Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MVLVH others(341): Show |
chr18 | 46329018 | 46468140 |
| a0002 | 0/0 | 346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | MVLVH others(341): Show |
chr18 | 46329018 | 46468140 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1038 | 252 | 79 | 48 | 83 | 8 | 33 | ARK2C_chr18_46329018_46468140 | ARK2C | ATGGT others(1033): Show |
chr18 | 46329018 | 46468140 | ||
| a0001c0002 | 0/1 | 1038 | 5 | 0 | 4 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATGGT others(1033): Show |
chr18 | 46329018 | 46468140 | ||
| a0001c0004 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATGGT others(1033): Show |
chr18 | 46329018 | 46468140 | ||
| a0001c0005 | 0/0 | 1038 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATGGT others(1033): Show |
chr18 | 46329018 | 46468140 | ||
| a0002c0003 | 0/0 | 1038 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATGGT others(1033): Show |
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 | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0002 | 0/0 | 7802 | 34 | 0 | 7 | 18 | 3 | 6 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0003 | 1/0 | 7802 | 22 | 18 | 2 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0004 | 0/0 | 7796 | 16 | 0 | 1 | 15 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0005 | 0/0 | 7802 | 13 | 1 | 7 | 1 | 1 | 3 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0006 | 0/0 | 7803 | 8 | 2 | 1 | 0 | 1 | 4 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0007 | 0/0 | 7802 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0008 | 0/0 | 7802 | 7 | 7 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0009 | 0/0 | 7796 | 7 | 0 | 2 | 4 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0010 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0011 | 0/0 | 7796 | 6 | 0 | 4 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0012 | 0/0 | 7802 | 4 | 4 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0013 | 0/0 | 7796 | 4 | 0 | 3 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0014 | 0/0 | 7804 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7799): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0015 | 0/0 | 7796 | 3 | 1 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0016 | 0/0 | 7803 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0017 | 0/0 | 7796 | 3 | 1 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0018 | 0/0 | 7802 | 3 | 3 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0019 | 0/0 | 7796 | 2 | 0 | 2 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0020 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0021 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0022 | 0/0 | 7796 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0023 | 0/0 | 7796 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0024 | 0/0 | 7802 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0025 | 0/0 | 7803 | 2 | 2 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0026 | 0/0 | 7797 | 2 | 0 | 0 | 2 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7792): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0027 | 0/0 | 7802 | 2 | 0 | 0 | 0 | 0 | 2 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0028 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0029 | 0/0 | 7797 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7792): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0030 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0031 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0032 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0033 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0034 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0035 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0036 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0037 | 0/0 | 7797 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7792): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0038 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0039 | 0/0 | 7797 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7792): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0040 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0041 | 0/0 | 7791 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7786): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0042 | 0/0 | 7804 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7799): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0043 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0044 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0045 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0046 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0047 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7799): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0048 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0049 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0050 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0051 | 0/0 | 7796 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0052 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0053 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0054 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0055 | 0/0 | 7797 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7792): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0056 | 0/0 | 7796 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0057 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0058 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7799): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0059 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0060 | 0/0 | 7802 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0061 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0062 | 0/0 | 7796 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0063 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0064 | 0/0 | 7796 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0065 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0066 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7798): Show |
chr18 | 46329018 | 46468140 |
| a0001c0001t0067 | 0/0 | 7802 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0002t0010 | 0/1 | 7802 | 5 | 0 | 4 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0004t0012 | 0/0 | 7802 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| a0001c0005t0001 | 0/0 | 7796 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7791): Show |
chr18 | 46329018 | 46468140 |
| a0002c0003t0005 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | ATTGG others(7797): Show |
chr18 | 46329018 | 46468140 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0136 | 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 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0007g0223 | 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 |
| a0001c0001t0008g0176 | 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 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0011g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0013g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0015g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0016g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0017g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0018g0208 | 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 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0020g0047 | 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 |
| a0001c0001t0021g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0022g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0023g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0024g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0025g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0026g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0026g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0027g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0028g0191 | 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 |
| a0001c0001t0030g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0031g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0032g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0033g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0034g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0035g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0036g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0037g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0038g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0039g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0040g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0041g0062 | 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 |
| a0001c0001t0043g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0044g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0045g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0046g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0047g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0048g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0049g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0050g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0051g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0052g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0053g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0054g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0055g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0056g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0057g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0058g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0059g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0060g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0061g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0062g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0063g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0064g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0065g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0066g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0001t0067g0224 | 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 |
| a0001c0002t0010g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0002t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0004t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| a0002c0003t0005g0115 | 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 | g0125 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00140 | hp1 | a0001 | c0001 | t0064 | g0148 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0154 | EUR | GBR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0143 | EUR | FIN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0008 | 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 | g0237 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00733 | hp2 | a0001 | c0001 | t0019 | g0159 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0158 | 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 | g0017 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01071 | hp1 | a0001 | c0002 | t0010 | g0085 | 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 | g0182 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01099 | hp2 | a0001 | c0001 | t0049 | g0034 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01106 | hp1 | a0001 | c0001 | t0044 | g0104 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0146 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0240 | 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 | g0226 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01175 | hp2 | a0001 | c0001 | t0039 | g0016 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0126 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01243 | hp2 | a0001 | c0001 | t0067 | g0224 | AMR | PUR | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01257 | hp2 | a0001 | c0001 | t0013 | g0166 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0228 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01358 | hp2 | a0001 | c0001 | t0010 | g0072 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01361 | hp1 | a0001 | c0001 | t0009 | g0137 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0076 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0257 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01496 | hp2 | a0001 | c0001 | t0050 | g0084 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | IBS | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0219 | 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 | g0030 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0197 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01981 | hp2 | a0001 | c0001 | t0056 | g0170 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0179 | 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 | g0150 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02145 | hp1 | a0001 | c0001 | t0025 | g0216 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0105 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CDX | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02155 | hp2 | a0001 | c0001 | t0034 | g0138 | EAS | CDX | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02257 | hp2 | a0001 | c0001 | t0028 | g0191 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02258 | hp2 | a0001 | c0001 | t0025 | g0056 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0066 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0059 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02300 | hp2 | a0001 | c0001 | t0051 | g0255 | AMR | PEL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0200 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02451 | hp2 | a0001 | c0001 | t0021 | g0081 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02523 | hp2 | a0001 | c0001 | t0059 | g0181 | EAS | KHV | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0218 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0042 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02615 | hp1 | a0001 | c0001 | t0043 | g0057 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0206 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0070 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0249 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02683 | hp2 | a0001 | c0001 | t0033 | g0053 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0047 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02717 | hp2 | a0001 | c0001 | t0036 | g0082 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0221 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0190 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0010 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0091 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0130 | 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 | g0203 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02818 | hp1 | a0001 | c0004 | t0012 | g0083 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02886 | hp1 | a0001 | c0001 | t0045 | g0205 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0198 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0060 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0208 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0239 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0044 | 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 | g0233 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0046 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0217 | AFR | ESN | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0204 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0222 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03225 | hp1 | a0001 | c0001 | t0035 | g0068 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03239 | hp1 | a0001 | c0001 | t0011 | g0149 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03486 | hp1 | a0001 | c0001 | t0058 | g0040 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0069 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0168 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03491 | hp2 | a0001 | c0001 | t0027 | g0011 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03492 | hp2 | a0002 | c0003 | t0005 | g0115 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03540 | hp1 | a0001 | c0001 | t0047 | g0045 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0173 | AFR | GWD | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03579 | hp1 | a0001 | c0001 | t0057 | g0220 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03654 | hp2 | a0001 | c0001 | t0040 | g0065 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0015 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03831 | hp1 | a0001 | c0001 | t0027 | g0078 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03942 | hp1 | a0001 | c0001 | t0041 | g0062 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04199 | hp1 | a0001 | c0001 | t0053 | g0102 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04199 | hp2 | a0001 | c0001 | t0038 | g0132 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0153 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04228 | hp1 | a0001 | c0001 | t0055 | g0092 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | STU | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18522 | hp1 | a0001 | c0001 | t0046 | g0043 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0234 | AFR | YRI | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18950 | hp2 | a0001 | c0001 | t0026 | g0029 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18960 | hp2 | a0001 | c0001 | t0017 | g0165 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18962 | hp1 | a0001 | c0001 | t0022 | g0183 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18963 | hp2 | a0001 | c0001 | t0026 | g0051 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18964 | hp1 | a0001 | c0001 | t0054 | g0241 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18970 | hp1 | a0001 | c0001 | t0017 | g0164 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18970 | hp2 | a0001 | c0001 | t0048 | g0147 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0097 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18993 | hp2 | a0001 | c0001 | t0022 | g0185 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | 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 | g0114 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0201 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19030 | hp2 | a0001 | c0001 | t0066 | g0120 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0202 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19060 | hp1 | a0001 | c0005 | t0001 | g0145 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19066 | hp2 | a0001 | c0001 | t0061 | g0123 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0187 | 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 | g0184 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19083 | hp1 | a0001 | c0001 | t0052 | g0172 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19084 | hp2 | a0001 | c0001 | t0060 | g0248 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19085 | hp2 | a0001 | c0001 | t0063 | g0032 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20129 | hp1 | a0001 | c0001 | t0017 | g0238 | AFR | ASW | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | ASW | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20905 | hp1 | a0001 | c0001 | t0023 | g0018 | SAS | GIH | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | GIH | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02109 | hp2 | a0001 | c0001 | t0062 | g0003 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | ACB | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG03471 | hp2 | a0001 | c0001 | t0031 | g0210 | AFR | MSL | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | USA | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | USA | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA21309 | hp1 | a0001 | c0001 | t0030 | g0209 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | LWK | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0010 | g0067 | REF | REF | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0036 | REF | REF | ARK2C_chr18_46329018_46468140 | ARK2C | chr18 | 46329018 | 46468140 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46435352 | A | G | 1 | a0001c0002 | 4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46456858 | A | G | 3 | a0001c0001t0065 a0001c0001t0066 a0001c0001t0067 |
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 | a0001c0001t0019 a0001c0001t0029 |
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 | a0001c0001t0014 a0001c0001t0020 a0001c0001t0030 others(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 | a0001c0001t0011 a0001c0001t0060 a0001c0001t0061 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0011 a0001c0001t0060 a0001c0001t0061 |
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 | a0001c0001t0011 a0001c0001t0060 a0001c0001t0061 |
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 | a0001c0001t0014 a0001c0001t0030 a0001c0001t0047 others(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 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0060 others(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 | a0001c0001t0011 a0001c0001t0060 a0001c0001t0061 |
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 | a0001c0001t0021 a0001c0001t0036 |
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 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0060 others(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 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0060 others(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 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0060 others(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 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0060 others(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 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0017 others(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 | a0001c0001t0037 a0001c0001t0062 |
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 | a0001c0001t0014 a0001c0001t0030 a0001c0001t0047 others(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 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0022 others(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 | a0001c0001t0026 a0001c0001t0029 a0001c0001t0037 others(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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0011 a0001c0001t0060 a0001c0001t0061 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0014 a0001c0001t0030 a0001c0001t0047 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0016 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(27): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): 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 | a0001c0001t0014 a0001c0001t0030 a0001c0001t0047 others(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 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0035 others(4): Show |
22 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(19): 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 | a0001c0001t0014 a0001c0001t0030 a0001c0001t0047 others(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 | a0001c0001t0015 a0001c0001t0039 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(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 | a0001c0001t0016 a0001c0001t0042 |
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 | a0001c0001t0011 a0001c0001t0061 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:46334475 | A | C | 197 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): 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 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0004g0253 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0021 a0001c0001t0005g0030 others(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 | a0001c0001t0001g0100 a0001c0001t0004g0096 a0001c0001t0007g0211 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0207 others(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 | a0001c0001t0002g0026 a0001c0001t0005g0152 |
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 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0015g0066 others(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 | a0001c0001t0002g0116 a0001c0001t0004g0106 a0001c0001t0021g0081 |
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 | a0001c0001t0003g0194 a0001c0001t0007g0190 a0001c0001t0008g0192 others(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 | 53 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): 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 | a0001c0001t0012g0069 a0001c0001t0016g0080 |
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 | a0001c0001t0003g0235 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0098 others(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 | a0001c0001t0036g0082 a0001c0001t0050g0084 a0001c0002t0010g0085 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0136 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0171 a0001c0001t0002g0189 others(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 | a0001c0001t0001g0193 a0001c0001t0008g0176 a0001c0001t0009g0178 others(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 | a0001c0001t0006g0117 | 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 | a0001c0001t0003g0225 a0001c0001t0007g0211 a0001c0001t0007g0223 others(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 | a0001c0001t0002g0127 a0001c0001t0004g0140 a0001c0001t0013g0197 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0009g0177 a0001c0001t0032g0173 |
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 | a0001c0001t0001g0199 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0003g0049 a0001c0001t0007g0058 a0001c0001t0014g0044 others(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 | a0001c0001t0001g0254 a0001c0001t0002g0252 a0001c0001t0003g0256 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0195 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0002g0236 |
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 | a0001c0001t0001g0229 a0001c0001t0003g0233 a0001c0001t0006g0226 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0004g0251 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0245 a0001c0001t0002g0243 a0001c0001t0002g0244 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0245 a0001c0001t0002g0243 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0233 a0001c0001t0003g0235 others(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 | a0001c0001t0035g0068 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | 168 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): 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 | 197 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): 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 | a0001c0001t0013g0197 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0199 a0001c0001t0014g0198 a0001c0001t0035g0068 |
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 | a0001c0001t0012g0069 | 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 | a0001c0001t0018g0070 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0004g0122 | 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 | a0001c0001t0003g0233 a0001c0001t0014g0234 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0246 a0001c0001t0006g0247 |
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 | a0001c0001t0045g0205 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0062g0003 | 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 | a0001c0001t0001g0124 a0001c0001t0061g0123 |
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 | a0001c0001t0003g0225 a0001c0001t0007g0223 a0001c0001t0016g0222 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
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 | a0001c0001t0003g0225 a0001c0001t0007g0223 a0001c0001t0016g0222 others(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 | a0001c0001t0005g0059 | 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 | a0001c0001t0056g0170 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0001t0016g0080 others(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 | a0001c0001t0006g0005 | 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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0036g0082 a0001c0001t0050g0084 a0001c0004t0012g0083 |
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 | a0001c0001t0043g0057 | 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 | a0001c0001t0016g0080 a0001c0001t0021g0081 |
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 | a0001c0001t0043g0057 | 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 | a0001c0001t0012g0069 | 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 | a0001c0001t0025g0056 | 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 | a0001c0001t0008g0217 a0001c0001t0012g0218 a0001c0001t0012g0219 others(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 | a0001c0001t0002g0006 a0001c0001t0012g0206 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0006g0247 | 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 | a0001c0001t0003g0194 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0242 a0001c0001t0002g0055 |
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 | a0001c0001t0002g0243 a0001c0001t0003g0256 a0001c0001t0006g0226 others(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 | 173 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0073 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0001t0001g0129 | 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 | 203 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0071 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.61+6789T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46341124 | |||||||
| chr18:46341206 | G | GA | 203 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0071 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): 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 | 205 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0073 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0001c0001t0052g0172 | 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 | a0001c0001t0003g0207 a0001c0001t0007g0058 a0001c0001t0014g0198 others(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 | 200 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0073 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): 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 | a0001c0001t0003g0207 a0001c0001t0007g0058 a0001c0001t0014g0198 others(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 | a0001c0001t0027g0078 | 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 | a0001c0001t0003g0054 a0001c0001t0006g0117 a0001c0001t0018g0070 |
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 | a0001c0001t0003g0049 a0001c0001t0003g0225 a0001c0001t0007g0223 others(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 | a0001c0001t0003g0130 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 |
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 | a0001c0001t0066g0120 | 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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0002g0243 | 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 | a0001c0001t0003g0130 | 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 | a0001c0001t0012g0206 | 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 | a0001c0001t0043g0057 | 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 | a0001c0001t0003g0207 a0001c0001t0007g0058 a0001c0001t0014g0198 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0043g0057 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0002g0131 | 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 | 206 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0073 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0001c0001t0007g0169 | 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 | a0001c0001t0004g0086 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0199 a0001c0001t0008g0200 a0001c0001t0008g0201 others(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 | a0001c0001t0043g0057 | 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 | a0001c0001t0007g0190 a0001c0001t0008g0192 a0001c0001t0028g0191 |
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 | a0001c0001t0005g0168 | 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 | a0001c0001t0002g0125 a0001c0001t0010g0072 |
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 | a0001c0001t0003g0225 a0001c0001t0067g0224 |
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 | 160 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): 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 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0008g0176 others(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 | a0001c0001t0032g0173 | 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 | a0001c0001t0009g0177 a0001c0001t0009g0178 |
2 | NA18966.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.61+9697G>A | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46344032 | |||||||
| chr18:46344335 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0005g0013 a0001c0001t0005g0015 |
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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 |
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 | a0002c0003t0005g0115 | 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 | a0001c0001t0038g0132 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0201 a0001c0001t0008g0202 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0016g0046 others(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 | a0001c0001t0015g0017 a0001c0001t0039g0016 |
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 | a0001c0001t0001g0199 a0001c0001t0003g0054 a0001c0001t0003g0207 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0201 a0001c0001t0008g0202 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0199 a0001c0001t0003g0054 a0001c0001t0003g0207 others(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 | a0001c0001t0018g0208 | 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 | a0001c0001t0007g0169 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0012g0206 | 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 | 172 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.61+11026G>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46345361 | |||||||
| chr18:46345683 | A | T | 159 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): 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 | a0001c0001t0003g0225 a0001c0001t0007g0223 a0001c0001t0016g0222 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0007g0190 | 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 | a0001c0001t0001g0133 | 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 | 171 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0001g0250 | 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 | 136 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | 167 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): 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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0002g0041 | 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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0001g0012 a0001c0001t0027g0011 |
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 | a0001c0001t0003g0225 a0001c0001t0007g0223 a0001c0001t0016g0222 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0020g0042 | 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 | a0001c0001t0062g0003 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(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 | a0001c0001t0024g0249 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0201 a0001c0001t0008g0202 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0246 a0001c0001t0006g0247 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0199 a0001c0001t0003g0054 a0001c0001t0003g0207 others(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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | 144 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0017g0238 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0167 |
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 | a0001c0001t0007g0190 a0001c0001t0007g0232 a0001c0001t0008g0192 others(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 | a0001c0001t0003g0008 | 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 | a0001c0001t0001g0199 a0001c0001t0003g0054 a0001c0001t0003g0207 others(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 | a0001c0001t0023g0018 | 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 | a0001c0001t0001g0048 a0001c0001t0014g0044 a0001c0001t0016g0046 others(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 | a0001c0001t0001g0199 a0001c0001t0003g0039 a0001c0001t0003g0054 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0193 others(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 | 162 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0245 a0001c0001t0002g0189 a0001c0001t0002g0236 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0193 others(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 | a0001c0001t0007g0058 a0001c0001t0014g0198 a0001c0001t0035g0068 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 139 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(136): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): 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 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0119 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0161 a0001c0001t0002g0243 others(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 | a0001c0001t0002g0028 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 118 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(115): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): 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 | a0001c0001t0001g0119 a0001c0001t0001g0196 a0001c0001t0002g0156 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0161 a0001c0001t0005g0160 others(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 | a0001c0001t0003g0225 a0001c0001t0007g0223 a0001c0001t0016g0222 others(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 | a0001c0001t0021g0221 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0246 a0001c0001t0006g0247 |
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 | a0001c0001t0016g0080 | 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 | a0001c0001t0001g0139 a0001c0001t0004g0140 a0001c0001t0013g0197 others(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 | a0001c0001t0066g0120 | 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 | a0001c0001t0005g0019 | 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 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0087 a0001c0001t0057g0220 |
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 | a0001c0001t0002g0155 a0001c0001t0003g0112 a0001c0001t0005g0077 others(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 | a0001c0001t0007g0211 a0001c0001t0008g0217 a0001c0001t0012g0206 others(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 | a0001c0001t0002g0111 | 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 | a0001c0001t0011g0239 | 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0001t0003g0207 others(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 | a0001c0001t0003g0054 a0001c0001t0014g0198 a0001c0001t0018g0070 |
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 | 193 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.61+16665C>T | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46351000 | |||||||
| chr18:46351009 | C | T | 135 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0003g0118 others(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 | a0001c0001t0005g0020 | 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 | a0001c0001t0025g0216 | 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 | a0001c0001t0012g0069 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0003g0118 others(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 | a0001c0001t0003g0207 | 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 | 144 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): 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 | a0001c0001t0003g0225 a0001c0001t0067g0224 |
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 | a0001c0001t0001g0171 | 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 | a0001c0001t0009g0093 | 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 | a0001c0001t0008g0217 a0001c0001t0012g0218 a0001c0001t0012g0219 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0090 others(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 | a0001c0001t0012g0069 | 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 | a0001c0001t0008g0204 a0001c0001t0008g0217 a0001c0001t0012g0218 others(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 | a0001c0001t0055g0092 | 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 | a0001c0001t0035g0068 | 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 | 254 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0006g0154 | 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 | a0001c0001t0005g0020 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0196 a0001c0001t0005g0020 |
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 | a0001c0001t0008g0204 a0001c0001t0008g0217 a0001c0001t0012g0218 others(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 | a0001c0001t0001g0196 a0001c0001t0005g0020 |
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 | a0001c0001t0002g0236 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0018g0231 a0001c0001t0065g0203 |
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 | a0001c0001t0012g0219 | 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0008g0204 | 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0001g0144 | 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 | 76 | a0001c0001t0001g0025 a0001c0001t0001g0073 a0001c0001t0001g0087 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): 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 | a0001c0001t0001g0196 a0001c0001t0002g0161 a0001c0001t0005g0020 others(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 | a0001c0001t0003g0207 | 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 | a0001c0001t0021g0081 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0201 a0001c0001t0008g0202 others(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 | a0001c0001t0001g0199 a0001c0001t0007g0211 a0001c0001t0030g0209 others(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 | 134 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0033 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0001c0001t0012g0069 | 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 | a0001c0005t0001g0145 | 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 | a0001c0001t0001g0199 a0001c0001t0007g0211 a0001c0001t0030g0209 others(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 | a0001c0001t0003g0207 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0001t0002g0236 | 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 | a0001c0001t0003g0118 a0001c0001t0066g0120 |
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 | a0001c0001t0006g0091 | 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 | a0001c0001t0003g0225 a0001c0001t0067g0224 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0012g0069 |
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 | a0001c0001t0005g0020 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0090 others(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 | a0001c0001t0066g0120 | 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 | a0001c0001t0014g0234 | 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 | a0001c0001t0004g0089 | 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 | a0001c0001t0001g0196 a0001c0001t0005g0020 |
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 | 127 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): 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 | a0001c0001t0006g0010 a0001c0001t0006g0154 |
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 | a0001c0001t0003g0225 a0001c0001t0067g0224 |
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 | a0001c0001t0048g0147 | 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 | 231 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0003g0118 others(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 | a0001c0001t0024g0249 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0066g0120 | 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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0199 a0001c0001t0007g0211 a0001c0001t0030g0209 others(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 | a0001c0001t0011g0239 | 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 | a0001c0001t0003g0038 | 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 | 231 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): 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 | a0002c0003t0005g0115 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0005g0020 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0088 others(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 | a0001c0001t0003g0207 a0001c0001t0035g0068 |
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 | 126 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0033 others(123): Show |
126 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(123): 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 | a0001c0001t0021g0081 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0036g0082 | 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 | a0001c0001t0019g0002 a0001c0001t0029g0002 |
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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0088 a0001c0001t0001g0196 a0001c0001t0002g0063 others(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 | a0001c0001t0001g0199 a0001c0001t0007g0211 a0001c0001t0030g0209 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
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 | 231 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): 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 | a0001c0001t0003g0194 a0001c0001t0007g0169 a0001c0001t0007g0223 others(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 | a0001c0001t0011g0149 | 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 | a0001c0001t0003g0235 | 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 | a0001c0001t0026g0051 | 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 | a0001c0001t0036g0082 | 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 | a0001c0001t0001g0199 a0001c0001t0003g0214 a0001c0001t0003g0215 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0055 a0001c0001t0005g0020 |
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 | a0001c0001t0002g0161 a0001c0001t0002g0236 a0001c0001t0005g0030 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0229 others(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 | a0001c0001t0035g0068 | 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 | a0001c0001t0025g0216 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0212 others(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 | a0001c0001t0003g0225 a0001c0001t0067g0224 |
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 | a0001c0001t0009g0143 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 |
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 | a0001c0001t0001g0196 a0001c0001t0002g0055 a0001c0001t0005g0020 |
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 | a0001c0001t0001g0196 a0001c0001t0002g0055 a0001c0001t0005g0020 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0196 a0001c0001t0002g0055 others(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 | a0001c0001t0003g0207 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0007g0190 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0003g0054 a0001c0001t0007g0058 a0001c0001t0018g0070 |
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 | a0001c0001t0045g0205 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0119 a0001c0001t0003g0038 a0001c0001t0057g0220 |
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 | a0001c0001t0001g0071 a0001c0001t0006g0010 a0001c0001t0006g0154 others(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 | a0001c0001t0020g0042 a0001c0001t0030g0209 |
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 | a0001c0001t0046g0043 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0121 a0001c0001t0003g0038 a0001c0001t0005g0077 others(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 | a0001c0001t0028g0191 | 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 | a0001c0001t0003g0038 a0001c0001t0028g0191 a0001c0005t0001g0145 |
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 | a0001c0001t0028g0191 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0071 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0196 a0001c0001t0002g0041 a0001c0001t0002g0055 others(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 | a0001c0001t0025g0216 a0001c0001t0035g0068 |
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 | a0001c0001t0007g0169 a0001c0001t0007g0223 a0001c0001t0007g0232 others(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 | a0001c0001t0003g0008 a0001c0001t0011g0228 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0003g0039 a0001c0001t0058g0040 |
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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0003g0039 a0001c0001t0025g0216 a0001c0001t0035g0068 others(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 | |||||||
| chr18:46364857 | C | A | 4 | a0001c0001t0001g0242 a0001c0001t0002g0156 a0001c0001t0003g0112 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0033 others(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 | 90 | a0001c0001t0001g0025 a0001c0001t0001g0087 a0001c0001t0001g0094 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): 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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0003g0038 a0001c0001t0057g0220 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0001g0195 a0001c0001t0012g0069 |
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 | a0001c0001t0007g0058 a0001c0001t0012g0219 a0001c0001t0021g0081 others(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 | a0001c0001t0001g0025 a0001c0001t0002g0024 |
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 | a0001c0001t0012g0219 a0001c0001t0021g0081 a0001c0001t0024g0060 others(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 | a0001c0001t0007g0058 | 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 | a0001c0001t0036g0082 | 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 | a0001c0001t0004g0122 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0015g0126 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0005g0168 | 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 | 11 | a0001c0001t0002g0061 a0001c0001t0002g0063 a0001c0001t0002g0103 others(8): Show |
11 | HG01123.hp1 HG01123.hp2 HG01433.hp1 others(8): 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 | a0001c0001t0002g0095 a0001c0001t0004g0089 a0001c0001t0017g0165 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0002g0074 a0001c0001t0002g0252 a0001c0001t0004g0253 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0054 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0136 a0001c0001t0004g0157 a0001c0001t0004g0182 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0006g0005 | 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 | a0001c0001t0003g0039 a0001c0001t0007g0058 a0001c0001t0012g0219 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0005g0152 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0225 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0225 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0036g0082 a0001c0001t0050g0084 a0001c0004t0012g0083 |
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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0033 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0002g0014 a0001c0001t0005g0013 |
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 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0002g0026 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0002g0026 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0002g0026 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0018g0208 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0254 a0001c0001t0013g0114 a0001c0001t0013g0240 others(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 | a0001c0001t0004g0134 | 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 | a0001c0004t0012g0083 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0002g0026 others(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 | a0001c0001t0012g0069 | 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 | a0001c0001t0003g0049 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0018g0070 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0136 a0001c0001t0001g0180 others(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 | a0001c0001t0003g0118 a0001c0001t0006g0005 a0001c0001t0007g0050 others(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 | a0001c0001t0001g0048 a0001c0001t0003g0039 a0001c0001t0016g0046 others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0018g0070 others(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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0018g0070 others(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 | a0001c0001t0047g0045 | 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 | a0001c0001t0036g0082 a0001c0001t0050g0084 a0001c0004t0012g0083 |
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 | a0001c0001t0004g0251 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0018g0208 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0135 others(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 | a0001c0001t0003g0039 a0001c0001t0058g0040 |
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 | a0001c0001t0002g0014 a0001c0001t0005g0013 a0001c0001t0005g0015 |
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 | a0001c0001t0002g0014 a0001c0001t0005g0013 a0001c0001t0005g0015 |
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 | a0001c0001t0037g0105 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0054 a0001c0001t0018g0070 others(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 | a0001c0001t0006g0247 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0135 others(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 | a0001c0001t0014g0234 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0007g0050 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0054 a0001c0001t0018g0070 a0001c0001t0028g0191 |
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 | a0001c0001t0003g0035 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0002g0099 others(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 | a0001c0001t0003g0118 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0090 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0007g0211 others(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 | a0001c0001t0025g0216 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0073 others(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 | |||||||
| chr18:46374641 | C | G | 1 | a0001c0001t0026g0029 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0124 a0001c0001t0061g0123 |
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 | a0001c0001t0001g0119 a0001c0001t0003g0039 a0001c0001t0003g0118 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0001t0006g0005 |
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 | a0001c0001t0004g0157 | 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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0001g0101 a0001c0001t0002g0074 a0001c0001t0015g0066 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0139 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0125 a0001c0001t0009g0137 a0001c0001t0014g0198 others(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 | 22 | a0001c0001t0001g0133 a0001c0001t0001g0196 a0001c0001t0002g0161 others(19): Show |
22 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(19): 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 | a0001c0001t0012g0206 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0038 | 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 | a0001c0001t0001g0167 | 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 | 192 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): 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 | a0001c0001t0036g0082 | 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 | a0001c0001t0034g0138 | 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 | a0001c0001t0046g0043 | 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 | a0001c0001t0002g0074 a0001c0001t0003g0130 |
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 | a0001c0001t0002g0061 | 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 | a0001c0001t0016g0080 | 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 | 78 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(75): 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 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0167 a0001c0001t0001g0179 others(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 | a0001c0001t0003g0039 a0001c0001t0005g0020 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0087 a0001c0001t0002g0006 a0001c0001t0004g0009 others(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 | a0001c0001t0037g0105 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0001t0006g0005 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0049g0034 | 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 | a0001c0001t0018g0208 | 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 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0207 others(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 | a0001c0001t0014g0198 a0001c0001t0016g0080 |
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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0167 a0001c0001t0001g0179 others(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 | a0001c0001t0046g0043 | 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 | a0001c0001t0038g0132 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0015g0066 a0001c0001t0015g0126 |
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 | a0001c0001t0003g0039 a0001c0001t0028g0191 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0129 a0001c0001t0001g0167 others(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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(108): Show |
111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): 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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0057g0220 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0214 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0003g0214 | 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 | 179 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.61+44687A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46379022 | |||||||
| chr18:46379062 | T | C | 179 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0001t0006g0005 |
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 | a0001c0001t0005g0160 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0056g0170 | 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 | a0001c0001t0009g0093 | 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 | a0001c0001t0046g0043 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0184 a0001c0001t0052g0172 |
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 | a0001c0001t0030g0209 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0041g0062 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0005g0023 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0012g0218 | 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 | a0001c0001t0001g0196 a0001c0001t0003g0038 a0001c0001t0003g0256 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0024g0249 | 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 | a0001c0002t0010g0001 a0001c0002t0010g0085 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0005g0160 | 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 | 183 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0046g0043 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0235 a0001c0001t0008g0200 a0001c0001t0008g0201 others(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 | 66 | a0001c0001t0001g0048 a0001c0001t0001g0129 a0001c0001t0001g0167 others(63): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): 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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0007g0058 a0001c0001t0007g0169 a0001c0001t0007g0223 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0218 |
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 | a0001c0001t0003g0035 a0001c0001t0007g0211 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0207 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0002g0244 | 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 | a0001c0001t0005g0023 | 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 | a0001c0002t0010g0001 a0001c0002t0010g0085 |
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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0071 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.61+48581A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46382916 | |||||||
| chr18:46382954 | T | C | 172 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): 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 | a0001c0001t0001g0098 a0001c0001t0009g0097 |
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 | a0001c0001t0014g0198 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0118 a0001c0001t0006g0005 |
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 | a0001c0001t0008g0217 | 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 | a0001c0001t0003g0233 a0001c0001t0008g0217 a0001c0001t0012g0206 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0071 others(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 | a0001c0001t0003g0039 a0001c0001t0003g0118 a0001c0001t0006g0005 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0098 a0001c0001t0002g0063 a0001c0001t0003g0214 others(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 | a0001c0001t0005g0019 | 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 | a0001c0001t0003g0225 a0001c0001t0009g0137 a0001c0001t0011g0158 others(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 | a0001c0001t0009g0137 a0001c0001t0011g0158 a0001c0001t0044g0104 |
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 | a0001c0001t0003g0225 a0001c0001t0012g0218 a0001c0001t0066g0120 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0184 a0001c0001t0002g0026 |
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 | a0001c0001t0007g0058 a0001c0001t0007g0169 a0001c0001t0007g0223 others(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 | 124 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(121): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.61+49320T>C | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46383655 | |||||||
| chr18:46383694 | A | G | 51 | a0001c0001t0002g0014 a0001c0001t0002g0125 a0001c0001t0002g0151 others(48): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): 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 | a0001c0001t0006g0117 a0001c0001t0046g0043 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | 150 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): 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 | a0001c0001t0003g0225 | 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 | a0001c0001t0007g0058 a0001c0001t0007g0169 a0001c0001t0007g0211 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0119 a0001c0001t0001g0124 others(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 | a0001c0001t0004g0122 a0001c0001t0004g0182 a0001c0001t0052g0172 |
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 | a0001c0001t0002g0022 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0002g0151 | 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 | a0001c0001t0009g0143 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0193 |
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 | a0001c0001t0002g0131 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | 11 | a0001c0001t0001g0229 a0001c0001t0003g0038 a0001c0001t0003g0052 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(8): 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0040g0065 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0003g0175 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0003g0175 | 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 | 8 | a0001c0001t0001g0229 a0001c0001t0003g0052 a0001c0001t0005g0023 others(5): Show |
8 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(5): 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 | a0001c0001t0001g0184 a0001c0001t0002g0006 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0129 a0001c0001t0001g0144 others(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 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0023g0153 |
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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0049g0034 | 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 | a0001c0001t0026g0029 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0088 others(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 | a0001c0001t0053g0102 | 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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0055 a0001c0001t0002g0063 others(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 | a0001c0001t0043g0057 | 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 | a0001c0001t0043g0057 | 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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | a0001c0001t0014g0198 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0030g0209 |
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 | a0001c0001t0003g0118 a0001c0001t0006g0117 a0001c0001t0012g0218 |
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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | a0001c0001t0027g0078 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | a0001c0001t0002g0026 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0047g0045 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0015g0017 others(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 | a0001c0001t0002g0244 | 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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0002g0074 a0001c0001t0003g0130 a0001c0001t0005g0015 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
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 | a0001c0001t0011g0149 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0002c0003t0005g0115 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0004g0140 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0043g0057 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0004g0140 | 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 | a0001c0001t0002g0125 a0001c0001t0041g0062 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0055 a0001c0001t0002g0063 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0088 others(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 | a0001c0001t0005g0020 | 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 | a0001c0001t0057g0220 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0207 a0001c0001t0018g0070 |
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 | a0001c0001t0002g0014 | 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 | a0001c0001t0035g0068 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | |||||||
| chr18:46391820 | A | G | 2 | a0001c0001t0012g0219 a0001c0001t0047g0045 |
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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | a0001c0001t0011g0149 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0180 a0001c0001t0013g0114 a0001c0001t0054g0241 |
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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0144 a0001c0001t0001g0163 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0055 a0001c0001t0002g0063 others(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 | a0001c0001t0005g0015 | 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 | a0001c0001t0043g0057 | 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 | a0001c0001t0012g0069 a0001c0001t0018g0208 a0001c0001t0018g0231 |
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 | a0001c0001t0003g0256 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0002g0244 a0001c0001t0003g0225 a0001c0001t0012g0069 others(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 | |||||||
| chr18:46392699 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0002g0107 |
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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0135 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0004g0134 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0016g0046 a0001c0001t0016g0222 a0001c0001t0042g0230 |
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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0100 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0005g0186 | 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 | a0001c0005t0001g0145 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0237 a0001c0001t0044g0104 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0016g0222 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0003g0174 a0001c0001t0003g0207 a0001c0001t0018g0070 |
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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0002g0252 | 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 | a0001c0001t0001g0098 a0001c0001t0003g0225 a0001c0001t0009g0097 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0002g0244 | 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 | a0001c0001t0003g0112 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0048 | 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 | a0001c0004t0012g0083 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0025g0056 a0001c0001t0025g0216 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0037g0105 | 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 | a0001c0001t0046g0043 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0112 | 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 | a0001c0001t0011g0228 a0001c0001t0012g0206 a0001c0001t0014g0044 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0007g0211 a0001c0001t0025g0056 a0001c0001t0032g0173 |
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 | a0001c0001t0043g0057 | 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 | a0001c0001t0004g0122 a0001c0001t0004g0182 a0001c0001t0007g0211 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0007g0211 a0001c0001t0025g0056 a0001c0001t0032g0173 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0007g0211 a0001c0001t0025g0056 a0001c0001t0032g0173 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0194 | 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 | a0001c0001t0007g0211 a0001c0001t0025g0056 a0001c0001t0032g0173 |
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 | a0001c0001t0007g0211 a0001c0001t0025g0056 a0001c0001t0032g0173 |
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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0001g0098 a0001c0001t0009g0097 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0001g0090 a0001c0001t0003g0256 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0051g0255 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0036g0082 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0033g0053 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0012g0219 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0057g0220 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0057g0220 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0171 | 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 | 15 | a0001c0001t0001g0071 a0001c0001t0001g0229 a0001c0001t0002g0074 others(12): Show |
15 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(12): 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 | a0001c0001t0004g0027 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | 119 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): 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 | a0001c0001t0035g0068 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0175 a0001c0001t0043g0057 |
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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0012 a0001c0001t0002g0064 a0001c0001t0005g0186 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0066g0120 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | 26 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0021 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(23): 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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0175 | 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 | 22 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0021 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(19): 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 | a0001c0001t0004g0110 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0009g0093 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0071 a0001c0001t0002g0074 a0001c0001t0003g0130 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0058g0040 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0021 others(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 | a0001c0001t0035g0068 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0008g0192 a0001c0001t0008g0200 a0001c0001t0008g0201 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0014 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0043g0057 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | a0001c0001t0043g0057 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0012 a0001c0001t0027g0011 |
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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0002g0055 a0001c0001t0002g0155 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0009g0143 | 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 | a0001c0001t0002g0103 a0001c0001t0034g0138 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | 7 | a0001c0001t0003g0052 a0001c0001t0005g0023 a0001c0001t0005g0077 others(4): Show |
7 | HG00140.hp1 HG00140.hp2 HG01192.hp2 others(4): 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 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0011g0257 others(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 | a0001c0001t0003g0035 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0006g0091 a0001c0001t0041g0062 |
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 | a0001c0001t0003g0207 | 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 | a0001c0001t0006g0227 | 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 | a0001c0001t0036g0082 | 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 | a0001c0001t0057g0220 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0037g0105 | 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 | a0001c0001t0001g0048 a0001c0001t0012g0206 a0001c0001t0014g0044 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0005g0077 a0001c0001t0006g0010 a0001c0001t0006g0154 |
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 | a0001c0001t0055g0092 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0005g0168 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0041g0062 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0006g0227 | 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0012g0069 | 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 | a0001c0001t0011g0228 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0008g0192 | 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 | a0001c0001t0057g0220 | 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 | a0001c0001t0043g0057 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0016g0046 a0001c0001t0016g0222 a0001c0001t0042g0230 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0004g0182 | 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 | a0001c0001t0025g0056 a0001c0001t0025g0216 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0025g0056 a0001c0001t0025g0216 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0038g0132 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0020g0047 | 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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0195 a0001c0001t0009g0093 |
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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0094 others(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 | a0001c0005t0001g0145 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0237 a0001c0001t0044g0104 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0243 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0057g0220 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
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 | a0001c0001t0002g0014 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0058g0040 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | 4 | a0001c0001t0005g0077 a0001c0001t0006g0010 a0001c0001t0006g0154 others(1): Show |
4 | HG00140.hp2 HG01192.hp2 HG02735.hp1 others(1): 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0256 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0188 a0001c0001t0009g0177 a0001c0001t0009g0178 |
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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0004g0089 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0001g0229 a0001c0001t0003g0035 a0001c0001t0003g0038 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0005g0013 | 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 | a0001c0001t0003g0054 a0001c0001t0003g0215 a0001c0001t0003g0235 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0012 a0001c0001t0002g0064 a0001c0001t0005g0186 others(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 | a0001c0001t0003g0052 a0001c0001t0005g0023 a0001c0001t0064g0148 |
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 | a0001c0001t0002g0161 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0109 a0001c0001t0001g0121 others(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 | a0001c0001t0049g0034 | 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 | a0001c0001t0011g0228 | 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 | a0001c0001t0003g0194 a0001c0001t0007g0058 a0001c0001t0007g0169 others(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 | a0001c0001t0053g0102 | 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 | a0001c0001t0063g0032 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | 122 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0001g0090 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0212 others(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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0007g0050 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0233 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0025g0056 | 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 | a0001c0001t0003g0225 a0001c0001t0012g0069 a0001c0001t0018g0208 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | 237 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0040g0065 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0007g0190 a0001c0001t0016g0046 a0001c0001t0016g0080 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0229 a0001c0001t0003g0038 a0001c0001t0046g0043 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0229 a0001c0001t0003g0035 a0001c0001t0003g0038 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0004g0086 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0214 |
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 | a0002c0003t0005g0115 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0109 a0001c0001t0001g0121 others(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 | a0001c0001t0004g0113 a0001c0001t0004g0140 |
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 | a0001c0001t0001g0229 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0180 a0001c0001t0002g0041 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0048 | 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 | 126 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0001g0090 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0024g0060 a0001c0001t0024g0249 |
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 | a0001c0001t0003g0175 | 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
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 | a0001c0001t0008g0204 | 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 | a0001c0001t0013g0114 a0001c0001t0054g0241 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0193 others(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 | a0001c0001t0059g0181 | 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 | a0001c0002t0010g0001 a0001c0002t0010g0085 |
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 | a0001c0001t0001g0109 | 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 | a0001c0001t0002g0142 | 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 | 233 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.62-9010A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | chr18 | 46424180 | |||||||
| chr18:46424202 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0006g0227 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0187 a0001c0001t0001g0245 others(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 | a0001c0001t0012g0206 a0001c0001t0014g0044 a0001c0001t0014g0198 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0163 a0001c0001t0001g0188 others(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 | 233 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0004g0089 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0071 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): 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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0002g0252 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0079 others(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 | a0001c0001t0026g0051 | 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 | 235 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(232): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0254 others(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 | a0001c0001t0057g0220 | 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 | a0001c0001t0050g0084 | 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 | a0001c0001t0002g0061 | 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 | 128 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0136 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): 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 | a0001c0001t0001g0229 a0001c0001t0003g0038 a0001c0001t0046g0043 |
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 | a0001c0001t0030g0209 | 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 | 148 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0090 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0215 a0001c0001t0003g0225 a0001c0001t0018g0070 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0009g0093 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0019g0002 a0001c0001t0029g0002 |
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 | a0001c0001t0023g0018 | 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 | a0001c0001t0003g0038 a0001c0001t0008g0192 a0001c0001t0008g0200 others(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 | 254 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0010g0072 | 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 | a0001c0001t0003g0038 a0001c0001t0008g0192 a0001c0001t0008g0200 others(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 | a0001c0001t0003g0215 | 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 | a0001c0001t0003g0038 a0001c0001t0008g0192 a0001c0001t0008g0200 others(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 | a0001c0001t0049g0034 | 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 | a0001c0001t0028g0191 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0012g0219 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0014g0198 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0027 a0001c0001t0004g0106 others(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 | a0001c0001t0006g0117 | 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 | a0001c0001t0054g0241 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0065g0203 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0193 |
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 | 2 | a0001c0002t0010g0001 a0001c0002t0010g0085 |
4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 a0001c0001t0020g0042 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(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 | a0001c0001t0004g0113 a0001c0001t0004g0140 |
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 | a0001c0001t0004g0113 a0001c0001t0004g0140 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0179 |
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 | a0001c0001t0028g0191 | 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 | a0001c0001t0001g0012 a0001c0001t0027g0011 |
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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0009g0076 | 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 | 2 | a0001c0002t0010g0001 a0001c0002t0010g0085 |
4 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(1): 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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0006g0091 a0001c0001t0041g0062 |
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 | 121 | a0001c0001t0001g0162 a0001c0001t0001g0188 a0001c0001t0001g0237 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0001c0001t0046g0043 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0003g0038 a0001c0001t0046g0043 |
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 | a0001c0001t0002g0064 | 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 | a0001c0001t0004g0086 a0001c0001t0004g0096 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0004g0106 a0001c0001t0004g0253 a0001c0001t0026g0029 |
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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0031g0210 | 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 | a0001c0001t0018g0070 a0001c0001t0018g0208 a0001c0001t0018g0231 |
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 | a0001c0001t0002g0041 a0001c0001t0002g0252 a0001c0001t0022g0183 others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0005g0013 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | 131 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0021 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): 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 | a0001c0001t0003g0054 a0001c0001t0003g0215 a0001c0001t0003g0225 others(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 | a0001c0001t0045g0205 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0002g0063 | 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 | a0001c0001t0006g0227 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0001c0001t0001g0195 |
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 | a0001c0001t0028g0191 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0064 a0001c0001t0002g0074 others(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 | a0001c0001t0004g0134 | 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 | a0001c0001t0003g0225 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | 158 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): 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 | a0001c0001t0001g0242 a0001c0001t0003g0052 |
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 | a0001c0001t0054g0241 | 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 | 130 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0021 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): 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 | a0001c0001t0001g0007 a0001c0001t0001g0237 a0001c0001t0050g0084 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0013g0197 | 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 | a0001c0001t0057g0220 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0006g0010 | 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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0004g0106 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0022g0183 a0001c0001t0022g0185 |
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 | a0001c0004t0012g0083 | 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 | a0001c0004t0012g0083 | 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | 130 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0021 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): 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 | a0001c0001t0003g0225 | 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 | a0001c0001t0008g0176 a0001c0001t0008g0217 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(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 | a0001c0001t0020g0042 a0001c0001t0020g0047 a0001c0001t0031g0210 |
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 | a0001c0005t0001g0145 | 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 | a0001c0001t0060g0248 | 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 | a0001c0001t0063g0032 | 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 | a0001c0001t0008g0200 | 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 | 140 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0090 others(137): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): 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 | a0001c0001t0002g0006 a0001c0001t0002g0041 a0001c0001t0002g0064 others(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 | a0001c0001t0020g0042 a0001c0001t0020g0047 a0001c0001t0031g0210 |
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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0005g0186 | 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 | a0001c0001t0066g0120 | 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 | 128 | a0001c0001t0001g0071 a0001c0001t0002g0006 a0001c0001t0002g0014 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0002g0041 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0058g0040 | 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 | a0001c0001t0005g0152 | 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 | a0001c0001t0002g0243 | 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 | a0001c0001t0053g0102 a0001c0001t0054g0241 |
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 | a0001c0001t0015g0017 a0001c0001t0015g0066 a0001c0001t0015g0126 others(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 | a0001c0001t0001g0195 a0001c0001t0011g0146 a0001c0001t0011g0149 others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0005g0059 | 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 | a0001c0001t0002g0142 a0001c0001t0002g0151 |
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 | a0001c0001t0015g0126 | 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 | a0001c0001t0011g0146 a0001c0001t0011g0158 a0001c0001t0011g0228 others(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 | a0001c0001t0004g0122 a0001c0001t0004g0182 a0001c0001t0017g0164 others(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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0045g0205 | 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 | a0001c0001t0002g0103 | 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 | 159 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0090 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): 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 | a0001c0001t0045g0205 | 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 | a0001c0001t0003g0256 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | 148 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): 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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0057g0220 | 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 | a0001c0001t0011g0158 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0045g0205 | 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 | a0001c0001t0002g0024 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0179 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0250 |
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 | a0001c0001t0002g0014 | 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 | 151 | a0001c0001t0001g0071 a0001c0001t0002g0006 a0001c0001t0002g0014 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): 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 | a0001c0001t0023g0018 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0060g0248 a0001c0001t0061g0123 |
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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0003g0174 | 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 | a0001c0001t0055g0092 | 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 | a0001c0001t0049g0034 | 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 | a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0004g0182 | 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 | a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0019g0002 a0001c0001t0019g0159 a0001c0001t0029g0002 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0017g0164 a0001c0001t0017g0165 a0001c0001t0017g0238 others(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 | a0001c0001t0028g0191 a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0045g0205 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0028g0191 | 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 | 119 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0021 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): 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 | a0001c0001t0001g0119 a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0014g0198 | 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 | 159 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0119 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0011g0228 | 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 | a0001c0001t0003g0054 a0001c0001t0003g0215 a0001c0001t0003g0225 |
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 | a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
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 | a0001c0001t0058g0040 | 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 | 128 | a0001c0001t0001g0071 a0001c0001t0002g0006 a0001c0001t0002g0014 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): 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 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0144 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0118 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0037 a0001c0001t0003g0039 others(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 | a0001c0001t0028g0191 a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0003g0233 | 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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0003g0054 a0001c0001t0003g0215 a0001c0001t0003g0225 |
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 | a0001c0001t0008g0176 a0001c0001t0008g0192 a0001c0001t0008g0200 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0002g0252 | 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 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0136 others(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 | a0001c0001t0014g0044 a0001c0001t0014g0198 a0001c0001t0014g0234 others(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 | a0001c0001t0028g0191 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0027 a0001c0001t0004g0086 others(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 | a0001c0001t0009g0076 a0001c0001t0009g0097 a0001c0001t0009g0137 others(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 | a0001c0001t0065g0203 a0001c0001t0067g0224 |
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 | a0001c0001t0001g0163 | 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 | a0001c0001t0003g0035 a0001c0001t0003g0049 |
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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0011g0146 a0001c0001t0011g0149 a0001c0001t0011g0158 others(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 | a0001c0001t0020g0042 a0001c0001t0020g0047 a0001c0001t0031g0210 |
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 | a0001c0001t0018g0070 a0001c0001t0018g0208 a0001c0001t0018g0231 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0136 others(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 | a0001c0001t0006g0154 | 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0003g0054 a0001c0001t0003g0215 a0001c0001t0003g0225 |
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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0011g0149 a0001c0001t0011g0239 |
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 | a0001c0001t0028g0191 a0001c0001t0047g0045 a0001c0001t0058g0040 |
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 | a0001c0001t0057g0220 | 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 | a0001c0001t0004g0108 a0001c0001t0004g0134 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.924-82A>G | ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 7/7 | chr18 | 46456437 |