Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55500 |
| ensemblid | ENSG00000139163.16 |
| hgncid | 24649 |
| symbol | ETNK1 |
| name | ethanolamine kinase 1 |
| refseq_nuc | NM_018638.5 |
| refseq_prot | NP_061108.3 |
| ensembl_nuc | ENST00000266517.9 |
| ensembl_prot | ENSP00000266517.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 22625171 |
| end | 22690665 |
| strand | + |
| ver | v1.2 |
| region | chr12:22625171-22690665 |
| region5000 | chr12:22620171-22695665 |
| regionname0 | ETNK1_chr12_22625171_22690665 |
| regionname5000 | ETNK1_chr12_22620171_22695665 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 363 | 310 | 96 | 58 | 116 | 7 | 31 | 94 | ETNK1_chr12_22620171_22695665 | ETNK1 | MANYI others(358): Show |
chr12 | 22620171 | 22695665 |
| a0002 | 0/0 | 363 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ETNK1_chr12_22620171_22695665 | ETNK1 | MANYI others(358): Show |
chr12 | 22620171 | 22695665 |
| a0003 | 0/0 | 363 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | MANYI others(358): Show |
chr12 | 22620171 | 22695665 |
| a0004 | 0/0 | 363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | MANYI others(358): Show |
chr12 | 22620171 | 22695665 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1089 | 218 | 79 | 49 | 59 | 5 | 24 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0002 | 0/0 | 1089 | 82 | 9 | 7 | 57 | 2 | 7 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0003 | 0/0 | 1089 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0005 | 0/0 | 1089 | 3 | 2 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0007 | 0/0 | 1089 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0008 | 0/0 | 1089 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0001c0009 | 0/0 | 1089 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0002c0004 | 0/0 | 1089 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0003c0006 | 0/0 | 1089 | 3 | 0 | 0 | 0 | 1 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 | ||
| a0004c0010 | 0/0 | 1089 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | ATGGC others(1084): Show |
chr12 | 22620171 | 22695665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7063 | 11 | 2 | 0 | 9 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0002 | 1/0 | 7063 | 45 | 14 | 15 | 4 | 3 | 8 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0003 | 0/1 | 7061 | 40 | 4 | 15 | 15 | 1 | 4 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7056): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0004 | 0/0 | 7062 | 18 | 0 | 5 | 6 | 1 | 6 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0005 | 0/0 | 7064 | 3 | 1 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0007 | 0/0 | 7064 | 9 | 6 | 0 | 2 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0008 | 0/0 | 7063 | 9 | 0 | 0 | 9 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0009 | 0/0 | 7061 | 8 | 8 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7056): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0010 | 0/0 | 7062 | 7 | 0 | 4 | 1 | 0 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0011 | 0/0 | 7065 | 4 | 2 | 1 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7060): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0012 | 0/0 | 7066 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7061): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0013 | 0/0 | 7064 | 6 | 4 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0014 | 0/0 | 7062 | 6 | 6 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0015 | 0/0 | 7062 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0017 | 0/0 | 7064 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0018 | 0/0 | 7062 | 3 | 1 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0019 | 0/0 | 7062 | 3 | 2 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0020 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0022 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0023 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7054): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0024 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0025 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0027 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0028 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0029 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0032 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0034 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7060): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0035 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0036 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0037 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0038 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0040 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0041 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0042 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0043 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0044 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0045 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0046 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0047 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0049 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0050 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0053 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0054 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7060): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0055 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0056 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0001t0057 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0001 | 0/0 | 7063 | 37 | 0 | 4 | 26 | 1 | 6 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0002 | 0/0 | 7063 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0005 | 0/0 | 7064 | 10 | 0 | 2 | 7 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0006 | 0/0 | 7063 | 11 | 0 | 0 | 10 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0012 | 0/0 | 7066 | 5 | 5 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7061): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0016 | 0/0 | 7062 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0021 | 0/0 | 7063 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0026 | 0/0 | 7065 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7060): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0030 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0031 | 0/0 | 7064 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0039 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0001c0002t0051 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0003t0007 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0003t0011 | 0/0 | 7065 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7060): Show |
chr12 | 22620171 | 22695665 |
| a0001c0005t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7061): Show |
chr12 | 22620171 | 22695665 |
| a0001c0005t0048 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0001c0005t0052 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7061): Show |
chr12 | 22620171 | 22695665 |
| a0001c0007t0003 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7056): Show |
chr12 | 22620171 | 22695665 |
| a0001c0008t0033 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7055): Show |
chr12 | 22620171 | 22695665 |
| a0001c0009t0023 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7054): Show |
chr12 | 22620171 | 22695665 |
| a0002c0004t0001 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0002c0004t0005 | 0/0 | 7064 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7059): Show |
chr12 | 22620171 | 22695665 |
| a0003c0006t0001 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0003c0006t0002 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0003c0006t0058 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7058): Show |
chr12 | 22620171 | 22695665 |
| a0004c0010t0004 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | GCGGC others(7057): Show |
chr12 | 22620171 | 22695665 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 1 | 2 | 3 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0016 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0012g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0022g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0022g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0024g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0024g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0025g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0025g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0027g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0028g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0028g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0029g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0029g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0032g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0034g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0035g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0036g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0037g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0038g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0040g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0041g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0042g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0043g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0044g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0045g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0046g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0047g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0049g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0050g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0053g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0054g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0055g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0056g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0057g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0003 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0012g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0026g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0026g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0030g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0031g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0039g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0051g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0011g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0048g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0052g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0007t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0008t0033g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0009t0023g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0058g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0004c0010t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0006 | t0002 | g0110 | EUR | GBR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0139 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00323 | hp2 | a0001 | c0002 | t0006 | g0062 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0008 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0060 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00423 | hp2 | a0001 | c0001 | t0024 | g0228 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0173 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00558 | hp2 | a0001 | c0001 | t0015 | g0029 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00621 | hp2 | a0001 | c0002 | t0006 | g0061 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0052 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00741 | hp1 | a0001 | c0001 | t0050 | g0196 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01071 | hp1 | a0001 | c0001 | t0044 | g0027 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01109 | hp1 | a0001 | c0001 | t0042 | g0208 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0037 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0038 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01175 | hp2 | a0001 | c0001 | t0035 | g0229 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01243 | hp2 | a0001 | c0005 | t0048 | g0004 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01358 | hp2 | a0001 | c0009 | t0023 | g0140 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0032 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01884 | hp2 | a0001 | c0003 | t0011 | g0019 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0218 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01934 | hp2 | a0001 | c0001 | t0010 | g0215 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01943 | hp1 | a0001 | c0001 | t0036 | g0097 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0146 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01952 | hp2 | a0001 | c0002 | t0051 | g0003 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0073 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0184 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02027 | hp2 | a0001 | c0002 | t0031 | g0002 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02129 | hp2 | a0001 | c0002 | t0016 | g0018 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02132 | hp1 | a0001 | c0002 | t0006 | g0055 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02135 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02145 | hp2 | a0001 | c0001 | t0047 | g0050 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0134 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02258 | hp2 | a0001 | c0005 | t0052 | g0111 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02273 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0219 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02293 | hp1 | a0001 | c0001 | t0053 | g0007 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02293 | hp2 | a0001 | c0001 | t0010 | g0154 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02451 | hp1 | a0001 | c0003 | t0007 | g0103 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0226 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02572 | hp1 | a0001 | c0001 | t0025 | g0031 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0042 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02602 | hp1 | a0001 | c0001 | t0049 | g0201 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02602 | hp2 | a0001 | c0001 | t0057 | g0114 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02615 | hp1 | a0001 | c0001 | t0028 | g0044 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02615 | hp2 | a0001 | c0001 | t0043 | g0211 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0177 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0010 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02647 | hp2 | a0001 | c0001 | t0041 | g0010 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0207 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0180 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02818 | hp1 | a0001 | c0005 | t0012 | g0004 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02886 | hp1 | a0001 | c0001 | t0045 | g0033 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02895 | hp2 | a0001 | c0001 | t0028 | g0045 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02896 | hp2 | a0001 | c0002 | t0012 | g0021 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0028 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0181 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0131 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0049 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0217 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0126 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0137 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0132 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0128 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0005 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0039 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03139 | hp1 | a0001 | c0002 | t0012 | g0004 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0179 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03195 | hp1 | a0001 | c0001 | t0023 | g0035 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03195 | hp2 | a0001 | c0008 | t0033 | g0155 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03209 | hp1 | a0001 | c0007 | t0003 | g0150 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03209 | hp2 | a0001 | c0001 | t0040 | g0047 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03225 | hp1 | a0001 | c0001 | t0038 | g0016 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03225 | hp2 | a0001 | c0001 | t0055 | g0130 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0048 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0041 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03516 | hp1 | a0001 | c0001 | t0054 | g0183 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0040 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03579 | hp1 | a0001 | c0001 | t0027 | g0010 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03654 | hp1 | a0003 | c0006 | t0001 | g0077 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03688 | hp2 | a0001 | c0002 | t0005 | g0076 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03834 | hp2 | a0003 | c0006 | t0058 | g0105 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0224 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03942 | hp1 | a0004 | c0010 | t0004 | g0227 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0135 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0102 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0178 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0234 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18942 | hp1 | a0001 | c0002 | t0016 | g0043 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18942 | hp2 | a0001 | c0002 | t0030 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18946 | hp1 | a0001 | c0002 | t0039 | g0120 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18946 | hp2 | a0001 | c0001 | t0015 | g0220 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0078 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18949 | hp2 | a0001 | c0002 | t0030 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18951 | hp2 | a0001 | c0001 | t0046 | g0093 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18954 | hp1 | a0002 | c0004 | t0001 | g0059 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18959 | hp1 | a0001 | c0002 | t0021 | g0090 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18961 | hp1 | a0001 | c0001 | t0008 | g0172 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18965 | hp2 | a0001 | c0002 | t0026 | g0187 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18978 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18978 | hp2 | a0001 | c0001 | t0015 | g0029 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18983 | hp2 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0069 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19004 | hp1 | a0001 | c0001 | t0037 | g0189 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19004 | hp2 | a0001 | c0002 | t0026 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19007 | hp1 | a0001 | c0002 | t0005 | g0079 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19007 | hp2 | a0002 | c0004 | t0005 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19011 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19012 | hp1 | a0001 | c0001 | t0024 | g0233 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0118 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19030 | hp2 | a0001 | c0002 | t0012 | g0004 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19043 | hp1 | a0001 | c0001 | t0034 | g0125 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0175 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19058 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19063 | hp1 | a0001 | c0002 | t0021 | g0066 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19065 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19068 | hp2 | a0001 | c0002 | t0021 | g0003 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0171 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19074 | hp2 | a0001 | c0002 | t0016 | g0046 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19075 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19075 | hp2 | a0002 | c0004 | t0005 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19076 | hp2 | a0001 | c0002 | t0016 | g0056 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19078 | hp1 | a0001 | c0002 | t0031 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0174 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19084 | hp2 | a0001 | c0002 | t0005 | g0108 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19085 | hp2 | a0001 | c0002 | t0005 | g0071 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19091 | hp1 | a0001 | c0001 | t0013 | g0176 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19240 | hp1 | a0001 | c0001 | t0022 | g0005 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0004 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ASW | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20129 | hp2 | a0001 | c0001 | t0032 | g0235 | AFR | ASW | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0100 | EUR | TSI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0225 | SAS | GIH | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0185 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02109 | hp1 | a0001 | c0001 | t0056 | g0117 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0129 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG06807 | hp2 | a0001 | c0003 | t0011 | g0104 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20300 | hp1 | a0001 | c0003 | t0011 | g0019 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0182 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA21309 | hp2 | a0001 | c0002 | t0012 | g0004 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0212 | REF | REF | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0016 | REF | REF | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22643805 | G | A | 1 | a0002 | 4 | NA18954.hp1 NA19007.hp2 NA19065.hp1 others(1): Show |
missense_variant | MODERATE | c.199G>A | p.Val67Met | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/8 | 459/7063 | 199/1092 | 67/363 | chr12 | 22643805 | |||
| chr12:22661089 | A | G | 1 | a0003 | 3 | HG00099.hp1 HG03654.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.584A>G | p.Gln195Arg | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 844/7063 | 584/1092 | 195/363 | chr12 | 22661089 | |||
| chr12:22673582 | A | T | 1 | a0004 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.867A>T | p.Lys289Asn | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/8 | 1127/7063 | 867/1092 | 289/363 | chr12 | 22673582 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625439 | T | C | 1 | a0001c0003 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.9T>C | p.Asn3Asn | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | 269/7063 | 9/1092 | 3/363 | chr12 | 22625439 | |||
| chr12:22625574 | G | A | 3 | a0001c0005 a0001c0007 a0001c0008 |
5 | HG01243.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.144G>A | p.Glu48Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | 404/7063 | 144/1092 | 48/363 | chr12 | 22625574 | |||
| chr12:22661102 | A | G | 3 | a0001c0002 a0001c0005 a0002c0004 |
89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.597A>G | p.Glu199Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 857/7063 | 597/1092 | 199/363 | chr12 | 22661102 | |||
| chr12:22661105 | G | A | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.600G>A | p.Glu200Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 860/7063 | 600/1092 | 200/363 | chr12 | 22661105 | |||
| chr12:22684909 | C | T | 1 | a0001c0009 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1047C>T | p.Tyr349Tyr | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1307/7063 | 1047/1092 | 349/363 | chr12 | 22684909 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625223 | C | T | 1 | a0003c0006t0058 | 1 | HG03834.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-208C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | chr12 | 22625223 | |||||||
| chr12:22685032 | T | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 78 | chr12 | 22685032 | ||||||
| chr12:22685291 | C | T | 1 | a0001c0001t0057 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 337 | chr12 | 22685291 | ||||||
| chr12:22685327 | A | C | 1 | a0001c0001t0056 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 373 | chr12 | 22685327 | ||||||
| chr12:22685751 | TATCA | T | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0023 others(3): Show |
50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*802delTCAA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 799 | INFO_REALIGN_3_PRIME | chr12 | 22685751 | |||||
| chr12:22685822 | T | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 868 | chr12 | 22685822 | ||||||
| chr12:22686584 | A | T | 4 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0022 others(1): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1630A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1630 | chr12 | 22686584 | ||||||
| chr12:22686647 | A | G | 8 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0029 others(5): Show |
34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1693A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1693 | chr12 | 22686647 | ||||||
| chr12:22686751 | T | C | 2 | a0001c0001t0015 a0001c0001t0024 |
6 | HG00423.hp2 HG00558.hp2 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1797T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1797 | chr12 | 22686751 | ||||||
| chr12:22686802 | G | A | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(17): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1848 | chr12 | 22686802 | ||||||
| chr12:22686819 | A | G | 1 | a0001c0001t0053 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1865 | chr12 | 22686819 | ||||||
| chr12:22686851 | A | AT | 17 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(14): Show |
65 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1925dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | |||||
| chr12:22686851 | A | ATT | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0024 others(6): Show |
54 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1924_*1925dupTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | |||||
| chr12:22686851 | A | ATTT | 5 | a0001c0001t0010 a0001c0001t0012 a0001c0002t0012 others(2): Show |
15 | HG01243.hp1 HG01934.hp2 HG01952.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1923_*1925dupTTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | |||||
| chr12:22686851 | AT | A | 7 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0019 others(4): Show |
21 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1925delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1925 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | |||||
| chr12:22686851 | ATT | A | 1 | a0001c0001t0009 | 8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1924_*1925delTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1924 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | |||||
| chr12:22686909 | A | G | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1955A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1955 | chr12 | 22686909 | ||||||
| chr12:22686966 | T | G | 1 | a0001c0001t0036 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2012 | chr12 | 22686966 | ||||||
| chr12:22686990 | G | C | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2036G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2036 | chr12 | 22686990 | ||||||
| chr12:22687042 | A | G | 1 | a0001c0001t0046 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2088 | chr12 | 22687042 | ||||||
| chr12:22687085 | C | T | 1 | a0001c0001t0045 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2131C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2131 | chr12 | 22687085 | ||||||
| chr12:22687158 | A | G | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(2): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2204A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2204 | chr12 | 22687158 | ||||||
| chr12:22687201 | A | G | 1 | a0001c0001t0044 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2247 | chr12 | 22687201 | ||||||
| chr12:22687211 | T | C | 2 | a0001c0001t0018 a0001c0001t0020 |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2257T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2257 | chr12 | 22687211 | ||||||
| chr12:22687324 | A | C | 1 | a0001c0002t0021 | 3 | NA18959.hp1 NA19063.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2370 | chr12 | 22687324 | ||||||
| chr12:22687494 | A | G | 1 | a0001c0002t0051 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2540 | chr12 | 22687494 | ||||||
| chr12:22687861 | A | G | 1 | a0001c0001t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2907A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2907 | chr12 | 22687861 | ||||||
| chr12:22688064 | C | T | 2 | a0001c0001t0043 a0001c0001t0050 |
2 | HG00741.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3110C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3110 | chr12 | 22688064 | ||||||
| chr12:22688065 | G | A | 1 | a0001c0001t0037 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3111G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3111 | chr12 | 22688065 | ||||||
| chr12:22688158 | A | C | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(2): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3204A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3204 | chr12 | 22688158 | ||||||
| chr12:22688173 | A | G | 1 | a0001c0001t0042 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3219A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3219 | chr12 | 22688173 | ||||||
| chr12:22688370 | C | T | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(2): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3416C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3416 | chr12 | 22688370 | ||||||
| chr12:22688412 | T | G | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3458T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3458 | chr12 | 22688412 | ||||||
| chr12:22688426 | A | C | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(2): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3472A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3472 | chr12 | 22688426 | ||||||
| chr12:22688553 | A | T | 4 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0022 others(1): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3599A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3599 | chr12 | 22688553 | ||||||
| chr12:22688589 | A | G | 1 | a0001c0001t0049 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3635A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3635 | chr12 | 22688589 | ||||||
| chr12:22688620 | A | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3666A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3666 | chr12 | 22688620 | ||||||
| chr12:22688730 | A | T | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3776A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3776 | chr12 | 22688730 | ||||||
| chr12:22688754 | G | A | 1 | a0001c0001t0038 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3800G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3800 | chr12 | 22688754 | ||||||
| chr12:22688821 | G | A | 1 | a0001c0002t0030 | 2 | NA18942.hp2 NA18949.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3867G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3867 | chr12 | 22688821 | ||||||
| chr12:22689043 | A | G | 3 | a0001c0001t0027 a0001c0001t0041 a0001c0005t0048 |
4 | HG01243.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4089A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4089 | chr12 | 22689043 | ||||||
| chr12:22689262 | CTA | C | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(2): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4310_*4311delAT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4310 | INFO_REALIGN_3_PRIME | chr12 | 22689262 | |||||
| chr12:22689340 | A | G | 2 | a0001c0001t0040 a0001c0001t0047 |
2 | HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4386A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4386 | chr12 | 22689340 | ||||||
| chr12:22689488 | A | G | 1 | a0001c0001t0037 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4534A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4534 | chr12 | 22689488 | ||||||
| chr12:22689625 | G | A | 1 | a0001c0002t0039 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4671G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4671 | chr12 | 22689625 | ||||||
| chr12:22689793 | G | A | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4839G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4839 | chr12 | 22689793 | ||||||
| chr12:22689844 | A | G | 7 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0024 others(4): Show |
29 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4890A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4890 | chr12 | 22689844 | ||||||
| chr12:22690077 | A | G | 1 | a0001c0001t0041 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5123A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5123 | chr12 | 22690077 | ||||||
| chr12:22690128 | C | T | 1 | a0001c0005t0052 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5174C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5174 | chr12 | 22690128 | ||||||
| chr12:22690273 | A | C | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0027 others(16): Show |
97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*5319A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5319 | chr12 | 22690273 | ||||||
| chr12:22690573 | C | T | 1 | a0001c0001t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5619C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5619 | chr12 | 22690573 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625601 | T | C | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+15T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625601 | |||||||
| chr12:22625651 | C | G | 2 | a0001c0001t0007g0234 a0001c0001t0032g0235 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.156+65C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625651 | |||||||
| chr12:22625653 | A | G | 1 | a0001c0001t0024g0233 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.156+67A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625653 | |||||||
| chr12:22625699 | C | T | 24 | a0001c0001t0002g0028 a0001c0001t0004g0030 a0001c0001t0004g0216 others(21): Show |
26 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.156+113C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625699 | |||||||
| chr12:22625767 | C | G | 37 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0002g0001 others(34): Show |
48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.156+181C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625767 | |||||||
| chr12:22625905 | A | G | 15 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(12): Show |
17 | HG00544.hp1 HG02622.hp1 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.156+319A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625905 | |||||||
| chr12:22626078 | T | A | 1 | a0001c0001t0004g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.156+492T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626078 | |||||||
| chr12:22626226 | CTG | C | 17 | a0001c0001t0004g0030 a0001c0001t0004g0216 a0001c0001t0004g0221 others(14): Show |
19 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.156+642_156+643del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22626226 | ||||||
| chr12:22626257 | A | G | 3 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 |
3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.156+671A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626257 | |||||||
| chr12:22626296 | G | A | 1 | a0001c0001t0045g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156+710G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626296 | |||||||
| chr12:22626297 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+711G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626297 | |||||||
| chr12:22626400 | C | A | 3 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 |
3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.156+814C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626400 | |||||||
| chr12:22626426 | CA | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(80): Show |
101 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.156+849delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22626426 | ||||||
| chr12:22626732 | G | T | 1 | a0001c0001t0003g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.156+1146G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626732 | |||||||
| chr12:22626892 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+1306T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626892 | |||||||
| chr12:22627150 | A | AT | 42 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(39): Show |
51 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.156+1574dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22627150 | ||||||
| chr12:22627150 | A | ATTT | 13 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(10): Show |
15 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.156+1572_156+1574d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22627150 | ||||||
| chr12:22627160 | T | TTA | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+1574_156+1575i others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627160 | |||||||
| chr12:22627174 | G | A | 251 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(248): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.156+1588G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627174 | |||||||
| chr12:22627189 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+1603G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627189 | |||||||
| chr12:22628193 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+2607G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628193 | |||||||
| chr12:22628596 | G | C | 1 | a0001c0001t0010g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.156+3010G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628596 | |||||||
| chr12:22628614 | C | T | 16 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(13): Show |
18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+3028C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628614 | |||||||
| chr12:22628746 | A | G | 9 | a0001c0002t0002g0004 a0001c0002t0002g0021 a0001c0002t0002g0112 others(6): Show |
12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+3160A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628746 | |||||||
| chr12:22628811 | T | A | 8 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+3225T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628811 | |||||||
| chr12:22628887 | A | G | 1 | a0001c0001t0009g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.156+3301A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628887 | |||||||
| chr12:22628984 | A | G | 1 | a0003c0006t0002g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.156+3398A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628984 | |||||||
| chr12:22629079 | A | G | 1 | a0001c0001t0054g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.156+3493A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629079 | |||||||
| chr12:22629088 | T | A | 2 | a0001c0002t0002g0021 a0001c0002t0012g0021 |
2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.156+3502T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629088 | |||||||
| chr12:22629290 | A | G | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.156+3704A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629290 | |||||||
| chr12:22629757 | C | T | 1 | a0001c0002t0006g0020 | 2 | NA18983.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.156+4171C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629757 | |||||||
| chr12:22629786 | A | G | 2 | a0001c0001t0032g0235 a0001c0001t0034g0125 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.156+4200A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629786 | |||||||
| chr12:22629889 | C | T | 1 | a0001c0001t0007g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.156+4303C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629889 | |||||||
| chr12:22629928 | T | A | 65 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(62): Show |
81 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.156+4342T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629928 | |||||||
| chr12:22630106 | A | G | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.156+4520A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630106 | |||||||
| chr12:22630118 | T | C | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+4532T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630118 | |||||||
| chr12:22630149 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+4563T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630149 | |||||||
| chr12:22630249 | C | T | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+4663C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630249 | |||||||
| chr12:22630255 | T | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+4669T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630255 | |||||||
| chr12:22630265 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.156+4679A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630265 | |||||||
| chr12:22630474 | A | C | 1 | a0001c0001t0004g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.156+4888A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630474 | |||||||
| chr12:22630504 | A | C | 1 | a0001c0002t0001g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.156+4918A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630504 | |||||||
| chr12:22630548 | G | GCTTA | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0005g0108 |
3 | NA18945.hp1 NA18987.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.156+4965_156+4968d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22630548 | ||||||
| chr12:22630629 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+5043T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630629 | |||||||
| chr12:22630720 | C | T | 1 | a0001c0002t0005g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.156+5134C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630720 | |||||||
| chr12:22630757 | T | G | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+5171T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630757 | |||||||
| chr12:22630759 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+5173C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630759 | |||||||
| chr12:22630811 | A | G | 69 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
85 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.156+5225A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630811 | |||||||
| chr12:22630881 | G | T | 1 | a0003c0006t0058g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.156+5295G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630881 | |||||||
| chr12:22630937 | A | G | 3 | a0001c0003t0007g0103 a0001c0003t0011g0019 a0001c0003t0011g0104 |
4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+5351A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630937 | |||||||
| chr12:22630977 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.156+5391G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630977 | |||||||
| chr12:22630989 | G | A | 1 | a0001c0002t0016g0043 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.156+5403G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630989 | |||||||
| chr12:22631177 | C | CT | 31 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(28): Show |
38 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+5605dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22631177 | ||||||
| chr12:22631335 | T | C | 91 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(88): Show |
112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.156+5749T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631335 | |||||||
| chr12:22631343 | T | C | 2 | a0001c0001t0028g0044 a0001c0001t0028g0045 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.156+5757T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631343 | |||||||
| chr12:22631499 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.156+5913C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631499 | |||||||
| chr12:22631629 | G | A | 1 | a0001c0002t0016g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.156+6043G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631629 | |||||||
| chr12:22631660 | G | A | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.156+6074G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631660 | |||||||
| chr12:22631785 | G | A | 1 | a0001c0001t0040g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156+6199G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631785 | |||||||
| chr12:22631954 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.156+6368A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631954 | |||||||
| chr12:22632014 | A | G | 1 | a0001c0001t0013g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+6428A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632014 | |||||||
| chr12:22632078 | A | AT | 140 | a0001c0001t0001g0074 a0001c0001t0001g0191 a0001c0001t0001g0192 others(137): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.156+6504dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632078 | ||||||
| chr12:22632078 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(5): Show |
10 | HG03453.hp2 NA18965.hp1 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+6504delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632078 | ||||||
| chr12:22632168 | G | A | 64 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(61): Show |
80 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.156+6582G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632168 | |||||||
| chr12:22632217 | A | T | 1 | a0001c0001t0002g0209 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.156+6631A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632217 | |||||||
| chr12:22632353 | A | G | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156+6767A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632353 | |||||||
| chr12:22632382 | C | G | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.156+6796C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632382 | |||||||
| chr12:22632482 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156+6896C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632482 | |||||||
| chr12:22632515 | C | CT | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+6939dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632515 | ||||||
| chr12:22632593 | T | TTGTACTC others(18): Show |
1 | a0001c0001t0010g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.156+7026_156+7027i others(27): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632593 | ||||||
| chr12:22632613 | G | C | 69 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
85 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.156+7027G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632613 | |||||||
| chr12:22632701 | C | T | 27 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(24): Show |
34 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+7115C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632701 | |||||||
| chr12:22632733 | T | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(25): Show |
35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.156+7147T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632733 | |||||||
| chr12:22632782 | G | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0133 a0001c0001t0014g0005 others(3): Show |
10 | HG01891.hp2 HG02818.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+7196G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632782 | |||||||
| chr12:22632837 | G | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+7251G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632837 | |||||||
| chr12:22632952 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(11): Show |
16 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+7366A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632952 | |||||||
| chr12:22633120 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0160 |
3 | HG02055.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.156+7534A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633120 | |||||||
| chr12:22633149 | T | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(11): Show |
16 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+7563T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633149 | |||||||
| chr12:22633174 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+7588C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633174 | |||||||
| chr12:22633547 | A | G | 1 | a0003c0006t0002g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.156+7961A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633547 | |||||||
| chr12:22633582 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+7996A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633582 | |||||||
| chr12:22633631 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.156+8045A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633631 | |||||||
| chr12:22633775 | G | A | 1 | a0001c0002t0006g0055 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.156+8189G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633775 | |||||||
| chr12:22633873 | A | G | 1 | a0001c0001t0042g0208 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.156+8287A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633873 | |||||||
| chr12:22633882 | A | G | 28 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(25): Show |
35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.156+8296A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633882 | |||||||
| chr12:22633967 | G | A | 1 | a0001c0001t0014g0022 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.156+8381G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633967 | |||||||
| chr12:22634440 | A | G | 1 | a0001c0001t0055g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+8854A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634440 | |||||||
| chr12:22634557 | T | C | 1 | a0001c0001t0003g0023 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.156+8971T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634557 | |||||||
| chr12:22634657 | C | T | 1 | a0001c0001t0019g0207 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.156+9071C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634657 | |||||||
| chr12:22634830 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(9): Show |
14 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-8933C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634830 | |||||||
| chr12:22634837 | A | G | 69 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
85 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.157-8926A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634837 | |||||||
| chr12:22634862 | T | C | 91 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(88): Show |
112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.157-8901T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634862 | |||||||
| chr12:22634905 | T | A | 3 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0016g0056 |
3 | HG02129.hp1 NA18951.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.157-8858T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634905 | |||||||
| chr12:22635145 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.157-8618A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635145 | |||||||
| chr12:22635239 | T | C | 69 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
85 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.157-8524T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635239 | |||||||
| chr12:22635269 | T | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(25): Show |
35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.157-8494T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635269 | |||||||
| chr12:22635349 | G | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0027 a0001c0001t0002g0095 others(12): Show |
18 | HG00639.hp1 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-8414G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635349 | |||||||
| chr12:22635432 | C | T | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-8331C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635432 | |||||||
| chr12:22635446 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-8317C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635446 | |||||||
| chr12:22635461 | T | C | 4 | a0001c0002t0005g0008 a0002c0004t0001g0008 a0002c0004t0001g0059 others(1): Show |
5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-8302T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635461 | |||||||
| chr12:22635479 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.157-8284G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635479 | |||||||
| chr12:22635638 | T | C | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-8125T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635638 | |||||||
| chr12:22635679 | G | A | 2 | a0001c0001t0028g0044 a0001c0001t0028g0045 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.157-8084G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635679 | |||||||
| chr12:22635839 | G | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-7924G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635839 | |||||||
| chr12:22635878 | T | A | 9 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(6): Show |
11 | HG00544.hp1 HG02602.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-7885T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635878 | |||||||
| chr12:22636004 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.157-7759C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636004 | |||||||
| chr12:22636130 | T | C | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-7633T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636130 | |||||||
| chr12:22636140 | G | T | 1 | a0001c0001t0003g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.157-7623G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636140 | |||||||
| chr12:22636309 | A | G | 1 | a0001c0001t0007g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.157-7454A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636309 | |||||||
| chr12:22636445 | A | G | 1 | a0001c0001t0013g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.157-7318A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636445 | |||||||
| chr12:22636522 | A | G | 2 | a0001c0002t0001g0100 a0001c0002t0001g0109 |
2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.157-7241A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636522 | |||||||
| chr12:22636709 | T | C | 67 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(64): Show |
83 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.157-7054T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636709 | |||||||
| chr12:22636726 | T | C | 8 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-7037T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636726 | |||||||
| chr12:22636815 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(19): Show |
29 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-6948G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636815 | |||||||
| chr12:22636883 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(19): Show |
29 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-6880G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636883 | |||||||
| chr12:22636919 | A | G | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-6844A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636919 | |||||||
| chr12:22636964 | G | T | 3 | a0001c0001t0003g0012 a0001c0001t0003g0157 a0001c0001t0003g0158 |
6 | NA18980.hp1 NA19003.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-6799G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636964 | |||||||
| chr12:22636990 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157-6773G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636990 | |||||||
| chr12:22637246 | C | A | 20 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(17): Show |
25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-6517C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637246 | |||||||
| chr12:22637598 | A | G | 3 | a0001c0003t0007g0103 a0001c0003t0011g0019 a0001c0003t0011g0104 |
4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-6165A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637598 | |||||||
| chr12:22637607 | C | A | 8 | a0001c0002t0006g0002 a0001c0002t0006g0020 a0001c0002t0006g0055 others(5): Show |
15 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-6156C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637607 | |||||||
| chr12:22637698 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.157-6065G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637698 | |||||||
| chr12:22637820 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.157-5943T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637820 | |||||||
| chr12:22637862 | C | CGA | 39 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(36): Show |
47 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.157-5889_157-5888d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22637862 | ||||||
| chr12:22638024 | A | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.157-5739A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638024 | |||||||
| chr12:22638051 | C | CA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5703dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638051 | ||||||
| chr12:22638063 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.157-5700A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638063 | |||||||
| chr12:22638255 | G | GT | 7 | a0001c0001t0001g0166 a0001c0001t0008g0174 a0001c0001t0008g0175 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-5494dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638255 | ||||||
| chr12:22638255 | GT | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.157-5494delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638255 | ||||||
| chr12:22638274 | C | A | 27 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(24): Show |
32 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5489C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638274 | |||||||
| chr12:22638347 | G | T | 27 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(24): Show |
32 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5416G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638347 | |||||||
| chr12:22638353 | A | G | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5410A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638353 | |||||||
| chr12:22638480 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157-5283G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638480 | |||||||
| chr12:22638513 | A | C | 37 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0002g0001 others(34): Show |
48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-5250A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638513 | |||||||
| chr12:22638613 | T | A | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5150T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638613 | |||||||
| chr12:22638755 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.157-5008T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638755 | |||||||
| chr12:22639036 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-4727A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639036 | |||||||
| chr12:22639072 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0157 a0001c0001t0003g0158 |
6 | NA18980.hp1 NA19003.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-4691T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639072 | |||||||
| chr12:22639178 | TTTG | T | 16 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(13): Show |
18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-4579_157-4577d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639178 | ||||||
| chr12:22639221 | A | T | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-4542A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639221 | |||||||
| chr12:22639225 | T | A | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-4538T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639225 | |||||||
| chr12:22639327 | A | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-4436A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639327 | |||||||
| chr12:22639364 | C | T | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.157-4399C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639364 | |||||||
| chr12:22639447 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.157-4316C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639447 | |||||||
| chr12:22639449 | G | T | 16 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(13): Show |
18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-4314G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639449 | |||||||
| chr12:22639487 | G | A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0138 a0001c0001t0003g0139 |
4 | HG00280.hp2 HG00733.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-4276G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639487 | |||||||
| chr12:22639538 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(6): Show |
11 | HG00621.hp1 HG02559.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-4225A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639538 | |||||||
| chr12:22639581 | G | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.157-4182G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639581 | |||||||
| chr12:22639609 | G | A | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.157-4154G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639609 | |||||||
| chr12:22639672 | C | CA | 9 | a0001c0002t0002g0004 a0001c0002t0002g0021 a0001c0002t0002g0112 others(6): Show |
12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-4080dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639672 | ||||||
| chr12:22639672 | CA | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(21): Show |
31 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.157-4080delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639672 | ||||||
| chr12:22639695 | A | G | 3 | a0001c0003t0007g0103 a0001c0003t0011g0019 a0001c0003t0011g0104 |
4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-4068A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639695 | |||||||
| chr12:22639759 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-4004G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639759 | |||||||
| chr12:22639836 | T | C | 1 | a0001c0001t0019g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.157-3927T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639836 | |||||||
| chr12:22639840 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(6): Show |
11 | HG00621.hp1 HG02559.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-3923A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639840 | |||||||
| chr12:22639910 | C | T | 8 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-3853C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639910 | |||||||
| chr12:22639934 | T | C | 3 | a0001c0001t0010g0137 a0001c0001t0010g0215 a0001c0009t0023g0140 |
3 | HG01358.hp2 HG01934.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.157-3829T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639934 | |||||||
| chr12:22639958 | G | C | 1 | a0001c0001t0003g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.157-3805G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639958 | |||||||
| chr12:22640115 | G | T | 20 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(17): Show |
25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-3648G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640115 | |||||||
| chr12:22640396 | CT | C | 15 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0009g0126 others(12): Show |
15 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.157-3350delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22640396 | ||||||
| chr12:22640620 | C | T | 1 | a0001c0001t0004g0231 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157-3143C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640620 | |||||||
| chr12:22640694 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3069G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640694 | |||||||
| chr12:22640723 | TAGAG | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3036_157-3033d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22640723 | ||||||
| chr12:22640742 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3021G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640742 | |||||||
| chr12:22641060 | G | GT | 24 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(21): Show |
33 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.157-2702dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22641060 | ||||||
| chr12:22641073 | C | T | 10 | a0001c0001t0002g0054 a0001c0001t0002g0063 a0001c0001t0002g0084 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-2690C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641073 | |||||||
| chr12:22641256 | G | A | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-2507G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641256 | |||||||
| chr12:22641289 | T | C | 63 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(60): Show |
79 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.157-2474T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641289 | |||||||
| chr12:22641293 | C | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-2470C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641293 | |||||||
| chr12:22641453 | G | A | 3 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0014g0128 |
3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.157-2310G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641453 | |||||||
| chr12:22641773 | C | T | 20 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(17): Show |
25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-1990C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641773 | |||||||
| chr12:22641913 | A | T | 1 | a0001c0001t0003g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.157-1850A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641913 | |||||||
| chr12:22641997 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.157-1766T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641997 | |||||||
| chr12:22642018 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.157-1745A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642018 | |||||||
| chr12:22642098 | G | T | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.157-1665G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642098 | |||||||
| chr12:22642303 | A | G | 1 | a0001c0001t0049g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157-1460A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642303 | |||||||
| chr12:22642367 | G | A | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-1396G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642367 | |||||||
| chr12:22642555 | T | C | 2 | a0001c0002t0001g0064 a0001c0002t0016g0046 |
2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.157-1208T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642555 | |||||||
| chr12:22642730 | T | G | 25 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(22): Show |
32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-1033T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642730 | |||||||
| chr12:22642773 | T | C | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-990T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642773 | |||||||
| chr12:22642838 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-925G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642838 | |||||||
| chr12:22642949 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157-814C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642949 | |||||||
| chr12:22643071 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157-692G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643071 | |||||||
| chr12:22643117 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0160 |
3 | HG02055.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.157-646A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643117 | |||||||
| chr12:22643353 | C | G | 1 | a0001c0002t0001g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.157-410C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643353 | |||||||
| chr12:22643381 | T | C | 16 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(13): Show |
18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-382T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643381 | |||||||
| chr12:22643403 | A | G | 1 | a0001c0001t0043g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.157-360A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643403 | |||||||
| chr12:22643499 | CAG | C | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-262_157-261del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22643499 | ||||||
| chr12:22644060 | A | AT | 245 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(242): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.416+38_416+39insT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644060 | |||||||
| chr12:22644150 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416+128G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644150 | |||||||
| chr12:22644599 | T | C | 64 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(61): Show |
80 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.416+577T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644599 | |||||||
| chr12:22644662 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416+640T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644662 | |||||||
| chr12:22644665 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.416+643T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644665 | |||||||
| chr12:22644687 | T | C | 1 | a0001c0002t0021g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.416+665T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644687 | |||||||
| chr12:22644709 | A | G | 1 | a0001c0001t0004g0030 | 2 | NA18970.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.416+687A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644709 | |||||||
| chr12:22644729 | A | G | 20 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0101 others(17): Show |
25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.416+707A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644729 | |||||||
| chr12:22644892 | G | T | 1 | a0001c0008t0033g0155 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.416+870G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644892 | |||||||
| chr12:22644955 | C | T | 1 | a0001c0001t0011g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.416+933C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644955 | |||||||
| chr12:22645011 | A | G | 1 | a0001c0002t0001g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.416+989A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645011 | |||||||
| chr12:22645110 | A | G | 2 | a0001c0001t0003g0153 a0001c0001t0010g0154 |
2 | HG02293.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.416+1088A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645110 | |||||||
| chr12:22645236 | G | A | 85 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(82): Show |
106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.416+1214G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645236 | |||||||
| chr12:22645321 | G | C | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.416+1299G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645321 | |||||||
| chr12:22645378 | C | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.416+1356C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645378 | |||||||
| chr12:22645378 | C | G | 1 | a0001c0001t0004g0230 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.416+1356C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645378 | |||||||
| chr12:22645511 | C | T | 2 | a0001c0001t0003g0143 a0001c0001t0003g0152 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.416+1489C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645511 | |||||||
| chr12:22645527 | C | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0165 others(20): Show |
30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.416+1505C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645527 | |||||||
| chr12:22645573 | A | T | 68 | a0001c0001t0001g0074 a0001c0001t0012g0010 a0001c0001t0027g0010 others(65): Show |
86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.416+1551A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645573 | |||||||
| chr12:22645707 | T | G | 2 | a0001c0001t0028g0044 a0001c0001t0028g0045 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.416+1685T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645707 | |||||||
| chr12:22645738 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0007g0190 others(1): Show |
4 | NA18984.hp2 NA19004.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.416+1716G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645738 | |||||||
| chr12:22645889 | T | C | 1 | a0001c0001t0007g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.416+1867T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645889 | |||||||
| chr12:22646012 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416+1990G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646012 | |||||||
| chr12:22646272 | G | C | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+2250G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646272 | |||||||
| chr12:22646411 | A | G | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.416+2389A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646411 | |||||||
| chr12:22646444 | G | A | 3 | a0001c0001t0003g0025 a0001c0001t0003g0145 a0001c0001t0010g0025 |
3 | NA18967.hp1 NA18987.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.416+2422G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646444 | |||||||
| chr12:22646663 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+2641T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646663 | |||||||
| chr12:22646995 | A | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.416+2973A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646995 | |||||||
| chr12:22647068 | C | T | 1 | a0001c0003t0011g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.416+3046C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647068 | |||||||
| chr12:22647155 | A | T | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.416+3133A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647155 | |||||||
| chr12:22647216 | A | G | 1 | a0003c0006t0058g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.416+3194A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647216 | |||||||
| chr12:22647300 | A | G | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.416+3278A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647300 | |||||||
| chr12:22647418 | A | G | 9 | a0001c0002t0002g0004 a0001c0002t0002g0021 a0001c0002t0002g0112 others(6): Show |
12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.416+3396A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647418 | |||||||
| chr12:22647718 | C | T | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416+3696C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647718 | |||||||
| chr12:22647828 | G | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+3806G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647828 | |||||||
| chr12:22647874 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.416+3852G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647874 | |||||||
| chr12:22647992 | A | G | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.416+3970A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647992 | |||||||
| chr12:22648012 | A | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+3990A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648012 | |||||||
| chr12:22648131 | C | A | 1 | a0001c0001t0008g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.416+4109C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648131 | |||||||
| chr12:22648347 | A | G | 155 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(152): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.416+4325A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648347 | |||||||
| chr12:22648349 | A | G | 1 | a0001c0001t0055g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.416+4327A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648349 | |||||||
| chr12:22648567 | T | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4545T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648567 | |||||||
| chr12:22648739 | C | T | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416+4717C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648739 | |||||||
| chr12:22648818 | T | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4796T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648818 | |||||||
| chr12:22648840 | C | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4818C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648840 | |||||||
| chr12:22649565 | C | T | 3 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0014g0128 |
3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.416+5543C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649565 | |||||||
| chr12:22649664 | C | G | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.416+5642C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649664 | |||||||
| chr12:22649682 | G | C | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+5660G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649682 | |||||||
| chr12:22649721 | T | C | 2 | a0001c0001t0018g0037 a0001c0001t0018g0038 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.416+5699T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649721 | |||||||
| chr12:22649734 | T | C | 1 | a0001c0001t0010g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.416+5712T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649734 | |||||||
| chr12:22649915 | G | A | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+5893G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649915 | |||||||
| chr12:22650176 | G | A | 2 | a0001c0001t0004g0221 a0001c0001t0004g0222 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416+6154G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650176 | |||||||
| chr12:22650232 | A | G | 1 | a0001c0001t0008g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416+6210A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650232 | |||||||
| chr12:22650353 | T | A | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.416+6331T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650353 | |||||||
| chr12:22650493 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.416+6471C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650493 | |||||||
| chr12:22650507 | A | G | 1 | a0001c0001t0010g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.416+6485A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650507 | |||||||
| chr12:22650733 | C | G | 1 | a0001c0001t0055g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.416+6711C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650733 | |||||||
| chr12:22650795 | A | C | 1 | a0001c0001t0002g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.416+6773A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650795 | |||||||
| chr12:22651259 | G | T | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.416+7237G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651259 | |||||||
| chr12:22651335 | G | C | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.416+7313G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651335 | |||||||
| chr12:22651339 | C | T | 1 | a0001c0001t0011g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.416+7317C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651339 | |||||||
| chr12:22651371 | T | C | 1 | a0001c0001t0019g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.416+7349T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651371 | |||||||
| chr12:22651379 | T | G | 25 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(22): Show |
34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.416+7357T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651379 | |||||||
| chr12:22651590 | A | G | 252 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(249): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.417-7424A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651590 | |||||||
| chr12:22651609 | T | C | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-7405T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651609 | |||||||
| chr12:22651630 | A | C | 3 | a0003c0006t0001g0077 a0003c0006t0002g0110 a0003c0006t0058g0105 |
3 | HG00099.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.417-7384A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651630 | |||||||
| chr12:22651646 | A | AT | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-7358dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651646 | ||||||
| chr12:22651656 | T | C | 3 | a0001c0001t0005g0099 a0001c0001t0028g0044 a0001c0001t0028g0045 |
3 | HG02615.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.417-7358T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651656 | |||||||
| chr12:22651682 | C | CT | 6 | a0001c0001t0002g0034 a0001c0001t0002g0051 a0001c0001t0007g0089 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.417-7312dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | ||||||
| chr12:22651682 | CTT | C | 63 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(60): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.417-7313_417-7312d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | ||||||
| chr12:22651682 | CTTT | C | 17 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(14): Show |
22 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.417-7314_417-7312d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | ||||||
| chr12:22651684 | T | C | 1 | a0001c0001t0017g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.417-7330T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651684 | |||||||
| chr12:22651685 | T | C | 43 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(40): Show |
52 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.417-7329T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651685 | |||||||
| chr12:22651731 | C | G | 1 | a0001c0001t0014g0022 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.417-7283C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651731 | |||||||
| chr12:22651837 | C | G | 1 | a0001c0001t0003g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.417-7177C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651837 | |||||||
| chr12:22651850 | C | T | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.417-7164C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651850 | |||||||
| chr12:22651966 | G | A | 4 | a0001c0002t0001g0009 a0001c0002t0001g0018 a0001c0002t0016g0018 others(1): Show |
7 | HG02129.hp2 HG03704.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.417-7048G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651966 | |||||||
| chr12:22651970 | G | A | 82 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(79): Show |
101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.417-7044G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651970 | |||||||
| chr12:22651992 | A | G | 2 | a0001c0002t0001g0018 a0001c0002t0016g0018 |
2 | HG02129.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.417-7022A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651992 | |||||||
| chr12:22652095 | G | A | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-6919G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652095 | |||||||
| chr12:22652193 | A | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(57): Show |
74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.417-6821A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652193 | |||||||
| chr12:22652360 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-6654G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652360 | |||||||
| chr12:22652387 | A | G | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-6627A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652387 | |||||||
| chr12:22652540 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.417-6474T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652540 | |||||||
| chr12:22652622 | T | A | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.417-6392T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652622 | |||||||
| chr12:22652624 | A | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-6390A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652624 | |||||||
| chr12:22652705 | A | T | 1 | a0001c0002t0002g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.417-6309A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652705 | |||||||
| chr12:22652708 | TGTG | T | 9 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(6): Show |
11 | HG00408.hp2 HG00673.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.417-6304_417-6302d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22652708 | ||||||
| chr12:22652825 | T | C | 1 | a0001c0003t0007g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.417-6189T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652825 | |||||||
| chr12:22652843 | C | T | 1 | a0001c0002t0005g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.417-6171C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652843 | |||||||
| chr12:22652947 | A | C | 15 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(12): Show |
20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.417-6067A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652947 | |||||||
| chr12:22653047 | T | C | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.417-5967T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653047 | |||||||
| chr12:22653099 | T | C | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.417-5915T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653099 | |||||||
| chr12:22653214 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-5800G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653214 | |||||||
| chr12:22653606 | C | T | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.417-5408C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653606 | |||||||
| chr12:22653721 | T | C | 35 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(32): Show |
45 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.417-5293T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653721 | |||||||
| chr12:22653742 | A | G | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-5272A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653742 | |||||||
| chr12:22653894 | A | T | 1 | a0001c0001t0003g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.417-5120A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653894 | |||||||
| chr12:22653991 | A | T | 1 | a0001c0001t0007g0184 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.417-5023A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653991 | |||||||
| chr12:22654053 | A | G | 1 | a0001c0001t0003g0139 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.417-4961A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654053 | |||||||
| chr12:22654122 | A | G | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-4892A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654122 | |||||||
| chr12:22654141 | T | A | 16 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(13): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-4873T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654141 | |||||||
| chr12:22654326 | C | G | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-4688C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654326 | |||||||
| chr12:22654399 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.417-4615G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654399 | |||||||
| chr12:22654460 | A | C | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-4554A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654460 | |||||||
| chr12:22654556 | A | T | 16 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(13): Show |
18 | HG00544.hp1 HG00673.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.417-4458A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654556 | |||||||
| chr12:22654773 | T | TAAC | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-4238_417-4236d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22654773 | ||||||
| chr12:22654957 | A | G | 1 | a0003c0006t0002g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.417-4057A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654957 | |||||||
| chr12:22655156 | C | CG | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3854dupG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655156 | ||||||
| chr12:22655209 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3805T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655209 | |||||||
| chr12:22655212 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3802T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655212 | |||||||
| chr12:22655328 | GT | G | 14 | a0001c0001t0002g0051 a0001c0001t0007g0234 a0001c0001t0008g0052 others(11): Show |
15 | HG00673.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.417-3662delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | ||||||
| chr12:22655328 | GTT | G | 42 | a0001c0001t0002g0034 a0001c0001t0004g0101 a0001c0001t0004g0223 others(39): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.417-3663_417-3662d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | ||||||
| chr12:22655328 | GTTT | G | 189 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(186): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.417-3664_417-3662d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | ||||||
| chr12:22655332 | T | G | 1 | a0001c0001t0008g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.417-3682T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655332 | |||||||
| chr12:22655333 | T | G | 9 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(6): Show |
11 | HG00673.hp2 HG03516.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.417-3681T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655333 | |||||||
| chr12:22655334 | T | G | 23 | a0001c0001t0008g0017 a0001c0001t0008g0170 a0001c0001t0008g0171 others(20): Show |
32 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.417-3680T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655334 | |||||||
| chr12:22655337 | T | G | 1 | a0001c0002t0001g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.417-3677T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655337 | |||||||
| chr12:22655338 | T | G | 122 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(119): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.417-3676T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655338 | |||||||
| chr12:22655339 | T | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3675T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655339 | |||||||
| chr12:22655346 | T | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3668T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655346 | |||||||
| chr12:22655358 | C | T | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.417-3656C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655358 | |||||||
| chr12:22655367 | G | A | 2 | a0001c0001t0040g0047 a0001c0001t0047g0050 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.417-3647G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655367 | |||||||
| chr12:22655483 | C | T | 3 | a0001c0003t0007g0103 a0001c0003t0011g0019 a0001c0003t0011g0104 |
4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-3531C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655483 | |||||||
| chr12:22655638 | A | T | 1 | a0001c0002t0001g0075 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.417-3376A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655638 | |||||||
| chr12:22655710 | C | A | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-3304C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655710 | |||||||
| chr12:22655829 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.417-3185C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655829 | |||||||
| chr12:22655921 | G | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0109 |
2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.417-3093G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655921 | |||||||
| chr12:22656097 | G | T | 3 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 |
3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.417-2917G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656097 | |||||||
| chr12:22656209 | A | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-2805A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656209 | |||||||
| chr12:22656242 | T | C | 1 | a0001c0001t0007g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.417-2772T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656242 | |||||||
| chr12:22656440 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.417-2574A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656440 | |||||||
| chr12:22656603 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.417-2411C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656603 | |||||||
| chr12:22656639 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-2375C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656639 | |||||||
| chr12:22656784 | A | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-2230A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656784 | |||||||
| chr12:22657062 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.417-1952T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657062 | |||||||
| chr12:22657088 | G | T | 3 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 |
3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.417-1926G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657088 | |||||||
| chr12:22657135 | C | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-1879C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657135 | |||||||
| chr12:22657145 | A | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-1869A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657145 | |||||||
| chr12:22657445 | G | C | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-1569G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657445 | |||||||
| chr12:22657539 | A | G | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.417-1475A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657539 | |||||||
| chr12:22657607 | A | AT | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.417-1403dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22657607 | ||||||
| chr12:22657739 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-1275C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657739 | |||||||
| chr12:22657895 | C | T | 1 | a0001c0001t0013g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.417-1119C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657895 | |||||||
| chr12:22657949 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.417-1065C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657949 | |||||||
| chr12:22658126 | A | G | 1 | a0001c0001t0003g0023 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.417-888A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658126 | |||||||
| chr12:22658128 | CAAG | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-883_417-881del others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22658128 | ||||||
| chr12:22658218 | A | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-796A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658218 | |||||||
| chr12:22658266 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.417-748C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658266 | |||||||
| chr12:22658366 | T | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-648T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658366 | |||||||
| chr12:22658439 | A | T | 1 | a0001c0001t0002g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.417-575A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658439 | |||||||
| chr12:22658512 | C | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-502C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658512 | |||||||
| chr12:22658607 | A | G | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.417-407A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658607 | |||||||
| chr12:22658685 | C | T | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-329C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658685 | |||||||
| chr12:22658833 | A | G | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.417-181A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658833 | |||||||
| chr12:22658898 | G | A | 1 | a0001c0002t0005g0078 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.417-116G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658898 | |||||||
| chr12:22658918 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-96G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658918 | |||||||
| chr12:22659316 | A | G | 1 | a0001c0002t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.557+162A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659316 | |||||||
| chr12:22659335 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.557+181C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659335 | |||||||
| chr12:22659337 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557+183C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659337 | |||||||
| chr12:22659421 | T | G | 243 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(240): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.557+267T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659421 | |||||||
| chr12:22659506 | A | C | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+352A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659506 | |||||||
| chr12:22659699 | A | C | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557+545A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659699 | |||||||
| chr12:22659832 | A | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(132): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.557+678A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659832 | |||||||
| chr12:22659984 | T | TA | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+830_557+831ins others(1): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659984 | |||||||
| chr12:22659998 | C | A | 2 | a0001c0001t0002g0084 a0001c0001t0007g0089 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.557+844C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659998 | |||||||
| chr12:22660022 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.557+868C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660022 | |||||||
| chr12:22660034 | T | TA | 6 | a0001c0001t0002g0204 a0001c0001t0028g0044 a0001c0001t0028g0045 others(3): Show |
6 | HG01257.hp2 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.557+901dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | ||||||
| chr12:22660034 | TA | T | 29 | a0001c0001t0001g0192 a0001c0001t0002g0186 a0001c0001t0002g0203 others(26): Show |
34 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.557+901delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | ||||||
| chr12:22660034 | TAA | T | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+900_557+901del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | ||||||
| chr12:22660047 | A | C | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557+893A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660047 | |||||||
| chr12:22660048 | A | C | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.557+894A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660048 | |||||||
| chr12:22660060 | G | A | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+906G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660060 | |||||||
| chr12:22660117 | G | A | 1 | a0001c0001t0004g0230 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.558-946G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660117 | |||||||
| chr12:22660309 | C | T | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-754C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660309 | |||||||
| chr12:22660354 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.558-709G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660354 | |||||||
| chr12:22660359 | A | G | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-704A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660359 | |||||||
| chr12:22660397 | T | C | 1 | a0001c0001t0056g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.558-666T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660397 | |||||||
| chr12:22660401 | G | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.558-662G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660401 | |||||||
| chr12:22660489 | C | T | 1 | a0001c0002t0001g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.558-574C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660489 | |||||||
| chr12:22660653 | T | A | 4 | a0001c0002t0005g0008 a0002c0004t0001g0008 a0002c0004t0001g0059 others(1): Show |
5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-410T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660653 | |||||||
| chr12:22660668 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.558-395G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660668 | |||||||
| chr12:22660965 | G | T | 1 | a0001c0009t0023g0140 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.558-98G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660965 | |||||||
| chr12:22661036 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.558-27A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22661036 | |||||||
| chr12:22661296 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.700+91T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661296 | |||||||
| chr12:22661392 | A | G | 1 | a0001c0001t0014g0022 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.700+187A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661392 | |||||||
| chr12:22661519 | A | G | 1 | a0001c0001t0024g0228 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.700+314A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661519 | |||||||
| chr12:22661904 | T | C | 1 | a0001c0002t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.700+699T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661904 | |||||||
| chr12:22662053 | CGCA | C | 8 | a0001c0001t0009g0005 a0001c0001t0009g0127 a0001c0001t0009g0133 others(5): Show |
12 | HG01891.hp2 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.700+849_700+851del others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662053 | |||||||
| chr12:22662056 | A | C | 1 | a0001c0001t0014g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.700+851A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662056 | |||||||
| chr12:22662056 | AC | A | 16 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(13): Show |
17 | HG00544.hp1 HG00673.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.700+862delC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662056 | ||||||
| chr12:22662056 | ACC | A | 210 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(207): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.700+861_700+862del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662056 | ||||||
| chr12:22662061 | C | G | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.700+856C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662061 | |||||||
| chr12:22662067 | C | T | 1 | a0001c0002t0016g0056 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.700+862C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662067 | |||||||
| chr12:22662077 | C | T | 74 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(71): Show |
93 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.700+872C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662077 | |||||||
| chr12:22662088 | A | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+883A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662088 | |||||||
| chr12:22662234 | A | C | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0014g0128 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1029A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662234 | |||||||
| chr12:22662242 | A | AT | 36 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(33): Show |
39 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.700+1062dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662242 | ||||||
| chr12:22662242 | AT | A | 12 | a0001c0001t0002g0034 a0001c0001t0002g0085 a0001c0001t0002g0194 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.700+1062delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662242 | ||||||
| chr12:22662276 | T | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+1071T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662276 | |||||||
| chr12:22662353 | G | A | 4 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+1148G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662353 | |||||||
| chr12:22662389 | TTCC | T | 10 | a0001c0001t0009g0005 a0001c0001t0009g0133 a0001c0001t0009g0134 others(7): Show |
15 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.700+1186_700+1188d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662389 | ||||||
| chr12:22662390 | TCC | T | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0014g0128 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1186_700+1187d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662390 | |||||||
| chr12:22662392 | C | CT | 131 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(128): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.700+1204dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662392 | ||||||
| chr12:22662394 | T | C | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0014g0128 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1189T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662394 | |||||||
| chr12:22662395 | T | C | 10 | a0001c0001t0009g0005 a0001c0001t0009g0133 a0001c0001t0009g0134 others(7): Show |
15 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.700+1190T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662395 | |||||||
| chr12:22662678 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.700+1473G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662678 | |||||||
| chr12:22662769 | A | T | 1 | a0001c0001t0014g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.700+1564A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662769 | |||||||
| chr12:22662853 | G | A | 3 | a0001c0001t0017g0217 a0001c0001t0017g0218 a0001c0001t0017g0219 |
3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.700+1648G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662853 | |||||||
| chr12:22662993 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+1788T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662993 | |||||||
| chr12:22663068 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+1863G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663068 | |||||||
| chr12:22663411 | C | T | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+2206C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663411 | |||||||
| chr12:22663470 | A | C | 3 | a0001c0001t0002g0197 a0001c0001t0043g0211 a0001c0001t0050g0196 |
3 | HG00741.hp1 HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.700+2265A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663470 | |||||||
| chr12:22663553 | G | GT | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+2349dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22663553 | ||||||
| chr12:22663769 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+2564T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663769 | |||||||
| chr12:22663860 | T | C | 7 | a0001c0002t0002g0004 a0001c0002t0002g0021 a0001c0002t0012g0004 others(4): Show |
10 | HG01243.hp2 HG02258.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.700+2655T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663860 | |||||||
| chr12:22663922 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.700+2717C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663922 | |||||||
| chr12:22663943 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+2738T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663943 | |||||||
| chr12:22664037 | G | A | 1 | a0001c0001t0004g0223 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.700+2832G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664037 | |||||||
| chr12:22664169 | T | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+2964T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664169 | |||||||
| chr12:22664330 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.700+3125A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664330 | |||||||
| chr12:22664345 | A | G | 1 | a0001c0001t0007g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.700+3140A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664345 | |||||||
| chr12:22664604 | T | A | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.700+3399T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664604 | |||||||
| chr12:22664691 | T | C | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.700+3486T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664691 | |||||||
| chr12:22664925 | A | T | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.700+3720A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664925 | |||||||
| chr12:22665130 | C | T | 1 | a0001c0001t0005g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.700+3925C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665130 | |||||||
| chr12:22665174 | T | C | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.700+3969T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665174 | |||||||
| chr12:22665280 | G | A | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.700+4075G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665280 | |||||||
| chr12:22665322 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700+4117C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665322 | |||||||
| chr12:22665396 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.700+4191A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665396 | |||||||
| chr12:22666033 | T | C | 1 | a0001c0001t0007g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700+4828T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666033 | |||||||
| chr12:22666079 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+4874C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666079 | |||||||
| chr12:22666097 | C | G | 3 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0175 |
3 | NA18998.hp2 NA19057.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.700+4892C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666097 | |||||||
| chr12:22666169 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.700+4964A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666169 | |||||||
| chr12:22666301 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.701-4971G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666301 | |||||||
| chr12:22666416 | TA | T | 8 | a0001c0002t0002g0004 a0001c0002t0002g0021 a0001c0002t0002g0112 others(5): Show |
11 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-4853delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22666416 | ||||||
| chr12:22666432 | C | T | 151 | a0001c0001t0001g0074 a0001c0001t0001g0192 a0001c0001t0002g0001 others(148): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.701-4840C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666432 | |||||||
| chr12:22666520 | A | G | 25 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(22): Show |
34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-4752A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666520 | |||||||
| chr12:22666589 | G | C | 66 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(63): Show |
80 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.701-4683G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666589 | |||||||
| chr12:22666860 | T | C | 1 | a0003c0006t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.701-4412T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666860 | |||||||
| chr12:22666959 | A | T | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.701-4313A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666959 | |||||||
| chr12:22667172 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701-4100G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667172 | |||||||
| chr12:22667250 | A | G | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.701-4022A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667250 | |||||||
| chr12:22667310 | C | T | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.701-3962C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667310 | |||||||
| chr12:22667416 | G | A | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-3856G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667416 | |||||||
| chr12:22667463 | G | A | 1 | a0003c0006t0058g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.701-3809G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667463 | |||||||
| chr12:22668116 | C | T | 1 | a0001c0002t0021g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.701-3156C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22668116 | |||||||
| chr12:22668150 | T | A | 2 | a0001c0001t0002g0084 a0001c0001t0007g0089 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.701-3122T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22668150 | |||||||
| chr12:22668492 | GT | G | 3 | a0001c0001t0002g0027 a0001c0001t0002g0204 a0001c0001t0044g0027 |
3 | HG00639.hp1 HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.701-2777delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22668492 | ||||||
| chr12:22669053 | T | C | 3 | a0001c0001t0003g0147 a0001c0001t0003g0148 a0001c0001t0003g0156 |
3 | NA18945.hp2 NA18954.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.701-2219T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669053 | |||||||
| chr12:22669201 | ATC | A | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-2067_701-2066d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669201 | ||||||
| chr12:22669339 | G | GA | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.701-1927dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669339 | ||||||
| chr12:22669436 | T | TC | 5 | a0001c0001t0013g0178 a0001c0001t0013g0179 a0001c0001t0013g0181 others(2): Show |
5 | HG02922.hp1 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-1835dupC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669436 | ||||||
| chr12:22669472 | C | G | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-1800C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669472 | |||||||
| chr12:22669686 | T | C | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-1586T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669686 | |||||||
| chr12:22669821 | GA | G | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.701-1443delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669821 | ||||||
| chr12:22670147 | T | C | 1 | a0001c0002t0026g0187 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.701-1125T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670147 | |||||||
| chr12:22670369 | A | AT | 16 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(13): Show |
25 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.701-889dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | ||||||
| chr12:22670369 | AT | A | 22 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(19): Show |
27 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.701-889delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | ||||||
| chr12:22670369 | ATT | A | 45 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(42): Show |
54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.701-890_701-889del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | ||||||
| chr12:22670417 | C | T | 1 | a0001c0002t0002g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701-855C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670417 | |||||||
| chr12:22670508 | C | T | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-764C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670508 | |||||||
| chr12:22670519 | T | C | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.701-753T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670519 | |||||||
| chr12:22670530 | T | C | 25 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(22): Show |
34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-742T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670530 | |||||||
| chr12:22670733 | G | A | 66 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(63): Show |
80 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.701-539G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670733 | |||||||
| chr12:22671074 | C | A | 1 | a0001c0005t0052g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.701-198C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22671074 | |||||||
| chr12:22671444 | G | C | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.784+89G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671444 | |||||||
| chr12:22671568 | G | A | 4 | a0001c0002t0005g0008 a0002c0004t0001g0008 a0002c0004t0001g0059 others(1): Show |
5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+213G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671568 | |||||||
| chr12:22671620 | C | T | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.784+265C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671620 | |||||||
| chr12:22671680 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.784+325T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671680 | |||||||
| chr12:22671705 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784+350G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671705 | |||||||
| chr12:22671815 | G | A | 46 | a0001c0001t0001g0192 a0001c0001t0002g0001 a0001c0001t0002g0007 others(43): Show |
57 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.784+460G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671815 | |||||||
| chr12:22671817 | C | T | 15 | a0001c0001t0004g0225 a0001c0001t0009g0005 a0001c0001t0009g0126 others(12): Show |
20 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+462C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671817 | |||||||
| chr12:22671820 | T | C | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+465T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671820 | |||||||
| chr12:22671841 | T | TA | 10 | a0001c0001t0002g0202 a0001c0001t0007g0086 a0001c0001t0007g0184 others(7): Show |
10 | HG01433.hp1 HG02027.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+508dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | ||||||
| chr12:22671841 | T | TAAAAA | 11 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(8): Show |
16 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.784+504_784+508dup others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | ||||||
| chr12:22671841 | TA | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0192 a0001c0001t0002g0193 others(9): Show |
12 | HG00323.hp2 HG03491.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+508delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | ||||||
| chr12:22671866 | A | C | 1 | a0001c0001t0009g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+511A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671866 | |||||||
| chr12:22671968 | C | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+613C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671968 | |||||||
| chr12:22671977 | A | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+622A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671977 | |||||||
| chr12:22672288 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784+933C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672288 | |||||||
| chr12:22672575 | C | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.785-925C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672575 | |||||||
| chr12:22672703 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.785-797G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672703 | |||||||
| chr12:22672760 | C | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.785-740C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672760 | |||||||
| chr12:22673001 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.785-499T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22673001 | |||||||
| chr12:22673345 | T | C | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.785-155T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22673345 | |||||||
| chr12:22673797 | T | A | 1 | a0001c0001t0011g0094 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.945+137T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673797 | |||||||
| chr12:22673817 | T | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(37): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.945+157T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673817 | |||||||
| chr12:22673839 | A | C | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+179A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673839 | |||||||
| chr12:22674408 | G | A | 2 | a0001c0002t0001g0064 a0001c0002t0016g0046 |
2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.945+748G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674408 | |||||||
| chr12:22674561 | A | C | 2 | a0001c0001t0002g0197 a0001c0001t0043g0211 |
2 | HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.945+901A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674561 | |||||||
| chr12:22674678 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.945+1018A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674678 | |||||||
| chr12:22674959 | C | T | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.945+1299C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674959 | |||||||
| chr12:22675002 | C | T | 1 | a0001c0001t0008g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.945+1342C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675002 | |||||||
| chr12:22675221 | A | G | 6 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+1561A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675221 | |||||||
| chr12:22675222 | AT | A | 66 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(63): Show |
80 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.945+1569delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22675222 | ||||||
| chr12:22675377 | A | T | 1 | a0001c0001t0002g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.945+1717A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675377 | |||||||
| chr12:22675418 | C | T | 1 | a0001c0001t0007g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.945+1758C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675418 | |||||||
| chr12:22675620 | G | A | 1 | a0001c0002t0005g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.945+1960G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675620 | |||||||
| chr12:22675758 | A | G | 3 | a0001c0001t0018g0037 a0001c0001t0018g0038 a0001c0001t0018g0041 |
3 | HG01168.hp1 HG01169.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.945+2098A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675758 | |||||||
| chr12:22675875 | T | C | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+2215T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675875 | |||||||
| chr12:22676051 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+2391G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676051 | |||||||
| chr12:22676094 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.945+2434T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676094 | |||||||
| chr12:22676404 | A | G | 2 | a0001c0001t0025g0031 a0001c0001t0025g0032 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.945+2744A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676404 | |||||||
| chr12:22676471 | G | A | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+2811G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676471 | |||||||
| chr12:22676725 | T | C | 1 | a0001c0001t0032g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+3065T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676725 | |||||||
| chr12:22676856 | GT | G | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.945+3206delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22676856 | ||||||
| chr12:22676856 | GTT | G | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.945+3205_945+3206d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22676856 | ||||||
| chr12:22677066 | A | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0145 a0001c0001t0010g0025 others(1): Show |
4 | NA18965.hp2 NA18967.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+3406A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677066 | |||||||
| chr12:22677091 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.945+3431G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677091 | |||||||
| chr12:22677574 | G | A | 3 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0152 |
3 | HG01257.hp1 HG01258.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.945+3914G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677574 | |||||||
| chr12:22677764 | C | T | 38 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(35): Show |
47 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.945+4104C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677764 | |||||||
| chr12:22677828 | G | A | 66 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(63): Show |
80 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.945+4168G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677828 | |||||||
| chr12:22677964 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.945+4304C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677964 | |||||||
| chr12:22678251 | C | T | 124 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(121): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.945+4591C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678251 | |||||||
| chr12:22678356 | A | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+4696A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678356 | |||||||
| chr12:22678425 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.945+4765A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678425 | |||||||
| chr12:22678529 | G | A | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.945+4869G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678529 | |||||||
| chr12:22678617 | A | G | 2 | a0001c0001t0003g0143 a0001c0001t0003g0152 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.945+4957A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678617 | |||||||
| chr12:22678781 | A | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(11): Show |
19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.945+5121A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678781 | |||||||
| chr12:22678858 | G | T | 1 | a0001c0002t0039g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.945+5198G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678858 | |||||||
| chr12:22678925 | A | G | 1 | a0001c0001t0035g0229 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.945+5265A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678925 | |||||||
| chr12:22679301 | T | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-5182T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679301 | |||||||
| chr12:22679320 | G | T | 1 | a0001c0001t0003g0159 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.946-5163G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679320 | |||||||
| chr12:22679444 | C | CT | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-5039_946-5038i others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679444 | |||||||
| chr12:22679616 | G | T | 1 | a0001c0001t0018g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.946-4867G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679616 | |||||||
| chr12:22679627 | G | T | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-4856G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679627 | |||||||
| chr12:22679670 | C | T | 1 | a0001c0001t0014g0022 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.946-4813C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679670 | |||||||
| chr12:22679701 | TG | T | 12 | a0001c0001t0009g0005 a0001c0001t0009g0127 a0001c0001t0009g0133 others(9): Show |
17 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.946-4781delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679701 | |||||||
| chr12:22679702 | G | GT | 21 | a0001c0001t0001g0166 a0001c0001t0002g0001 a0001c0001t0002g0083 others(18): Show |
24 | HG00673.hp2 HG01169.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.946-4765dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | ||||||
| chr12:22679702 | G | T | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-4781G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679702 | |||||||
| chr12:22679702 | GT | G | 23 | a0001c0001t0003g0026 a0001c0001t0003g0139 a0001c0001t0004g0011 others(20): Show |
29 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-4765delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | ||||||
| chr12:22679702 | GTT | G | 42 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(39): Show |
50 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.946-4766_946-4765d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | ||||||
| chr12:22679733 | C | T | 1 | a0001c0001t0014g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.946-4750C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679733 | |||||||
| chr12:22679739 | C | T | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-4744C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679739 | |||||||
| chr12:22679884 | G | T | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-4599G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679884 | |||||||
| chr12:22679953 | G | A | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-4530G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679953 | |||||||
| chr12:22680012 | AATAC | A | 80 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(77): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.946-4464_946-4461d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680012 | ||||||
| chr12:22680120 | G | A | 1 | a0001c0002t0005g0069 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.946-4363G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680120 | |||||||
| chr12:22680202 | G | A | 1 | a0001c0001t0055g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.946-4281G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680202 | |||||||
| chr12:22680291 | T | G | 4 | a0001c0002t0005g0008 a0002c0004t0001g0008 a0002c0004t0001g0059 others(1): Show |
5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-4192T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680291 | |||||||
| chr12:22680430 | C | G | 17 | a0001c0001t0008g0017 a0001c0001t0008g0052 a0001c0001t0008g0170 others(14): Show |
19 | HG00544.hp1 HG00673.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.946-4053C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680430 | |||||||
| chr12:22680473 | C | G | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-4010C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680473 | |||||||
| chr12:22680584 | T | C | 1 | a0001c0001t0011g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.946-3899T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680584 | |||||||
| chr12:22680595 | A | T | 1 | a0001c0001t0020g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.946-3888A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680595 | |||||||
| chr12:22680723 | T | C | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-3760T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680723 | |||||||
| chr12:22680754 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.946-3729C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680754 | |||||||
| chr12:22680889 | TTC | T | 9 | a0001c0001t0004g0096 a0001c0001t0004g0101 a0001c0001t0004g0102 others(6): Show |
10 | HG00558.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.946-3593_946-3592d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680889 | |||||||
| chr12:22680889 | TTCC | T | 11 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0216 others(8): Show |
15 | HG00323.hp1 HG00423.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.946-3593_946-3591d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680889 | |||||||
| chr12:22680890 | T | TC | 63 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0002g0001 others(60): Show |
67 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.946-3588dupC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680890 | ||||||
| chr12:22680890 | T | TCC | 15 | a0001c0001t0001g0168 a0001c0001t0002g0206 a0001c0001t0007g0190 others(12): Show |
15 | HG00408.hp1 HG00621.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.946-3589_946-3588d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680890 | ||||||
| chr12:22680893 | CCCG | C | 26 | a0001c0001t0003g0012 a0001c0001t0003g0138 a0001c0001t0003g0147 others(23): Show |
34 | HG00733.hp2 HG01175.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.946-3587_946-3585d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680893 | ||||||
| chr12:22680894 | CCG | C | 19 | a0001c0001t0002g0083 a0001c0001t0003g0006 a0001c0001t0003g0023 others(16): Show |
22 | HG01074.hp2 HG01081.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.946-3587_946-3586d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680894 | ||||||
| chr12:22680895 | C | A | 1 | a0001c0001t0007g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.946-3588C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680895 | |||||||
| chr12:22680895 | CG | C | 31 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0166 others(28): Show |
35 | HG00741.hp2 HG01081.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.946-3587delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680895 | |||||||
| chr12:22680896 | G | C | 180 | a0001c0001t0001g0074 a0001c0001t0001g0165 a0001c0001t0001g0167 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.946-3587G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680896 | |||||||
| chr12:22680896 | G | T | 3 | a0001c0003t0007g0103 a0001c0003t0011g0019 a0001c0003t0011g0104 |
4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-3587G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680896 | |||||||
| chr12:22680897 | C | A | 1 | a0001c0001t0019g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946-3586C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680897 | |||||||
| chr12:22680900 | C | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-3583C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680900 | |||||||
| chr12:22680905 | T | C | 46 | a0001c0001t0002g0034 a0001c0001t0003g0006 a0001c0001t0003g0012 others(43): Show |
55 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.946-3578T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680905 | |||||||
| chr12:22681205 | TG | T | 44 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(41): Show |
53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-3276delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22681205 | ||||||
| chr12:22681472 | G | A | 1 | a0001c0001t0014g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.946-3011G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22681472 | |||||||
| chr12:22681843 | T | C | 2 | a0001c0001t0028g0044 a0001c0001t0028g0045 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.946-2640T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22681843 | |||||||
| chr12:22682145 | C | A | 1 | a0001c0002t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.946-2338C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22682145 | |||||||
| chr12:22682399 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.946-2084T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22682399 | |||||||
| chr12:22682730 | CCTTGA | C | 18 | a0001c0001t0001g0192 a0001c0002t0001g0014 a0001c0002t0001g0057 others(15): Show |
19 | HG00408.hp1 HG00639.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.946-1749_946-1745d others(7): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22682730 | ||||||
| chr12:22683118 | G | T | 67 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(64): Show |
81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.946-1365G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683118 | |||||||
| chr12:22683553 | C | G | 15 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(12): Show |
20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-930C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683553 | |||||||
| chr12:22683845 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.946-638G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683845 | |||||||
| chr12:22683965 | A | G | 41 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0023 others(38): Show |
50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.946-518A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683965 | |||||||
| chr12:22684007 | G | A | 160 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0163 others(157): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.946-476G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684007 | |||||||
| chr12:22684027 | A | G | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-456A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684027 | |||||||
| chr12:22684166 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.946-317T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684166 | |||||||
| chr12:22684219 | A | G | 4 | a0001c0002t0001g0015 a0001c0002t0001g0072 a0001c0002t0001g0080 others(1): Show |
6 | HG00558.hp1 HG02132.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.946-264A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684219 | |||||||
| chr12:22684308 | G | A | 1 | a0001c0001t0034g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-175G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684308 | |||||||
| chr12:22684323 | C | T | 13 | a0001c0001t0009g0005 a0001c0001t0009g0126 a0001c0001t0009g0127 others(10): Show |
18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-160C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684323 | |||||||
| chr12:22684327 | CG | C | 3 | a0001c0001t0003g0147 a0001c0001t0003g0148 a0001c0001t0003g0156 |
3 | NA18945.hp2 NA18954.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.946-155delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684327 | |||||||
| chr12:22684348 | A | G | 21 | a0001c0001t0004g0011 a0001c0001t0004g0030 a0001c0001t0004g0096 others(18): Show |
26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-135A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684348 | |||||||
| chr12:22684388 | A | G | 1 | a0001c0001t0014g0022 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.946-95A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684388 | |||||||
| chr12:22684475 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.946-8C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684475 | |||||||
| chr12:22684583 | C | T | 1 | a0001c0001t0020g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1019+27C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684583 | |||||||
| chr12:22684718 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1019+162G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684718 | |||||||
| chr12:22684791 | G | A | 2 | a0001c0001t0029g0177 a0001c0001t0029g0180 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1020-91G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684791 |