451.hp2 HG02717.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2933G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2933 | chr18 | 46459569 | |||||
| chr18:46459607
|
T | C | 4 | a0001c0001t0011a0001c0001t0028a0001c0001t0060others(1): Show | 9 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2971T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2971 | chr18 | 46459607 | |||||
| chr18:46459619
|
C | T | 4 | a0001c0001t0011a0001c0001t0028a0001c0001t0060others(1): Show | 9 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2983C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 2983 | chr18 | 46459619 | |||||
| chr18:46459680
|
G | A | 1 | a0001c0001t0050 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3044G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3044 | chr18 | 46459680 | |||||
| chr18:46459726
|
C | T | 1 | a0001c0001t0045 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3090C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3090 | chr18 | 46459726 | |||||
| chr18:46459844
|
C | A | 1 | a0001c0001t0017 | 3 | NA18960.hp2 NA18970.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3208C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3208 | chr18 | 46459844 | |||||
| chr18:46460247
|
G | A | 1 | a0001c0001t0051 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3611G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3611 | chr18 | 46460247 | |||||
| chr18:46460252
|
T | C | 4 | a0001c0001t0011a0001c0001t0028a0001c0001t0060others(1): Show | 9 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3616T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3616 | chr18 | 46460252 | |||||
| chr18:46460253
|
A | C | 4 | a0001c0001t0011a0001c0001t0028a0001c0001t0060others(1): Show | 9 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3617A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3617 | chr18 | 46460253 | |||||
| chr18:46460384
|
A | C | 1 | a0001c0001t0024 | 2 | HG02647.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3748A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3748 | chr18 | 46460384 | |||||
| chr18:46460512
|
T | G | 1 | a0001c0001t0033 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3876 | chr18 | 46460512 | |||||
| chr18:46460596
|
G | A | 6 | a0001c0001t0004a0001c0001t0013a0001c0001t0017others(3): Show | 27 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3960G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3960 | chr18 | 46460596 | |||||
| chr18:46460634
|
C | A | 2 | a0001c0001t0037a0001c0001t0062 | 2 | HG02109.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 3998 | chr18 | 46460634 | |||||
| chr18:46460651
|
G | A | 1 | a0001c0001t0038 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4015 | chr18 | 46460651 | |||||
| chr18:46460656
|
C | CA | 4 | a0001c0001t0014a0001c0001t0030a0001c0001t0047others(1): Show | 6 | HG02896.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4030dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4031 | INFO_REALIGN_3_PRIME | chr18 | 46460656 | ||||
| chr18:46460697
|
T | C | 16 | a0001c0001t0002a0001c0001t0015a0001c0001t0022others(13): Show | 53 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4061T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4061 | chr18 | 46460697 | |||||
| chr18:46460812
|
C | T | 1 | a0001c0001t0057 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4176C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4176 | chr18 | 46460812 | |||||
| chr18:46460903
|
A | AC | 8 | a0001c0001t0026a0001c0001t0029a0001c0001t0037others(5): Show | 9 | HG01069.hp1 HG01109.hp2 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4274dupC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4275 | INFO_REALIGN_3_PRIME | chr18 | 46460903 | ||||
| chr18:46460910
|
C | A | 13 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(10): Show | 36 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4274C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4274 | chr18 | 46460910 | |||||
| chr18:46460993
|
C | G | 1 | a0001c0001t0007 | 7 | HG02723.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4357C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4357 | chr18 | 46460993 | |||||
| chr18:46461187
|
A | G | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(26): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*4551A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4551 | chr18 | 46461187 | |||||
| chr18:46461267
|
G | T | 1 | a0001c0001t0028 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4631G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4631 | chr18 | 46461267 | |||||
| chr18:46461302
|
C | T | 3 | a0001c0001t0011a0001c0001t0060a0001c0001t0061 | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4666C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4666 | chr18 | 46461302 | |||||
| chr18:46461357
|
A | G | 1 | a0001c0001t0056 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4721A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4721 | chr18 | 46461357 | |||||
| chr18:46461432
|
A | G | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(26): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4796A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4796 | chr18 | 46461432 | |||||
| chr18:46461434
|
C | T | 4 | a0001c0001t0014a0001c0001t0030a0001c0001t0047others(1): Show | 6 | HG02896.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4798C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4798 | chr18 | 46461434 | |||||
| chr18:46461519
|
T | C | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(26): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4883T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 4883 | chr18 | 46461519 | |||||
| chr18:46461646
|
C | CA | 9 | a0001c0001t0006a0001c0001t0014a0001c0001t0016others(6): Show | 21 | HG00140.hp2 HG01109.hp2 HG01169.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5031dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5032 | INFO_REALIGN_3_PRIME | chr18 | 46461646 | ||||
| chr18:46461646
|
CAAAAAA | C | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(23): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*5026_*5031delAAAA others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5026 | INFO_REALIGN_3_PRIME | chr18 | 46461646 | ||||
| chr18:46461646
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0041 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5021_*5031delAAAA others(7): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5021 | INFO_REALIGN_3_PRIME | chr18 | 46461646 | ||||
| chr18:46461709
|
C | G | 30 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(27): Show | 121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*5073C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5073 | chr18 | 46461709 | |||||
| chr18:46461839
|
G | A | 4 | a0001c0001t0014a0001c0001t0030a0001c0001t0047others(1): Show | 6 | HG02896.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5203G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5203 | chr18 | 46461839 | |||||
| chr18:46461947
|
A | G | 1 | a0001c0001t0031 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5311A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5311 | chr18 | 46461947 | |||||
| chr18:46462004
|
T | G | 7 | a0001c0001t0005a0001c0001t0010a0001c0001t0035others(4): Show | 23 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5368T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5368 | chr18 | 46462004 | |||||
| chr18:46462232
|
G | C | 1 | a0001c0001t0013 | 4 | HG01109.hp1 HG01257.hp2 HG01928.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5596G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5596 | chr18 | 46462232 | |||||
| chr18:46462591
|
T | G | 4 | a0001c0001t0014a0001c0001t0030a0001c0001t0047others(1): Show | 6 | HG02896.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5955T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5955 | chr18 | 46462591 | |||||
| chr18:46462605
|
A | T | 1 | a0001c0001t0044 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5969A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5969 | chr18 | 46462605 | |||||
| chr18:46462626
|
C | T | 2 | a0001c0001t0015a0001c0001t0039 | 4 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5990C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 5990 | chr18 | 46462626 | |||||
| chr18:46462842
|
C | A | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(23): Show | 108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*6206C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 6206 | chr18 | 46462842 | |||||
| chr18:46462916
|
T | C | 2 | a0001c0001t0016a0001c0001t0042 | 4 | HG01109.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6280T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 6280 | chr18 | 46462916 | |||||
| chr18:46463041
|
G | A | 2 | a0001c0001t0011a0001c0001t0061 | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6405G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 8/8 | 6405 | chr18 | 46463041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46334475
|
A | C | 198 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.61+140A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334475 | ||||||
| chr18:46334671
|
C | CGT | 5 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0002g0055others(2): Show | 5 | HG01517.hp1 HG01517.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+380_61+381dupTG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
C | CGTGT | 5 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0004g0257others(2): Show | 5 | HG02630.hp2 HG02897.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+378_61+381dupTG others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
CGT | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0002g0016others(8): Show | 11 | HG00673.hp2 HG01099.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+380_61+381delTG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
CGTGT | C | 6 | a0001c0001t0001g0007a0001c0001t0002g0004a0001c0001t0005g0005others(3): Show | 6 | HG00733.hp1 HG01081.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+378_61+381delTG others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
CGTGTGTG others(1): Show |
C | 16 | a0001c0001t0001g0100a0001c0001t0004g0099a0001c0001t0007g0064others(13): Show | 16 | HG00544.hp2 HG01884.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.61+374_61+381delTG others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
CGTGTGTG others(3): Show |
C | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0086others(7): Show | 10 | HG00140.hp1 HG01106.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+372_61+381delTG others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334671
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0002g0003a0001c0001t0005g0065 | 2 | HG01361.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.61+370_61+381delTG others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334671 | |||||
| chr18:46334703
|
TGTGTGTG others(7): Show |
T | 5 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0015g0070others(2): Show | 5 | HG02280.hp1 HG03239.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+370_61+383delTG others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334703 | |||||
| chr18:46334705
|
TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0002g0094a0001c0001t0004g0093a0001c0001t0021g0092 | 3 | HG02451.hp2 HG03669.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.61+372_61+383delTG others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334705 | |||||
| chr18:46334705
|
TGTGTGTG others(9): Show |
T | 4 | a0001c0001t0003g0098a0001c0001t0007g0095a0001c0001t0008g0097others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+372_61+387delTG others(14): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334705 | |||||
| chr18:46334707
|
TGTGTGTG others(3): Show |
T | 54 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.61+374_61+383delTG others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334707 | |||||
| chr18:46334707
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0012g0155a0001c0001t0016g0156 | 2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.61+374_61+385delTG others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334707 | |||||
| chr18:46334707
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0003g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.61+374_61+387delTG others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334707 | |||||
| chr18:46334709
|
TGTGTGTG others(1): Show |
T | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0165others(12): Show | 15 | HG00741.hp1 HG01106.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.61+376_61+383delTG others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334709 | |||||
| chr18:46334709
|
TGTGTGTG others(3): Show |
T | 4 | a0001c0001t0036g0173a0001c0001t0050g0175a0001c0002t0010g0176others(1): Show | 4 | HG01071.hp1 HG01496.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+376_61+385delTG others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334709 | |||||
| chr18:46334711
|
TGTGTGA | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0002g0182others(1): Show | 4 | HG01978.hp1 NA18950.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+378_61+383delTG others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334711 | |||||
| chr18:46334711
|
TGTGTGAG others(1): Show |
T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0189others(2): Show | 5 | HG02083.hp1 HG02132.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+378_61+385delTG others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334711 | |||||
| chr18:46334711
|
TGTGTGAG others(3): Show |
T | 5 | a0001c0001t0001g0194a0001c0001t0008g0192a0001c0001t0009g0193others(2): Show | 5 | HG02109.hp1 NA18980.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+378_61+387delTG others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334711 | |||||
| chr18:46334711
|
TGTGTGAG others(5): Show |
T | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61+378_61+389delTG others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334711 | |||||
| chr18:46334713
|
T | A | 7 | a0001c0001t0003g0180a0001c0001t0007g0064a0001c0001t0007g0178others(4): Show | 7 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+378T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334713 | ||||||
| chr18:46334713
|
TGTGA | T | 4 | a0001c0001t0002g0199a0001c0001t0004g0201a0001c0001t0013g0202others(1): Show | 4 | HG01928.hp2 HG02155.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+380_61+383delTG others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334713 | |||||
| chr18:46334713
|
TGTGAGA | T | 5 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0207others(2): Show | 5 | HG02015.hp1 HG04204.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+380_61+385delTG others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334713 | |||||
| chr18:46334713
|
TGTGAGAG others(1): Show |
T | 10 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0001t0001g0212others(7): Show | 10 | HG01074.hp2 HG02129.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+380_61+387delTG others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334713 | |||||
| chr18:46334713
|
TGTGAGAG others(3): Show |
T | 2 | a0001c0001t0009g0219a0001c0001t0032g0218 | 2 | HG03540.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.61+380_61+389delTG others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334713 | |||||
| chr18:46334715
|
T | A | 25 | a0001c0001t0001g0197a0001c0001t0003g0011a0001c0001t0003g0012others(22): Show | 25 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.61+380T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334715 | ||||||
| chr18:46334715
|
T | TGA | 7 | a0001c0001t0003g0029a0001c0001t0007g0031a0001c0001t0014g0026others(4): Show | 7 | HG02258.hp2 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+394_61+395dupAG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334715 | |||||
| chr18:46334715
|
TGA | T | 7 | a0001c0001t0001g0247a0001c0001t0002g0246a0001c0001t0003g0254others(4): Show | 7 | HG01433.hp2 HG02300.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+394_61+395delAG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334715 | |||||
| chr18:46334715
|
TGAGA | T | 14 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0238others(11): Show | 14 | HG00609.hp2 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+392_61+395delAG others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334715 | |||||
| chr18:46334715
|
TGAGAGA | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0233 | 3 | HG01346.hp2 NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.61+390_61+395delAG others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334715 | |||||
| chr18:46334715
|
TGAGAGAG others(1): Show |
T | 9 | a0001c0001t0001g0229a0001c0001t0003g0234a0001c0001t0006g0226others(6): Show | 9 | HG01109.hp2 HG01169.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+388_61+395delAG others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334715 | |||||
| chr18:46334717
|
A | T | 6 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0004g0253others(3): Show | 6 | HG01496.hp1 HG02071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+382A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334717 | ||||||
| chr18:46334719
|
A | T | 12 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0255others(9): Show | 12 | HG01433.hp2 HG01496.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+384A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334719 | ||||||
| chr18:46334721
|
A | T | 21 | a0001c0001t0001g0238a0001c0001t0001g0243a0001c0001t0001g0247others(18): Show | 21 | HG00609.hp2 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.61+386A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334721 | ||||||
| chr18:46334723
|
A | T | 5 | a0001c0001t0001g0251a0001c0001t0002g0249a0001c0001t0002g0250others(2): Show | 5 | HG00609.hp2 HG01123.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+388A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334723 | ||||||
| chr18:46334729
|
A | AGC | 12 | a0001c0001t0001g0229a0001c0001t0001g0251a0001c0001t0002g0249others(9): Show | 12 | HG00609.hp2 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+404_61+405dupCG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334729 | |||||
| chr18:46334729
|
A | C | 4 | a0001c0001t0002g0233a0001c0001t0003g0157a0001c0001t0003g0234others(1): Show | 4 | HG01346.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+394A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334729 | ||||||
| chr18:46334732
|
G | A | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61+397G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334732 | ||||||
| chr18:46334783
|
A | G | 29 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0197others(26): Show | 29 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.61+448A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334783 | ||||||
| chr18:46334812
|
A | ATTTC | 169 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.61+479_61+480insTC others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46334812 | |||||
| chr18:46334824
|
T | G | 198 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.61+489T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334824 | ||||||
| chr18:46334946
|
C | T | 1 | a0001c0001t0013g0202 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.61+611C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46334946 | ||||||
| chr18:46335045
|
C | CGT | 110 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0147others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.61+731_61+732dupGT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46335045 | |||||
| chr18:46335045
|
CGT | C | 3 | a0001c0001t0001g0197a0001c0001t0014g0236a0001c0001t0035g0196 | 3 | HG02896.hp2 HG03225.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.61+731_61+732delGT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46335045 | |||||
| chr18:46335047
|
T | C | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+712T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46335047 | ||||||
| chr18:46335280
|
T | C | 1 | a0001c0001t0018g0221 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61+945T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46335280 | ||||||
| chr18:46335379
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.61+1044C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46335379 | ||||||
| chr18:46335556
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.61+1221C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46335556 | ||||||
| chr18:46335676
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.61+1341C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46335676 | ||||||
| chr18:46336191
|
G | A | 2 | a0001c0001t0003g0234a0001c0001t0014g0235 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61+1856G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46336191 | ||||||
| chr18:46336384
|
CA | C | 78 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0194others(75): Show | 78 | HG00609.hp2 HG00642.hp2 HG01074.hp2 others(75): Show |
intron_variant | MODIFIER | c.61+2058delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46336384 | |||||
| chr18:46336389
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.61+2054A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46336389 | ||||||
| chr18:46336590
|
A | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0252a0001c0001t0006g0237 | 3 | HG03669.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.61+2255A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46336590 | ||||||
| chr18:46336608
|
T | G | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.61+2273T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46336608 | ||||||
| chr18:46336865
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+2530A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46336865 | ||||||
| chr18:46337444
|
G | A | 1 | a0001c0001t0062g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61+3109G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337444 | ||||||
| chr18:46337469
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0061g0128 | 2 | NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.61+3134G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337469 | ||||||
| chr18:46337479
|
C | T | 4 | a0001c0001t0003g0180a0001c0001t0007g0178a0001c0001t0016g0177others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3144C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337479 | ||||||
| chr18:46337805
|
CT | C | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0130others(7): Show | 10 | HG00099.hp1 HG01169.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+3482delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46337805 | |||||
| chr18:46337883
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0199 | 2 | NA18964.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.61+3548G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337883 | ||||||
| chr18:46337883
|
G | C | 4 | a0001c0001t0003g0180a0001c0001t0007g0178a0001c0001t0016g0177others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3548G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337883 | ||||||
| chr18:46337942
|
C | G | 1 | a0001c0001t0005g0009 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.61+3607C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46337942 | ||||||
| chr18:46338118
|
A | G | 1 | a0001c0001t0056g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61+3783A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338118 | ||||||
| chr18:46338227
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.61+3892T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338227 | ||||||
| chr18:46338250
|
C | A | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61+3915C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338250 | ||||||
| chr18:46338277
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.61+3942A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338277 | ||||||
| chr18:46338607
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.61+4272T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338607 | ||||||
| chr18:46338625
|
T | C | 4 | a0001c0001t0001g0209a0001c0001t0003g0208a0001c0001t0016g0156others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+4290T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338625 | ||||||
| chr18:46338747
|
G | A | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+4412G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338747 | ||||||
| chr18:46338770
|
A | C | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+4435A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338770 | ||||||
| chr18:46338895
|
C | A | 3 | a0001c0001t0036g0173a0001c0001t0050g0175a0001c0004t0012g0174 | 3 | HG01496.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.61+4560C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338895 | ||||||
| chr18:46338924
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+4589C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338924 | ||||||
| chr18:46338970
|
C | G | 2 | a0001c0001t0016g0156a0001c0001t0021g0092 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+4635C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46338970 | ||||||
| chr18:46339012
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+4677C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339012 | ||||||
| chr18:46339157
|
C | T | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+4822C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339157 | ||||||
| chr18:46339186
|
A | G | 1 | a0001c0001t0025g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61+4851A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339186 | ||||||
| chr18:46339683
|
G | T | 7 | a0001c0001t0008g0077a0001c0001t0012g0078a0001c0001t0012g0079others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+5348G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339683 | ||||||
| chr18:46339807
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0012g0220 | 2 | HG02615.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.61+5472G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339807 | ||||||
| chr18:46339888
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.61+5553T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46339888 | ||||||
| chr18:46340039
|
C | T | 27 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0197others(24): Show | 27 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.61+5704C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340039 | ||||||
| chr18:46340213
|
A | C | 1 | a0001c0001t0006g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.61+5878A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340213 | ||||||
| chr18:46340305
|
A | G | 1 | a0001c0001t0003g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61+5970A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340305 | ||||||
| chr18:46340367
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.61+6032T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340367 | ||||||
| chr18:46340540
|
A | G | 5 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0094others(2): Show | 5 | HG03239.hp2 HG03654.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+6205A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340540 | ||||||
| chr18:46340615
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.61+6280G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340615 | ||||||
| chr18:46340710
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0002g0054 | 2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.61+6375G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340710 | ||||||
| chr18:46340728
|
T | C | 6 | a0001c0001t0002g0249a0001c0001t0003g0254a0001c0001t0006g0226others(3): Show | 6 | HG01123.hp2 HG01169.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+6393T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340728 | ||||||
| chr18:46340784
|
G | T | 174 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0104others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.61+6449G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46340784 | ||||||
| chr18:46341010
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.61+6675G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341010 | ||||||
| chr18:46341124
|
T | C | 204 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0087others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.61+6789T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341124 | ||||||
| chr18:46341206
|
G | GA | 204 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0087others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.61+6872dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46341206 | |||||
| chr18:46341319
|
AG | A | 206 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0088others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.61+6990delG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46341319 | |||||
| chr18:46341325
|
G | C | 1 | a0001c0001t0052g0191 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.61+6990G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341325 | ||||||
| chr18:46341335
|
CG | C | 5 | a0001c0001t0003g0086a0001c0001t0007g0031a0001c0001t0014g0236others(2): Show | 5 | HG02257.hp1 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+7001delG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341335 | ||||||
| chr18:46341336
|
G | T | 201 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0088others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.61+7001G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341336 | ||||||
| chr18:46341338
|
G | T | 5 | a0001c0001t0003g0086a0001c0001t0007g0031a0001c0001t0014g0236others(2): Show | 5 | HG02257.hp1 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+7003G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341338 | ||||||
| chr18:46341477
|
C | T | 1 | a0001c0001t0027g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.61+7142C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341477 | ||||||
| chr18:46341586
|
C | T | 3 | a0001c0001t0003g0060a0001c0001t0006g0195a0001c0001t0018g0221 | 3 | HG02559.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.61+7251C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341586 | ||||||
| chr18:46341595
|
G | T | 7 | a0001c0001t0003g0029a0001c0001t0003g0180a0001c0001t0007g0178others(4): Show | 7 | HG01243.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+7260G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341595 | ||||||
| chr18:46341657
|
T | C | 1 | a0001c0001t0003g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.61+7322T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341657 | ||||||
| chr18:46341744
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0003g0208 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.61+7409T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341744 | ||||||
| chr18:46341855
|
T | C | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+7520T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341855 | ||||||
| chr18:46341955
|
G | A | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+7620G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341955 | ||||||
| chr18:46341963
|
C | G | 1 | a0001c0001t0002g0249 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.61+7628C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341963 | ||||||
| chr18:46342064
|
G | T | 1 | a0001c0001t0003g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.61+7729G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342064 | ||||||
| chr18:46342237
|
T | C | 1 | a0001c0001t0012g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+7902T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342237 | ||||||
| chr18:46342319
|
G | A | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+7984G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342319 | ||||||
| chr18:46342338
|
TCC | T | 5 | a0001c0001t0003g0086a0001c0001t0007g0031a0001c0001t0014g0236others(2): Show | 5 | HG02257.hp1 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+8005_61+8006del others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46342338 | |||||
| chr18:46342384
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.61+8049C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342384 | ||||||
| chr18:46342514
|
A | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+8179A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342514 | ||||||
| chr18:46342555
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.61+8220G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342555 | ||||||
| chr18:46342583
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.61+8248G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342583 | ||||||
| chr18:46342682
|
C | T | 207 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0088others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.61+8347C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342682 | ||||||
| chr18:46342820
|
A | T | 1 | a0001c0001t0007g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.61+8485A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342820 | ||||||
| chr18:46342901
|
G | C | 1 | a0001c0001t0004g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.61+8566G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46342901 | ||||||
| chr18:46343084
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.61+8749A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343084 | ||||||
| chr18:46343096
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0008g0071a0001c0001t0008g0072others(3): Show | 6 | HG02451.hp1 HG02809.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+8761A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343096 | ||||||
| chr18:46343164
|
G | A | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+8829G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343164 | ||||||
| chr18:46343195
|
C | T | 3 | a0001c0001t0007g0095a0001c0001t0008g0097a0001c0001t0028g0096 | 3 | HG02257.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.61+8860C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343195 | ||||||
| chr18:46343219
|
G | T | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.61+8884G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343219 | ||||||
| chr18:46343231
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0010g0101 | 2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.61+8896G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343231 | ||||||
| chr18:46343781
|
C | T | 2 | a0001c0001t0003g0180a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+9446C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343781 | ||||||
| chr18:46343888
|
A | G | 161 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.61+9553A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46343888 | ||||||
| chr18:46344000
|
T | C | 4 | a0001c0001t0003g0187a0001c0001t0003g0210a0001c0001t0008g0192others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+9665T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344000 | ||||||
| chr18:46344025
|
G | A | 1 | a0001c0001t0032g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+9690G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344025 | ||||||
| chr18:46344032
|
G | A | 2 | a0001c0001t0009g0193a0001c0001t0009g0219 | 2 | NA18966.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.61+9697G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344032 | ||||||
| chr18:46344112
|
C | T | 1 | a0001c0002t0010g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.61+9777C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344112 | ||||||
| chr18:46344335
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0005g0039a0001c0001t0005g0056 | 3 | HG01517.hp1 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61+10000G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344335 | ||||||
| chr18:46344441
|
C | T | 3 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.61+10106C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344441 | ||||||
| chr18:46344551
|
C | T | 1 | a0002c0003t0005g0125 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.61+10216C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344551 | ||||||
| chr18:46344609
|
G | C | 1 | a0001c0001t0038g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61+10274G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344609 | ||||||
| chr18:46344679
|
C | T | 5 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+10344C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344679 | ||||||
| chr18:46344698
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0016g0028others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+10363C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344698 | ||||||
| chr18:46344823
|
G | A | 2 | a0001c0001t0015g0041a0001c0001t0039g0040 | 2 | HG01069.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.61+10488G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344823 | ||||||
| chr18:46345010
|
C | G | 13 | a0001c0001t0001g0197a0001c0001t0003g0060a0001c0001t0003g0086others(10): Show | 13 | HG01243.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+10675C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345010 | ||||||
| chr18:46345085
|
G | GGCAGGGG others(10): Show |
18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+10764_61+10780d others(19): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46345085 | |||||
| chr18:46345085
|
G | GGCAGGGG others(27): Show |
5 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+10780_61+10781i others(36): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46345085 | |||||
| chr18:46345093
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.61+10758T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345093 | ||||||
| chr18:46345099
|
G | A | 13 | a0001c0001t0001g0197a0001c0001t0003g0060a0001c0001t0003g0086others(10): Show | 13 | HG01243.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+10764G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345099 | ||||||
| chr18:46345116
|
C | G | 1 | a0001c0001t0018g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+10781C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345116 | ||||||
| chr18:46345193
|
C | T | 1 | a0001c0001t0007g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.61+10858C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345193 | ||||||
| chr18:46345231
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.61+10896C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345231 | ||||||
| chr18:46345359
|
A | C | 1 | a0001c0001t0012g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+11024A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345359 | ||||||
| chr18:46345361
|
G | C | 173 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.61+11026G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345361 | ||||||
| chr18:46345683
|
A | T | 160 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.61+11348A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345683 | ||||||
| chr18:46345810
|
G | A | 4 | a0001c0001t0003g0180a0001c0001t0007g0178a0001c0001t0016g0177others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11475G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345810 | ||||||
| chr18:46345859
|
G | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+11524G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345859 | ||||||
| chr18:46345959
|
G | A | 1 | a0001c0001t0007g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.61+11624G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345959 | ||||||
| chr18:46345983
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61+11648G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345983 | ||||||
| chr18:46345990
|
C | T | 172 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.61+11655C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345990 | ||||||
| chr18:46346096
|
G | A | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+11761G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346096 | ||||||
| chr18:46346184
|
G | A | 18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+11849G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346184 | ||||||
| chr18:46346217
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+11882G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346217 | ||||||
| chr18:46346443
|
A | AG | 137 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.61+12111dupG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46346443 | |||||
| chr18:46346484
|
A | T | 168 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.61+12149A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346484 | ||||||
| chr18:46346493
|
G | A | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12158G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346493 | ||||||
| chr18:46346543
|
C | G | 1 | a0001c0001t0002g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.61+12208C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346543 | ||||||
| chr18:46346705
|
C | T | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12370C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346705 | ||||||
| chr18:46346763
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0027g0014 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.61+12428C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346763 | ||||||
| chr18:46346793
|
G | A | 4 | a0001c0001t0003g0180a0001c0001t0007g0178a0001c0001t0016g0177others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12458G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346793 | ||||||
| chr18:46346840
|
G | A | 27 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(24): Show | 27 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.61+12505G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346840 | ||||||
| chr18:46346877
|
G | A | 1 | a0001c0001t0020g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61+12542G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346877 | ||||||
| chr18:46346884
|
T | G | 1 | a0001c0001t0062g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61+12549T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46346884 | ||||||
| chr18:46347143
|
G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(28): Show | 33 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.61+12808G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347143 | ||||||
| chr18:46347175
|
G | A | 1 | a0001c0001t0024g0245 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.61+12840G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347175 | ||||||
| chr18:46347446
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.61+13111C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347446 | ||||||
| chr18:46347503
|
G | A | 5 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+13168G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347503 | ||||||
| chr18:46347577
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.61+13242C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347577 | ||||||
| chr18:46347583
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0252a0001c0001t0006g0237 | 3 | HG03669.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.61+13248G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347583 | ||||||
| chr18:46347599
|
A | C | 18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+13264A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347599 | ||||||
| chr18:46347637
|
C | T | 23 | a0001c0001t0001g0194a0001c0001t0001g0224a0001c0001t0001g0225others(20): Show | 23 | HG00609.hp2 HG01109.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+13302C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347637 | ||||||
| chr18:46347809
|
T | C | 10 | a0001c0001t0001g0197a0001c0001t0003g0060a0001c0001t0003g0086others(7): Show | 10 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+13474T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347809 | ||||||
| chr18:46347857
|
A | G | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+13522A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46347857 | ||||||
| chr18:46348073
|
G | C | 18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+13738G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348073 | ||||||
| chr18:46348180
|
A | T | 145 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.61+13845A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348180 | ||||||
| chr18:46348234
|
G | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+13899G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348234 | ||||||
| chr18:46348235
|
G | A | 1 | a0001c0001t0017g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.61+13900G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348235 | ||||||
| chr18:46348311
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG02015.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.61+13976G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348311 | ||||||
| chr18:46348333
|
G | T | 4 | a0001c0001t0007g0095a0001c0001t0007g0232a0001c0001t0008g0097others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+13998G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348333 | ||||||
| chr18:46348358
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.61+14023T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348358 | ||||||
| chr18:46348381
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0003g0060a0001c0001t0003g0086others(7): Show | 10 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+14046C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348381 | ||||||
| chr18:46348382
|
G | A | 1 | a0001c0001t0023g0042 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.61+14047G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348382 | ||||||
| chr18:46348423
|
C | A | 8 | a0001c0001t0001g0050a0001c0001t0014g0026a0001c0001t0016g0028others(5): Show | 8 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+14088C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348423 | ||||||
| chr18:46348607
|
C | T | 12 | a0001c0001t0001g0197a0001c0001t0003g0012a0001c0001t0003g0060others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+14272C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348607 | ||||||
| chr18:46348743
|
T | C | 25 | a0001c0001t0001g0194a0001c0001t0001g0224a0001c0001t0001g0225others(22): Show | 25 | HG00609.hp2 HG01109.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.61+14408T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348743 | ||||||
| chr18:46348821
|
G | T | 163 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.61+14486G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348821 | ||||||
| chr18:46348898
|
TTCTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0251a0001c0001t0002g0189a0001c0001t0002g0233others(1): Show | 4 | HG01346.hp2 HG02132.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+14565_61+14572d others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348898 | |||||
| chr18:46348898
|
TTCTGTGT others(3): Show |
T | 15 | a0001c0001t0001g0194a0001c0001t0001g0224a0001c0001t0001g0225others(12): Show | 15 | HG01109.hp1 HG01433.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.61+14565_61+14574d others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348898 | |||||
| chr18:46348898
|
TTCTGTGT others(7): Show |
T | 4 | a0001c0001t0007g0031a0001c0001t0014g0236a0001c0001t0035g0196others(1): Show | 4 | HG02896.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+14565_61+14578d others(16): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348898 | |||||
| chr18:46348900
|
CTG | C | 30 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0186others(27): Show | 30 | HG01361.hp1 HG01517.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.61+14612_61+14613d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348900 | |||||
| chr18:46348900
|
CTGTG | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.61+14610_61+14613d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348900 | |||||
| chr18:46348900
|
CTGTGTG | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0207others(25): Show | 28 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.61+14608_61+14613d others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348900 | |||||
| chr18:46348900
|
CTGTGTGT others(1): Show |
C | 15 | a0001c0001t0002g0054a0001c0001t0002g0135a0001c0001t0002g0249others(12): Show | 15 | HG01123.hp2 HG01243.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+14606_61+14613d others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348900 | |||||
| chr18:46348900
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0002g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.61+14600_61+14613d others(16): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46348900 | |||||
| chr18:46348909
|
T | C | 1 | a0001c0001t0004g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.61+14574T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348909 | ||||||
| chr18:46348911
|
T | C | 24 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0186others(21): Show | 24 | HG01361.hp1 HG01884.hp1 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.61+14576T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348911 | ||||||
| chr18:46348913
|
T | C | 119 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0100others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+14578T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348913 | ||||||
| chr18:46348915
|
T | C | 12 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0002g0136others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+14580T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348915 | ||||||
| chr18:46348917
|
T | C | 4 | a0001c0001t0002g0054a0001c0001t0002g0135a0001c0001t0005g0134others(1): Show | 4 | HG01243.hp1 HG01257.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+14582T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348917 | ||||||
| chr18:46348974
|
G | T | 4 | a0001c0001t0003g0180a0001c0001t0007g0178a0001c0001t0016g0177others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+14639G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46348974 | ||||||
| chr18:46349126
|
C | G | 1 | a0001c0001t0021g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+14791C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349126 | ||||||
| chr18:46349204
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0252a0001c0001t0006g0237 | 3 | HG03669.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.61+14869C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349204 | ||||||
| chr18:46349353
|
G | C | 1 | a0001c0001t0016g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.61+15018G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349353 | ||||||
| chr18:46349592
|
G | C | 4 | a0001c0001t0001g0139a0001c0001t0004g0201a0001c0001t0013g0202others(1): Show | 4 | HG01928.hp2 HG02155.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+15257G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349592 | ||||||
| chr18:46349772
|
C | T | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+15437C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349772 | ||||||
| chr18:46349817
|
C | A | 1 | a0001c0001t0005g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+15482C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349817 | ||||||
| chr18:46349895
|
C | A | 5 | a0001c0001t0001g0238a0001c0001t0001g0243a0001c0001t0002g0054others(2): Show | 7 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+15560C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46349895 | ||||||
| chr18:46350229
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0057g0080 | 2 | HG00544.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.61+15894A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350229 | ||||||
| chr18:46350280
|
C | T | 6 | a0001c0001t0002g0145a0001c0001t0003g0121a0001c0001t0005g0103others(3): Show | 6 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+15945C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350280 | ||||||
| chr18:46350289
|
C | T | 14 | a0001c0001t0007g0064a0001c0001t0008g0077a0001c0001t0012g0078others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+15954C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350289 | ||||||
| chr18:46350409
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.61+16074G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350409 | ||||||
| chr18:46350524
|
G | A | 1 | a0001c0001t0011g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.61+16189G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350524 | ||||||
| chr18:46350544
|
A | G | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+16209A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350544 | ||||||
| chr18:46350630
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+16295G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350630 | ||||||
| chr18:46350644
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+16309G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350644 | ||||||
| chr18:46350831
|
A | G | 16 | a0001c0001t0001g0209a0001c0001t0003g0086a0001c0001t0003g0208others(13): Show | 16 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.61+16496A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350831 | ||||||
| chr18:46350888
|
A | G | 3 | a0001c0001t0003g0060a0001c0001t0014g0236a0001c0001t0018g0221 | 3 | HG02622.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.61+16553A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46350888 | ||||||
| chr18:46351000
|
C | T | 194 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.61+16665C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351000 | ||||||
| chr18:46351009
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.61+16674C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351009 | ||||||
| chr18:46351148
|
A | C | 11 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0003g0208others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+16813A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351148 | ||||||
| chr18:46351157
|
A | G | 1 | a0001c0001t0005g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.61+16822A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351157 | ||||||
| chr18:46351207
|
T | G | 1 | a0001c0001t0025g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.61+16872T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351207 | ||||||
| chr18:46351217
|
G | A | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+16882G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351217 | ||||||
| chr18:46351279
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0003g0208others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+16944A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351279 | ||||||
| chr18:46351541
|
A | G | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+17206A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351541 | ||||||
| chr18:46351614
|
C | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.61+17279C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351614 | ||||||
| chr18:46351666
|
G | C | 2 | a0001c0001t0003g0180a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+17331G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351666 | ||||||
| chr18:46351827
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+17492G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351827 | ||||||
| chr18:46351865
|
C | A | 1 | a0001c0001t0009g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.61+17530C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351865 | ||||||
| chr18:46351944
|
A | G | 1 | a0001c0001t0042g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61+17609A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351944 | ||||||
| chr18:46352036
|
C | T | 7 | a0001c0001t0008g0077a0001c0001t0012g0078a0001c0001t0012g0079others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+17701C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352036 | ||||||
| chr18:46352041
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+17706C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352041 | ||||||
| chr18:46352329
|
C | T | 82 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0122others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.61+17994C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352329 | ||||||
| chr18:46352473
|
G | C | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+18138G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352473 | ||||||
| chr18:46352506
|
G | C | 8 | a0001c0001t0008g0074a0001c0001t0008g0077a0001c0001t0012g0078others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+18171G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352506 | ||||||
| chr18:46352637
|
C | T | 1 | a0001c0001t0055g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.61+18302C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352637 | ||||||
| chr18:46352695
|
G | A | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61+18360G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352695 | ||||||
| chr18:46352707
|
C | T | 255 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.61+18372C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352707 | ||||||
| chr18:46352881
|
C | T | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+18546C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352881 | ||||||
| chr18:46352940
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+18605C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46352940 | ||||||
| chr18:46353074
|
G | A | 1 | a0001c0001t0006g0144 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.61+18739G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353074 | ||||||
| chr18:46353178
|
G | C | 1 | a0001c0001t0005g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.61+18843G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353178 | ||||||
| chr18:46353244
|
T | G | 22 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0012others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.61+18909T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353244 | ||||||
| chr18:46353535
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.61+19200G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353535 | ||||||
| chr18:46353586
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0005g0044 | 2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+19251C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353586 | ||||||
| chr18:46353661
|
C | T | 8 | a0001c0001t0008g0074a0001c0001t0008g0077a0001c0001t0012g0078others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+19326C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353661 | ||||||
| chr18:46353739
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0005g0044 | 2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+19404C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353739 | ||||||
| chr18:46353797
|
C | A | 1 | a0001c0001t0002g0233 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.61+19462C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353797 | ||||||
| chr18:46353840
|
T | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.61+19505T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353840 | ||||||
| chr18:46353982
|
G | A | 2 | a0001c0001t0018g0231a0001c0001t0065g0198 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.61+19647G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46353982 | ||||||
| chr18:46354095
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.61+19760A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46354095 | ||||||
| chr18:46354419
|
C | T | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+20084C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46354419 | ||||||
| chr18:46354475
|
G | A | 1 | a0001c0001t0008g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.61+20140G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46354475 | ||||||
| chr18:46355077
|
G | C | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+20742G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355077 | ||||||
| chr18:46355244
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61+20909G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355244 | ||||||
| chr18:46355251
|
C | A | 77 | a0001c0001t0001g0019a0001c0001t0001g0100a0001c0001t0001g0106others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.61+20916C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355251 | ||||||
| chr18:46355262
|
A | AT | 5 | a0001c0001t0001g0207a0001c0001t0002g0135a0001c0001t0005g0044others(2): Show | 5 | HG01175.hp1 HG01978.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+20936dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46355262 | |||||
| chr18:46355377
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+21042G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355377 | ||||||
| chr18:46355425
|
C | T | 1 | a0001c0001t0021g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61+21090C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355425 | ||||||
| chr18:46355651
|
C | T | 4 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(1): Show | 4 | HG02145.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+21316C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355651 | ||||||
| chr18:46355733
|
C | G | 7 | a0001c0001t0001g0197a0001c0001t0007g0064a0001c0001t0030g0062others(4): Show | 7 | HG01496.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+21398C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355733 | ||||||
| chr18:46355743
|
TCCAC | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.61+21412_61+21415d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46355743 | |||||
| chr18:46355827
|
C | T | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+21492C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355827 | ||||||
| chr18:46355875
|
G | A | 1 | a0001c0005t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.61+21540G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355875 | ||||||
| chr18:46355929
|
T | A | 7 | a0001c0001t0001g0197a0001c0001t0007g0064a0001c0001t0030g0062others(4): Show | 7 | HG01496.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+21594T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46355929 | ||||||
| chr18:46356211
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+21876C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356211 | ||||||
| chr18:46356305
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.61+21970G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356305 | ||||||
| chr18:46356492
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.61+22157G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356492 | ||||||
| chr18:46356567
|
G | A | 2 | a0001c0001t0003g0208a0001c0001t0066g0190 | 2 | HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.61+22232G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356567 | ||||||
| chr18:46356610
|
C | T | 1 | a0001c0001t0006g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.61+22275C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356610 | ||||||
| chr18:46356690
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+22355G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356690 | ||||||
| chr18:46356771
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0012g0155 | 3 | HG02896.hp1 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.61+22436G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356771 | ||||||
| chr18:46356788
|
C | T | 1 | a0001c0001t0005g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.61+22453C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356788 | ||||||
| chr18:46356868
|
C | T | 47 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0122others(44): Show | 49 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.61+22533C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356868 | ||||||
| chr18:46356869
|
G | T | 48 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0122others(45): Show | 50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.61+22534G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46356869 | ||||||
| chr18:46357120
|
T | C | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+22785T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357120 | ||||||
| chr18:46357167
|
A | G | 1 | a0001c0001t0014g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61+22832A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357167 | ||||||
| chr18:46357243
|
C | G | 1 | a0001c0001t0004g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.61+22908C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357243 | ||||||
| chr18:46357244
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0005g0044 | 2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+22909C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357244 | ||||||
| chr18:46357304
|
C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.61+22969C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357304 | ||||||
| chr18:46357323
|
C | A | 2 | a0001c0001t0006g0038a0001c0001t0006g0144 | 2 | HG00140.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.61+22988C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357323 | ||||||
| chr18:46357490
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+23155G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357490 | ||||||
| chr18:46357685
|
G | A | 1 | a0001c0001t0048g0141 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.61+23350G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46357685 | ||||||
| chr18:46358085
|
G | A | 232 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.61+23750G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358085 | ||||||
| chr18:46358094
|
T | G | 1 | a0001c0001t0001g0224 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.61+23759T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358094 | ||||||
| chr18:46358252
|
T | A | 11 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0003g0208others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+23917T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358252 | ||||||
| chr18:46358332
|
A | T | 1 | a0001c0001t0024g0245 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.61+23997A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358332 | ||||||
| chr18:46358344
|
T | C | 37 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209others(34): Show | 37 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+24009T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358344 | ||||||
| chr18:46358349
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.61+24014G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358349 | ||||||
| chr18:46358383
|
C | T | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+24048C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358383 | ||||||
| chr18:46358556
|
G | A | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61+24221G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358556 | ||||||
| chr18:46358925
|
C | T | 8 | a0001c0001t0001g0197a0001c0001t0007g0064a0001c0001t0030g0062others(5): Show | 8 | HG01496.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+24590C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46358925 | ||||||
| chr18:46359169
|
C | T | 1 | a0001c0001t0011g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.61+24834C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359169 | ||||||
| chr18:46359315
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.61+24980C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359315 | ||||||
| chr18:46359327
|
A | G | 232 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.61+24992A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359327 | ||||||
| chr18:46359530
|
G | T | 1 | a0002c0003t0005g0125 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.61+25195G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359530 | ||||||
| chr18:46359591
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.61+25256C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359591 | ||||||
| chr18:46359725
|
G | C | 1 | a0001c0001t0005g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.61+25390G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46359725 | ||||||
| chr18:46360010
|
G | C | 61 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0122others(58): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.61+25675G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360010 | ||||||
| chr18:46360046
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0035g0196 | 2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.61+25711A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360046 | ||||||
| chr18:46360102
|
C | T | 127 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0036others(124): Show | 127 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.61+25767C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360102 | ||||||
| chr18:46360154
|
C | G | 1 | a0001c0001t0021g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61+25819C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360154 | ||||||
| chr18:46360185
|
T | G | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+25850T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360185 | ||||||
| chr18:46360196
|
AG | A | 12 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0089others(9): Show | 12 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+25864delG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46360196 | |||||
| chr18:46360299
|
G | A | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61+25964G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360299 | ||||||
| chr18:46360335
|
C | A | 2 | a0001c0001t0019g0002a0001c0001t0029g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.61+26000C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360335 | ||||||
| chr18:46360533
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.61+26198A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360533 | ||||||
| chr18:46360710
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0001g0207a0001c0001t0002g0067others(1): Show | 4 | HG03239.hp2 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+26375T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360710 | ||||||
| chr18:46360756
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0007g0064a0001c0001t0030g0062others(1): Show | 4 | HG03471.hp2 HG04184.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+26421G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360756 | ||||||
| chr18:46360768
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0199 | 2 | NA18964.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.61+26433G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360768 | ||||||
| chr18:46360793
|
A | G | 232 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.61+26458A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360793 | ||||||
| chr18:46360837
|
A | G | 6 | a0001c0001t0003g0098a0001c0001t0007g0154a0001c0001t0007g0178others(3): Show | 6 | HG02809.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+26502A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360837 | ||||||
| chr18:46360895
|
G | A | 1 | a0001c0001t0011g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.61+26560G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360895 | ||||||
| chr18:46360944
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.61+26609C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360944 | ||||||
| chr18:46360970
|
A | G | 1 | a0001c0001t0026g0052 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.61+26635A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46360970 | ||||||
| chr18:46361118
|
G | C | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61+26783G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46361118 | ||||||
| chr18:46361531
|
G | T | 8 | a0001c0001t0001g0197a0001c0001t0003g0089a0001c0001t0003g0090others(5): Show | 8 | HG01496.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+27196G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46361531 | ||||||
| chr18:46361768
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+27433T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46361768 | ||||||
| chr18:46361981
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+27646C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46361981 | ||||||
| chr18:46362003
|
A | C | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+27668A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362003 | ||||||
| chr18:46362020
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0002g0054a0001c0001t0005g0044 | 3 | HG01175.hp1 HG01243.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+27685G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362020 | ||||||
| chr18:46362101
|
G | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0233a0001c0001t0005g0005others(3): Show | 6 | HG01257.hp1 HG01257.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+27766G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362101 | ||||||
| chr18:46362104
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0229others(19): Show | 22 | HG00639.hp1 HG00733.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.61+27769T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362104 | ||||||
| chr18:46362276
|
G | T | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61+27941G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362276 | ||||||
| chr18:46362424
|
T | C | 1 | a0001c0001t0025g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.61+28089T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362424 | ||||||
| chr18:46362444
|
G | A | 32 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0197others(29): Show | 32 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.61+28109G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362444 | ||||||
| chr18:46362446
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+28111G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362446 | ||||||
| chr18:46362548
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.61+28213A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362548 | ||||||
| chr18:46362634
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0003g0208 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.61+28299G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362634 | ||||||
| chr18:46362642
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0002g0054a0001c0001t0005g0044 | 3 | HG01175.hp1 HG01243.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+28307G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362642 | ||||||
| chr18:46362672
|
G | T | 3 | a0001c0001t0001g0207a0001c0001t0002g0054a0001c0001t0005g0044 | 3 | HG01175.hp1 HG01243.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.61+28337G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362672 | ||||||
| chr18:46362720
|
G | C | 14 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0002g0054others(11): Show | 14 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.61+28385G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362720 | ||||||
| chr18:46362723
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+28388T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362723 | ||||||
| chr18:46362822
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+28487C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362822 | ||||||
| chr18:46362907
|
A | G | 7 | a0001c0001t0007g0064a0001c0001t0007g0095a0001c0001t0020g0013others(4): Show | 7 | HG02145.hp1 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+28572A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362907 | ||||||
| chr18:46362947
|
G | A | 3 | a0001c0001t0003g0060a0001c0001t0007g0031a0001c0001t0018g0221 | 3 | HG02622.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.61+28612G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362947 | ||||||
| chr18:46362982
|
C | A | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.61+28647C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46362982 | ||||||
| chr18:46363111
|
CATA | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0100a0001c0001t0001g0110others(17): Show | 20 | HG00544.hp2 HG00609.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+28781_61+28783d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46363111 | |||||
| chr18:46363463
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0003g0011a0001c0001t0057g0080 | 3 | HG02055.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.61+29128C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363463 | ||||||
| chr18:46363546
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0006g0038a0001c0001t0006g0144others(2): Show | 5 | HG00140.hp2 HG01099.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+29211T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363546 | ||||||
| chr18:46363609
|
G | A | 2 | a0001c0001t0020g0013a0001c0001t0030g0062 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.61+29274G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363609 | ||||||
| chr18:46363780
|
G | A | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+29445G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363780 | ||||||
| chr18:46363838
|
C | T | 20 | a0001c0001t0001g0019a0001c0001t0001g0100a0001c0001t0001g0110others(17): Show | 20 | HG00544.hp2 HG00609.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+29503C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363838 | ||||||
| chr18:46363897
|
C | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+29562C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363897 | ||||||
| chr18:46363923
|
C | CT | 59 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0100others(56): Show | 59 | HG00140.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+29597dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46363923 | |||||
| chr18:46363923
|
C | CTT | 6 | a0001c0001t0001g0181a0001c0001t0003g0011a0001c0001t0005g0103others(3): Show | 6 | HG01192.hp2 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+29596_61+29597d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46363923 | |||||
| chr18:46363923
|
C | T | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+29588C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363923 | ||||||
| chr18:46363933
|
C | T | 3 | a0001c0001t0003g0011a0001c0001t0028g0096a0001c0005t0001g0204 | 3 | HG02055.hp1 HG02257.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.61+29598C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363933 | ||||||
| chr18:46363940
|
C | T | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+29605C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46363940 | ||||||
| chr18:46363945
|
C | CT | 58 | a0001c0001t0001g0019a0001c0001t0001g0087a0001c0001t0001g0088others(55): Show | 58 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.61+29626dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46363945 | |||||
| chr18:46363945
|
C | CTT | 6 | a0001c0001t0001g0207a0001c0001t0002g0023a0001c0001t0002g0054others(3): Show | 6 | HG01175.hp1 HG01243.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+29625_61+29626d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46363945 | |||||
| chr18:46364061
|
C | A | 2 | a0001c0001t0025g0091a0001c0001t0035g0196 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.61+29726C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364061 | ||||||
| chr18:46364134
|
A | C | 4 | a0001c0001t0007g0154a0001c0001t0007g0178a0001c0001t0007g0232others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+29799A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364134 | ||||||
| chr18:46364201
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0011g0227 | 2 | HG00639.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.61+29866G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364201 | ||||||
| chr18:46364223
|
T | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(147): Show | 152 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.61+29888T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364223 | ||||||
| chr18:46364305
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.61+29970C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364305 | ||||||
| chr18:46364356
|
G | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(154): Show | 159 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.61+30021G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364356 | ||||||
| chr18:46364405
|
TA | T | 147 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(144): Show | 149 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.61+30083delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46364405 | |||||
| chr18:46364518
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0058g0048 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+30183T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364518 | ||||||
| chr18:46364598
|
A | C | 5 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+30263A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364598 | ||||||
| chr18:46364728
|
C | T | 7 | a0001c0001t0003g0012a0001c0001t0025g0091a0001c0001t0035g0196others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+30393C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364728 | ||||||
| chr18:46364735
|
A | T | 1 | a0001c0002t0010g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.61+30400A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364735 | ||||||
| chr18:46364857
|
C | A | 4 | a0001c0001t0001g0243a0001c0001t0002g0136a0001c0001t0003g0121others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+30522C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46364857 | ||||||
| chr18:46365002
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0033others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.61+30667G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365002 | ||||||
| chr18:46365041
|
T | G | 91 | a0001c0001t0001g0019a0001c0001t0001g0100a0001c0001t0001g0106others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.61+30706T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365041 | ||||||
| chr18:46365046
|
T | C | 5 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+30711T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365046 | ||||||
| chr18:46365089
|
T | C | 2 | a0001c0001t0003g0011a0001c0001t0057g0080 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.61+30754T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365089 | ||||||
| chr18:46365383
|
C | A | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+31048C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365383 | ||||||
| chr18:46365508
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0012g0155 | 2 | HG03486.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.61+31173G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365508 | ||||||
| chr18:46365531
|
G | C | 8 | a0001c0001t0007g0031a0001c0001t0012g0079a0001c0001t0021g0092others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+31196G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365531 | ||||||
| chr18:46365549
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0002g0018 | 2 | NA18984.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.61+31214C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46365549 | ||||||
| chr18:46366011
|
G | A | 4 | a0001c0001t0012g0079a0001c0001t0021g0092a0001c0001t0024g0061others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+31676G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366011 | ||||||
| chr18:46366020
|
C | T | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+31685C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366020 | ||||||
| chr18:46366083
|
A | G | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61+31748A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366083 | ||||||
| chr18:46366149
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.61+31814G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366149 | ||||||
| chr18:46366188
|
A | G | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+31853A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366188 | ||||||
| chr18:46366200
|
G | A | 1 | a0001c0001t0015g0131 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.61+31865G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366200 | ||||||
| chr18:46366218
|
G | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+31883G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366218 | ||||||
| chr18:46366249
|
G | A | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.61+31914G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366249 | ||||||
| chr18:46366292
|
C | CA | 12 | a0001c0001t0002g0024a0001c0001t0002g0067a0001c0001t0002g0115others(9): Show | 12 | HG01123.hp1 HG01123.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+31984dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
C | CAA | 5 | a0001c0001t0002g0164a0001c0001t0004g0123a0001c0001t0017g0150others(2): Show | 5 | HG02083.hp2 HG03654.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+31983_61+31984d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
C | CAAA | 29 | a0001c0001t0001g0033a0001c0001t0001g0113a0001c0001t0001g0148others(26): Show | 29 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.61+31982_61+31984d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
C | CAAAA | 5 | a0001c0001t0002g0160a0001c0001t0002g0246a0001c0001t0004g0257others(2): Show | 5 | HG01981.hp2 HG03831.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+31981_61+31984d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
CA | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0100others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.61+31984delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
CAA | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(50): Show | 53 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+31983_61+31984d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366292
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 12 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+31975_61+31984d others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366292 | |||||
| chr18:46366305
|
AAAAAAAA others(10): Show |
A | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+31972_61+31988d others(19): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46366305 | |||||
| chr18:46366314
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0002g0018others(1): Show | 4 | NA18980.hp1 NA18984.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+31979A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366314 | ||||||
| chr18:46366324
|
G | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+31989G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366324 | ||||||
| chr18:46366351
|
C | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0060others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+32016C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366351 | ||||||
| chr18:46366512
|
G | A | 5 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+32177G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366512 | ||||||
| chr18:46366874
|
T | C | 47 | a0001c0001t0001g0033a0001c0001t0001g0113a0001c0001t0001g0148others(44): Show | 49 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.61+32539T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366874 | ||||||
| chr18:46366898
|
C | T | 74 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0100others(71): Show | 76 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.61+32563C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46366898 | ||||||
| chr18:46367024
|
GA | G | 7 | a0001c0001t0001g0184a0001c0001t0004g0169a0001c0001t0004g0213others(4): Show | 7 | HG01074.hp2 HG02080.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+32695delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46367024 | |||||
| chr18:46367253
|
C | T | 59 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0087others(56): Show | 59 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+32918C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367253 | ||||||
| chr18:46367490
|
G | C | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+33155G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367490 | ||||||
| chr18:46367635
|
G | C | 11 | a0001c0001t0003g0012a0001c0001t0007g0031a0001c0001t0012g0079others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+33300G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367635 | ||||||
| chr18:46367702
|
T | G | 51 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(48): Show | 51 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.61+33367T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367702 | ||||||
| chr18:46367778
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.61+33443T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367778 | ||||||
| chr18:46367842
|
G | A | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0180others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+33507G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367842 | ||||||
| chr18:46367917
|
T | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0003g0180others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+33582T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46367917 | ||||||
| chr18:46368055
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0002g0018others(10): Show | 13 | HG00609.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+33720A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368055 | ||||||
| chr18:46368060
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+33725C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368060 | ||||||
| chr18:46368065
|
G | A | 3 | a0001c0001t0036g0173a0001c0001t0050g0175a0001c0004t0012g0174 | 3 | HG01496.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.61+33730G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368065 | ||||||
| chr18:46368136
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.61+33801T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368136 | ||||||
| chr18:46368161
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0002g0018others(10): Show | 13 | HG00609.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+33826C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368161 | ||||||
| chr18:46368322
|
T | C | 167 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0036others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.61+33987T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368322 | ||||||
| chr18:46368324
|
C | G | 167 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0036others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.61+33989C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368324 | ||||||
| chr18:46368350
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+34015C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368350 | ||||||
| chr18:46368384
|
C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(51): Show | 54 | HG00280.hp1 HG00642.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.61+34049C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368384 | ||||||
| chr18:46368515
|
C | G | 2 | a0001c0001t0002g0055a0001c0001t0005g0039 | 2 | HG01517.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.61+34180C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368515 | ||||||
| chr18:46368580
|
C | T | 34 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0002g0003others(31): Show | 34 | HG01074.hp2 HG01928.hp2 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.61+34245C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368580 | ||||||
| chr18:46368601
|
A | T | 68 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0100others(65): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.61+34266A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368601 | ||||||
| chr18:46368619
|
C | T | 120 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.61+34284C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368619 | ||||||
| chr18:46368645
|
C | T | 34 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0002g0003others(31): Show | 34 | HG01074.hp2 HG01928.hp2 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.61+34310C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368645 | ||||||
| chr18:46368648
|
T | C | 34 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0002g0003others(31): Show | 34 | HG01074.hp2 HG01928.hp2 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.61+34313T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368648 | ||||||
| chr18:46368715
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0002g0018others(5): Show | 8 | HG00609.hp1 HG02071.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+34380G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46368715 | ||||||
| chr18:46369017
|
A | G | 141 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(138): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.61+34682A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369017 | ||||||
| chr18:46369350
|
A | G | 144 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(141): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.61+35015A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369350 | ||||||
| chr18:46369366
|
GGT | G | 96 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.61+35043_61+35044d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46369366 | |||||
| chr18:46369568
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0110a0001c0001t0001g0113others(56): Show | 61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+35233C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369568 | ||||||
| chr18:46369575
|
C | T | 96 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.61+35240C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369575 | ||||||
| chr18:46369633
|
C | T | 96 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.61+35298C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369633 | ||||||
| chr18:46369949
|
G | A | 1 | a0001c0001t0018g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+35614G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369949 | ||||||
| chr18:46369968
|
C | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0002g0018others(6): Show | 9 | HG00609.hp1 HG02071.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+35633C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369968 | ||||||
| chr18:46369984
|
A | T | 5 | a0001c0001t0001g0247a0001c0001t0013g0124a0001c0001t0013g0241others(2): Show | 5 | HG01109.hp1 HG01433.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+35649A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46369984 | ||||||
| chr18:46370217
|
G | A | 1 | a0001c0001t0004g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.61+35882G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370217 | ||||||
| chr18:46370325
|
T | C | 1 | a0001c0004t0012g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61+35990T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370325 | ||||||
| chr18:46370381
|
G | C | 27 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0002g0003others(24): Show | 27 | HG01074.hp2 HG01928.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.61+36046G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370381 | ||||||
| chr18:46370518
|
G | A | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+36183G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370518 | ||||||
| chr18:46370575
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.61+36240G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370575 | ||||||
| chr18:46370646
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.61+36311C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370646 | ||||||
| chr18:46370746
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0018g0221others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+36411A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370746 | ||||||
| chr18:46370824
|
A | C | 39 | a0001c0001t0001g0184a0001c0001t0001g0209a0001c0001t0001g0212others(36): Show | 39 | HG01074.hp2 HG01928.hp2 HG02080.hp1 others(36): Show |
intron_variant | MODIFIER | c.61+36489A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370824 | ||||||
| chr18:46370848
|
G | A | 8 | a0001c0001t0003g0208a0001c0001t0006g0034a0001c0001t0007g0053others(5): Show | 8 | HG01243.hp2 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+36513G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46370848 | ||||||
| chr18:46371132
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0003g0012a0001c0001t0016g0028others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+36797C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371132 | ||||||
| chr18:46371276
|
C | A | 1 | a0001c0001t0002g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.61+36941C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371276 | ||||||
| chr18:46371487
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0018g0221others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+37152G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371487 | ||||||
| chr18:46371489
|
G | GAGA | 4 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0018g0221others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+37157_61+37159d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46371489 | |||||
| chr18:46371581
|
C | T | 1 | a0001c0001t0047g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61+37246C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371581 | ||||||
| chr18:46371824
|
C | G | 3 | a0001c0001t0036g0173a0001c0001t0050g0175a0001c0004t0012g0174 | 3 | HG01496.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.61+37489C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371824 | ||||||
| chr18:46371992
|
G | C | 1 | a0001c0001t0004g0253 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.61+37657G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46371992 | ||||||
| chr18:46372194
|
G | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+37859G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372194 | ||||||
| chr18:46372259
|
GC | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(13): Show | 16 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.61+37927delC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46372259 | |||||
| chr18:46372499
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+38164C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372499 | ||||||
| chr18:46372507
|
G | T | 1 | a0001c0001t0018g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+38172G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372507 | ||||||
| chr18:46372517
|
T | A | 91 | a0001c0001t0001g0110a0001c0001t0001g0152a0001c0001t0001g0159others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.61+38182T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372517 | ||||||
| chr18:46372684
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0058g0048 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+38349G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372684 | ||||||
| chr18:46372739
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0005g0039a0001c0001t0005g0056 | 3 | HG01517.hp1 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61+38404T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372739 | ||||||
| chr18:46372745
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0005g0039a0001c0001t0005g0056 | 3 | HG01517.hp1 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61+38410G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372745 | ||||||
| chr18:46372802
|
C | T | 1 | a0001c0001t0037g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.61+38467C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372802 | ||||||
| chr18:46372823
|
A | T | 4 | a0001c0001t0001g0209a0001c0001t0003g0060a0001c0001t0018g0221others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+38488A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372823 | ||||||
| chr18:46372981
|
C | T | 1 | a0001c0001t0006g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.61+38646C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46372981 | ||||||
| chr18:46373116
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(12): Show | 15 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+38781T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373116 | ||||||
| chr18:46373188
|
G | T | 63 | a0001c0001t0001g0110a0001c0001t0001g0152a0001c0001t0001g0159others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.61+38853G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373188 | ||||||
| chr18:46373249
|
T | C | 1 | a0001c0001t0014g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61+38914T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373249 | ||||||
| chr18:46373309
|
C | G | 1 | a0001c0001t0004g0169 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61+38974C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373309 | ||||||
| chr18:46373488
|
T | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(12): Show | 15 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+39153T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373488 | ||||||
| chr18:46373492
|
G | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(8): Show | 11 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+39157G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373492 | ||||||
| chr18:46373579
|
G | A | 1 | a0001c0001t0007g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.61+39244G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373579 | ||||||
| chr18:46373607
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61+39272G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373607 | ||||||
| chr18:46373625
|
G | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(8): Show | 11 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+39290G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373625 | ||||||
| chr18:46373651
|
C | T | 3 | a0001c0001t0003g0060a0001c0001t0018g0221a0001c0001t0028g0096 | 3 | HG02257.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.61+39316C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373651 | ||||||
| chr18:46373768
|
G | T | 1 | a0001c0001t0003g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.61+39433G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46373768 | ||||||
| chr18:46374055
|
G | T | 6 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0002g0112others(3): Show | 6 | NA18964.hp2 NA19002.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+39720G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374055 | ||||||
| chr18:46374062
|
G | A | 1 | a0001c0001t0003g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.61+39727G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374062 | ||||||
| chr18:46374083
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(12): Show | 15 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+39748C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374083 | ||||||
| chr18:46374141
|
T | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0045a0001c0001t0007g0064others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+39806T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374141 | ||||||
| chr18:46374239
|
T | C | 1 | a0001c0001t0025g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.61+39904T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374239 | ||||||
| chr18:46374408
|
C | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0108others(84): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.61+40073C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374408 | ||||||
| chr18:46374629
|
TG | T | 257 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.61+40295delG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374629 | ||||||
| chr18:46374641
|
C | G | 1 | a0001c0001t0026g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.61+40306C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374641 | ||||||
| chr18:46374859
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.61+40524C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374859 | ||||||
| chr18:46374897
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0061g0128 | 2 | NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.61+40562G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374897 | ||||||
| chr18:46374907
|
T | C | 17 | a0001c0001t0001g0209a0001c0001t0003g0012a0001c0001t0003g0180others(14): Show | 17 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+40572T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46374907 | ||||||
| chr18:46375001
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+40666G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375001 | ||||||
| chr18:46375148
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0003g0208a0001c0001t0006g0034 | 3 | HG02622.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.61+40813C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375148 | ||||||
| chr18:46375180
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61+40845G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375180 | ||||||
| chr18:46375277
|
G | GTGGCTGG others(3): Show |
4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+40942_61+40943i others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375277 | ||||||
| chr18:46375278
|
C | G | 4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+40943C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375278 | ||||||
| chr18:46375307
|
C | A | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.61+40972C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375307 | ||||||
| chr18:46375447
|
A | T | 1 | a0001c0001t0018g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+41112A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375447 | ||||||
| chr18:46375553
|
C | CTAA | 4 | a0001c0001t0001g0113a0001c0001t0002g0160a0001c0001t0015g0070others(1): Show | 4 | HG02071.hp1 HG02280.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+41261_61+41263d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375553
|
CTAA | C | 141 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.61+41261_61+41263d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375553
|
CTAATAA | C | 35 | a0001c0001t0001g0019a0001c0001t0001g0139a0001c0001t0001g0171others(32): Show | 37 | HG00140.hp2 HG00609.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+41258_61+41263d others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375553
|
CTAATAAT others(2): Show |
C | 5 | a0001c0001t0002g0130a0001c0001t0009g0146a0001c0001t0014g0236others(2): Show | 5 | HG00099.hp1 HG01361.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+41255_61+41263d others(11): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375553
|
CTAATAAT others(5): Show |
C | 23 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0002g0135others(20): Show | 23 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+41252_61+41263d others(14): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375553
|
CTAATAAT others(14): Show |
C | 1 | a0001c0001t0012g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+41243_61+41263d others(23): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46375553 | |||||
| chr18:46375641
|
G | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+41306G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375641 | ||||||
| chr18:46375643
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.61+41308C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375643 | ||||||
| chr18:46375688
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.61+41353C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375688 | ||||||
| chr18:46375738
|
T | G | 193 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0036others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.61+41403T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375738 | ||||||
| chr18:46375931
|
A | C | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61+41596A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375931 | ||||||
| chr18:46375975
|
T | A | 1 | a0001c0001t0034g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.61+41640T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375975 | ||||||
| chr18:46375979
|
C | T | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+41644C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375979 | ||||||
| chr18:46375983
|
G | C | 2 | a0001c0001t0002g0160a0001c0001t0003g0132 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.61+41648G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46375983 | ||||||
| chr18:46376173
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.61+41838C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376173 | ||||||
| chr18:46376425
|
G | T | 1 | a0001c0001t0016g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.61+42090G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376425 | ||||||
| chr18:46376664
|
C | CT | 79 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0088others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.61+42354dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46376664 | |||||
| chr18:46376664
|
C | CTT | 45 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0113others(42): Show | 45 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.61+42353_61+42354d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46376664 | |||||
| chr18:46376664
|
C | CTTT | 41 | a0001c0001t0001g0152a0001c0001t0001g0211a0001c0001t0001g0222others(38): Show | 43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.61+42352_61+42354d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46376664 | |||||
| chr18:46376664
|
C | CTTTT | 7 | a0001c0001t0003g0012a0001c0001t0005g0044a0001c0001t0009g0193others(4): Show | 7 | HG01099.hp2 HG01175.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+42351_61+42354d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46376664 | |||||
| chr18:46376664
|
CT | C | 8 | a0001c0001t0001g0106a0001c0001t0002g0035a0001c0001t0004g0010others(5): Show | 8 | HG00544.hp1 HG02083.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+42354delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46376664 | |||||
| chr18:46376723
|
G | A | 1 | a0001c0001t0037g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.61+42388G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376723 | ||||||
| chr18:46376759
|
C | A | 3 | a0001c0001t0001g0209a0001c0001t0003g0208a0001c0001t0006g0034 | 3 | HG02622.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.61+42424C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376759 | ||||||
| chr18:46376871
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61+42536A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376871 | ||||||
| chr18:46376905
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+42570C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376905 | ||||||
| chr18:46376906
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.61+42571G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376906 | ||||||
| chr18:46376959
|
G | C | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+42624G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46376959 | ||||||
| chr18:46377042
|
G | A | 1 | a0001c0001t0049g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.61+42707G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377042 | ||||||
| chr18:46377367
|
A | G | 1 | a0001c0001t0018g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+43032A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377367 | ||||||
| chr18:46377451
|
C | A | 8 | a0001c0001t0003g0086a0001c0001t0003g0187a0001c0001t0003g0210others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+43116C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377451 | ||||||
| chr18:46377462
|
A | G | 2 | a0001c0001t0014g0236a0001c0001t0016g0156 | 2 | HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61+43127A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377462 | ||||||
| chr18:46377688
|
G | T | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+43353G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377688 | ||||||
| chr18:46377858
|
G | A | 37 | a0001c0001t0001g0152a0001c0001t0001g0211a0001c0001t0001g0222others(34): Show | 39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.61+43523G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377858 | ||||||
| chr18:46377962
|
T | C | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+43627T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46377962 | ||||||
| chr18:46378097
|
G | A | 1 | a0001c0001t0038g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61+43762G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378097 | ||||||
| chr18:46378156
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.61+43821G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378156 | ||||||
| chr18:46378171
|
C | G | 2 | a0001c0001t0015g0070a0001c0001t0015g0131 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.61+43836C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378171 | ||||||
| chr18:46378174
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0028g0096 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.61+43839T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378174 | ||||||
| chr18:46378188
|
T | C | 39 | a0001c0001t0001g0050a0001c0001t0001g0152a0001c0001t0001g0211others(36): Show | 41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.61+43853T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378188 | ||||||
| chr18:46378210
|
G | A | 112 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.61+43875G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378210 | ||||||
| chr18:46378440
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+44105G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378440 | ||||||
| chr18:46378484
|
T | G | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.61+44149T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378484 | ||||||
| chr18:46378546
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+44211A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378546 | ||||||
| chr18:46378548
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+44213G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378548 | ||||||
| chr18:46378802
|
C | G | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+44467C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378802 | ||||||
| chr18:46378981
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+44646C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378981 | ||||||
| chr18:46378982
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+44647C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46378982 | ||||||
| chr18:46379022
|
A | G | 180 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0050others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.61+44687A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379022 | ||||||
| chr18:46379062
|
T | C | 180 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0050others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.61+44727T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379062 | ||||||
| chr18:46379087
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+44752A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379087 | ||||||
| chr18:46379170
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0003g0208a0001c0001t0006g0034 | 3 | HG02622.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.61+44835T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379170 | ||||||
| chr18:46379246
|
G | A | 1 | a0001c0001t0005g0134 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.61+44911G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379246 | ||||||
| chr18:46379304
|
A | T | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+44969A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379304 | ||||||
| chr18:46379358
|
C | T | 1 | a0001c0001t0056g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61+45023C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379358 | ||||||
| chr18:46379392
|
A | G | 1 | a0001c0001t0009g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.61+45057A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379392 | ||||||
| chr18:46379437
|
C | T | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+45102C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379437 | ||||||
| chr18:46379439
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.61+45104C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379439 | ||||||
| chr18:46379546
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0052g0191 | 2 | NA19082.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.61+45211G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379546 | ||||||
| chr18:46379602
|
C | T | 1 | a0001c0001t0030g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+45267C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379602 | ||||||
| chr18:46379740
|
C | T | 96 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(93): Show | 96 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.61+45405C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379740 | ||||||
| chr18:46379895
|
CT | C | 4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+45561delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379895 | ||||||
| chr18:46379926
|
C | T | 1 | a0001c0001t0041g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.61+45591C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379926 | ||||||
| chr18:46379969
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+45634C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379969 | ||||||
| chr18:46380064
|
G | C | 4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+45729G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380064 | ||||||
| chr18:46380236
|
A | G | 94 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(91): Show | 94 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.61+45901A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380236 | ||||||
| chr18:46380307
|
G | A | 1 | a0001c0001t0005g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.61+45972G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380307 | ||||||
| chr18:46380349
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.61+46014G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380349 | ||||||
| chr18:46380394
|
T | G | 1 | a0001c0001t0012g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.61+46059T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380394 | ||||||
| chr18:46380550
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0003g0011a0001c0001t0003g0254others(2): Show | 5 | HG02055.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+46215G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380550 | ||||||
| chr18:46380870
|
C | T | 88 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.61+46535C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380870 | ||||||
| chr18:46380975
|
C | T | 1 | a0001c0001t0024g0245 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.61+46640C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46380975 | ||||||
| chr18:46381086
|
T | C | 2 | a0001c0002t0010g0001a0001c0002t0010g0176 | 4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+46751T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381086 | ||||||
| chr18:46381201
|
C | G | 89 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(86): Show | 89 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.61+46866C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381201 | ||||||
| chr18:46381293
|
T | C | 1 | a0001c0001t0005g0134 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.61+46958T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381293 | ||||||
| chr18:46381315
|
T | C | 184 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0036others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.61+46980T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381315 | ||||||
| chr18:46381344
|
G | A | 4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+47009G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381344 | ||||||
| chr18:46381448
|
C | G | 88 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.61+47113C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381448 | ||||||
| chr18:46381462
|
C | T | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+47127C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381462 | ||||||
| chr18:46381601
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.61+47266C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381601 | ||||||
| chr18:46381818
|
G | A | 9 | a0001c0001t0003g0157a0001c0001t0008g0071a0001c0001t0008g0072others(6): Show | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+47483G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46381818 | ||||||
| chr18:46381830
|
C | CA | 67 | a0001c0001t0001g0050a0001c0001t0001g0152a0001c0001t0001g0222others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.61+47506dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46381830 | |||||
| chr18:46382021
|
G | A | 89 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(86): Show | 89 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.61+47686G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382021 | ||||||
| chr18:46382097
|
C | T | 8 | a0001c0001t0007g0031a0001c0001t0007g0154a0001c0001t0007g0178others(5): Show | 8 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+47762C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382097 | ||||||
| chr18:46382101
|
G | C | 2 | a0001c0001t0003g0180a0001c0001t0012g0078 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.61+47766G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382101 | ||||||
| chr18:46382605
|
T | C | 4 | a0001c0001t0003g0045a0001c0001t0007g0064a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+48270T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382605 | ||||||
| chr18:46382653
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0194others(7): Show | 10 | HG00609.hp1 HG02071.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+48318C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382653 | ||||||
| chr18:46382707
|
T | A | 8 | a0001c0001t0003g0086a0001c0001t0003g0187a0001c0001t0003g0210others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+48372T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382707 | ||||||
| chr18:46382714
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+48379G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382714 | ||||||
| chr18:46382789
|
C | G | 1 | a0001c0001t0002g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.61+48454C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382789 | ||||||
| chr18:46382793
|
A | G | 1 | a0001c0001t0005g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.61+48458A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382793 | ||||||
| chr18:46382877
|
C | T | 2 | a0001c0002t0010g0001a0001c0002t0010g0176 | 4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+48542C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382877 | ||||||
| chr18:46382916
|
A | G | 147 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0087others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.61+48581A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382916 | ||||||
| chr18:46382954
|
T | C | 173 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0050others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.61+48619T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382954 | ||||||
| chr18:46383052
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0009g0111 | 2 | NA18986.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.61+48717G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383052 | ||||||
| chr18:46383123
|
G | C | 1 | a0001c0001t0014g0236 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.61+48788G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383123 | ||||||
| chr18:46383288
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.61+48953T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383288 | ||||||
| chr18:46383388
|
G | A | 2 | a0001c0001t0003g0208a0001c0001t0006g0034 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.61+49053G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383388 | ||||||
| chr18:46383404
|
T | C | 1 | a0001c0001t0008g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.61+49069T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383404 | ||||||
| chr18:46383454
|
A | G | 9 | a0001c0001t0003g0234a0001c0001t0008g0077a0001c0001t0012g0220others(6): Show | 9 | HG01496.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+49119A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383454 | ||||||
| chr18:46383550
|
G | GT | 67 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0087others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.61+49237dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46383550 | |||||
| chr18:46383550
|
G | GTT | 5 | a0001c0001t0003g0012a0001c0001t0003g0208a0001c0001t0006g0034others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+49236_61+49237d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46383550 | |||||
| chr18:46383550
|
GT | G | 37 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0104others(34): Show | 37 | HG00741.hp2 HG01081.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.61+49237delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46383550 | |||||
| chr18:46383550
|
GTT | G | 6 | a0001c0001t0001g0165a0001c0001t0002g0067a0001c0001t0003g0089others(3): Show | 6 | HG01517.hp2 HG01981.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+49236_61+49237d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46383550 | |||||
| chr18:46383551
|
T | G | 1 | a0001c0001t0005g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+49216T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383551 | ||||||
| chr18:46383608
|
A | G | 6 | a0001c0001t0003g0180a0001c0001t0009g0146a0001c0001t0011g0137others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+49273A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383608 | ||||||
| chr18:46383614
|
G | A | 3 | a0001c0001t0009g0146a0001c0001t0011g0137a0001c0001t0044g0166 | 3 | HG00741.hp2 HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.61+49279G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383614 | ||||||
| chr18:46383615
|
T | C | 3 | a0001c0001t0003g0180a0001c0001t0012g0078a0001c0001t0066g0190 | 3 | HG02559.hp1 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.61+49280T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383615 | ||||||
| chr18:46383618
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0215a0001c0001t0002g0003 | 3 | HG02922.hp2 NA18995.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.61+49283G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383618 | ||||||
| chr18:46383624
|
A | G | 7 | a0001c0001t0007g0031a0001c0001t0007g0154a0001c0001t0007g0178others(4): Show | 7 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+49289A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383624 | ||||||
| chr18:46383655
|
T | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(122): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.61+49320T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383655 | ||||||
| chr18:46383694
|
A | G | 52 | a0001c0001t0002g0055a0001c0001t0002g0130a0001c0001t0002g0135others(49): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.61+49359A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383694 | ||||||
| chr18:46383701
|
G | C | 2 | a0001c0001t0006g0195a0001c0001t0046g0025 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.61+49366G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383701 | ||||||
| chr18:46383715
|
C | T | 61 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0106others(58): Show | 61 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+49380C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383715 | ||||||
| chr18:46383721
|
A | C | 151 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0036others(148): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.61+49386A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383721 | ||||||
| chr18:46383755
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.61+49420C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383755 | ||||||
| chr18:46383786
|
C | T | 17 | a0001c0001t0007g0031a0001c0001t0007g0064a0001c0001t0007g0154others(14): Show | 17 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-49404C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383786 | ||||||
| chr18:46383798
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.62-49392A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383798 | ||||||
| chr18:46383802
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.62-49388T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383802 | ||||||
| chr18:46383824
|
C | T | 96 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0050others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.62-49366C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383824 | ||||||
| chr18:46383841
|
G | A | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62-49349G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383841 | ||||||
| chr18:46383843
|
G | A | 18 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0209others(15): Show | 18 | HG01243.hp2 HG01884.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.62-49347G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383843 | ||||||
| chr18:46384182
|
C | G | 3 | a0001c0001t0004g0127a0001c0001t0004g0213a0001c0001t0052g0191 | 3 | HG01074.hp2 HG02129.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.62-49008C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384182 | ||||||
| chr18:46384358
|
G | T | 1 | a0001c0001t0002g0017 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.62-48832G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384358 | ||||||
| chr18:46384398
|
G | C | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-48792G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384398 | ||||||
| chr18:46384413
|
T | A | 1 | a0001c0001t0002g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-48777T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384413 | ||||||
| chr18:46384468
|
G | A | 1 | a0001c0001t0009g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.62-48722G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384468 | ||||||
| chr18:46384515
|
T | C | 100 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.62-48675T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384515 | ||||||
| chr18:46384735
|
G | A | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-48455G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46384735 | ||||||
| chr18:46385020
|
C | A | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-48170C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385020 | ||||||
| chr18:46385048
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0194 | 2 | NA18980.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.62-48142G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385048 | ||||||
| chr18:46385068
|
C | A | 1 | a0001c0001t0002g0182 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.62-48122C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385068 | ||||||
| chr18:46385277
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62-47913G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385277 | ||||||
| chr18:46385298
|
G | A | 12 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0003g0059others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-47892G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385298 | ||||||
| chr18:46385375
|
C | T | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-47815C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385375 | ||||||
| chr18:46385431
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0238 | 2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.62-47759A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385431 | ||||||
| chr18:46385481
|
T | C | 98 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.62-47709T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385481 | ||||||
| chr18:46385528
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-47662T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385528 | ||||||
| chr18:46385663
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-47527G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385663 | ||||||
| chr18:46385787
|
C | T | 1 | a0001c0001t0040g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.62-47403C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385787 | ||||||
| chr18:46385813
|
C | G | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-47377C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385813 | ||||||
| chr18:46385866
|
T | C | 15 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(12): Show | 15 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-47324T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385866 | ||||||
| chr18:46385889
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0207 | 2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.62-47301C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385889 | ||||||
| chr18:46385932
|
T | A | 51 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0100others(48): Show | 51 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.62-47258T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385932 | ||||||
| chr18:46385985
|
A | C | 9 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0003g0180others(6): Show | 9 | HG02258.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-47205A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46385985 | ||||||
| chr18:46386163
|
G | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-47027G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386163 | ||||||
| chr18:46386190
|
T | C | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-47000T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386190 | ||||||
| chr18:46386207
|
G | A | 9 | a0001c0001t0001g0229a0001c0001t0003g0059a0001c0001t0005g0057others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-46983G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386207 | ||||||
| chr18:46386537
|
A | AC | 20 | a0001c0001t0001g0215a0001c0001t0002g0035a0001c0001t0002g0054others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-46647dupC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46386537 | |||||
| chr18:46386570
|
T | TCATCCAC others(1): Show |
3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62-46618_62-46617i others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46386570 | |||||
| chr18:46386573
|
C | CCCACCCA others(1): Show |
254 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.62-46605_62-46598d others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46386573 | |||||
| chr18:46386573
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62-46617C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386573 | ||||||
| chr18:46386639
|
C | T | 51 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0171others(48): Show | 53 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.62-46551C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386639 | ||||||
| chr18:46386806
|
C | G | 3 | a0001c0001t0006g0226a0001c0001t0006g0228a0001c0001t0023g0085 | 3 | HG01169.hp1 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.62-46384C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46386806 | ||||||
| chr18:46387023
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-46167A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387023 | ||||||
| chr18:46387082
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-46108C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387082 | ||||||
| chr18:46387371
|
G | A | 1 | a0001c0001t0049g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.62-45819G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387371 | ||||||
| chr18:46387611
|
C | G | 1 | a0001c0001t0026g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.62-45579C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387611 | ||||||
| chr18:46387635
|
G | C | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-45555G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387635 | ||||||
| chr18:46387647
|
C | T | 1 | a0001c0001t0053g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.62-45543C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387647 | ||||||
| chr18:46387728
|
G | C | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-45462G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387728 | ||||||
| chr18:46387739
|
T | C | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-45451T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387739 | ||||||
| chr18:46387752
|
C | T | 18 | a0001c0001t0002g0035a0001c0001t0002g0054a0001c0001t0002g0067others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.62-45438C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387752 | ||||||
| chr18:46387819
|
G | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-45371G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387819 | ||||||
| chr18:46387860
|
T | C | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-45330T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387860 | ||||||
| chr18:46387893
|
A | G | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-45297A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46387893 | ||||||
| chr18:46388052
|
A | G | 1 | a0001c0001t0014g0236 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.62-45138A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388052 | ||||||
| chr18:46388121
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-45069A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388121 | ||||||
| chr18:46388252
|
G | A | 3 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0030g0062 | 3 | HG02615.hp2 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.62-44938G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388252 | ||||||
| chr18:46388294
|
T | C | 3 | a0001c0001t0003g0208a0001c0001t0006g0195a0001c0001t0012g0078 | 3 | HG02559.hp2 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.62-44896T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388294 | ||||||
| chr18:46388322
|
C | T | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-44868C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388322 | ||||||
| chr18:46388336
|
A | G | 1 | a0001c0001t0027g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.62-44854A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388336 | ||||||
| chr18:46388372
|
T | C | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-44818T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388372 | ||||||
| chr18:46388408
|
C | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-44782C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388408 | ||||||
| chr18:46388570
|
T | A | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(6): Show | 9 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-44620T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388570 | ||||||
| chr18:46388785
|
G | T | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-44405G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388785 | ||||||
| chr18:46388960
|
G | GTTTATTG others(6112): Show |
1 | a0001c0001t0002g0003 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.62-44214_62-44213i others(6121): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46388960 | |||||
| chr18:46388991
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-44199T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388991 | ||||||
| chr18:46388994
|
C | T | 1 | a0001c0001t0047g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.62-44196C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388994 | ||||||
| chr18:46388995
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0003g0045 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.62-44195G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46388995 | ||||||
| chr18:46389002
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0015g0041others(4): Show | 7 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-44188G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389002 | ||||||
| chr18:46389047
|
C | A | 1 | a0001c0001t0002g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.62-44143C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389047 | ||||||
| chr18:46389235
|
G | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-43955G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389235 | ||||||
| chr18:46389271
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.62-43919G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389271 | ||||||
| chr18:46389317
|
A | G | 1 | a0001c0001t0005g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.62-43873A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389317 | ||||||
| chr18:46389459
|
G | A | 4 | a0001c0001t0002g0160a0001c0001t0003g0132a0001c0001t0005g0056others(1): Show | 4 | HG02738.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-43731G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389459 | ||||||
| chr18:46389459
|
G | T | 2 | a0001c0001t0002g0168a0001c0001t0002g0199 | 2 | NA18964.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.62-43731G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389459 | ||||||
| chr18:46389572
|
G | A | 1 | a0001c0001t0011g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-43618G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389572 | ||||||
| chr18:46389575
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62-43615G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389575 | ||||||
| chr18:46389746
|
T | TC | 13 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(10): Show | 13 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-43443dupC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46389746 | |||||
| chr18:46389976
|
C | T | 1 | a0002c0003t0005g0125 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.62-43214C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46389976 | ||||||
| chr18:46390008
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(10): Show | 13 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-43182G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390008 | ||||||
| chr18:46390050
|
G | T | 1 | a0001c0001t0004g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62-43140G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390050 | ||||||
| chr18:46390122
|
T | A | 76 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(73): Show | 76 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.62-43068T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390122 | ||||||
| chr18:46390153
|
C | A | 75 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(72): Show | 75 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.62-43037C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390153 | ||||||
| chr18:46390260
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-42930C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390260 | ||||||
| chr18:46390302
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.62-42888A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390302 | ||||||
| chr18:46390659
|
C | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0194 | 2 | NA18980.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.62-42531C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390659 | ||||||
| chr18:46390695
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(10): Show | 13 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-42495G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390695 | ||||||
| chr18:46390729
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62-42461T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46390729 | ||||||
| chr18:46391134
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0041g0066 | 2 | HG00099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.62-42056C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391134 | ||||||
| chr18:46391146
|
G | T | 14 | a0001c0001t0002g0035a0001c0001t0002g0054a0001c0001t0002g0067others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-42044G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391146 | ||||||
| chr18:46391175
|
C | G | 29 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(26): Show | 29 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-42015C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391175 | ||||||
| chr18:46391218
|
A | G | 1 | a0001c0001t0005g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.62-41972A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391218 | ||||||
| chr18:46391373
|
C | T | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-41817C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391373 | ||||||
| chr18:46391400
|
C | T | 57 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0100others(54): Show | 57 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.62-41790C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391400 | ||||||
| chr18:46391416
|
G | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0210a0001c0001t0018g0221 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.62-41774G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391416 | ||||||
| chr18:46391648
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.62-41542T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391648 | ||||||
| chr18:46391656
|
T | C | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62-41534T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391656 | ||||||
| chr18:46391717
|
C | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-41473C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391717 | ||||||
| chr18:46391722
|
T | C | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-41468T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391722 | ||||||
| chr18:46391741
|
A | C | 257 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.62-41449A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391741 | ||||||
| chr18:46391820
|
A | G | 2 | a0001c0001t0012g0079a0001c0001t0047g0027 | 2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.62-41370A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391820 | ||||||
| chr18:46391861
|
C | T | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-41329C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391861 | ||||||
| chr18:46391886
|
T | C | 5 | a0001c0001t0003g0180a0001c0001t0003g0187a0001c0001t0012g0155others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-41304T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391886 | ||||||
| chr18:46391938
|
C | T | 1 | a0001c0001t0011g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-41252C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391938 | ||||||
| chr18:46391947
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-41243C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391947 | ||||||
| chr18:46391948
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0013g0124a0001c0001t0054g0242 | 3 | NA18964.hp1 NA19007.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.62-41242G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46391948 | ||||||
| chr18:46392003
|
T | C | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-41187T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392003 | ||||||
| chr18:46392011
|
C | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-41179C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392011 | ||||||
| chr18:46392011
|
C | T | 44 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0100others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.62-41179C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392011 | ||||||
| chr18:46392081
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-41109C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392081 | ||||||
| chr18:46392099
|
C | T | 39 | a0001c0001t0001g0148a0001c0001t0001g0171a0001c0001t0001g0222others(36): Show | 41 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.62-41091C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392099 | ||||||
| chr18:46392100
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0002g0054a0001c0001t0002g0067others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-41090G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392100 | ||||||
| chr18:46392162
|
C | T | 1 | a0001c0001t0005g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.62-41028C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392162 | ||||||
| chr18:46392220
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-40970C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392220 | ||||||
| chr18:46392292
|
A | T | 3 | a0001c0001t0012g0155a0001c0001t0018g0076a0001c0001t0018g0231 | 3 | HG02965.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62-40898A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392292 | ||||||
| chr18:46392387
|
C | A | 1 | a0001c0001t0003g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.62-40803C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392387 | ||||||
| chr18:46392422
|
C | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-40768C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392422 | ||||||
| chr18:46392453
|
C | T | 5 | a0001c0001t0002g0250a0001c0001t0003g0180a0001c0001t0012g0155others(2): Show | 5 | HG00609.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-40737C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392453 | ||||||
| chr18:46392571
|
A | AG | 257 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.62-40618dupG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46392571 | |||||
| chr18:46392699
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0002g0116 | 2 | HG02015.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.62-40491T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392699 | ||||||
| chr18:46392835
|
C | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-40355C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392835 | ||||||
| chr18:46392941
|
C | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-40249C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392941 | ||||||
| chr18:46392954
|
A | C | 17 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0186others(14): Show | 17 | HG00673.hp2 HG02071.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-40236A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392954 | ||||||
| chr18:46392968
|
G | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-40222G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392968 | ||||||
| chr18:46392970
|
A | G | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-40220A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46392970 | ||||||
| chr18:46393312
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(5): Show | 8 | HG03491.hp2 HG03492.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-39878C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393312 | ||||||
| chr18:46393328
|
C | T | 1 | a0001c0001t0004g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.62-39862C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393328 | ||||||
| chr18:46393355
|
C | T | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-39835C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393355 | ||||||
| chr18:46393375
|
C | T | 12 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0035others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-39815C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393375 | ||||||
| chr18:46393380
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.62-39810C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393380 | ||||||
| chr18:46393445
|
C | T | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-39745C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393445 | ||||||
| chr18:46393463
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.62-39727T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393463 | ||||||
| chr18:46393513
|
C | G | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-39677C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393513 | ||||||
| chr18:46393541
|
C | A | 3 | a0001c0001t0016g0028a0001c0001t0016g0177a0001c0001t0042g0230 | 3 | HG01109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-39649C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393541 | ||||||
| chr18:46393806
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-39384G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393806 | ||||||
| chr18:46393955
|
T | C | 103 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.62-39235T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46393955 | ||||||
| chr18:46394171
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0129others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-39019G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394171 | ||||||
| chr18:46394174
|
G | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-39016G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394174 | ||||||
| chr18:46394317
|
T | C | 41 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.62-38873T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394317 | ||||||
| chr18:46394323
|
T | C | 41 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.62-38867T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394323 | ||||||
| chr18:46394349
|
C | T | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62-38841C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394349 | ||||||
| chr18:46394387
|
C | T | 1 | a0001c0001t0005g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.62-38803C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394387 | ||||||
| chr18:46394400
|
C | A | 1 | a0001c0005t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.62-38790C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394400 | ||||||
| chr18:46394855
|
G | C | 62 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0100others(59): Show | 62 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.62-38335G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394855 | ||||||
| chr18:46394902
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0238a0001c0001t0044g0166others(1): Show | 4 | HG00642.hp2 HG01106.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-38288A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394902 | ||||||
| chr18:46394954
|
C | T | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-38236C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46394954 | ||||||
| chr18:46395096
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-38094C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395096 | ||||||
| chr18:46395133
|
G | T | 1 | a0001c0001t0016g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.62-38057G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395133 | ||||||
| chr18:46395240
|
C | G | 1 | a0001c0001t0002g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-37950C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395240 | ||||||
| chr18:46395281
|
AC | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0210a0001c0001t0018g0221 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.62-37907delC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46395281 | |||||
| chr18:46395292
|
A | G | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-37898A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395292 | ||||||
| chr18:46395333
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62-37857C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395333 | ||||||
| chr18:46395410
|
A | C | 37 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(34): Show | 37 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-37780A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395410 | ||||||
| chr18:46395616
|
C | A | 1 | a0001c0001t0002g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.62-37574C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395616 | ||||||
| chr18:46395624
|
C | T | 6 | a0001c0001t0001g0165a0001c0001t0003g0180a0001c0001t0009g0111others(3): Show | 6 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-37566C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395624 | ||||||
| chr18:46395635
|
C | T | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-37555C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395635 | ||||||
| chr18:46395839
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.62-37351G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395839 | ||||||
| chr18:46395876
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.62-37314G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395876 | ||||||
| chr18:46395908
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62-37282G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46395908 | ||||||
| chr18:46396012
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-37178G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396012 | ||||||
| chr18:46396018
|
C | G | 1 | a0001c0004t0012g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.62-37172C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396018 | ||||||
| chr18:46396284
|
T | C | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-36906T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396284 | ||||||
| chr18:46396300
|
AGTT | A | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-36884_62-36882d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46396300 | |||||
| chr18:46396356
|
G | A | 2 | a0001c0001t0025g0030a0001c0001t0025g0091 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.62-36834G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396356 | ||||||
| chr18:46396571
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-36619A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396571 | ||||||
| chr18:46396587
|
C | T | 1 | a0001c0001t0037g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.62-36603C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396587 | ||||||
| chr18:46396676
|
G | A | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-36514G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396676 | ||||||
| chr18:46396740
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.62-36450A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396740 | ||||||
| chr18:46396745
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-36445A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396745 | ||||||
| chr18:46396765
|
C | T | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.62-36425C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396765 | ||||||
| chr18:46396786
|
C | T | 30 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(27): Show | 30 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.62-36404C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396786 | ||||||
| chr18:46396798
|
G | C | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-36392G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396798 | ||||||
| chr18:46396811
|
C | T | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-36379C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396811 | ||||||
| chr18:46396841
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.62-36349T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396841 | ||||||
| chr18:46396884
|
G | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-36306G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396884 | ||||||
| chr18:46396922
|
T | G | 37 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(34): Show | 37 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-36268T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46396922 | ||||||
| chr18:46397120
|
T | G | 41 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.62-36070T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397120 | ||||||
| chr18:46397201
|
G | A | 32 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(29): Show | 32 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-35989G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397201 | ||||||
| chr18:46397420
|
G | C | 1 | a0001c0001t0003g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.62-35770G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397420 | ||||||
| chr18:46397453
|
G | GGT | 5 | a0001c0001t0011g0227a0001c0001t0012g0220a0001c0001t0014g0026others(2): Show | 5 | HG01346.hp1 HG02615.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-35721_62-35720d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397453 | |||||
| chr18:46397453
|
G | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(22): Show | 25 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-35737G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397453 | ||||||
| chr18:46397489
|
G | GGGGT | 33 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0104others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-35700_62-35699i others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397489 | |||||
| chr18:46397489
|
G | GGT | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-35685_62-35684d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397489 | |||||
| chr18:46397489
|
G | GGTGT | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(6): Show | 9 | HG02615.hp1 HG03491.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-35687_62-35684d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397489 | |||||
| chr18:46397489
|
G | GGTGTGT | 14 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0154others(11): Show | 14 | HG02145.hp1 HG02451.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-35689_62-35684d others(8): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397489 | |||||
| chr18:46397491
|
T | G | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-35699T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397491 | ||||||
| chr18:46397499
|
TGTGTGTG others(21): Show |
T | 3 | a0001c0001t0007g0064a0001c0001t0025g0030a0001c0001t0032g0218 | 3 | HG02258.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-35683_62-35656d others(30): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397499 | |||||
| chr18:46397532
|
G | A | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-35658G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397532 | ||||||
| chr18:46397539
|
G | T | 6 | a0001c0001t0004g0127a0001c0001t0004g0213a0001c0001t0007g0064others(3): Show | 6 | HG01074.hp2 HG02129.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-35651G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397539 | ||||||
| chr18:46397539
|
GGGTCATG others(29): Show |
G | 40 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(37): Show | 40 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.62-35604_62-35569d others(38): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397539 | |||||
| chr18:46397550
|
G | A | 3 | a0001c0001t0007g0064a0001c0001t0025g0030a0001c0001t0032g0218 | 3 | HG02258.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-35640G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397550 | ||||||
| chr18:46397555
|
TGAGGGTG others(1390): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-35633_62-34237d others(2): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397555 | |||||
| chr18:46397557
|
AG | A | 3 | a0001c0001t0007g0064a0001c0001t0025g0030a0001c0001t0032g0218 | 3 | HG02258.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-35630delG | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397557 | |||||
| chr18:46397559
|
G | GGT | 17 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0035others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-35615_62-35614d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397559 | |||||
| chr18:46397559
|
GGTGTGTG others(31): Show |
G | 32 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(29): Show | 32 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-35615_62-35578d others(40): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397559 | |||||
| chr18:46397559
|
GGTGTGTG others(35): Show |
G | 1 | a0001c0001t0003g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.62-35619_62-35578d others(44): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397559 | |||||
| chr18:46397562
|
GT | G | 3 | a0001c0001t0007g0064a0001c0001t0025g0030a0001c0001t0032g0218 | 3 | HG02258.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-35627delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397562 | ||||||
| chr18:46397575
|
T | G | 3 | a0001c0001t0007g0064a0001c0001t0025g0030a0001c0001t0032g0218 | 3 | HG02258.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-35615T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397575 | ||||||
| chr18:46397631
|
G | GGTGT | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-35547_62-35544d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397631 | |||||
| chr18:46397643
|
T | G | 2 | a0001c0001t0001g0165a0001c0001t0009g0111 | 2 | NA18986.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.62-35547T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397643 | ||||||
| chr18:46397645
|
T | G | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-35545T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397645 | ||||||
| chr18:46397666
|
T | TTG | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-35505_62-35504d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397666 | |||||
| chr18:46397666
|
TTG | T | 2 | a0001c0001t0001g0108a0001c0001t0003g0254 | 2 | HG00280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.62-35505_62-35504d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46397666 | |||||
| chr18:46397894
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(5): Show | 8 | HG03491.hp2 HG03492.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-35296G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397894 | ||||||
| chr18:46397974
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-35216G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46397974 | ||||||
| chr18:46398086
|
G | T | 1 | a0001c0001t0051g0248 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62-35104G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398086 | ||||||
| chr18:46398098
|
A | T | 1 | a0001c0001t0004g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.62-35092A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398098 | ||||||
| chr18:46398131
|
G | A | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.62-35059G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398131 | ||||||
| chr18:46398279
|
T | C | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-34911T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398279 | ||||||
| chr18:46398313
|
G | A | 1 | a0001c0001t0033g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.62-34877G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398313 | ||||||
| chr18:46398454
|
C | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-34736C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398454 | ||||||
| chr18:46398769
|
G | A | 32 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(29): Show | 32 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-34421G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46398769 | ||||||
| chr18:46399193
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-33997C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399193 | ||||||
| chr18:46399272
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-33918C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399272 | ||||||
| chr18:46399411
|
C | T | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-33779C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399411 | ||||||
| chr18:46399457
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.62-33733G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399457 | ||||||
| chr18:46399464
|
C | T | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-33726C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399464 | ||||||
| chr18:46399476
|
C | T | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-33714C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399476 | ||||||
| chr18:46399690
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-33500G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399690 | ||||||
| chr18:46399736
|
A | G | 87 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(84): Show | 87 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-33454A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399736 | ||||||
| chr18:46399743
|
G | A | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-33447G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399743 | ||||||
| chr18:46399957
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-33233C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399957 | ||||||
| chr18:46399962
|
C | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-33228C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399962 | ||||||
| chr18:46399975
|
T | G | 38 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.62-33215T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46399975 | ||||||
| chr18:46400113
|
C | T | 37 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(34): Show | 37 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-33077C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400113 | ||||||
| chr18:46400296
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.62-32894T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400296 | ||||||
| chr18:46400349
|
A | G | 16 | a0001c0001t0001g0158a0001c0001t0001g0229a0001c0001t0002g0160others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.62-32841A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400349 | ||||||
| chr18:46400650
|
T | A | 1 | a0001c0001t0004g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.62-32540T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400650 | ||||||
| chr18:46400707
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-32483C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400707 | ||||||
| chr18:46400836
|
A | G | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-32354A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400836 | ||||||
| chr18:46400932
|
T | G | 37 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(34): Show | 37 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-32258T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400932 | ||||||
| chr18:46400956
|
G | A | 120 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.62-32234G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400956 | ||||||
| chr18:46400994
|
G | A | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62-32196G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46400994 | ||||||
| chr18:46401019
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-32171C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46401019 | ||||||
| chr18:46401684
|
G | A | 2 | a0001c0001t0003g0187a0001c0001t0043g0008 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.62-31506G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46401684 | ||||||
| chr18:46401764
|
A | C | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-31426A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46401764 | ||||||
| chr18:46401788
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-31402T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46401788 | ||||||
| chr18:46401985
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0002g0068a0001c0001t0005g0217others(3): Show | 6 | HG03491.hp2 HG03492.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-31205T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46401985 | ||||||
| chr18:46402020
|
T | C | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-31170T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402020 | ||||||
| chr18:46402230
|
C | A | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-30960C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402230 | ||||||
| chr18:46402268
|
T | C | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-30922T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402268 | ||||||
| chr18:46402315
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-30875C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402315 | ||||||
| chr18:46402331
|
A | AT | 50 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(47): Show | 50 | HG01069.hp2 HG01081.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.62-30855dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46402331 | |||||
| chr18:46402509
|
A | G | 84 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(81): Show | 84 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.62-30681A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402509 | ||||||
| chr18:46402517
|
G | GT | 10 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-30664dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46402517 | |||||
| chr18:46402519
|
T | G | 27 | a0001c0001t0001g0229a0001c0001t0002g0004a0001c0001t0002g0017others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.62-30671T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402519 | ||||||
| chr18:46402557
|
C | T | 50 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(47): Show | 50 | HG01069.hp2 HG01081.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.62-30633C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402557 | ||||||
| chr18:46402567
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-30623C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402567 | ||||||
| chr18:46402620
|
A | G | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-30570A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402620 | ||||||
| chr18:46402626
|
C | T | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-30564C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402626 | ||||||
| chr18:46402691
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-30499A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402691 | ||||||
| chr18:46402902
|
G | A | 23 | a0001c0001t0001g0229a0001c0001t0002g0004a0001c0001t0002g0017others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-30288G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402902 | ||||||
| chr18:46402945
|
G | A | 1 | a0001c0001t0004g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.62-30245G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402945 | ||||||
| chr18:46402990
|
C | T | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-30200C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46402990 | ||||||
| chr18:46403037
|
C | CT | 86 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(83): Show | 86 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.62-30151dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46403037 | |||||
| chr18:46403143
|
C | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-30047C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403143 | ||||||
| chr18:46403157
|
G | A | 1 | a0001c0001t0009g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.62-30033G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403157 | ||||||
| chr18:46403172
|
C | A | 35 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(32): Show | 35 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.62-30018C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403172 | ||||||
| chr18:46403212
|
G | A | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-29978G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403212 | ||||||
| chr18:46403230
|
A | T | 7 | a0001c0001t0001g0158a0001c0001t0002g0160a0001c0001t0003g0132others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-29960A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403230 | ||||||
| chr18:46403252
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-29938T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403252 | ||||||
| chr18:46403373
|
G | A | 34 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(31): Show | 34 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.62-29817G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403373 | ||||||
| chr18:46403389
|
G | C | 1 | a0001c0001t0058g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-29801G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403389 | ||||||
| chr18:46403738
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-29452C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403738 | ||||||
| chr18:46403739
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.62-29451G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403739 | ||||||
| chr18:46403955
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-29235C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403955 | ||||||
| chr18:46403991
|
G | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(120): Show | 123 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-29199G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403991 | ||||||
| chr18:46403992
|
T | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(120): Show | 123 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-29198T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46403992 | ||||||
| chr18:46404080
|
T | C | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-29110T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404080 | ||||||
| chr18:46404184
|
G | A | 20 | a0001c0001t0001g0229a0001c0001t0002g0004a0001c0001t0002g0017others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-29006G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404184 | ||||||
| chr18:46404217
|
C | T | 1 | a0001c0001t0035g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62-28973C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404217 | ||||||
| chr18:46404462
|
G | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(120): Show | 123 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-28728G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404462 | ||||||
| chr18:46404488
|
T | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-28702T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404488 | ||||||
| chr18:46404559
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-28631G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404559 | ||||||
| chr18:46404607
|
G | T | 7 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(4): Show | 7 | HG02451.hp1 HG02886.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-28583G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404607 | ||||||
| chr18:46404722
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-28468C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404722 | ||||||
| chr18:46404746
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.62-28444C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404746 | ||||||
| chr18:46404787
|
T | TACACACA others(5): Show |
14 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-28401_62-28390d others(14): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46404787 | |||||
| chr18:46404787
|
T | TACACACA others(7): Show |
1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-28390_62-28389i others(16): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46404787 | |||||
| chr18:46404815
|
AAAAC | A | 28 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0104others(25): Show | 28 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.62-28360_62-28357d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46404815 | |||||
| chr18:46404823
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-28367C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404823 | ||||||
| chr18:46404956
|
A | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(86): Show | 89 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.62-28234A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404956 | ||||||
| chr18:46404975
|
G | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(12): Show | 15 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-28215G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46404975 | ||||||
| chr18:46405070
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0027g0014 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.62-28120A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405070 | ||||||
| chr18:46405145
|
A | C | 17 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-28045A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405145 | ||||||
| chr18:46405263
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-27927C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405263 | ||||||
| chr18:46405565
|
G | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-27625G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405565 | ||||||
| chr18:46405589
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-27601C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405589 | ||||||
| chr18:46405741
|
T | C | 30 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(27): Show | 30 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.62-27449T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405741 | ||||||
| chr18:46405754
|
C | G | 1 | a0001c0001t0002g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.62-27436C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405754 | ||||||
| chr18:46405873
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.62-27317C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405873 | ||||||
| chr18:46405882
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0145 | 2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.62-27308C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405882 | ||||||
| chr18:46405952
|
T | C | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-27238T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46405952 | ||||||
| chr18:46406034
|
C | T | 1 | a0001c0001t0009g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.62-27156C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406034 | ||||||
| chr18:46406119
|
T | A | 2 | a0001c0001t0002g0115a0001c0001t0034g0200 | 2 | HG02155.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.62-27071T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406119 | ||||||
| chr18:46406242
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-26948C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406242 | ||||||
| chr18:46406279
|
C | T | 8 | a0001c0001t0003g0059a0001c0001t0005g0057a0001c0001t0005g0103others(5): Show | 8 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-26911C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406279 | ||||||
| chr18:46406317
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0011g0256others(5): Show | 8 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-26873G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406317 | ||||||
| chr18:46406384
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.62-26806C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406384 | ||||||
| chr18:46406638
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-26552G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406638 | ||||||
| chr18:46406696
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-26494T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406696 | ||||||
| chr18:46406889
|
CTTACCCT others(15): Show |
C | 2 | a0001c0001t0006g0109a0001c0001t0041g0066 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.62-26300_62-26279d others(24): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46406889 | ||||||
| chr18:46407055
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.62-26135C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407055 | ||||||
| chr18:46407306
|
T | A | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.62-25884T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407306 | ||||||
| chr18:46407485
|
G | A | 1 | a0001c0001t0036g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.62-25705G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407485 | ||||||
| chr18:46407612
|
G | C | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-25578G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407612 | ||||||
| chr18:46407816
|
G | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-25374G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407816 | ||||||
| chr18:46407880
|
C | A | 1 | a0001c0001t0037g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.62-25310C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407880 | ||||||
| chr18:46407912
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0012g0220a0001c0001t0014g0026others(2): Show | 5 | HG02615.hp2 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-25278C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407912 | ||||||
| chr18:46407972
|
G | A | 39 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(36): Show | 39 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-25218G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46407972 | ||||||
| chr18:46408192
|
G | A | 3 | a0001c0001t0005g0103a0001c0001t0006g0038a0001c0001t0006g0144 | 3 | HG00140.hp2 HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.62-24998G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408192 | ||||||
| chr18:46408238
|
G | A | 1 | a0001c0001t0055g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.62-24952G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408238 | ||||||
| chr18:46408242
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-24948G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408242 | ||||||
| chr18:46408333
|
T | G | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-24857T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408333 | ||||||
| chr18:46408339
|
T | C | 1 | a0001c0001t0018g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62-24851T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408339 | ||||||
| chr18:46408370
|
G | T | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.62-24820G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408370 | ||||||
| chr18:46408482
|
G | C | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.62-24708G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408482 | ||||||
| chr18:46408492
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(12): Show | 15 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-24698A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408492 | ||||||
| chr18:46408512
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-24678G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408512 | ||||||
| chr18:46408520
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-24670G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408520 | ||||||
| chr18:46408669
|
A | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.62-24521A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408669 | ||||||
| chr18:46408728
|
C | T | 1 | a0001c0001t0041g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.62-24462C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408728 | ||||||
| chr18:46408837
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-24353T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408837 | ||||||
| chr18:46408893
|
T | C | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.62-24297T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46408893 | ||||||
| chr18:46409161
|
T | C | 1 | a0001c0001t0005g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.62-24029T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409161 | ||||||
| chr18:46409249
|
G | A | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.62-23941G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409249 | ||||||
| chr18:46409334
|
G | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-23856G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409334 | ||||||
| chr18:46409374
|
T | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-23816T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409374 | ||||||
| chr18:46409406
|
G | A | 1 | a0001c0001t0012g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-23784G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409406 | ||||||
| chr18:46409577
|
A | AACCAGAG others(17): Show |
1 | a0001c0001t0011g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.62-23611_62-23588d others(26): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46409577 | |||||
| chr18:46409892
|
A | C | 44 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0104others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.62-23298A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46409892 | ||||||
| chr18:46410104
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-23086G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410104 | ||||||
| chr18:46410150
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-23040C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410150 | ||||||
| chr18:46410452
|
C | T | 1 | a0001c0001t0008g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62-22738C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410452 | ||||||
| chr18:46410683
|
T | C | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-22507T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410683 | ||||||
| chr18:46410805
|
C | T | 1 | a0001c0001t0043g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.62-22385C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410805 | ||||||
| chr18:46410816
|
T | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.62-22374T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410816 | ||||||
| chr18:46410848
|
C | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-22342C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410848 | ||||||
| chr18:46410941
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0036others(57): Show | 60 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.62-22249G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46410941 | ||||||
| chr18:46411148
|
A | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.62-22042A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411148 | ||||||
| chr18:46411179
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-22011C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411179 | ||||||
| chr18:46411259
|
C | T | 3 | a0001c0001t0016g0028a0001c0001t0016g0177a0001c0001t0042g0230 | 3 | HG01109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-21931C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411259 | ||||||
| chr18:46411279
|
G | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-21911G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411279 | ||||||
| chr18:46411303
|
A | G | 2 | a0001c0001t0002g0168a0001c0001t0002g0199 | 2 | NA18964.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.62-21887A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411303 | ||||||
| chr18:46411325
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.62-21865G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411325 | ||||||
| chr18:46411393
|
G | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.62-21797G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411393 | ||||||
| chr18:46411499
|
G | A | 1 | a0001c0001t0004g0213 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.62-21691G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411499 | ||||||
| chr18:46411500
|
A | T | 2 | a0001c0001t0025g0030a0001c0001t0025g0091 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.62-21690A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411500 | ||||||
| chr18:46411502
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-21688T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411502 | ||||||
| chr18:46411566
|
G | T | 76 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.62-21624G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411566 | ||||||
| chr18:46411703
|
G | A | 2 | a0001c0001t0025g0030a0001c0001t0025g0091 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.62-21487G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46411703 | ||||||
| chr18:46412060
|
T | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(11): Show | 14 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-21130T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412060 | ||||||
| chr18:46412095
|
C | T | 1 | a0001c0001t0038g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.62-21095C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412095 | ||||||
| chr18:46412134
|
G | C | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-21056G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412134 | ||||||
| chr18:46412468
|
G | A | 1 | a0001c0001t0020g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.62-20722G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412468 | ||||||
| chr18:46412519
|
A | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-20671A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412519 | ||||||
| chr18:46412636
|
T | C | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-20554T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412636 | ||||||
| chr18:46412739
|
C | G | 2 | a0001c0001t0001g0223a0001c0001t0009g0163 | 2 | NA18981.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.62-20451C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412739 | ||||||
| chr18:46412806
|
T | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-20384T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412806 | ||||||
| chr18:46412835
|
A | G | 16 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0100others(13): Show | 16 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.62-20355A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412835 | ||||||
| chr18:46412928
|
C | T | 1 | a0001c0001t0007g0232 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.62-20262C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412928 | ||||||
| chr18:46412939
|
C | G | 1 | a0001c0005t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.62-20251C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46412939 | ||||||
| chr18:46413259
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(45): Show | 48 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.62-19931C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46413259 | ||||||
| chr18:46413388
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-19802A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46413388 | ||||||
| chr18:46413523
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0238a0001c0001t0044g0166others(1): Show | 4 | HG00642.hp2 HG01106.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-19667C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46413523 | ||||||
| chr18:46413870
|
C | G | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-19320C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46413870 | ||||||
| chr18:46413901
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(47): Show | 50 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.62-19289G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46413901 | ||||||
| chr18:46414434
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.62-18756C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414434 | ||||||
| chr18:46414453
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(45): Show | 48 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.62-18737C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414453 | ||||||
| chr18:46414512
|
C | G | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-18678C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414512 | ||||||
| chr18:46414579
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-18611C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414579 | ||||||
| chr18:46414691
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-18499T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414691 | ||||||
| chr18:46414736
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-18454C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414736 | ||||||
| chr18:46414871
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0017 | 2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.62-18319T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414871 | ||||||
| chr18:46414880
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.62-18310A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414880 | ||||||
| chr18:46414906
|
C | T | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-18284C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46414906 | ||||||
| chr18:46415052
|
G | A | 1 | a0001c0001t0058g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-18138G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415052 | ||||||
| chr18:46415117
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(113): Show | 116 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.62-18073G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415117 | ||||||
| chr18:46415136
|
C | G | 5 | a0001c0001t0005g0103a0001c0001t0006g0038a0001c0001t0006g0144others(2): Show | 5 | HG00140.hp2 HG01192.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-18054C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415136 | ||||||
| chr18:46415145
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-18045A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415145 | ||||||
| chr18:46415212
|
G | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(45): Show | 48 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.62-17978G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415212 | ||||||
| chr18:46415337
|
G | T | 4 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-17853G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415337 | ||||||
| chr18:46415418
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.62-17772C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415418 | ||||||
| chr18:46415442
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(5): Show | 8 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-17748C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415442 | ||||||
| chr18:46415504
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-17686C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415504 | ||||||
| chr18:46415508
|
A | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(46): Show | 49 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.62-17682A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415508 | ||||||
| chr18:46415543
|
T | A | 1 | a0001c0001t0003g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.62-17647T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415543 | ||||||
| chr18:46415547
|
A | T | 39 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0104others(36): Show | 39 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-17643A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415547 | ||||||
| chr18:46415599
|
A | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(113): Show | 116 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.62-17591A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415599 | ||||||
| chr18:46415616
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-17574C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415616 | ||||||
| chr18:46415617
|
G | A | 43 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0104others(40): Show | 43 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-17573G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415617 | ||||||
| chr18:46415796
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-17394C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46415796 | ||||||
| chr18:46416046
|
A | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0036others(53): Show | 56 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.62-17144A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416046 | ||||||
| chr18:46416073
|
G | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-17117G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416073 | ||||||
| chr18:46416227
|
C | T | 115 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(112): Show | 115 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.62-16963C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416227 | ||||||
| chr18:46416380
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0009g0193a0001c0001t0009g0219 | 3 | NA18966.hp1 NA18986.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.62-16810G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416380 | ||||||
| chr18:46416422
|
T | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-16768T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416422 | ||||||
| chr18:46416465
|
T | G | 116 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(113): Show | 116 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.62-16725T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416465 | ||||||
| chr18:46416501
|
A | G | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-16689A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416501 | ||||||
| chr18:46416531
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.62-16659C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416531 | ||||||
| chr18:46416538
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-16652C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416538 | ||||||
| chr18:46416611
|
C | A | 9 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0003g0012others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-16579C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416611 | ||||||
| chr18:46416666
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.62-16524A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416666 | ||||||
| chr18:46416679
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(40): Show | 43 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.62-16511C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416679 | ||||||
| chr18:46416882
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-16308C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416882 | ||||||
| chr18:46416906
|
G | A | 113 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(110): Show | 113 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.62-16284G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416906 | ||||||
| chr18:46416982
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-16208A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46416982 | ||||||
| chr18:46417258
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62-15932T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417258 | ||||||
| chr18:46417376
|
C | T | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62-15814C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417376 | ||||||
| chr18:46417498
|
G | T | 8 | a0001c0001t0003g0060a0001c0001t0003g0090a0001c0001t0003g0157others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-15692G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417498 | ||||||
| chr18:46417717
|
A | G | 94 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(91): Show | 94 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.62-15473A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417717 | ||||||
| chr18:46417764
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0002g0068a0001c0001t0005g0217others(3): Show | 6 | HG03491.hp2 HG03492.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-15426G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417764 | ||||||
| chr18:46417772
|
G | A | 3 | a0001c0001t0003g0059a0001c0001t0005g0057a0001c0001t0064g0084 | 3 | HG00140.hp1 HG01517.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-15418G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417772 | ||||||
| chr18:46417820
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.62-15370A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417820 | ||||||
| chr18:46417980
|
A | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(129): Show | 132 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.62-15210A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46417980 | ||||||
| chr18:46417999
|
TA | T | 43 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0036others(40): Show | 43 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-15180delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46417999 | |||||
| chr18:46418271
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-14919C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418271 | ||||||
| chr18:46418272
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-14918G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418272 | ||||||
| chr18:46418341
|
G | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0170others(48): Show | 51 | HG00609.hp2 HG00673.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.62-14849G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418341 | ||||||
| chr18:46418569
|
A | G | 1 | a0001c0001t0049g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.62-14621A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418569 | ||||||
| chr18:46418768
|
C | A | 1 | a0001c0001t0011g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.62-14422C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418768 | ||||||
| chr18:46418868
|
T | C | 18 | a0001c0001t0003g0098a0001c0001t0007g0031a0001c0001t0007g0064others(15): Show | 18 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.62-14322T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418868 | ||||||
| chr18:46418947
|
C | T | 1 | a0001c0001t0053g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.62-14243C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46418947 | ||||||
| chr18:46419044
|
G | A | 1 | a0001c0001t0063g0043 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.62-14146G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419044 | ||||||
| chr18:46419301
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(109): Show | 112 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.62-13889T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419301 | ||||||
| chr18:46419460
|
C | T | 123 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0106others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.62-13730C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419460 | ||||||
| chr18:46419492
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(5): Show | 8 | HG00280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-13698C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419492 | ||||||
| chr18:46419539
|
C | A | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-13651C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419539 | ||||||
| chr18:46419639
|
G | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(7): Show | 10 | HG01496.hp1 HG03491.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-13551G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419639 | ||||||
| chr18:46419841
|
C | G | 1 | a0001c0001t0007g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-13349C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419841 | ||||||
| chr18:46419885
|
C | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-13305C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419885 | ||||||
| chr18:46419942
|
G | A | 73 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(70): Show | 73 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.62-13248G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46419942 | ||||||
| chr18:46420016
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.62-13174G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420016 | ||||||
| chr18:46420023
|
G | A | 74 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(71): Show | 74 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.62-13167G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420023 | ||||||
| chr18:46420152
|
A | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-13038A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420152 | ||||||
| chr18:46420192
|
C | T | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-12998C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420192 | ||||||
| chr18:46420345
|
G | A | 1 | a0001c0001t0025g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.62-12845G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420345 | ||||||
| chr18:46420580
|
C | T | 4 | a0001c0001t0003g0180a0001c0001t0012g0155a0001c0001t0018g0076others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-12610C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420580 | ||||||
| chr18:46420632
|
T | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(69): Show | 72 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.62-12558T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420632 | ||||||
| chr18:46420776
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.62-12414T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420776 | ||||||
| chr18:46420892
|
C | T | 238 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.62-12298C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420892 | ||||||
| chr18:46420947
|
A | C | 1 | a0001c0001t0040g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.62-12243A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420947 | ||||||
| chr18:46420963
|
C | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(69): Show | 72 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.62-12227C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46420963 | ||||||
| chr18:46420990
|
CCCAATGC others(3): Show |
C | 7 | a0001c0001t0007g0095a0001c0001t0016g0028a0001c0001t0016g0156others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-12196_62-12187d others(12): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46420990 | |||||
| chr18:46421029
|
C | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(54): Show | 57 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.62-12161C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421029 | ||||||
| chr18:46421098
|
T | G | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.62-12092T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421098 | ||||||
| chr18:46421285
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0046g0025 | 3 | HG01884.hp2 HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-11905T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421285 | ||||||
| chr18:46421365
|
A | ATCAT | 62 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0118others(59): Show | 62 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.62-11797_62-11794d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46421365 | |||||
| chr18:46421365
|
ATCAT | A | 31 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(28): Show | 31 | HG01081.hp1 HG01346.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.62-11797_62-11794d others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46421365 | |||||
| chr18:46421365
|
ATCATTCA others(1): Show |
A | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-11801_62-11794d others(10): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46421365 | |||||
| chr18:46421563
|
G | A | 13 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0003g0012others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.62-11627G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421563 | ||||||
| chr18:46421572
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(9): Show | 12 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-11618G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421572 | ||||||
| chr18:46421608
|
A | T | 70 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(67): Show | 70 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-11582A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421608 | ||||||
| chr18:46421613
|
C | T | 1 | a0001c0001t0004g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.62-11577C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421613 | ||||||
| chr18:46421783
|
G | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(8): Show | 11 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-11407G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421783 | ||||||
| chr18:46421884
|
T | C | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-11306T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421884 | ||||||
| chr18:46421894
|
T | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0187 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-11296T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421894 | ||||||
| chr18:46421897
|
C | G | 1 | a0002c0003t0005g0125 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.62-11293C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421897 | ||||||
| chr18:46421968
|
T | C | 13 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0110others(10): Show | 13 | HG01081.hp1 HG01346.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-11222T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421968 | ||||||
| chr18:46421974
|
T | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(69): Show | 72 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.62-11216T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421974 | ||||||
| chr18:46421998
|
G | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0170others(36): Show | 39 | HG00609.hp2 HG00673.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-11192G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46421998 | ||||||
| chr18:46422016
|
A | T | 2 | a0001c0001t0004g0107a0001c0001t0004g0201 | 2 | HG00609.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.62-11174A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422016 | ||||||
| chr18:46422037
|
C | A | 5 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0003g0012others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-11153C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422037 | ||||||
| chr18:46422221
|
C | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0023 | 2 | NA19007.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.62-10969C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422221 | ||||||
| chr18:46422239
|
G | A | 35 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(32): Show | 35 | HG01081.hp1 HG01346.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-10951G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422239 | ||||||
| chr18:46422305
|
C | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(67): Show | 70 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-10885C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422305 | ||||||
| chr18:46422337
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-10853G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422337 | ||||||
| chr18:46422357
|
C | G | 127 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0106others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.62-10833C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422357 | ||||||
| chr18:46422458
|
G | C | 71 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(68): Show | 71 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.62-10732G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422458 | ||||||
| chr18:46422546
|
C | T | 2 | a0001c0001t0024g0061a0001c0001t0024g0245 | 2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.62-10644C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422546 | ||||||
| chr18:46422606
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-10584G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422606 | ||||||
| chr18:46422937
|
G | A | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.62-10253G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46422937 | ||||||
| chr18:46423150
|
C | A | 2 | a0001c0001t0003g0187a0001c0001t0003g0210 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-10040C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423150 | ||||||
| chr18:46423160
|
G | A | 1 | a0001c0001t0008g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.62-10030G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423160 | ||||||
| chr18:46423163
|
G | T | 2 | a0001c0001t0013g0124a0001c0001t0054g0242 | 2 | NA18964.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.62-10027G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423163 | ||||||
| chr18:46423464
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0194others(6): Show | 9 | HG01496.hp1 HG03491.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-9726G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423464 | ||||||
| chr18:46423524
|
C | T | 1 | a0001c0001t0059g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.62-9666C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423524 | ||||||
| chr18:46423815
|
G | A | 2 | a0001c0002t0010g0001a0001c0002t0010g0176 | 4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-9375G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423815 | ||||||
| chr18:46423896
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.62-9294C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46423896 | ||||||
| chr18:46424084
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.62-9106A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424084 | ||||||
| chr18:46424180
|
A | G | 234 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.62-9010A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424180 | ||||||
| chr18:46424202
|
G | A | 238 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.62-8988G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424202 | ||||||
| chr18:46424281
|
C | T | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.62-8909C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424281 | ||||||
| chr18:46424565
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0251others(1): Show | 4 | NA18970.hp2 NA19012.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-8625C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424565 | ||||||
| chr18:46424600
|
C | T | 4 | a0001c0001t0012g0220a0001c0001t0014g0026a0001c0001t0014g0236others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-8590C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424600 | ||||||
| chr18:46424763
|
G | T | 19 | a0001c0001t0001g0148a0001c0001t0001g0171a0001c0001t0001g0225others(16): Show | 19 | HG00741.hp1 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-8427G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424763 | ||||||
| chr18:46424995
|
T | C | 234 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.62-8195T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424995 | ||||||
| chr18:46425119
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.62-8071C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46425119 | ||||||
| chr18:46425312
|
G | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0087others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.62-7878G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46425312 | ||||||
| chr18:46425379
|
C | A | 48 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0104others(45): Show | 48 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.62-7811C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46425379 | ||||||
| chr18:46425780
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.62-7410C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46425780 | ||||||
| chr18:46425990
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-7200G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46425990 | ||||||
| chr18:46426238
|
C | A | 1 | a0001c0001t0003g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.62-6952C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46426238 | ||||||
| chr18:46426413
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.62-6777C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46426413 | ||||||
| chr18:46426440
|
G | A | 33 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0106others(30): Show | 33 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-6750G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46426440 | ||||||
| chr18:46426516
|
C | T | 1 | a0001c0001t0026g0052 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.62-6674C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46426516 | ||||||
| chr18:46426973
|
A | T | 236 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.62-6217A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46426973 | ||||||
| chr18:46427166
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0181a0001c0001t0001g0247others(2): Show | 5 | HG01358.hp1 HG01433.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-6024G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427166 | ||||||
| chr18:46427310
|
G | A | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-5880G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427310 | ||||||
| chr18:46427325
|
C | A | 1 | a0001c0001t0050g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.62-5865C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427325 | ||||||
| chr18:46427364
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.62-5826G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427364 | ||||||
| chr18:46427389
|
C | G | 129 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.62-5801C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427389 | ||||||
| chr18:46427642
|
G | GC | 3 | a0001c0001t0001g0229a0001c0001t0003g0011a0001c0001t0046g0025 | 3 | HG01884.hp2 HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-5547dupC | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46427642 | |||||
| chr18:46427885
|
T | C | 1 | a0001c0001t0030g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-5305T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46427885 | ||||||
| chr18:46428057
|
C | T | 149 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0087others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.62-5133C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428057 | ||||||
| chr18:46428078
|
G | A | 48 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0104others(45): Show | 48 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.62-5112G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428078 | ||||||
| chr18:46428170
|
G | C | 5 | a0001c0001t0003g0090a0001c0001t0003g0180a0001c0001t0018g0076others(2): Show | 5 | HG02559.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-5020G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428170 | ||||||
| chr18:46428238
|
G | A | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-4952G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428238 | ||||||
| chr18:46428302
|
G | A | 1 | a0001c0001t0009g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.62-4888G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428302 | ||||||
| chr18:46428345
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.62-4845A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428345 | ||||||
| chr18:46428395
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-4795G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428395 | ||||||
| chr18:46428633
|
C | T | 2 | a0001c0001t0019g0002a0001c0001t0029g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.62-4557C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428633 | ||||||
| chr18:46428720
|
T | C | 1 | a0001c0001t0023g0042 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.62-4470T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428720 | ||||||
| chr18:46428839
|
T | C | 9 | a0001c0001t0003g0011a0001c0001t0008g0071a0001c0001t0008g0072others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-4351T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428839 | ||||||
| chr18:46428876
|
T | C | 255 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.62-4314T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428876 | ||||||
| chr18:46428888
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.62-4302G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46428888 | ||||||
| chr18:46429216
|
A | G | 7 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-3974A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46429216 | ||||||
| chr18:46429377
|
C | T | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-3813C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46429377 | ||||||
| chr18:46429441
|
T | A | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62-3749T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46429441 | ||||||
| chr18:46429768
|
CT | C | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-3413delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46429768 | |||||
| chr18:46429862
|
C | T | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62-3328C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46429862 | ||||||
| chr18:46429894
|
G | T | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-3296G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46429894 | ||||||
| chr18:46430264
|
A | G | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-2926A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430264 | ||||||
| chr18:46430331
|
G | A | 16 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(13): Show | 16 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.62-2859G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430331 | ||||||
| chr18:46430416
|
C | A | 7 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-2774C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430416 | ||||||
| chr18:46430771
|
G | T | 1 | a0001c0001t0010g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.62-2419G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430771 | ||||||
| chr18:46430786
|
G | C | 9 | a0001c0001t0003g0011a0001c0001t0008g0071a0001c0001t0008g0072others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-2404G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430786 | ||||||
| chr18:46430813
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.62-2377T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430813 | ||||||
| chr18:46430997
|
A | G | 9 | a0001c0001t0003g0011a0001c0001t0008g0071a0001c0001t0008g0072others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-2193A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46430997 | ||||||
| chr18:46431295
|
C | G | 1 | a0001c0001t0049g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.62-1895C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431295 | ||||||
| chr18:46431412
|
G | A | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.62-1778G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431412 | ||||||
| chr18:46431471
|
A | G | 33 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(30): Show | 33 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.62-1719A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431471 | ||||||
| chr18:46431490
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-1700A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431490 | ||||||
| chr18:46431548
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.62-1642G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431548 | ||||||
| chr18:46431629
|
CCTG | C | 7 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-1557_62-1555del others(3): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46431629 | |||||
| chr18:46431837
|
G | A | 1 | a0001c0001t0014g0236 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.62-1353G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46431837 | ||||||
| chr18:46432113
|
A | G | 9 | a0001c0001t0004g0010a0001c0001t0004g0021a0001c0001t0004g0093others(6): Show | 9 | HG00673.hp1 HG02080.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-1077A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432113 | ||||||
| chr18:46432140
|
C | T | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-1050C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432140 | ||||||
| chr18:46432333
|
T | C | 1 | a0001c0001t0054g0242 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.62-857T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432333 | ||||||
| chr18:46432447
|
A | G | 28 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(25): Show | 28 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.62-743A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432447 | ||||||
| chr18:46432588
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.62-602G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432588 | ||||||
| chr18:46432651
|
G | A | 1 | a0001c0001t0065g0198 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.62-539G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432651 | ||||||
| chr18:46432723
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0194 | 2 | NA18980.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.62-467C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432723 | ||||||
| chr18:46432867
|
T | C | 3 | a0001c0002t0010g0001a0001c0002t0010g0126a0001c0002t0010g0176 | 5 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-323T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432867 | ||||||
| chr18:46432874
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.62-316G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432874 | ||||||
| chr18:46432939
|
C | T | 5 | a0001c0001t0003g0029a0001c0001t0003g0045a0001c0001t0020g0013others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-251C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432939 | ||||||
| chr18:46432970
|
A | AT | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(10): Show | 13 | HG00280.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-220_62-219insT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432970 | ||||||
| chr18:46432970
|
A | ATAAAT | 7 | a0001c0001t0001g0050a0001c0001t0001g0171a0001c0001t0001g0209others(4): Show | 7 | HG00741.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-220_62-219insTA others(3): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46432970 | ||||||
| chr18:46433007
|
G | A | 128 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.62-183G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46433007 | ||||||
| chr18:46433119
|
T | C | 2 | a0001c0001t0004g0107a0001c0001t0004g0201 | 2 | HG00609.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.62-71T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46433119 | ||||||
| chr18:46433127
|
AGGGTCAG others(6): Show |
A | 2 | a0001c0001t0004g0107a0001c0001t0004g0201 | 2 | HG00609.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.62-60_62-48delGTCA others(9): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 46433127 | |||||
| chr18:46433637
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0222 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.377+132T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46433637 | ||||||
| chr18:46433645
|
T | C | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.377+140T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46433645 | ||||||
| chr18:46433723
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0027g0014 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.377+218T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46433723 | ||||||
| chr18:46433845
|
G | A | 7 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(4): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.377+340G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46433845 | ||||||
| chr18:46433929
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.377+424C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46433929 | ||||||
| chr18:46434119
|
G | A | 1 | a0001c0001t0009g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.377+614G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46434119 | ||||||
| chr18:46434335
|
C | G | 3 | a0001c0002t0010g0001a0001c0002t0010g0126a0001c0002t0010g0176 | 5 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.377+830C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46434335 | ||||||
| chr18:46434473
|
G | A | 7 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-816G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 2/7 | chr18 | 46434473 | ||||||
| chr18:46435674
|
A | G | 2 | a0001c0001t0006g0109a0001c0001t0041g0066 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.485+278A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46435674 | ||||||
| chr18:46435680
|
C | T | 122 | a0001c0001t0001g0147a0001c0001t0001g0225a0001c0001t0001g0238others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.485+284C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46435680 | ||||||
| chr18:46435900
|
C | A | 1 | a0001c0001t0046g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485+504C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46435900 | ||||||
| chr18:46436175
|
C | T | 28 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(25): Show | 28 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+779C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46436175 | ||||||
| chr18:46436217
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.485+821A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46436217 | ||||||
| chr18:46436296
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0046g0025 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.485+900A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46436296 | ||||||
| chr18:46436724
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+1328T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46436724 | ||||||
| chr18:46436774
|
C | G | 2 | a0001c0001t0004g0099a0001c0001t0004g0105 | 2 | HG00544.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.485+1378C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46436774 | ||||||
| chr18:46437011
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG00280.hp1 HG00741.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+1615C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437011 | ||||||
| chr18:46437138
|
T | TCCCTGCC others(21): Show |
7 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+1750_485+1777d others(30): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46437138 | |||||
| chr18:46437295
|
G | A | 3 | a0001c0001t0004g0093a0001c0001t0004g0257a0001c0001t0026g0022 | 3 | NA18950.hp2 NA18993.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.485+1899G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437295 | ||||||
| chr18:46437377
|
G | T | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.485+1981G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437377 | ||||||
| chr18:46437567
|
C | G | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.485+2171C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437567 | ||||||
| chr18:46437691
|
T | TAGAGAGG others(9): Show |
1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.485+2295_485+2296i others(18): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437691 | ||||||
| chr18:46437735
|
C | T | 1 | a0001c0001t0031g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.485+2339C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437735 | ||||||
| chr18:46437763
|
T | A | 3 | a0001c0001t0018g0076a0001c0001t0018g0221a0001c0001t0018g0231 | 3 | HG02622.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.485+2367T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437763 | ||||||
| chr18:46437929
|
C | T | 5 | a0001c0001t0002g0023a0001c0001t0002g0246a0001c0001t0022g0214others(2): Show | 5 | HG02155.hp2 NA18962.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+2533C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437929 | ||||||
| chr18:46437935
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.485+2539C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46437935 | ||||||
| chr18:46438009
|
G | A | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485+2613G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438009 | ||||||
| chr18:46438051
|
C | T | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+2655C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438051 | ||||||
| chr18:46438101
|
G | A | 4 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2705G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438101 | ||||||
| chr18:46438205
|
T | A | 132 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0016others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.485+2809T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438205 | ||||||
| chr18:46438296
|
A | G | 21 | a0001c0001t0003g0060a0001c0001t0003g0090a0001c0001t0003g0180others(18): Show | 21 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.485+2900A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438296 | ||||||
| chr18:46438334
|
C | T | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485+2938C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438334 | ||||||
| chr18:46438341
|
C | A | 4 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2945C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438341 | ||||||
| chr18:46438683
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.485+3287G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438683 | ||||||
| chr18:46438702
|
A | G | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.485+3306A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438702 | ||||||
| chr18:46438808
|
G | A | 1 | a0001c0001t0006g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485+3412G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46438808 | ||||||
| chr18:46439074
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0139a0001c0001t0001g0223 | 3 | HG00544.hp1 NA18981.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.485+3678C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439074 | ||||||
| chr18:46439222
|
G | C | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.485+3826G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439222 | ||||||
| chr18:46439282
|
C | T | 8 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3886C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439282 | ||||||
| chr18:46439420
|
G | A | 8 | a0001c0001t0002g0035a0001c0001t0002g0068a0001c0001t0002g0136others(5): Show | 8 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+4024G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439420 | ||||||
| chr18:46439565
|
C | T | 1 | a0001c0001t0004g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.485+4169C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439565 | ||||||
| chr18:46439641
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.485+4245C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439641 | ||||||
| chr18:46439663
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.485+4267A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439663 | ||||||
| chr18:46439704
|
TA | T | 159 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.485+4316delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46439704 | |||||
| chr18:46439710
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0003g0059 | 2 | HG01081.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.485+4314A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439710 | ||||||
| chr18:46439961
|
G | C | 1 | a0001c0001t0054g0242 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485+4565G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46439961 | ||||||
| chr18:46440011
|
G | A | 131 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0016others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.485+4615G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440011 | ||||||
| chr18:46440273
|
T | TGA | 5 | a0001c0001t0001g0036a0001c0001t0001g0238a0001c0001t0050g0175others(2): Show | 5 | HG00140.hp1 HG00642.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+4900_485+4901d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46440273 | |||||
| chr18:46440273
|
TGA | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+4900_485+4901d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46440273 | |||||
| chr18:46440312
|
C | T | 1 | a0001c0001t0013g0202 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.485+4916C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440312 | ||||||
| chr18:46440579
|
G | A | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.485+5183G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440579 | ||||||
| chr18:46440710
|
T | TTCGG | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5314_485+5315i others(6): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440710 | ||||||
| chr18:46440713
|
C | CTG | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5317_485+5318i others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440713 | ||||||
| chr18:46440714
|
A | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5318A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440714 | ||||||
| chr18:46440715
|
A | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5319A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46440715 | ||||||
| chr18:46441026
|
G | T | 1 | a0001c0001t0006g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.485+5630G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441026 | ||||||
| chr18:46441051
|
C | G | 1 | a0001c0001t0006g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.485+5655C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441051 | ||||||
| chr18:46441119
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.485+5723G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441119 | ||||||
| chr18:46441267
|
C | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5871C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441267 | ||||||
| chr18:46441274
|
G | A | 8 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+5878G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441274 | ||||||
| chr18:46441292
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.485+5896G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441292 | ||||||
| chr18:46441336
|
T | C | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+5940T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441336 | ||||||
| chr18:46441338
|
G | A | 1 | a0001c0001t0004g0093 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.485+5942G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441338 | ||||||
| chr18:46441492
|
A | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-6071A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441492 | ||||||
| chr18:46441503
|
T | C | 2 | a0001c0001t0022g0214a0001c0001t0022g0216 | 2 | NA18962.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.486-6060T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441503 | ||||||
| chr18:46441576
|
G | C | 1 | a0001c0004t0012g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.486-5987G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441576 | ||||||
| chr18:46441579
|
C | G | 1 | a0001c0004t0012g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.486-5984C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441579 | ||||||
| chr18:46441616
|
C | T | 1 | a0001c0001t0005g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.486-5947C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441616 | ||||||
| chr18:46441760
|
C | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-5803C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441760 | ||||||
| chr18:46441861
|
C | CAAA | 16 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(13): Show | 16 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.486-5685_486-5683d others(5): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46441861 | |||||
| chr18:46441861
|
CAAAAAAA others(2): Show |
C | 131 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0016others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.486-5691_486-5683d others(11): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46441861 | |||||
| chr18:46441878
|
A | G | 1 | a0001c0001t0003g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.486-5685A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441878 | ||||||
| chr18:46441892
|
C | T | 2 | a0001c0001t0008g0077a0001c0001t0008g0192 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.486-5671C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441892 | ||||||
| chr18:46441940
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG00280.hp1 HG00741.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-5623G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441940 | ||||||
| chr18:46441986
|
A | T | 3 | a0001c0001t0020g0013a0001c0001t0020g0049a0001c0001t0031g0063 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486-5577A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46441986 | ||||||
| chr18:46442031
|
C | T | 1 | a0001c0005t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.486-5532C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442031 | ||||||
| chr18:46442044
|
T | C | 1 | a0001c0001t0060g0244 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.486-5519T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442044 | ||||||
| chr18:46442052
|
A | G | 1 | a0001c0001t0063g0043 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.486-5511A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442052 | ||||||
| chr18:46442128
|
G | A | 1 | a0001c0001t0008g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486-5435G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442128 | ||||||
| chr18:46442162
|
C | CA | 141 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(138): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.486-5387dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46442162 | |||||
| chr18:46442162
|
C | CAA | 18 | a0001c0001t0002g0023a0001c0001t0002g0035a0001c0001t0002g0068others(15): Show | 18 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.486-5388_486-5387d others(4): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46442162 | |||||
| chr18:46442191
|
C | A | 3 | a0001c0001t0020g0013a0001c0001t0020g0049a0001c0001t0031g0063 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486-5372C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442191 | ||||||
| chr18:46442267
|
C | G | 8 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-5296C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442267 | ||||||
| chr18:46442300
|
C | T | 1 | a0001c0001t0005g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.486-5263C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442300 | ||||||
| chr18:46442342
|
A | G | 1 | a0001c0001t0066g0190 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.486-5221A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442342 | ||||||
| chr18:46442434
|
A | G | 129 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.486-5129A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442434 | ||||||
| chr18:46442541
|
T | C | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-5022T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442541 | ||||||
| chr18:46442611
|
A | T | 6 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(3): Show | 6 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-4952A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442611 | ||||||
| chr18:46442638
|
A | G | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-4925A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442638 | ||||||
| chr18:46442677
|
C | T | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-4886C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442677 | ||||||
| chr18:46442748
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.486-4815G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442748 | ||||||
| chr18:46442897
|
C | T | 1 | a0001c0001t0002g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.486-4666C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442897 | ||||||
| chr18:46442979
|
A | G | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-4584A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46442979 | ||||||
| chr18:46443058
|
C | G | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-4505C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46443058 | ||||||
| chr18:46443204
|
T | C | 8 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-4359T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46443204 | ||||||
| chr18:46443858
|
T | C | 1 | a0001c0001t0058g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-3705T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46443858 | ||||||
| chr18:46443892
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.486-3671T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46443892 | ||||||
| chr18:46444049
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.486-3514T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444049 | ||||||
| chr18:46444162
|
T | C | 2 | a0001c0001t0053g0114a0001c0001t0054g0242 | 2 | HG04199.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.486-3401T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444162 | ||||||
| chr18:46444589
|
T | C | 4 | a0001c0001t0015g0041a0001c0001t0015g0070a0001c0001t0015g0131others(1): Show | 4 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-2974T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444589 | ||||||
| chr18:46444638
|
A | AT | 18 | a0001c0001t0001g0223a0001c0001t0011g0083a0001c0001t0011g0137others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-2910dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46444638 | |||||
| chr18:46444751
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486-2812G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444751 | ||||||
| chr18:46444765
|
G | A | 1 | a0001c0001t0005g0009 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.486-2798G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444765 | ||||||
| chr18:46444820
|
C | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0183 | 2 | HG02155.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.486-2743C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46444820 | ||||||
| chr18:46445193
|
C | T | 1 | a0001c0001t0015g0131 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.486-2370C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445193 | ||||||
| chr18:46445250
|
T | A | 4 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0227others(1): Show | 4 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-2313T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445250 | ||||||
| chr18:46445306
|
G | T | 6 | a0001c0001t0004g0127a0001c0001t0004g0213a0001c0001t0017g0149others(3): Show | 6 | HG01074.hp2 HG02129.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-2257G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445306 | ||||||
| chr18:46445615
|
G | T | 8 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-1948G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445615 | ||||||
| chr18:46445643
|
C | T | 7 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(4): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-1920C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445643 | ||||||
| chr18:46445664
|
C | T | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.486-1899C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445664 | ||||||
| chr18:46445668
|
C | G | 1 | a0001c0001t0002g0115 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.486-1895C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445668 | ||||||
| chr18:46445719
|
A | G | 160 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.486-1844A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445719 | ||||||
| chr18:46445798
|
A | G | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.486-1765A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445798 | ||||||
| chr18:46445855
|
AACTATCA others(65): Show |
A | 1 | a0001c0001t0003g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-1707_486-1636d others(74): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46445855 | ||||||
| chr18:46445902
|
C | CT | 8 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-1649dupT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46445902 | |||||
| chr18:46445902
|
CT | C | 149 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0108others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-1649delT | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46445902 | |||||
| chr18:46446217
|
A | G | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-1346A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446217 | ||||||
| chr18:46446271
|
T | C | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-1292T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446271 | ||||||
| chr18:46446437
|
G | A | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.486-1126G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446437 | ||||||
| chr18:46446483
|
C | A | 1 | a0001c0001t0011g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.486-1080C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446483 | ||||||
| chr18:46446593
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.486-970C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446593 | ||||||
| chr18:46446606
|
G | A | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.486-957G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446606 | ||||||
| chr18:46446643
|
C | T | 1 | a0001c0001t0002g0018 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.486-920C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446643 | ||||||
| chr18:46446655
|
A | T | 1 | a0001c0001t0002g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.486-908A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446655 | ||||||
| chr18:46446670
|
C | CA | 26 | a0001c0001t0001g0104a0001c0001t0001g0148a0001c0001t0001g0170others(23): Show | 26 | HG00642.hp2 HG00733.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.486-869dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46446670 | |||||
| chr18:46446670
|
CA | C | 21 | a0001c0001t0001g0211a0001c0001t0003g0090a0001c0001t0003g0208others(18): Show | 21 | HG00140.hp2 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.486-869delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46446670 | |||||
| chr18:46446701
|
GA | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0212others(3): Show | 6 | HG03486.hp1 HG03540.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-851delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 46446701 | |||||
| chr18:46446708
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0255 | 2 | NA18966.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.486-855A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446708 | ||||||
| chr18:46446827
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.486-736T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46446827 | ||||||
| chr18:46447230
|
A | G | 152 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.486-333A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46447230 | ||||||
| chr18:46447248
|
G | A | 1 | a0001c0001t0023g0042 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.486-315G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46447248 | ||||||
| chr18:46447262
|
T | C | 7 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(4): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-301T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46447262 | ||||||
| chr18:46447377
|
T | C | 2 | a0001c0001t0060g0244a0001c0001t0061g0128 | 2 | NA19066.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.486-186T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46447377 | ||||||
| chr18:46447390
|
G | A | 4 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-173G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 3/7 | chr18 | 46447390 | ||||||
| chr18:46447721
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.615+29G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46447721 | ||||||
| chr18:46447728
|
G | C | 1 | a0001c0001t0055g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.615+36G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46447728 | ||||||
| chr18:46448035
|
C | G | 1 | a0001c0001t0049g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.615+343C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448035 | ||||||
| chr18:46448107
|
C | T | 2 | a0001c0001t0047g0027a0001c0001t0058g0048 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.615+415C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448107 | ||||||
| chr18:46448112
|
C | T | 1 | a0001c0001t0004g0213 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.615+420C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448112 | ||||||
| chr18:46448250
|
C | A | 2 | a0001c0001t0047g0027a0001c0001t0058g0048 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.615+558C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448250 | ||||||
| chr18:46448350
|
C | T | 3 | a0001c0001t0019g0002a0001c0001t0019g0138a0001c0001t0029g0002 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.615+658C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448350 | ||||||
| chr18:46448449
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.615+757C>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448449 | ||||||
| chr18:46448595
|
T | A | 7 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(4): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+903T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448595 | ||||||
| chr18:46448670
|
G | T | 4 | a0001c0001t0017g0149a0001c0001t0017g0150a0001c0001t0017g0239others(1): Show | 4 | NA18960.hp2 NA18970.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+978G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448670 | ||||||
| chr18:46448722
|
T | G | 3 | a0001c0001t0028g0096a0001c0001t0047g0027a0001c0001t0058g0048 | 3 | HG02257.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.615+1030T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448722 | ||||||
| chr18:46448772
|
T | G | 1 | a0001c0001t0045g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.615+1080T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46448772 | ||||||
| chr18:46449264
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.616-1032G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46449264 | ||||||
| chr18:46449678
|
G | T | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.616-618G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46449678 | ||||||
| chr18:46449691
|
G | T | 120 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0016others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.616-605G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46449691 | ||||||
| chr18:46449803
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0209 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.616-493T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46449803 | ||||||
| chr18:46449875
|
G | A | 1 | a0001c0001t0014g0236 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.616-421G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46449875 | ||||||
| chr18:46450081
|
C | T | 160 | a0001c0001t0001g0050a0001c0001t0001g0087a0001c0001t0001g0088others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.616-215C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46450081 | ||||||
| chr18:46450280
|
G | A | 4 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-16G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 4/7 | chr18 | 46450280 | ||||||
| chr18:46450651
|
A | G | 1 | a0001c0001t0011g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.721-53A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 5/7 | chr18 | 46450651 | ||||||
| chr18:46450941
|
A | C | 3 | a0001c0001t0003g0060a0001c0001t0003g0090a0001c0001t0003g0180 | 3 | HG02559.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.816+142A>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46450941 | ||||||
| chr18:46451036
|
C | T | 2 | a0001c0001t0047g0027a0001c0001t0058g0048 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.816+237C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46451036 | ||||||
| chr18:46451687
|
C | G | 8 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+888C>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46451687 | ||||||
| chr18:46452250
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.816+1451T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452250 | ||||||
| chr18:46452343
|
G | A | 1 | a0001c0001t0058g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.816+1544G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452343 | ||||||
| chr18:46452393
|
C | T | 129 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.816+1594C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452393 | ||||||
| chr18:46452488
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(2): Show | 5 | HG00280.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1689C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452488 | ||||||
| chr18:46452524
|
C | T | 7 | a0001c0001t0003g0012a0001c0001t0003g0047a0001c0001t0003g0086others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+1725C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452524 | ||||||
| chr18:46452761
|
G | A | 12 | a0001c0001t0003g0012a0001c0001t0003g0029a0001c0001t0003g0045others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+1962G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452761 | ||||||
| chr18:46452987
|
C | T | 3 | a0001c0001t0028g0096a0001c0001t0047g0027a0001c0001t0058g0048 | 3 | HG02257.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.816+2188C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46452987 | ||||||
| chr18:46453303
|
G | T | 1 | a0001c0001t0003g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816+2504G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453303 | ||||||
| chr18:46453607
|
A | T | 7 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(4): Show | 7 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-2367A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453607 | ||||||
| chr18:46453751
|
G | A | 3 | a0001c0001t0003g0060a0001c0001t0003g0090a0001c0001t0003g0180 | 3 | HG02559.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.817-2223G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453751 | ||||||
| chr18:46453858
|
G | A | 9 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-2116G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453858 | ||||||
| chr18:46453863
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.817-2111T>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453863 | ||||||
| chr18:46453910
|
T | C | 1 | a0001c0001t0005g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.817-2064T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453910 | ||||||
| chr18:46453920
|
C | T | 1 | a0001c0001t0018g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817-2054C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453920 | ||||||
| chr18:46453923
|
G | A | 1 | a0001c0001t0002g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.817-2051G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46453923 | ||||||
| chr18:46454110
|
C | CA | 32 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0129others(29): Show | 32 | HG00544.hp1 HG00733.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.817-1836dupA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr18 | 46454110 | |||||
| chr18:46454110
|
CA | C | 13 | a0001c0001t0001g0122a0001c0001t0001g0158a0001c0001t0001g0184others(10): Show | 13 | HG00673.hp2 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-1836delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr18 | 46454110 | |||||
| chr18:46454110
|
CAAAAAAA | C | 9 | a0001c0001t0014g0026a0001c0001t0014g0235a0001c0001t0014g0236others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-1842_817-1836d others(9): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr18 | 46454110 | |||||
| chr18:46454110
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0028g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.817-1849_817-1836d others(16): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr18 | 46454110 | |||||
| chr18:46454160
|
A | T | 15 | a0001c0001t0004g0010a0001c0001t0004g0021a0001c0001t0004g0093others(12): Show | 15 | HG00544.hp2 HG00673.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-1814A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454160 | ||||||
| chr18:46454248
|
CA | C | 6 | a0001c0001t0009g0102a0001c0001t0009g0111a0001c0001t0009g0140others(3): Show | 6 | HG00280.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1719delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr18 | 46454248 | |||||
| chr18:46454251
|
A | G | 2 | a0001c0001t0065g0198a0001c0001t0067g0179 | 2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.817-1723A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454251 | ||||||
| chr18:46454328
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.817-1646A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454328 | ||||||
| chr18:46454431
|
C | T | 2 | a0001c0001t0003g0029a0001c0001t0003g0045 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.817-1543C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454431 | ||||||
| chr18:46454769
|
A | G | 18 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.817-1205A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454769 | ||||||
| chr18:46454975
|
C | T | 8 | a0001c0001t0011g0083a0001c0001t0011g0137a0001c0001t0011g0142others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-999C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46454975 | ||||||
| chr18:46455152
|
GA | G | 3 | a0001c0001t0020g0013a0001c0001t0020g0049a0001c0001t0031g0063 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.817-821delA | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455152 | ||||||
| chr18:46455383
|
A | G | 3 | a0001c0001t0018g0076a0001c0001t0018g0221a0001c0001t0018g0231 | 3 | HG02622.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.817-591A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455383 | ||||||
| chr18:46455570
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0001t0001g0147others(1): Show | 4 | HG02015.hp2 NA18981.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-404C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455570 | ||||||
| chr18:46455573
|
A | G | 1 | a0001c0001t0006g0144 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.817-401A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455573 | ||||||
| chr18:46455680
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.817-294A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455680 | ||||||
| chr18:46455725
|
A | T | 3 | a0001c0001t0003g0060a0001c0001t0003g0090a0001c0001t0003g0180 | 3 | HG02559.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.817-249A>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455725 | ||||||
| chr18:46455771
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.817-203G>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455771 | ||||||
| chr18:46455791
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.817-183C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455791 | ||||||
| chr18:46455932
|
T | A | 2 | a0001c0001t0011g0142a0001c0001t0011g0240 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.817-42T>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 6/7 | chr18 | 46455932 | ||||||
| chr18:46456220
|
T | C | 3 | a0001c0001t0028g0096a0001c0001t0047g0027a0001c0001t0058g0048 | 3 | HG02257.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.923+140T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 7/7 | chr18 | 46456220 | ||||||
| chr18:46456426
|
G | C | 1 | a0001c0001t0057g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.924-93G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 7/7 | chr18 | 46456426 | ||||||
| chr18:46456437
|
A | G | 2 | a0001c0001t0004g0117a0001c0001t0004g0206 | 2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.924-82A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 7/7 | chr18 | 46456437 |